B. P. Leroy

Two cases of acute macular neuroretinopathy (2007)

Corver, H.D., Ruys, J., Leroy, B.P.

Purpose To report chorioretinal vasoconstriction as a potential pathogenic mechanism in acute macular neuroretinopathy (AMNR). To describe a time lag between the onset of functional deficits and that...

Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome (2005)

Beysen, D., Raes, J., Leroy, B. P., Lucassen, A., Yates, J. R., Clayton-Smith, J., ...

The expression of a gene requires not only a normal coding sequence but also intact regulatory regions, which can be located at large distances from the target genes, as demonstrated for an...

FOXL2 and BPES: Mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation (2003)

Baere, E. De, Beysen, D., Oley, C., Lorenz, B., Cocquet, J., Sutter, P. De, ...

Clinical and electrophysiological findings in autosomal dominant vitreoretinochoroidopathy: report of a new pedigree (2001)

Loeys, B, Leroy, B P, De Laey, J J, Kestelyn, P

PURPOSE: To report the clinical and electrophysiological findings in a three-generation pedigree with autosomal dominant vitreoretinochoroidopathy. METHODS: Sixteen members of a three-generation...

Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation (2001)

Dixon, M J, Small, K W, Jabs, E W, Leroy, B P, ...

Mutations in FOXL2, a forkhead transcription factor gene, have recently been shown to cause blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) types I and II, a rare genetic disorder. In...

Rapid recovery of night blindness due to obesity surgery after vitamin A repletion therapy

Spits, Y, De Laey, J-J, Leroy, B P