Stefan Eber

Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis

Stefan Eber, Jennifer M. Reingle González, Marcia L. Lux et al. · Nature Genetics · 1996 · 218 citations

Life Sciences, Genetics, Molecular Genetics +4

THROMBO‐EMBOLIC DISEASE AFTER SPLENECTOMY FOR HEREDITARY STOMATOCYTOSIS

Gordon W. Stewart, John Amess, Stefan Eber et al. · British Journal of Haematology · 1996 · 208 citations

Medicine, Hematology, Surgery +14

Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study

Rachael F. Grace, Paola Bianchi, Eduard J. van Beers et al. · Blood · 2018 · 163 citations · Full text

Life Sciences, Biochemistry, Physiology +9

Variable clinical severity of hereditary spherocytosis: Relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis

Stefan Eber, R. Armbrust, W. Schröter · The Journal of Pediatrics · 1990 · 151 citations

Medicine, Cell Biology, Hematology +13

Short stature and failure of pubertal development in thalassaemia major: evidence for hypothalamic neurosecretory dysfunction of growth hormone secretion and defective pituitary gonadotropin secretion

Christian Roth, Arnulf Pekrun, Miriam Cristine Machado Bartz et al. · European Journal of Pediatrics · 1997 · 106 citations

Medicine, Endocrinology, Physiology +17