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France
HCP Center: OPHTARA – AP-HP, Hôpital Necker-Enfants Malades, Paris, France
Working Group(s): Retinal Rare Eye Diseases (WG1), Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7)
France
HCP Center: Reference Center Rare Diseases ‘Genetic Sensory Diseases’, MAOLYA, Montpellier, France
Working Group(s): Retinal Rare Eye Diseases (WG1)
Spain
HCP Center: Hospital Sant Joan de Déu, Spain
Working Group(s): Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), Research (TWG8), CPMS & Digital Medecine (TWG10)
Spain
HCP Center: Hospital Universitario La Paz, Spain
Working Group(s): Retinal Rare Eye Diseases (WG1), Registries & Epidemiology (TWG7)
Representative
Spain
HCP Center: Hospital Sant Joan de Déu, Spain
Working Group(s): CPMS & Digital Medecine (TWG10)
Representative
Italy
HCP Center: ASST Santi Paolo e Carlo, Milan, Italy
France
HCP Center: OPHTARA – Hôpital Cochin, Paris, France
Working Group(s): Retinal Rare Eye Diseases (WG1)
France
HCP Center: CARGO, Hôpitaux Universitaires de Strasbourg, France
Working Group(s): CPMS & Digital Medecine (TWG10)
France
HCP Center: Reference Center Rare Diseases ‘Genetic Sensory Diseases’, MAOLYA, Montpellier, France
Working Group(s): Retinal Rare Eye Diseases (WG1)
Substitute
Germany
HCP Center: Klinikum der Universität München, Germany
