W. Schröter

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

Hyperphagia in children with craniopharyngioma is associated with hyperleptinaemia and a failure in the downregulation of appetite

Christian Roth, B. Wilken, F. Hanefeld et al. · European Journal of Endocrinology · 1998 · 162 citations · Full text

Medicine, Endocrinology, Neurosurgery +13

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

Prevalence of increased osmotic fragility of erythrocytes in German blood donors: Screening using a modified glycerol lysis test

Stefan Eber, Arnulf Pekrun, A. Neufeldt et al. · Annals of Hematology · 1992 · 95 citations

Medicine, Hematology, Physiology +10