Publications by authors named "Maria Inmaculada Martin-Merida"

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Identification of new families and variants in autosomal dominant macular dystrophy associated with THRB.
Lidia Fernández-Caballero, Fiona Blanco-Kelly, Saoud Tahsin Swafiri, María Inmaculada Martín-Mérida, Mathieu Quinodoz

Sci Rep· April 2025

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-associated retinopathy: genotype-phenotype correlations - study group report 3.
Thales A C de Guimaraes, Michalis Georgiou, Anthony G Robson, Kaoru Fujinami, Ajoy Vincent, Maria Inmaculada Martin-Merida

Br J Ophthalmol· July 2024

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KCNV2-Associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints-KCNV2 Study Group Report 2.
Michalis Georgiou, Kaoru Fujinami, Ajoy Vincent, Fadi Nasser, Samer Khateb, Maria Inmaculada Martin-Merida

Am J Ophthalmol· October 2021

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KCNV2-Associated Retinopathy: Genetics, Electrophysiology, and Clinical Course-KCNV2 Study Group Report 1.
Michalis Georgiou, Anthony G Robson, Kaoru Fujinami, Shaun M Leo, Ajoy Vincent, Maria Inmaculada Martin-Merida

Am J Ophthalmol· May 2021

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Derivation of a human DOA iPSC line, IISHDOi006-A, with a mutation in the ACO2 gene: c.1999G>A; p.Glu667Lys.
Victoria Cerrada, Marta García-López, Ana Moreno-Izquierdo, Cristina Villaverde, Olga Zurita, Maria Inmaculada Martin-Merida

Stem Cell Res· October 2019

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