ereprof. dr. Philippe Kestelyn
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Exome-based panel testing as an efficient method to diagnose the highly heterogeneous ocular disorder spectrum Microphthalmia, Anophthalmia, Coloboma and Anterior Segment Dysgenesis (MAC-ASD)
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Expanding the differential diagnosis of primary congenital glaucoma : molecular lessons learned from a large consanguineous family
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Expanding the CPAMD8-associated eye disease spectrum to primary congenital glaucoma : lessons learned from a large consanguineous family with pseudodominance
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Switch from BAK-preserved to preservative-free latanoprost decreases anterior chamber flare in POAG patients
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Fuchs’ Uveitis syndrome : no longer a syndrome?
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Novel FRMD7 mutations and genomic rearrangement expand the molecular pathogenesis of X-linked idiopathic infantile nystagmus
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Efficacy and safety of deep sclerectomy in childhood glaucoma in Saudi Arabia
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Identity-by-descent mapping and exome sequencing reveals a new candidate gene for the primary congenital glaucoma locus GLC3E
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Identity-by-descent mapping and exome sequencing reveals a new candidate gene for the primary congenital glaucoma locus GLC3E
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- Conference Paper
- C3
- open access
Proptosis and blindness caused by meningioma in a patient treated with cyproterone acetate