සාමාජික තොරතුරු
Pr José-Alain Sahel
ප්රංශය
කණ්ඩායම
Pr Isabelle Audo
ප්රංශය
Dr Christina Zeitz
ප්රංශය
Dr Catherine Vignal-Clermont
ප්රංශය
HCP මධ්යස්ථානය
අමතන්න
RÉFÉRET National Hospital of Ophthalmology of Quinze-Vingts, Paris, France
සායනික පරීක්ෂණ
A Post-Authorization, Multicenter, Multinational, Longitudinal,Observational Safety Registry Study for Patients Treated with Voretigene Neparvovec.
A Study to Determine the Long Term Safety, Tolerability and Biological Activity of SAR422459 in Patients With Stargardt’s Macular Degeneration.
An Open-Label Study to Determine the Long Term Safety, Tolerability and Biological Activity of UshStat® in Patients With Usher Syndrome Type 1B.
Argus® II Retinal Prosthesis System: Post-Market Study
Argus® II Retinal Stimulation System Feasibility Protocol.
Autosomal Dominant Retinitis Pigmentosa: Prevalence of Known Genes Identification of New Loci/Genes.
Clinical and Genetic Examination of Usher Syndrome Patients’ Cohort in Europe.
Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy.
Leber Hereditary Optic Neuropathy (LHON) Historical Case Record Survey.
Phase I/IIa Study of SAR422459 in Patients With Stargardt’s Macular Degeneration.
Prospective Natural History Study of Retinitis Pigmentosa (PHENOROD2)
Study of UshStat in Patients With Retinitis Pigmentosa Associated With Usher Syndrome Type 1B.
Prospective study of visual function in USHER syndrome induced by MYO7A mutation and retinotosis pigmentosa.
විද්යාත්මක ප්රකාශන
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F‐mediated inherited retinal disorders
ජාන-කේතකරණ කලාපවල සෘජු සැන්ගර් අනුක්රමය යොදන විස්තීරණ අධ්යයනයක්, එක්සෝම් සහ ජෙනෝම් අනුක්රමණය විශාල සමූහයකට අදාළ වේ.
Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 Years
SP හි ප්රමාණාත්මක මිනුම් වසර 2ක් පුරා USH2A ආශ්රිත දෘෂ්ටි විතානයේ සැලකිය යුතු ලෙස අඩු විය...
Shedding light on myopia by studying complete congenital stationary night blindness
ප්රතිඵල ඖෂධීය මයෝපියාව වර්ධනය කිරීමට මඟ පෙන්වීම සඳහා පදනමක් සපයයි.