Skip Navigation, or press ALT and K together and then press enter.Welcome to the OMC website. This site has been developed for both the visually impaired and non visually impaired. If you would like to use the visually impaired version of this site please go to omc.gov.ie/viewtxt.asp, or press ALT and I together and then press enter

Irish Child Health Database - Peer Reviewed Papers

Database Search


Irish Child Health Database » » B » Brain/pathology

Brain/pathology

Your search returns 6 documents

  • 1.   Acute demyelinating events with rhombencephalitis: a high-risk subgroup in children

    The aim of this study was to examine four children who had cerebellar involvement with significant mass effect in posterior fossa on CT and MRI brain - finding acute demyelinating events with rhombencephalitis

    Eur J Paediatr Neurol, Vol: 12 Page: 137-40 March 2008
    S. Tirupathi; N. Lynch; E. Phelan; J. Mc Menamin; D. Webb

    [Preview] [Read]

  • 2.   Bilateral subdural collections--an unusual feature of possible Kawasaki disease

    This case report discusses a case of possible Kawasaki disease which presented with bilateral subdural collections

    Eur J Paediatr Neurol, Vol: 5 Page: 79-81 2001
    N. M. Bailie; O. J. Hensey; S. Ryan; D. Allcut; M. D. King

    [Preview] [Read]

  • 3.   Cardiomyopathy and cardiomegaly in stillborn infants of diabetic mothers

    The aim of the study was to examine the cardiomyopathy and cardiomegaly in stillborn infants of diabetic mothers

    Pediatr Dev Pathol, Vol: 11 Page: 10-4 2008 Jan-Feb
    N. E. Russell; P. Holloway; S. Quinn; M. Foley; P. Kelehan; F. M. McAuliffe

    [Preview] [Read]

  • 4.   Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype

    This case report discusses profound neurological presentation resulting from homozygosity - for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype

    J Inherit Metab Dis, Vol: 26 Page: 72-4 2003
    E. P. Treacy; A. Lee-Chong; G. Roche; B. Lynch; S. Ryan; S. Goodman

    [Preview] [Read]

  • 5.   Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects

    This article discusses progressive myoclonic epilepsies

    Lancet Neurol, Vol: 4 Page: 239-48 April 2005
    A. Shahwan; M. Farrell; N. Delanty

    [Preview] [Read]

  • 6.   Rasmussen's syndrome associated with chronic brain stem encephalitis

    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

    Eur J Paediatr Neurol, Vol: 5 Page: 203-6 2001
    D. McDonald; Farrell; J. McMenamin

    [Preview] [Read]