M E Fabry

Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.

Dominique Labie, J. Pagnier, Claudine Lapouméroulie et al. · Proceedings of the National Academy of Sciences · 1985 · 232 citations · Full text

Life Sciences, Genetics, Hematology +17

Erythrocytes in sickle cell anemia are heterogeneous in their rheological and hemodynamic characteristics.

Dhananjay K. Kaul, M E Fabry, Péter Windisch et al. · Journal of Clinical Investigation · 1983 · 228 citations · Full text

Veterinary Medicine, Hematology, Physiology +17

In vivo demonstration of red cell-endothelial interaction, sickling and altered microvascular response to oxygen in the sickle transgenic mouse.

Dhananjay K. Kaul, M E Fabry, Frank Costantini et al. · Journal of Clinical Investigation · 1995 · 132 citations · Full text

Life Sciences, Cell Biology, Physiology +17

Heterogeneity of red cells in the sickler: a characteristic with practical clinical and pathophysiological implications.

M E Fabry, R L Nagel · PubMed · 1982 · 111 citations

Medicine, Cell Biology, Hematology +14

High expression of human beta S- and alpha-globins in transgenic mice: erythrocyte abnormalities, organ damage, and the effect of hypoxia.

M E Fabry, Frank Costantini, A Pachnis et al. · Proceedings of the National Academy of Sciences · 1992 · 100 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13