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Helvetica Paediatrica Acta|May 1, 1975
Catalytically inactive sucrase antigen of rabbit small intestine: the enzyme precursorR Dubs, R Gitzelmann, B Steinmann, et al.Helvetica Paediatrica Acta|September 1, 1981
The diagnosis of hereditary fructose intoleranceB Steinmann, R GitzelmannHelvetica Paediatrica Acta|January 1, 1979
Strychnine treatment attempted in newborn twins with severe nonketotic hyperglycinemiaB Steinmann, R GitzelmannEnzyme|January 1, 1984
Galactosemia: how does long-term treatment change the outcome?R Gitzelmann, B SteinmannClinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1983
Zonal differences of alpha-glucosidases in human kidney: studies in controls and in patients with glycogenosis type IIK Pfister, R Gitzelmann, B SteinmannClinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1989
Patients with hereditary fructose intolerance have normal erythrocyte aldolase activityR Gitzelmann, B Steinmann, P TuchschmidEnzyme|January 1, 1992
Essential fructosuria: increased levels of fructose 3-phosphate in erythrocytesA Petersen, B Steinmann, R GitzelmannHelvetica Paediatrica Acta|January 1, 1979
Skin and bone lesions (dermato-osteolathyrism), possible side effects of D-penicillamine treatment, in a boy with cystinuriaB Steinmann, A Otten, R GitzelmannClinica Chimica Acta; International Journal of Clinical Chemistry|May 9, 1983
Hepatic glycogen synthetase deficiency not expressed in cultured skin fibroblastsR Gitzelmann, B Steinmann, A Aynsley-GreenProceedings of the National Academy of Sciences of the United States of America|December 1, 1975
Reversal of UDP-galactose 4-epimerase deficiency of human leukocytes in cultureB Mitchell, E Haigis, B Steinmann, et al.Pageof 22