Liikmete teave
Pr Hélène Dollfus
Prantsusmaa
MEIST
meeskond
Dr Dorothée Leroux
Prantsusmaa
Dr Isabella Vacchi
Prantsusmaa
Dr Amélie Gavard
Prantsusmaa
Caroline Wernert-Iberg
Prantsusmaa
HCP keskus
kontakt
CARGO, Hôpitaux Universitaires de Strasbourg, France
Kliinilised uuringud
Argus® II Retinal Prosthesis System: Post-Market Study
Autosomal Dominant Retinitis Pigmentosa: Prevalence of Known Genes Identification of New Loci/Genes.
Bardet-Biedl Syndrome Study: Clinical and Genetic Epidemiology Study in Adults.
Clinical implication of Retinitis Pigmentosa molecular diagnostic using high throughput sequencing (RP-SEQ-HD).
Clinical Study of a single ciliopathy: Alström Syndrome.
Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy.
Historical Case Record Survey of Visual Acuity Data From Patients With Leber’s Hereditary Optic Neuropathy (LHON).
Setmelanotide (RM-493), Melanocortin-4 Receptor (MC4R) Agonist, in Bardet-BiedlSyndrome (BBS) and Alström Syndrome (AS) Patients With Moderate to Severe Obesity.
Trisomy 21 in Adulthood : a medical and social situation in Alsace.