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 · 216 citations

Major Cause, Developmental Biology, Genetic Disorder +7

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 · 160 citations · Full text

Obesity, Metabolic Syndrome, Gastrointestinal Peptide Hormone +15

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 · 150 citations

Health Sciences, Inherited Metabolic Disease, Physiology +6

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

Developmental Biology, Growth Hormone Secretion, Short Stature +10

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 · 93 citations

Glycerol Lysis Test, Physiology, Hematology +10