M Garbarz

Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.

William Tse, Marie‐Christine Lecomte, Fernando Ferreira Costa et al. · Journal of Clinical Investigation · 1990 · 106 citations · Full text

Allelic Variant, Family Members, Genetic Disorder +13

Spectrin beta-chain variant associated with hereditary elliptocytosis.

D Dhermy, Marie‐Christine Lecomte, M Garbarz et al. · Journal of Clinical Investigation · 1982 · 66 citations · Full text

Genetics, Pathology, Molecular Genetics +21

Polymorphisms of the Tissue Factor Pathway Inhibitor (TFPI) Gene in Patients With Acute Coronary Syndromes and in Healthy Subjects

Didier Moatti, Patrick Seknadji, Colette Galand et al. · Arteriosclerosis Thrombosis and Vascular Biology · 1999 · 59 citations · Full text

Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin

Clement Glele‐Kakai, M Garbarz, Marie‐Christine Lecomte et al. · British Journal of Haematology · 1996 · 55 citations

Genetics, Genetic Epidemiology, Human Polymorphism +17

Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects

D Dhermy, Colette Galand, Odile Bournier et al. · British Journal of Haematology · 1997 · 48 citations · Full text