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Irish Child Health Database - Peer Reviewed Papers

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Your search returns 3 documents

• 1.   A genome-wide scan for genes involved in primary vesicoureteric reflux

  The aim of this study was to examine a genome-wide linkage scan using 4710 single-nucleotide polymorphisms in families with more then one member with Vesicoureteric reflux

  

  Abstract:

  BACKGROUND: Vesicoureteric reflux (VUR) is the retrograde flow of urine from the bladder into the ureters. It is the most common urological anomaly in children, and a major cause of end-stage renal failure and hypertension in both children and adults. VUR is seen in approximately 1-2% of Caucasian newborns and is frequently familial. Objective and METHODS: In order to search for genetic more...

  International Classification:

  Other - genome-wide linkage scan

  Categories:

  genome-wide linkage scan

  Geography:

  Republic of Ireland

  J Med Genet, Vol: 44 Page: 710-7 November 2007
  H. Kelly; C. M. Molony; J. M. Darlow; M. E. Pirker; A. Yoneda; A. J. Green; P. Puri; D. E. Barton

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• 2.   Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14

  The aim of this study was to describe a genome-wide search on individuals with early-onset homogeneous bipolar affective disorder type I proband

  

  Abstract:

  Preliminary studies suggested that age at onset (AAO) may help to define homogeneous bipolar affective disorder (BPAD) subtypes. This candidate symptom approach might be useful to identify vulnerability genes. Thus, the probability of detecting major disease-causing genes might be increased by focusing on families with early-onset BPAD type I probands. This study was conducted as part more...

  International Classification:

  Mental and behavioural disorders - Mood [affective] disorders - bipolar affective disorder

  Categories:

  homogeneous bipolar affective disorder

  Geography:

  International

  Mol Psychiatry, Vol: 11 Page: 685-94 July 2006
  B. Etain; F. Mathieu; M. Rietschel; W. Maier; M. Albus; P. McKeon; S. Roche; C. Kealey; D. Blackwood; W. Muir; F. Bellivier; C. Henry; C. Dina; S. Gallina; H. Gurling; A. Malafosse; M. Preisig; F. Ferrero; S. Cichon; J. Schumacher; S. Ohlraun; M. Borrmann-Hassenbach; P. Propping; R. Abou Jamra; T. G. Schulze; A. Marusic; Z. M. Dernovsek; B. Giros; T. Bourgeron; A. Lemainque; D. Bacq; C. Betard; C. Charon; M. M. Nothen; M. Lathrop; M. Leboyer

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• 3.   Linkage of a gene causing familial membranoproliferative glomerulonephritis type III to chromosome 1

  The aim of this study was to examine linkage of a gene causing familial membranoproliferative glomerulonephritis type III to chromosome 1

  

  Abstract:

  Membranoproliferative glomerulonephritis (MPGN) type III is a chronic progressive renal disease of unknown cause. The diagnosis is based on renal pathologic features (specifically immunofluorescence staining patterns and ultrastructural appearance). Mesangial cell proliferation and subendothelial and subepithelial deposits characterize the renal disease. Although the actual prevalence more...

  International Classification:

  Diseases of the genitourinay system - Glomerular diseases - membranoproliferative glomerulonephritis type III

  Categories:

  familial membranoproliferative glomerulonephritis type III

  Geography:

  Republic of Ireland

  J Am Soc Nephrol, Vol: 13 Page: 2052-7 August 2002
  J. J. Neary; P. J. Conlon; D. Croke; A. Dorman; M. Keogan; F. Y. Zhang; J. M. Vance; M. A. Pericak-Vance; W. K. Scott; M. P. Winn

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