C. Schwartz

Homozygous Nonsense Mutation in the FOXE3 Gene as a Cause of Congenital Primary Aphakia in Humans

Sophie Valleix, Florence Niel, Brigitte Nédelec et al. · The American Journal of Human Genetics · 2006 · 101 citations · Full text

Developmental Anomaly, Congenital Primary Aphakia, Developmental Biology +12

CHOROIDAL THICKNESS MEASUREMENT IN CHILDREN USING OPTICAL COHERENCE TOMOGRAPHY

Mélanie Bidaut-Garnier, C. Schwartz, Marc Puyraveau et al. · Retina · 2013 · 90 citations

Constitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1.

Sonja A. Rasmussen, Steven D. Colman, Vikki Ho et al. · Journal of Medical Genetics · 1998 · 89 citations · Full text

Nf1 Gene Deletion, Mendelian Disorder, Genetic Disorder +13

Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.

Anouk Dansault, Gabriel David, C. Schwartz et al. · PubMed · 2007 · 74 citations

Intravenous high‐dose methotrexate based systemic therapy in the treatment of isolated primary vitreoretinal lymphoma: An <scp>LOC</scp> network study

Marion Lam, Valérie Touitou, Sylvain Choquet et al. · American Journal of Hematology · 2021 · 62 citations · Full text

Lymphoid Neoplasia, Primary Vitreoretinal Lymphoma, Iv Hd‐mtx +13