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Schweizerische Medizinische Wochenschrift|December 27, 1975
[Telemetric ECG control of the heart during the rehabilitation of hemiplegics]B Steinmann, R Schwarz, E KunzCurrent Molecular Medicine|April 13, 2002
Fanconi-Bickel syndrome--a congenital defect of facilitative glucose transportR Santer, B Steinmann, J SchaubZookeys|May 6, 2024
A new troglomorphic species of Larca (Pseudoscorpiones, Larcidae) from ColoradoMark S Harvey, David B SteinmannJournal of Molecular Biology|February 25, 1994
Delayed triple helix formation of mutant collagen from patients with osteogenesis imperfectaM Raghunath, P Bruckner, 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 GitzelmannAmerican Journal of Human Genetics|August 1, 1986
Processing of types I and III procollagen in Ehlers-Danlos syndrome type VIIR Halila, B Steinmann, L PeltonenClinical Genetics|May 8, 2010
Stüve-Wiedemann syndrome: long-term follow-up and genetic heterogeneityC Jung, N Dagoneau, G Baujat, et al.American Journal of Human Genetics|July 1, 1996
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13Y Gong, M Vikkula, L Boon, et al.Clinical Genetics|December 16, 2010
Clinical and molecular characterization of Diastrophic Dysplasia in the Portuguese populationM Barbosa, A B Sousa, A Medeira, et al.Pageof 25