
Dr Agathe Robertie
France
HCP Center: Reference Center Rare Diseases ‘Genetic Sensory Diseases’, MAOLYA, Montpellier, France
Working Group(s): Retinal Rare Eye Diseases (WG1)
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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

France
HCP Center: RÉFÉRET National Hospital of Ophthalmology of Quinze-Vingts, Paris, France
Working Group(s): Retinal Rare Eye Diseases (WG1), Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Low Vision Daily Life and Patients Groups (TWG5), Genetic Diagnostics (TWG6), Registries & Epidemiology (TWG7), Research (TWG8)