Irish Child Health Database - Peer Reviewed Papers
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- A case of ADHD and a major Y chromosome abnormality
- A case of coarctation in a right aortic arch with an aneurysmal right subclavian artery and aberrant left brachiocephalic artery
- A case of disseminated miliary tuberculosis in a five-year-old child
- A case of pneumomediastinum in paediatric ARDS: to oscillate or not?
- A confused child. Diagnosis: urinary tract infection, dilated urinary system and associated hyperammonaemic encephalopathy
- A frightening complication of general anaesthesia for paediatric dental extractions
- A long-term follow up of spontaneously healed root fractures later subjected to orthodontic forces - two case reports
- A new technique for treatment of a non-union of a lateral humeral condyle
- A novel constellation of cardiac findings for Kabuki syndrome: hypoplastic left heart syndrome and partial anomalous pulmonary venous drainage
- A novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation, and features of VATER association
- A recurrent splice-site mutation in the human hairless gene underlies congenital atrichia in Irish families
- A seasonal sign: angel-shaped phalango-epiphyseal dysplasia
- A steroid cell tumor outside the ovary is a rare cause of virilization
- Abdominal pain in a 9-year-old: omental torsion masquerading as appendicitis
- Achieving optimal diabetic control in adolescence: the continuing enigma
- Acute lymphoblastic leukemia: A diagnosis easily missed [1]
- Agenesis of the corpus callosum with interhemispheric cyst, hepatic haemangioma and trisomy 21
- Airway evaluation on placental support
- Airway management in a baby with femoral hypoplasia-unusual facies syndrome
- Ameloblastic fibroma of the anterior maxilla presenting as a complication of tooth eruption: a case report
- Amitriptyline poisoning in a 2-year old
- An atypical case suggesting the possibility of overlap between Malpuech and Juberg-Hayward syndromes
- An Irish three-generation family of Cornelia de Lange syndrome displaying autosomal dominant inheritance
- An unusual case of anaemia and dyspnoea
- An unusual cause of respiratory symptoms in a toddler
- An unusual orthopaedic presentation of acute lymphoblastic leukemia
- Anesthesia for sickle cell disease and congenital myopathy in combination
- Aneursymal bone cyst of the proximal phalanx of the thumb in a child
- Anorexia nervosa or otherwise? The usefulness of adult diagnostic systems in child and adolescent eating disorders
- Antenatal diagnosis of deletion chromosome 11(q23-qter) (Jacobsen syndrome)
- Anterior mitral leaflet reconstruction with pericardium in a 1.9 kg infant with endocarditis
- Antley-Bixler syndrome with radioulnar synostosis
- Article 18 of the Adoption (Northern Ireland) Order 1987: the appointment of expert witnesses; and the Children Order Advisory Committee Best Practice Guidance
- Article 53(3) of the Children (NI) Order 1995 and Rules 4.19 and 4.24 of the Family Proceedings Rules (NI) 1996: the need for an expert witness
- Article 9 of the Adoption (Northern Ireland) Order 1987 and the Adoption of Children from Overseas Regulations (Northern Ireland) 2002: the right of an applicant to adopt a non-resident child from a non-Convention country
- Articles 9 and 18 of the Adoption Order (Northern Ireland) Order 1987: importance of placing siblings together; weight to be attached to child's wish not to be adopted; views of older siblings regarding adoption of family member; and the relative
- Aspiration of an avulsed primary incisor: a case report
- Asplenia in ATR-X syndrome: a second report
- Assessment of the influence of background noise on escape-maintained problem behavior and pain behavior in a child with Williams syndrome
- Asymptomatic ascariasis infection in a child
- Atrioventricular block after transcatheter closure of perimembranous ventricular septal defects
- Atypical Mycobacterial infections in children: the case for early diagnosis
- Autoamputation of a congenital oropharyngeal hairy polyp
- Autoimmune progesterone dermatitis in a parturient for emergency caesarean section
- Autosomal dominant early childhood seizures associated with chondrocalcinosis and a mutation in the ANKH Gene
- Avascular necrosis of the talus after a minimally displaced neck of talus fracture in a 6 year old child
- Barriers to inclusion: A case study of a pupil with severe learning difficulties in Ireland
- Bilateral microtia with severe cardiac defect: a new syndrome, or a severe manifestation of the oculoauriculovertebral spectrum?
- Bilateral optic disk swelling in the 4q34 deletion syndrome
- Bilateral serous retinal detachments following diode laser treatment for retinopathy of prematurity
- Bilateral subdural collections--an unusual feature of possible Kawasaki disease
- Bilateral wrist dislocation in trisomy 21: a case report
- Bone marrow transplantation corrects osteopetrosis in the carbonic anhydrase II deficiency syndrome
- Botulinum toxin for treatment of glandular hypersecretory disorders
- Broad thumbs and halluces with deafness: a patient with Keipert syndrome
- Bronchoscopically administered recombinant human DNase for lobar atelectasis in cystic fibrosis
- Calcified occlusion of the right coronary artery in Kawasaki disease: evidence of myocardial ischaemia using cardiac technetium-99m-tetrofosmin perfusion single-photon emission computed tomography
- Calcinosis associated with dermatomyositis
- Can classic metaphyseal lesions follow uncomplicated caesarean section?
- Carbonic anhydrase II deficiency: a rare autosomal recessive disorder of osteopetrosis, renal tubular acidosis, and cerebral calcification
- Cardiac diverticulum with pericardial effusion: report of two new cases treated by in-utero pericardiocentesis and a review of the literature
- Case of Sjogren reticular dystrophy
- Case report: an unusal cause of stridor in a post-liver transplant 6-year old
- Cellist's finger dermatitis
- Central hypoventilation syndrome after Haemophilus influenzae type b meningitis and herpes infection
- Cerebral palsy and juvenile-onset bipolar disorder. A preliminary report
- Characterization of optical coherence topography findings in Kenny-Caffey syndrome
- Cherubism and its charlatans
- Child seduction and self-representation on the Internet
- Children's experience and adjustment to political conflict in Northern Ireland
- Choanal atresia - a recurrent feature of foetal carbimazole syndrome
- Chondro-osseous respiratory epithelial adenomatoid hamartoma of the nasal cavity: a case report
- Choroid plexus adenoma: case report and review of the literature
- Cleft palate and congenital synechiae syndrome: a case report
- Clinical and molecular findings in IPEX syndrome
- Complete vascular ring detected by barium esophagography
- Complex branchial fistula: a variant arch anomaly
- Complications in paediatric airway management
- Congenital cardiac disease as a core feature of cranio-osteoarthropathy
- Congenital depression of the neonatal skull: a self limiting condition
- Congenital erosive and vesicular dermatosis
- Congenital insensitivity to pain--review and report of a case with dental implications
- Congenital methaemoglobinaemia Type I in a Turkish infant due to a novel mutation, Pro144Ser, in NADH-cytochrome b5 reductase
- Congenital ptosis with esotropia in brothers
- Congenital subglotic haemingiomas
- Cryptogenic, multifocal, ulcerous, and stenosing enteritis as a manifestation of enterocolic venopathy
- Deafness associated with bilateral facial diplegia, ptosis and hypermobile joints--A new autosomal recessive condition?
- Delayed union and non-union of the ulna following intramedullary nailing in children
- Delaying preterm delivery at the threshold of viability
- Developing fluency and endurance in a child diagnosed with attention deficit hyperactivity disorder
- Diencephalic cachexia of infancy: Russell's syndrome
- Double vagina with sex reversal, congenital diaphragmatic hernia, pulmonary and cardiac malformations--another case of Meacham syndrome
- Duplication of the optic disc: true or pseudo? A coloboma or not a coloboma?
- Early continuous video-EEG in acute near-total intrauterine asphyxia
- Early onset of Friedreich's ataxia in a compound heterozygote
- Early restenosis following biodegradable stent implantation in an aortopulmonary collateral of a patient with pulmonary atresia and hypoplastic pulmonary arteries
- Elbow dislocation with ipsilateral open radial and ulnar diaphyseal fractures--a rare combination
- Emergency department ultrasound (EDU): clinical adjunct or plaything?
- Erythema induratum of Bazin and episcleritis in a 6 year old girl
- Establishment of functional B cell memory against parvovirus B19 capsid proteins may be associated with resolution of persistent infection
- Evaluation of video feedback and self-management to decrease schoolyard aggression and increase pro-social behaviour in two students with behavioural disorders
- Ex utero intrapartum treatment (EXIT) procedure and simultaneous excision of oral teratoma
- External inflammatory and replacement resorption of luxated, and avulsed replanted permanent incisors: a review and case presentation
- Extracutaneous Sweet syndrome involving the gastrointestinal tract in a patient with Fanconi anemia
- Extraventricular choroid plexus papilloma in a neonate
- Failure of cutting balloon angioplasty to prevent restenosis in childhood pulmonary venous stenosis
- False positive Kleihauer tests and unnecessary administration of anti-D immunoglobulin
- Familial childhood onset neuropathy and cirrhosis with the 4977bp mitochondrial DNA deletion
- Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene
- Familial membranoproliferative glomerulonephritis type III
- Familial Prader-Willi syndrome: case report and a literature review
- Fatal presentation of ornithine transcarbamylase deficiency in a 62-year-old man and family studies
- Female monozygotic twins with selective mutism--a case report
- Fetal hydrops due to supraventricular tachycardia - Successful outcome in a difficult case
- Fetal meconium peritonitis: the "vanishing hydrocele" sign
- Foam eater
- Focal upper limb neuropathy in a child
- Follow up of patients with ocular scarring secondary to LOC syndrome treated by amniotic membrane transplantation
- Freeman-Sheldon syndrome: a case report
- Further case of microdeletion of 8q24 with phenotype overlapping Langer-Giedion without TRPS1 deletion
- Gastric lymphoid hyperplasia: radiological evidence of childhood Helicobacter pylori infection
- Gastric stromal tumors in children
- General paediatric surgery in Ireland: a crisis in evolution
- Genetic abnormalities in a pre and post-chemotherapy hepatoblastoma
- Genitopatellar syndrome: a recognizable phenotype
- Gianotti-crosti syndrome following meningococcal septicaemia
- Giant inflammatory polyposis coli as a manifestation of Crohn's disease in patients with coexistent cystic fibrosis
- Giant left atrial appendage with a common ventricular-appendicular wall and an abnormal course of the circumflex coronary artery in an asymptomatic 18-month-old girl
- Haemangioma presenting as perianal ulcer in neonates
- Hair-thread tourniquet syndrome in an infant with bony erosion: a case report, literature review, and meta-analysis
- Hangman's fracture caused by suspected child abuse. A case report
- Hashimoto's thyroiditis--a rare but treatable cause of encephalopathy in children
- Hereditary cerebral cavernous angiomas: Presentation as idiopathic familial epilepsy
- High prevalence of Cohen syndrome among Irish travellers
- Histopathology of the teeth in segmental odontomaxillary dysplasia: new findings
- Hypoglycemia due to adrenal suppression secondary to high-dose nebulized corticosteroid
- Hypopituitarism following cerebral oedema with diabetic ketoacidosis
- Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b(5) reductase: an aid to determine recessive congenital methemoglobinemia status in an infant
- Impaired IgG responses in a child with homozygous C2 deficiency and recurrent pneumococcal septicaemia
- Implications for anaesthesia in a patient established on clozapine treatment
- Imported malaria to Northern Ireland: improving surveillance for better intervention
- Impossible laryngeal intubation in an infant with Fraser syndrome
- Incidental detection of parvovirus myocarditis at time of resection of discrete subaortic stenosis
- Incidental finding of endocarditis in a preterm neonate
- Inequalities in health: evaluation and effectiveness in practice... four research case studies
- Infantile pyoderma gangrenosum
- Inherited myoclonus-dystonia and epilepsy: further evidence of an association?
- Interferon-gamma receptor deficiency mimicking Langerhans' cell histiocytosis
- Intracervical application of synthetic hydrogel sealant for preterm prelabor rupture of membranes: a case report
- Intractable pulmonary aspiration in children: which operation?
- Intussusception associated with bacterial meningitis
- Invasive rhino-maxillary mucormycosis diagnosed before HSCT
- Is a once daily dose of gentamicin safe and effective in the treatment of uti in infants and children?
- Isolated bilateral orbital neurofibromatosis in a twelve-year-old
- Isoparaffin poisoning in an 18 month old girl
- Job syndrome masquerading as non-accidental injury
- Kallmann syndrome presenting as congenital ptosis in brothers
- Kartagener's syndrome in pregnancy
- Knobloch syndrome: novel intra-oral findings
- Langerhans' cell histiocytosis of the clivus: case report and literature review
- Late-onset central hypoventilation syndrome: a family genetic study
- Latex allergy: two educational cases
- Laurence Stephen Lowry and Asperger's syndrome
- Left atrial appendage mimicking an intra-cardiac vegetation in preterm neonates
- Legal notes: Northern Ireland
- Lightening can Strike Twice: The Case for the Management and Control of Violent Offenders against Children in Northern Ireland
- Locality Matters: Ethnic Segregation and Community Conflict the Experience of Protestant Girls in Belfast
- Long chain fatty acid oxidation defects in children: importance of detection and treatment options
- Long-term support with milrinone prior to cardiac transplantation in a neonate with left ventricular noncompaction cardiomyopathy
- Low-grade fibromyxoid sarcoma: yet another malignancy associated with Kabuki syndrome
- Malignant transformation of a lipomyelocele into a rhabdomyosarcoma?
- Malpuech syndrome: facial features in the absence of clefting
- Management of a large bronchial haemangioma in an infant
- Management of an unerupted canine associated with a central giant cell granuloma
- Maternal brain death, pregnancy and the foetus: the medico-legal implications for Ireland
- Maturity Onset Diabetes in the Young (MODY) type 3 [1]
- Megaprepuce associated with vesicoureteric reflux
- Microgastria-limb reduction anomaly with total amelia
- Miliary neonatal hemangiomatosis with fulminant heart failure and cardiac septal hypertrophy in two infants
- Misidentification of a genomovar of Burkholderia cepacia by recA restriction fragment length polymorphism
- Moebius sequence and hypogonadotrophic hypogonadism
- Multifocal infantile myofibromatosis and generalized fibromuscular dysplasia in a child: evidence for a common pathologic process?
- Multifocal Langerhans' cell histiocytosis: a case report
- Multiple airway abnormalities in a patient with Rothmund-Thomson syndrome
- Multiple vertebral collapse as a presentation of childhood acute lymphoblastic leukaemia
- Murder, mercury, mental illness: infanticide in nineteenth-century Ireland
- Nasal chondromesynchymal hamartoma presenting in an adolescent
- Neonatal abstinence syndrome due to prolonged administration of fentanyl in pregnancy
- Neonatal alloimmune thrombocytopenia due to HPA-3a antibodies: a case report
- Neonatal diagnostic difficulty in hereditary spherocytosis [2]
- Neonatal respiratory distress secondary to bilateral intranasal dacryocystocoeles
- Neonatal seizures and limb malformations associated with liver-specific complex IV respiratory chain deficiency
- Neonatal sigmoid volvulus: a complication of anal stenosis
- Nephrocalcinosis and disordered calcium metabolism in two children with SHORT syndrome
- Nodular fascitis of the maxilla in a child
- Non-invasive investigation and management of aortic saddle embolus in a 7-month-old infant
- Normal neurologic and developmental outcome after an accidental intravenous infusion of expressed breast milk in a neonate
- Northern Ireland
- Occlusion of a Sano shunt using the amplatzer duct occluder
- Occlusion of an aberrant artery to a pulmonary sequestration using a duct occluder
- Oculo-facio-cardio-dental syndrome in a mother and daughter
- Odontogenic keratocysts in a 5-year-old: initial manifestations of nevoid basal cell carcinoma syndrome
- One to make the diagnosis. A case of non tuberculous mycobacterial mastoiditis in a nine year old female
- Osteoid osteoma of the scapular neck: a case report
- Osteomyelitis of the ischiopubic synchondrosis: imaging findings
- Paediatric trauma associated with all-terrain vehicles
- PANDAS (Paediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcal Infection)
- Paroxetine induced mania in pre-adolescence
- Parry-Romberg syndrome: a report of the dental findings in a child followed up for 9 years
- Partial lipodystrophy and renal disease
- Parvovirus B19 infection associated with dilated cardiomyopathy in patients with previous anthracycline exposure
- Patent omphalomesenteric duct presenting as an umbilical discharge
- 'Peeling paint' dermatitis as a presenting sign of cystic fibrosis
- Pelvic girdle sepsis in childhood. An illustrative case of the difficulty in diagnosis
- Penetrating ocular injuries from fish-hooks
- Penile malignant peripheral nerve sheath tumour (schwannoma) in a three-year-old child without evidence of neurofibromatosis
- Perinatal hepatic infarction in twin-twin transfusion
- Peritoneography in the assessment of peritoneal cerebrospinal fluid absorption potential for distal ventriculoperitoneal shunt catheter placement: technical case report
- Pneumatosis intestinalis and portal-venous gas: an unusual presentation of acute appendicitis
- Polyuria, polydipsia, polypopsia: "Mummy I want a drink"
- Post traumatic intra-abdominal pseudo-aneurysms in children
- Presence of two Lactobacillus and Bifidobacterium probiotic strains in the neonatal ileum
- Primary desmoplastic small round cell tumor of bone: report of a case with cytogenetic confirmation
- Primary middle-ear lymphoma in a child
- Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype
- Pseudoarthrosis of the clavicle and copper beaten skull associated with chromosome 10p11.21p12.1 microdeletion
- Pseudomonas aeruginosa endophthalmitis in a preterm infant
- Psychosocial study of a surviving conjoined twin
- Pure alcohol injection of a congenital splenic cyst: a valid alternative?
- Putting Harry Potter on the Couch
- Radiological case of the month. Perforation of the inferior cava as a cause of neonatal free intra-abdominal air
- Radiological findings in cyclical administration of intravenous pamidronate in children with osteoporosis
- Rasmussen's syndrome associated with chronic brain stem encephalitis
- Recessive congenital methaemoglobinaemia: functional characterization of the novel D239G mutation in the NADH-binding lobe of cytochrome b5 reductase
- Recurrent congenital haemangiopericytoma in a child
- Recurrent postdural puncture headache
- Response covariation of escape-maintained aberrant behavior correlated with sleep deprivation
- Response to IL-1-receptor antagonist in a child with familial cold autoinflammatory syndrome
- Reversible multiorgan system involvement in a neonate with complex IV deficiency
- Rhinocerebral zygomycosis in childhood acute lymphoblastic leukaemia
- Rhombencephalosynapsis: prenatal imaging and autopsy findings
- Rights of patients: comparative perspectives from five countries
- Ruptured abdominal aortic aneurysm in a 12-month-old boy
- Second premolars: a review and case report of two impaction cases
- Section 29 of the Family Law Act 1986, Article 8 of the Children (Northern Ireland) Order 1995, Article 13 of the Hague Convention, Article 12 of the United Nations Convention on the Rights of the Child and Article 8 of the European Convention on
- Septo-optic dysplasia with digital anomalies--a recurrent pattern syndrome
- Severe osteopenia with recurrent fractures after bone marrow transplant for Wiskott-Aldrich syndrome: a case report
- Short segment posterior locking cervical plate fixation after kyphectomy for myelomeningocoele-associated kyphosis
- Short-chain acyl-CoA dehydrogenase deficiency associated with early onset severe axonal neuropathy
- Skin-coloured lumps in childhood
- Small bowel infarction secondary to volvulus during pregnancy: a case report
- Spina bifida occulta in isthmic spondylolisthesis: a surgical trap
- Staphylococcal diaphyseal subacute osteomyelitis of the ulna in a child: an unusual cause of post-traumatic forearm swelling
- Straight-chain acyl-CoA oxidase deficiency presenting with dysmorphia, neurodevelopmental autistic-type regression and a selective pattern of leukodystrophy
- Successful ex utero intrapartum treatment (EXIT) procedure for congenital high airway obstruction syndrome (CHAOS) owing to a large oropharyngeal teratoma
- Successful long-term outcome of kidney transplantation in a child with Kabuki syndrome
- Successful surgical resection of intrapericardial extralobar pulmonary sequestration with congenital pulmonary adenomatoid malformation type II
- Successful surgical treatment of Moya Moya Syndrome in a child
- Successful treatment of florid cutaneous warts with intravenous cidofovir in an 11-year-old girl
- Superior mesenteric artery syndrome (Wilkie's syndrome) complicating recovery from posterior fossa surgery in a child--a rare phenomenon
- Supralabyrinthine approach to petrosal cholesteatoma
- Surgical and radiological significance of variants of Buhler's anastomotic artery: a report of three cases
- Surgical management of giant left atrial diverticulum
- Suspected child abuse: communicating with a child and her mother
- Symptomatic anal anomalies in chromosome 22q11 deletion syndrome: a report of three patients
- Systemic absorption of lithium following ingestion of a lithium button battery
- Temporary arrest of root development in a premolar of a child with hypodontia and extensive caries
- The Adoption (Northern Ireland) Order 1987: the best interests of the child and post-adoption contact; arrangements for direct sibling contact
- The Children (Northern Ireland) Order 1995, Article 50: the best interests of the child; alleged parental culpability; medical evidence; and the rules governing publicity
- The Children (Northern Ireland) Order 1995: Article 50(2) and the importance of a care plan; welfare of child following death of sibling by NAI; carers with learning disability; risks of kinship care; role of independent consultants; social work
- The combined use of a Fogarty balloon with extraction forceps for the controlled retrieval of an endobronchial foreign body
- The dental management of five paediatric patients with a history of acute intermittent porphyria
- The Internet and offending behaviour: A case study
- The KBG syndrome, characteristic dental findings: a case report
- The management of traumatic ankylosis during orthodontics: a case report
- The novel use of small intestinal submucosal matrix for chest wall reconstruction following Ewing's tumour resection
- The panda naevus: management of synchronous upper- and lower-eyelid pigmented naevi
- The role of primary prophylactic factor replacement therapy in children with severe factor X deficiency
- The treatment of flexion contracture of the knee using the Ilizarov technique in a child with haemophilia B
- The Walker-Warburg phenotype and genotype among Irish Travellers
- Three-dimensional morphology of gut innervation in total intestinal aganglionosis using whole-mount preparation
- Tibial hemimelia of a different class
- Train of four fade in a child with stiff baby syndrome
- Transient renal failure in twins with maternal Cox-1/Cox-2 use in pregnancy
- Transpericardial extra-anatomic intrathoracic aortic bypass conduits in the management of coarctation of the aorta
- Traumatic posterior dislocation of hip in children
- Traumatic rupture of the aorta in an 11-year-old patient: surgical considerations in the technique of repair
- Treating food refusal in a child with Williams syndrome using the parent as therapist in the home setting
- Treatment of early onset bipolar disorder NOS, with low dose carbamazepine
- Triple pelvic osteotomy in Legg-Calve-Perthes disease using a single anterolateral incision
- Tuberculous osteomyelitis of the sternum in an infant: a case report and review of the literature
- Tumor Necrosis Factor Receptor-Associated Periodic Syndrome or Familial Hibernian Fever: Presentation in a Four-Day-Old Infant
- Turner's syndrome and benign intracranial hypertension with or without growth hormone treatment
- Unrehearsed circuit failure during neonatal ECMO: critical trans-heat exchanger pressure
- Upper airway obstruction in infectious mononucleosis
- Use of self-motivating and delayed feedback to increase on-task behavior in a post-institutionalized child within regular classroom settings
- Using a Time Timertrade mark to increase appropriate waiting behavior in a child with developmental disabilities
- Using the Roper-Logan-Tierney model in neonatal transport
- Vein of Galen aneurysm malformation (VGAM): Closing the management loop
- What is the best treatment for hyperkalaemia in a preterm infant?
- When is a pneumothorax not a pneumothorax?
- Working with a Child Exposed to Community and Domestic Violence in Northern Ireland: An Illustrated Case Example
Aims and Ojectives
- The article discusses a court case concerning an appeal from a British High Court decision that articles 14 and 15 of the Adoption Order 1987 did not contravene the rights of the appellants under article 8
- The article discusses a court case involving a Trust application for a care order for a child of a teenage single mother whose previous child had died in Northern Ireland
- The article discusses a court case on the right of an applicant to adopt a non-resident child for a non-Convention country pursuant to article 9 of the Adoption (Northern Ireland) Order 1987
- The article discusses the ruling of the Northern Ireland High Court of Justice in a case about an appeal against an order made by a Master of the High Court refusing leave to the father of a children
- The article focuses on an adoption case in Northern Ireland related to the Articles 9 and 18 of the Adoption Order of 1987
- The article focuses on some of the medico-legal issues that arose as a result of a situation which occurred in May 2001 in Ireland when a woman who was a British citizen and who was fourteen weeks pregnant collapsed and suffered a brain haemorrhage
- The article focuses on the ruling on the wishes of a child and legal representation concerning her decision to live in Northern Ireland
- The article presents a case concerning an application for a freeing order filed by a Health and Social Services Trust under the Adoption Order 1987 in Northern Ireland.
- The article provides information on a court case in Northern Ireland involving adoption application, parental reasonableness in withholding consent, welfare interests and the right to family life.
- These case report discuss 4 cases of rhombencephalosynapsis with correlation of prenatal and postnatal imaging and autopsy findings
- These case report discuss four cases of penetrating ocular injuries from fish-hooks
- These case report discuss two children with Nephrocalcinosis and disordered calcium metabolism and an Adult with SHORT syndrome
- These case reports discuss 2 cases of the left atrial appendage rarely mimicking a posterior mitral valve leaflet vegetation, leading to an erroneous diagnosis of infective endocarditis
- These case reports discuss 4 patients in whom megaprepuce was associated with vesicoureteric reflux
- These case reports discuss a novel G to A mutation at position 15,635 in the DIAI gene of a 4-month-old baby that results in a glycine to serine substitution at codon 75 in the cytochrome b(5) reductase protein
- These case reports discuss a novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation, and features of VATER association
- These case reports discuss a patient presenting with mental retardation and asplenia who has been shown to have a mutation at the ATR-X locus
- These case reports discuss cases of latex allergy in children
- These case reports discuss coarctation of the aorta. The second case was a fifth time reoperation in a 12-year-old girl with recurrent coarctating
- These case reports discuss delayed union and non-union of the ulna following intramedullary nailing in children
- These case reports discuss five case studies in the patient rights area from Malaysia, Ireland, South Africa, Indonesia and the United States, respectively
- These case reports discuss four cases of paediatric trauma associated with All-Terrain vehicles
- These case reports discuss four patients presenting with rare synchronous upper- and lower-eyelid naevi.
- These case reports discuss nasal chondromesynchymal hamartoma presenting in an adolescent
- These case reports discuss the case of a neonate who presented with acute liver failure and fulminant lactic acidosis with profound complex IV deficiency documented in muscle and liver biopsies andsubsequent clinical resolution by 3 months of age
- These case reports discuss the cases of 2 related Irish families with clinically severe carbonic anhydrase II deficiency syndrome deficiency in whom the gene mutation has been fully elucidated
- These case reports discuss the dental management of 5 children with a diagnosis of latent acute intermittent porphyria or a family history of same
- These case reports discuss the occurrence of giant inflammatory polyposis in 2 boys attending a tertiary care hospital, with an established diagnosis of cystic fibrosis who subsequently developed Crohn's disease
- These case reports discuss three cases of arterial anastomoses between the celiac trunk and superior mesenteric artery
- These case reports discuss three cases of subglottic haemingiomas all of which represented different clinical management strategies
- These case reports discuss three children with symptoms of polyuria, polydipsia, polypopsia
- These case reports discuss two cases of cardiac diverticulum with pericardial effusion: treated by in-utero pericardiocentesis and a review of the literature
- These case reports discuss two cases of haemangioma presenting as perianal ulcer in neonates
- These case reports discuss two cases of Kenny-Caffey syndrome with an ellipsoid macular fold orientated horizontally involving the fovea and document this unusual feature with optical coherence topography
- These case reports discuss two cases of osteomyelitis of the ischiopubic synchondrosis and describe findings on radiographs, isotope bone scan, computed tomograph and magnetic resonance imaging
- These case reports discuss two cases of selective serotonin reuptake inhibitor-induced mania
- These case reports discuss two cases of spastic diplegia of prematurity comorbid with juvenile onset bipolar disorder, which highlight some of the diagnostic difficulties in these cases
- These case reports discuss two cases of traumatic posterior dislocation of hip in children aged 3 and 14 years
- These case reports discuss two cases of upper airway obstruction in infectious mononucleosis
- These case reports discuss two children with previous anthracycline exposure for cancer who presented with acute decompensated left ventricular dysfunction due to Parvovirus B19 infection
- These case reports discuss two infants with miliary neonatal hemangiomatosis who had fulminant cardiac failure and cardiac septal hypertrophy
- These case reports discuss two unrelated patients with features of cranio-osteoarthropathy, both of whom also had a history of congenital heart disease
- These case reports two individual cases where spontaneous root fracture healing was observed and this healing was apparently not compromised by later orthodontic tooth movement
- This article describes the difficulties frequently encountered in managing glycaemic control in the transition periods from childhood through adolescence to adulthood, with a description of four cases illustrating these points
- This article discusses a court case concerning an adoption application for two children whose birth parents and siblings seek direct contact post adoption.
- This article discusses a court case which concerns an application by a Trust for an order under Article 50 of the Children (N. Ireland) Order 1995 in relation to three children after one child was admitted for intra-abdominal tumour
- This case report 2 mutations, E255- and G291D, identified in the nicotinamide adenine dinucleotide -binding lobe of cytb(5)r in previously reported patients, and detection of a further novel mutation, D239G, in this lobe in two unrelated Irish families
- This case report describes the pattern of early childhood seizures within a family with autosomal dominant chondrocalcinosis (CCAL, which causes adult-onset arthritis)
- This case report discuss giant left atrial appendage with a common ventricular-appendicular wall and an abnormal course of the circumflex coronary artery in an asymptomatic 18-month-old girl
- This case report discusses 11-year old girl presented with history of scaling on fingers
- This case report discusses a 10 year old girl with "odd shaped" skull and family history of craniosynostois
- This case report discusses a 13-year-old boy who, after exercise, had respiratory distress and left upper quadrant abdominal pain
- This case report discusses a 1-day-old baby girl with a cleft of the secondary palate and a soft tissue band connecting the upper and lower jaws and preventing mouth opening
- This case report discusses a 21-month-old asthmatic boy who had a hypoglycemic seizure during a proven acute adrenal crisis secondary to high-dose nebulized budesonide treatment.
- This case report discusses a 2-week-old female who infant presented with acute decompensated left ventricular failure
- This case report discusses a 2-year-old child presenting with Multifocal Langerhans' cell histiocytosis and review the literature concerning this rare disease
- This case report discusses a 3 year old boy with Septo-optic dysplasia and digital anomalies
- This case report discusses a 3-day-old infant with bilateral intranasal lacrimal duct cysts causing nasal obstruction and intermittent respiratory compromise
- This case report discusses a 3-year-old boy of Romanian origin with an unusual orthopaedic presentation of acute lymphoblastic leukemia
- This case report discusses a 3-year-old boy with a clinical picture of Rasmussen's encephalitis who had clinical, radiological and pathological evidence of brain stem involvement resulting in death
- This case report discusses a 3-year-old girl with severe microgastria and total amelia who has been managed conservatively with minimal surgical intervention.
- This case report discusses a 5-year-old boy with presented with an infected left-sided branchial fistula
- This case report discusses a 5-year-old girl with Langerhans' cell histiocytosis of the clivus.
- This case report discusses a 6-year-old boy who presented with tic and hemi-chorea associated with Group A beta haemolytic streptococcal infection of the throat
- This case report discusses a 7-day-old boy referred to our institution with tachypnea and cardiomegaly who was discovered to have an intrapericardial extra-lobar pulmonary sequestration containing a cystic pulmonary adenomatoid malformation type II
- This case report discusses a 7-year-old boy who avulsed and inhaled a primary maxillary incisor
- This case report discusses a 8 year old girl with cystic fibrosis presented with a pulmonary exacerbation from which Burkholderia cepacia was cultured
- This case report discusses a 8-month-old infant with macrocephaly was found to have hydrocephalus and a cystic third ventricular tumour; biopsy of the tumour showed a choroid plexus adenoma
- This case report discusses a 9-year-old girl with focal upper limb neuropathy preceding a diffuse demyelinating process by several years
- This case report discusses a boy with an oligo array-cgh characterised small microdeletion involving EXT1 alone but with some features of Langer-giedion syndrome suggesting a functional disturbance of TRPS1
- This case report discusses a carbonic anhydrase II deficiency: a rare autosomal recessive disorder of osteopetrosis, renal tubular acidosis, and cerebral calcification
- This case report discusses a case a congenital erosive and vesicular dermatosis evident only 8-year after diagnosis
- This case report discusses a case arising in an 11-year-old male patient, who presented with a 6-month history of right-sided nasal obstruction
- This case report discusses a case example to illustrate the need for robust arrangements to manage violent offenders against children in Northern Ireland
- This case report discusses a case of 4q deletion syndrome, presenting with asymptomatic bilateral disk swelling
- This case report discusses a case of 7-year-old girl presented with the non-specific findings of subtle dysmorphism, short stature and developmental delay
- This case report discusses a case of a de novo 10p11.21p12.1 microdeletion in a boy with multiple problems including a beaten copper appearance of the cranium on skull X-ray and pseudoarthrosis of the right clavicle
- This case report discusses a case of a double aortic arch in a 9-month-old girl that was diagnosed by barium esophagography
- This case report discusses a case of a five year old boy who presented with a lower motor neurone facial nerve palsy secondary to primary non-Hodgkin's lymphoma of the middle ear
- This case report discusses a case of a giant oropharyngeal teratoma diagnosed in a fetus of 19 weeks gestation
- This case report discusses a case of a large oral teratoma in a foetus diagnosed on antenatal ultrasound
- This case report discusses a case of a successful emergency caesarean section in a schizophrenic patient on clozapine treatment.
- This case report discusses a case of a twin pregnancy which was complicated by a twin-twin transfusion in which the recipient twin was noted to have an intra-abdominal echogenic mass
- This case report discusses a case of ameloblastic fibroma of the anterior maxilla presenting as a complication of tooth eruption
- This case report discusses a case of an infant with Fraser syndrome who required a surgical airway because of a severe stenosis of her airway secondary to a glottic web
- This case report discusses a case of aneursymal bone cyst of the proximal phalanx of the thumb in a child
- This case report discusses a case of asymptomatic ascariasis in a child
- This case report discusses a case of atypical case of Mycobacteria
- This case report discusses a case of autoimmune progesterone dermatitis in a parturient who required emergency caesarean section
- This case report discusses a case of bilateral microtia with severe cardiac defect questioning if this represents a new syndrome, or a severe manifestation of the oculoauriculovertebral spectrum
- This case report discusses a case of choanal atresia - a recurrent feature of foetal carbimazole syndrome
- This case report discusses a case of clinical characteristics of cherubism and their variable expression in addition to distinguishing cherubism from central giant cell granuloma and giant cell tumour of the jaws, with which it holds a false synonymity
- This case report discusses a case of dental treatment carried out successfully under local anaesthetic for a young child with Freeman-Sheldon syndrome.
- This case report discusses a case of desmoplastic small round cell tumor occurring in the right ilium of a 13-year-old boy
- This case report discusses a case of Diencephalic cachexia of infancy
- This case report discusses a case of fetal meconium peritonitis
- This case report discusses a case of genetic abnormailites in pre and post-chemotherapy hepatoblastoma
- This case report discusses a case of hypopituitarism and executive dysfunction which developed two years after cerebral oedema complicating diabetic ketoacidosis in a 12 year old with type 1 diabetes.
- This case report discusses a case of infanticide for 19th century Ireland and explore related diagnostic, therapeutic and judicial issues
- This case report discusses a case of intergeneration familial membranoproliferative glomerulonephritis type III
- This case report discusses a case of isolated bilateral orbital neurofibromatosis in a twelve-year-old
- This case report discusses a case of Jacobsen syndrome, suspected antenatally on the grounds of trigonocephaly and hypoplastic left heart syndrome.
- This case report discusses a case of Job syndrome masquerading as a non-accidental injury
- This case report discusses a case of late-onset central hypoventilation syndrome: a family genetic study
- This case report discusses a case of Moebius sequence and hypogonadotrophic hypogonadism with detailed neurologic, endocrine, and autopsy findings
- This case report discusses a case of multiple ventriculoperitoneal shunt placement procedures and a diagnostic dilemma with respect to distal shunt placement
- This case report discusses a case of neonatal alloimmune thrombocytopenia due to HPA-3a antibodies
- This case report discusses a case of neonatal seizures and limb malformations associated with liver-specific complex IV respiratory chain deficiency
- This case report discusses a case of oculo-facio-cardio-dental syndrome in a mother and daughter
- This case report discusses a case of otherwise typical cutaneous Sweet syndrome accompanied by an extracutaneous manifestation in the ileum.
- This case report discusses a case of partial lipodystrophy and renal disease
- This case report discusses a case of patent omphalomesenteric duct presenting as an umbilical discharge
- This case report discusses a case of peeling paint' dermatitis as a presenting sign of cystic fibrosis
- This case report discusses a case of possible Kawasaki disease which presented with bilateral subdural collections
- This case report discusses a case of prelabor rupture of membranes at 20 weeks' gestation where a hydrogel sealant was applied to the cervical canal in order to maintain an adequate liquor volume in the second trimester
- This case report discusses a case of recurrent congenital haemangiopericytoma in a child
- This case report discusses a case of ruptured abdominal aortic aneurysm in a 12-month-old boy
- This case report discusses a case of sigmoid volvulus in a neonate secondary to anal stenosis and review the diagnosis and management of this serious condition
- This case report discusses a case of spina bifida occulta in an 11-year old girl presenting with isthmic spondylolisthesis
- This case report discusses a case of successful allogeneic hematopoietic stem cell transplantation with full myeloablative conditioning in a patient with pre-existing invasive mucormycosis.
- This case report discusses a case of successful renal transplantation in a child with Kabuki syndrome
- This case report discusses a case of systemic absorption of lithium following ingestion of a lithium button battery
- This case report discusses a case of temporary arrest of root development in a premolar of a child with hypodontia and extensive caries
- This case report discusses a case of traumatic Hangman's fracture in a child under the age of 3 years and the only case where there is a strong probability of child abuse
- This case report discusses a case of unrehearsed circuit failure during neonatal extracorporeal membrane oxygenation
- This case report discusses a case of young female monozygotic twins who presented with selective mutism and their treatment
- This case report discusses a case treatment - conventional ventilation - of a case of pneumomediastinum in paediatric acute respiratory distress syndrome
- This case report discusses a case where an antenatal scan showed a cerebral vessel dilatation consistent with a vein of Galen malformation
- This case report discusses a case where multiple vertebral collapse was the presenting symptom of childhood acute lymphoblastic leukaemia
- This case report discusses a cases of Turner's syndrome and benign intracranial hypertension with or without growth hormone treatment
- This case report discusses a cause of familial epilepsy that also emphasises the importance of MRI as the modality of choice in investigating seizures in children - Hereditary cerebral cavernous angiomas
- This case report discusses a child with central hypoventilation syndrome after Haemophilus influenzae type b meningitis and herpes infection
- This case report discusses a child with stiff baby syndrome who underwent open reduction and femoral shortening of congenital dislocated hip under general anaesthesia
- This case report discusses a classically affected neonate with de Lange syndrome, an affected mother and probably affected maternal grandmother
- This case report discusses a congenital methaemoglobinaemia Type I in a Turkish infant due to a novel mutation, Pro144Ser, in NADH-cytochrome b5 reductase
- This case report discusses a diagnosis of 5 cases of Cohen Syndrome among 3 families from the Irish Traveller Community in the West of Ireland
- This case report discusses a diagnostically challenging case of a 14-year-old boy presenting with an atraumatic painful limp and pyrexia
- This case report discusses a eight year old child who developed subcutaneous emphysema, bilateral pneumothorax, pneumomediastinum and pneumoperitonium in recovery room after apparently uneventful general anaesthesia for eight primary teeth extractions
- This case report discusses a female child with C2 deficiency that presented at the age of 3 months with recurrent pneumococcal septicaemia
- This case report discusses a female infant with a rare chromosome defect, del. 12 (q22-24.1), who has severe pulmonary valve stenosis, an atrial septal defect, and a small muscular ventricular septal defect
- This case report discusses a female who presented in childhood with symptoms and signs of hyperandrogenism secondary to an extraovarian steroid cell tumor
- This case report discusses a girl with Malpuech Syndrome
- This case report discusses a male child with attention deficit disorder with hyperactivity and a major de-novo Y chromosome abnormality consisting of deletion of the long arm and duplication of the short arm
- This case report discusses a man charged with the offense of downloading child pornography from the Internet.
- This case report discusses a new technique for treatment of a non-union of a lateral humeral condyle
- This case report discusses a newborn boy with Antley-Bixler syndrome, is a rare disorder characterized mainly by craniosynostosis and multiple joint contractures including radiohumeral synostosis
- This case report discusses a nine year old of Asian descent who presented with clinical mastoiditis where the pathogenic organism was Mycobacterium Gordonae
- This case report discusses a novel use of small intestinal submucosal matrix for chest wall reconstruction following Ewing's tumour resection
- This case report discusses a pair of siblings affected by Prader-Wili Syndrome
- This case report discusses a patient in whom Infantile myofibromatosis was diagnosed, on the basis of multiple soft tissue tumours present from birth, who subsequently developed generalized and ultimately fatal fibromuscular dysplasia
- This case report discusses a patient whose clinical presentation closely resembles the profile of Malpuech syndrome, but whose radiological features are more in keeping with published observations in Juberg-Hayward patients.
- This case report discusses a positive Mantoux test and a chest x-ray consistent with miliary tuberculosis.
- This case report discusses a preterm infant who developed pseudomonas endophthalmitis, septicemia, and meningitis after a corneal abrasion.
- This case report discusses a rare case of straight-chain acyl-CoA oxidase deficiency (McKusick 264470) presenting with dysmorphism, neurodevelopmental regression and leukodystrophy
- This case report discusses a selection of cases managed with botulinum toxin and review the current data on use of the toxin to treat salivary gland disorders - Frey's syndrome, excessive salivation, hyperhidrosis, lacrimation and chronic rhinitis.
- This case report discusses a successful treatment of florid cutaneous warts with intravenous cidofovir in an 11-year-old girl
- This case report discusses abdominal pain in a 9-year-old: omental torsion masquerading as appendicitis
- This case report discusses absidia corymbifera infection causing rhinocerebral zygomycosis in two children with acute lymphoblastic leukaemia, early in the induction phase of treatment and within a 3-month interval, in the same oncology unit
- This case report discusses acute lymphoblastic leukemia
- This case report discusses agenesis of the corpus callosum with interhemispheric cyst, hepatic haemangioma and trisomy 21
- This case report discusses airway management in a baby with femoral hypoplasia-unusual facies syndrome
- This case report discusses an 11 year old girl with dark lump of pigment at each fovea Case of Sjogren reticular dystrophy
- This case report discusses an 11-year-old child who presented with a traumatic aortic transaction
- This case report discusses an 18 month girl who presented having ingested and aspirated a mouthful of Isoparaffin stored in a bottle of mineral water
- This case report discusses an 8-month-old infant whose pyoderma gangrenosum was aggressive and unresponsive to systemic steroids
- This case report discusses an 8-year-old girl, diagnosed with Familial cold auto-inflammatory syndrome
- This case report discusses an asymptomatic 18-month-old boy who underwent surgical resection of the discrete subaortic stenosis with Incidental detection of parvovirus myocarditis at time of resection of discrete subaortic stenosis
- This case report discusses an exceptional case of petrosal cholesteatomas occurring in a seven-year old girl who presented with a unilateral conductive hearing loss, despite normal tympanic membrane appearance
- This case report discusses an incidental finding of endocarditis in a preterm neonate
- This case report discusses an infant, with a strong family history of this hereditary periodic febrile syndromes, who presented on day-of-life 4 with high fever, irritability, diarrhea, lethargy, and raised acute phase reactants
- This case report discusses an interview with children, reporting self-reported experience of a number of negative life events
- This case report discusses an unusual case of anemia and dyspnoea
- This case report discusses an unusual case of optic disc pseudoduplication with colobomata
- This case report discusses an unusual case of respiratory symptoms in a toddler
- This case report discusses an unusual case where imaging revealed extensive pneumatosis intestinalis and portal venous gas in a patient with acute appendicitis
- This case report discusses an unusual cause of stridor in a post-liver transplant 6-year old
- This case report discusses an unusual form of "pseudodominant" inheritance to illustrate how a diagnosis of Friedreich's ataxia in a parent does not preclude the diagnosis in the child.
- This case report discusses angel-shaped phalango-epiphyseal dysplasia in a 2 yrs female with failure to thrive - angel-shaped phalango-epiphyseal dysplasia
- This case report discusses Asperger's syndrome
- This case report discusses atrioventricular block after transcatheter closure of perimembranous ventricular septal defects
- This case report discusses avascular necrosis of the talus after a minimally displaced neck of talus fracture in a 6 year old child
- This case report discusses bilateral pulmonary vein stenosis in a 5-year-old boy
- This case report discusses bilateral serous retinal detachments following diode laser treatment for retinopathy of prematurity
- This case report discusses bilateral wrist dislocation in trisomy 21
- This case report discusses bronchoscopically administered recombinant human DNase for lobar atelectasis in cystic fibrosis
- This case report discusses calcinosis associated with dermatomyositis
- This case report discusses clinical and molecular findings in IPEX syndrome
- This case report discusses complications in paediatric airway management
- This case report discusses congenital depression of the neonatal skull
- This case report discusses cryptogenic, multifocal, ulcerous, and stenosing enteritis as a manifestation of enterocolic venopathy
- This case report discusses early continuous video-electroencephalography from 3 hours after birth in an infant with the characteristic clinical and radiologic features of acute near-total intrauterine asphyxia
- This case report discusses elbow dislocation with ipsilateral open radial and ulnar diaphyseal fractures
- This case report discusses external inflammatory resorption and replacement resorption trauma entities, factors that influence the occurrence of resorption and to describe the most appropriate treatment
- This case report discusses extraventricular choroid plexus papilloma in a neonate
- This case report discusses fetal hydrops due to supraventricular tachycardia
- This case report discusses gianotti-crosti syndrome following meningococcal septicaemia
- This case report discusses hashimoto's thyroiditis--a rare but treatable cause of encephalopathy in children
- This case report discusses how effectively high-frequency ultrasound can identify an aortic saddle embolus in a 7-month-old infant, and to demonstrate its usefulness in monitoring the efficacy of treatment
- This case report discusses how the classic metaphyseal lesion may occur following simple lower segment caesarean section
- This case report discusses how the value judgments of the health professionals involved affected the interaction between themselves and a mother with her injured child who presented at an accident and emergency department
- This case report discusses inequalities in health
- This case report discusses Kabuki Syndrome with a confirmed diagnosis of a low grade fibromyxoid sarcoma.
- This case report discusses Kallmann Syndrome presenting as congenital ptosis in brothers
- This case report discusses Katargener's Syndrome in pregnancy
- This case report discusses Knobloch syndrome
- This case report discusses maturity onset diabetes in the young - type 3
- This case report discusses Moya Moya Syndrome in a child
- This case report discusses multiple airway abnormalities in a patient with Rothmund-Thomson syndrome
- This case report discusses neonatal abstinence syndrome due to prolonged administration of fentanyl in pregnancy
- This case report discusses neonatal diagnostic difficulty in hereditary spherocytosis
- This case report discusses new findings on the histopathology of the teeth in segmental odontomaxillary dysplasia
- This case report discusses nodular fascitis of the maxilla in a child
- This case report discusses pathological features of gastric stromal tumors in children
- This case report discusses patients identified as having gastric lymphoid hyperplasia on double contrast barium studies - Helicobacter pylori infection
- This case report discusses penile malignant peripheral nerve sheath tumour (schwannoma) in a three-year-old child without evidence of neurofibromatosis
- This case report discusses profound neurological presentation resulting from homozygosity - for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype
- This case report discusses radiological findings in cyclical administration of intravenous pamidronate in children with osteoporosis
- This case report discusses recurrent postdural puncture headache
- This case report discusses recurrent splice-site mutation in the human hairless gene underlies congenital atrichia in Irish families
- This case report discusses respiratory distress in a newborn infant
- This case report discusses skin-coloured lumps in childhood
- This case report discusses surgical management of giant left atrial diverticulum
- This case report discusses the anterior mitral leaflet reconstruction with pericardium in a 1.9 kg infant with endocarditis
- This case report discusses the authors experience with ultrasound (US)-guided aspiration and injection of a congenital splenic cyst
- This case report discusses the author's multi-modal therapeutic practice with a 7-year-old boy referred to the Family Trauma Centre, following paramilitary assaults on his father.
- This case report discusses the autoamputation of a congenital oropharyngeal hairy polyp
- This case report discusses the best treatment for hyperkalaemia in a preterm infant
- This case report discusses the case of a 12-year-old child with residual acetabular dysplasia, resulting from Legg-Calve-Perthes disease, which was treated by a triple pelvic osteotomy performed by a small single anterolateral incision
- This case report discusses the case of a 14-year-old boy who developed Kawasaki disease at 5 months of age and subsequent calcified occlusion of the right coronary artery in Kawasaki disease
- This case report discusses the case of a 2-year-old boy who ingested 35 mg.kg(-1) of amitriptyline.
- This case report discusses the case of a 3-month-old baby girl with hair-thread tourniquet syndrome in whom a hair cheese-wired through the skin and soft tissue of the toe and caused bony erosion of the underlying phalanx
- This case report discusses the case of a boy who developed osteopenia and sustained multiple long-bone fractures over a 5-year period after bone marrow transplant for Wiskott-Aldrich syndrome
- This case report discusses the case of a child who had persistent vomiting after surgery for posterior fossa astrocytoma complicated by low pressure hydrocephalus
- This case report discusses the case of a child with Kabuki syndrome, hypoplastic left heart syndrome, and right-sided partial anomalous pulmonary venous drainage to the inferior vena cava
- This case report discusses the case of a non-ambulant, 13-year-old boy from Chernobyl, who did not have access to early replacement therapy, and whose deformity was managed using the Ilizarov external fixator
- This case report discusses the case of a patient with congenital insensitivity to pain that presented with self-mutilation injuries to his hands and oral tissues caused by biting
- This case report discusses the case of a three-year-old girl referred to our fracture clinic as an occult osteomyelitis fracture following trauma to her forearm with normal initial radiographs
- This case report discusses the case of an 11-year-old girl, who presented with an osteoid osteoma at the neck of the glenoid
- This case report discusses the clinical and pathological findings in two siblings in whom the 4977 base pair mitochondrial DNA deletion was identified in muscle-derived mitochondrial DNA
- This case report discusses the clinical, radiological, and audiological features are described in a boy whose condition closely parallels the profile of patients previously described with Keipert syndrome
- This case report discusses the combination of sensorineural deafness with facial diplegia, ptosis and hypermobile joints in a brother and sister
- This case report discusses the delaying preterm delivery at the threshold of viability
- This case report discusses the dental findings in a child followed up for 9 years: Parry-Romberg syndrome
- This case report discusses the diagnosis of a confused child - urinary tract infection, dilated urinary system and associated hyperammonaemic encephalopathy
- This case report discusses the effectiveness of a behavioural intervention which included escape extinction and differential reinforcement of each bite eaten to treat non-organic food refusal in a child with Williams syndrome
- This case report discusses the effectiveness of video-feedback and self-management interventions on the aggressive and pro-social behaviour of two primary school children
- This case report discusses the establishment of functional B cell memory against parvovirus B19 capsid proteins which may be associated with resolution of persistent infection
- This case report discusses the examination of a 3-dimensional morphology of the myentric plexus of the entire gastrointestinal tract in a newborn with total intestinal aganglionosis
- This case report discusses the experience of two cases of post traumatic intra-abdominal pseudoaneurysms which were managed conservatively
- This case report discusses the fatal late-onset presentation of ornithine transcarbamylase deficiency in a 62-year-old man with the V337L mutation, also in his grandson and negative clinical and biochemical screening of the proband's three daughters
- This case report discusses the first case of intrapartum management of prenatal airway obstruction attempted in Ireland
- This case report discusses the genitopatellar syndrome
- This case report discusses the inclusion of a pupil with a severe general learning difficulty in a four-teacher mainstream primary school, located in rural Ireland
- This case report discusses the initial phase of the introduction of emergency department ultrasound with three illustrative case reports and a discussion on the pitfalls and benefits of Emergency department ultrasound
- This case report discusses the journey of one child in getting hospital treatment and broadens to discuses general paediatric surgery in Ireland
- This case report discusses the lactobacilli and bifidobacteria microbiota in the human ileum at a very early stage of life
- This case report discusses the long term outcome of a new ophthalmic treatment for laryngo-onycho-cutaneous (LOC) syndrome
- This case report discusses the management of a large bronchial haemangioma in an infant
- This case report discusses the management of a malocclusion, complicated by an ankylosed maxillary central incisor, which arose during orthodontic treatment, following an acute traumatic injury
- This case report discusses the management of an unerupted canine associated with a central giant cell granuloma
- This case report discusses the manner in which pregnancy may mask the signs and symptoms of intestinal obstruction
- This case report discusses the neurologic and developmental outcome of an infant after an accidental intravenous infusion of expressed breast milk
- This case report discusses the occurrence of odontogenic keratocysts in a young child
- This case report discusses the perioperative management of anesthesia and analgesia in a child with sickle cell disease and a congenital myopathy, presenting for corrective orthopedic surgery
- This case report discusses the presentation of erythema induratum of Bazin (EIB) a cutaneous hypersensitivity reaction to internal tuberculosis infection known as tuberculids.
- This case report discusses the presentation, monitoring and successful treatment of an eight year old girl with bipolar disorder, with low dose carbamazepine
- This case report discusses the psychosocial functioning of an 8-yr-old surviving conjoined twin
- This case report discusses the role of primary prophylactic factor replacement therapy in children with severe factor X deficiency
- This case report discusses the second M-D family in which several clinically affected epsilon-sarcoglycan gene (SGCE) mutation carriers have seizures in addition to myoclonus and dystonia
- This case report discusses the second reported case of coarctation in a right aortic arch with an aberrant left brachiocephalic artery
- This case report discusses the significance of locality and of girls experience of sectarian residential segregation and community conflict in Belfast
- This case report discusses the underlying medical condition of a child who presented as a "Foam eater" - Pica
- This case report discusses the unusual transformation of a lipomyelocele to a rhabdomyosarcoma in a 3-year-old boy
- This case report discusses the use of a predictive stimulus and delayed reinforcement to increase appropriate waiting behaviour in a child with developmental disabilities and problem behavior maintained by access to tangible items and activities
- This case report discusses the use of posterior cervical locking plate fixation after apical vertebral excision for congenital lumbar kyphosis in a 3-year-old male myelomeningocoele patient
- This case report discusses the usefulness of adult diagnostic systems in child and adolescent eating disorders
- This case report discusses three cases of long chain fatty acid oxidation defects in children: importance of detection and treatment options
- This case report discusses three patients presenting to paediatric services with symptoms attributed initially to symptomatic anal stenosis/atresia.
- This case report discusses transient renal failure in twins with maternal Cox-1/Cox-2 use in pregnancy
- This case report discusses tuberculous osteomyelitis of the sternum in an infant
- This case report discusses two brothers congenital ptosis and esotropia, one of whom also has polythelia
- This case report discusses two cases and a paper review which describes a variant of tibial hemimelia, previously undescribed in the literature and not classifiable by either of the established classification systems
- This case report discusses two cases of intussusception associated with bacterial meningitis
- This case report discusses two patients who were initially given a diagnosis of Langerhans' cell histiocytosis on the basis of the clinical, radiologic, and biopsy findings had mycobacterial infection subsequently identified
- This case report discusses two unusual cases of axonal neuropathy associated with short-chain acyl-CoA dehydrogenase deficiency are described.
- This case report discusses use of a Fogarty balloon with extraction forceps for the controlled retrieval of an endobronchial foreign body
- This case report discusses use of an Amplatzer Ductal Occluder Device to occlude a residual Sano shunt in an infant with a variant of hypoplastic left heart syndrome
- This case report discusses use of self-motivating and delayed feedback to increase on-task behaviour in a post-institutionalized child within regular classroom settings
- This case report discusses Walker-Warburg phenotype and genotype among Irish Travellers
- This case report discusses whether a once daily dose of gentamicin safe and effective in the treatment of urinary tract infection in infants and children
- This case report discusses which operation to undertake for intractable pulmonary aspiration in children
- This case report examine the influence of background noise on levels of problem behaviour and pain behaviour under functional analysis conditions for a child with a diagnosis of Williams syndrome and hyperacusis
- This case report examine the relation between sleep deprivation and changes in level and allocation of aberrant behaviour (aggression and self-injury) for a child with moderate mental retardation
- This case report examines the effect of a teaching method on skill fluency and on-task endurance of a 9-year-old boy who had been diagnosed with attention deficit hyperactivity disorder.
- This case report explores the use of the Roper-Logan-Tierney (RLT) nursing model in a neonatal transport setting
- This case report investigates whether Harry Potter stories can be clinically employed to assist in psychotheraputic work with children and adolescents
- This case report is used to illustrate a process-focused model of offending, using interview material to demonstrate how the offender represented and accounted for his behaviour
- This case report the management of two patients who presented with impacted premolars
- This case reports a 2-month-old girl with pulmonary atresia, ventricular septal defect, multiple aorto-pulmonary collaterals with severely hypoplastic pulmonary arteries
- This case reports a female infant of 42 weeks gestation with diaphragmatic hernia and hypoplastic left heart. A double vagina, absent uterus & abnormal male gonads were found in the presence of normal external female genitalia - Meacham Syndrome
- This obstetric case shows two false negative Kleihauer tests and two persistently positive Kleihauer tests leading to unnecessary administration of anti-D immunoglobulin
- This study sought to evaluate the current surveillance arrangements in Northern Ireland, describe the epidemiology of malaria and make appropriate recommendations
International Classification
- Behavioural and emotional disorders with onset usually occurring in childhood and adolescence - Report
- Certain conditions originating in the perinatal period - Report
- Certain infectious and parasitic diseases - Report
- Congenital malformations, deformations and chromosomal abnormalities - Report
- Dental
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism - Report
- Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism - Report
- Diseases of the circulatory system - Report
- Diseases of the digestive system - gastric lymphoid hyperplasia
- Diseases of the digestive system - Report
- Diseases of the ear and mastoid process - Report
- Diseases of the eye and adnexa - Report
- Diseases of the genitourinary system - Renal tubulo-interstitial diseases - vesicoureteric reflux-Report
- Diseases of the genitourinary system - Report
- Diseases of the musculoskeletal system and connective tissue - cranio-osteoarthropathy
- Diseases of the musculoskeletal system and connective tissue - Report
- Diseases of the musculoskeletal system and connective tissue-Sjogren reticular dystrophy
- Diseases of the nervous system - Report
- Diseases of the respiratory system - Report
- Diseases of the skin and subcutaneous tissue - Report
- Endocrine, nutritional and metabolic diseases-Report
- External causes of morbidity and mortality-Report
- Health service provision
- ICD-O: 9540/3 - Penile malignant peripheral nerve sheath tumour Neurofibrosarcoma ICD-O: 9540/3
- ICD-O:Connective/soft tissue tumors and sarcomas (ICD-O 8800-9059)
- Injury, poisoning and certain other consequences of external causes
- Injury, poisoning and certain other consequences of external causes - Report
- Legal or care issues
- Mental and behavioural disorders - Behavioural syndromes associated with physiological disturbances and physical factors - eating disorders - Report
- Mental and behavioural disorders - mania-Report
- Mental and behavioural disorders - Mood [affective] disorders - bipolar disorder - Report
- Mental and behavioural disorders - Report
- Mental and behavioural disorders - Schizophrenia, schizotypal and delusional disorders - schizophrenia Report
- Neoplasm - Report
- Neoplasms-Malignant
- Neurological
- Organ transplants
- Organ transplants - liver
- Other - carbonic anhydrase II deficiency-condiction
- Other - Community-segration and conflict
- Other - complex IV respiratory chain deficiency
- Other - Diagnostically challenging case
- Other - enterocolic venopathy
- Other - gastric stromal tumors
- Other - Growth and development-craniosynostois
- Other - hyperandrogenism-condiction
- Other - iatrogenic event
- Other - Kidney Diseases
- Other - Latex allergy
- Other - lipomyelocele
- Other - long chain fatty acid oxidation defects
- Other - microgastria
- Other - microtia
- Other - nasal chondromesynchymal hamartoma
- Other - Nephrocalcinosis
- Other - parvovirus B19
- Other - raised acute phase reactants
- Other-rhombencephalosynapsis
- Other-severe factor X deficiency-condiction
- Pregnancy, childbirth and the puerperium
- Procedure - chest wall reconstruction
- Procedure - postdural puncture headache
- Procedure - surgery, arterial anastomoses
- Psychosocial functioning
- Syndrome
- Syndrome V.A.T.E.R. syndrome Vertebrae, Anus, Trachea, Esophagus, and Renal