Bp Leroy | Researchain

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Featured researches published by Bp Leroy.

Archive | 2010

Molecular analysis in a large cohort of patients with anterior segment malformations: expanding the spectrum of FOXC1/PITX2 mutations and copy number changes

Barbara D'haene; B Menten; Ilse Claerhout; Françoise Meire; Hester Y. Kroes; Astrid S. Plomp; Yvonne Arens; Thomy de Ravel de l'Argentière; Ingele Casteels; Wim Wuyts; Hermine E. Veenstra-Knol; Rogier A. Oldenburg; Jacques C. Giltay; Jb Verhey; A. De Paepe; P Kesteleyn; Bp Leroy; E De Baere

Journal of The International Neuropsychological Society | 1995

Neuropsychological test performance versus postconcussional complaints after moderate to severe head injury: a two-year follow up

Engelien Lannoo; A De Paepe; Bp Leroy; Evert Thiery

Online abstracts | 2015

An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

Miriam Bauwens; Frauke Coppieters; J De Zaeytijd; Nicole Weisschuh; Susanne Kohl; Karin Dahan; Fanny Depasse; M. De Rademaeker; B Loeys; Françoise Meire; Thomy de Ravel de l'Argentière; Wouter Steyaert; S De Jaegere; Bp Leroy; E De Baere

Abstract book | 2015

Novel FRMD7 mutations and genomic rearrangement expand the molecularathogenesis of X-linked idiopathic infantile nystagmus

B Almoallem; Miriam Bauwens; Sophie Walraedt; Patricia Delbeke; J De Zaeytijd; P. Kestelyn; Françoise Meire; Koenraad Devriendt; Bp Leroy; E De Baere

ASHG Meeting Abstracts | 2015

Comprehensive evaluation of the FBN1, LTBP2 and ADAMTSL4 genes in 207 patients with ectopia lentis

Bert Callewaert; S Van Nuffel; L De Potter; E De Bals; J. De Backer; Olivier Vanakker; Hilde Van Esch; Martine Biervliet; J Desir; J Vandenende; A. De Paepe; Bp Leroy; Paul Coucke

Acta Ophthalmologica | 2014

FRO 2014: Exploring the role of a novel disease gene EML4 in autosomal recessive retinitis pigmentosa

K Van Schil; Bp Leroy; E De Baere

Acta Ophthalmologica | 2012

Genetic retinal diseases

Bp Leroy

Acta Ophthalmologica | 2012

Inherited retinal disease

Bp Leroy

Abstract book | 2012

Combined Identity-by-descent Mapping And Exome Sequencing Identifies A Novel MERTK Mutation In Autosomal Recessive Retinitis Pigmentosa

Frauke Coppieters; K Van Schil; Steve Lefever; J De Zaeytijd; Bp Leroy; Ingele Casteels; Thomy de Ravel de l'Argentière; E De Baere

Investigative Ophthalmology & Visual Science | 2009

Mutations in a Gene Encoding a Mitochondrial Protein as a First Cause of Recessively Inherited Simple Optic Atrophy

Sylvain Hanein; Isabelle Perrault; O. Roche; Sylvie Gerber; Bp Leroy; Françoise Meire; Arnold Munnich; Jean-Louis Dufier; Josseline Kaplan; Jean Michel Rozet

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