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Pr Isabelle MEUNIER

In this page

Member info

Pr Isabelle MEUNIER

Representative

France

Working Group(s): Retinal Rare Eye Diseases (WG1)

Team

Dr Catherine Blanchet

France

Retinal Rare Eye Diseases (WG1)
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Dr Agathe Robertie

France

Retinal Rare Eye Diseases (WG1)
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Dr Anne-Françoise Roux

France

Retinal Rare Eye Diseases (WG1)
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HCP Center

Labelized in 2004, MAOLYA is a national reference center for the diagnosis and management of multisensory inherited diseases with isolated or...

contact

Reference Center Rare Diseases ‘Genetic Sensory Diseases’, MAOLYA, Montpellier, France

Hôpital Gui de ChauliacService Ophtalmologie80, avenue Augustin Fliche 1er étage, bureau 1414
34 295 Montpellier Cedex 5
France

Clinical trials

NCT02994368 Recruiting Active

A Multicenter Prospective Observational « Natural History » Study in Patients With Choroideremia.

Observational
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NCT01235624 Completed

Autosomal Dominant Retinitis Pigmentosa: Prevalence of Known Genes Identification of New Loci/Genes.

Interventional
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NCT01461213 Completed

Gene therapy study on choroideremia : to assess the safety and tolerability of the AAV.REP1 vector, administered at two different doses to the retina in patients with a diagnosis of choroideremia.

Interventional
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NCT03328130 Recruiting Active

Safety and Efficacy of a Unilateral Subretinal Administration of HORA-PDE6B in Patients With Retinitis Pigmentosa Harbouring Mutations in the PDE6B Gene Leading to a Defect in PDE6B Expression

Interventional
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NCT03314207 Recruiting Active

Natural history of the progression of X-linked retinitis pigmentosa.

Observational
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