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B Steinmann

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Biochemical and Biophysical Research Communications|August 19, 1974
Antibody activation of mutant human fructosediphosphate aldolase B in liver extracts of patients with hereditary fructose intoleranceR Gitzelmann, B Steinmann, C Bally, et al.
Human Genetics|January 1, 1993
Decreased extracellular deposition of fibrillin and decorin in neonatal Marfan syndrome fibroblastsM Raghunath, A Superti-Furga, M Godfrey, et al.
Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 1, 1988
[Brittle cornea syndrome: a hereditary disease of connective tissue with spontaneous corneal perforation]U Steinhorst, A Kohlschütter, B Steinmann, et al.
International Journal of Microcirculation, Clinical and Experimental|August 1, 1992
Microangiopathy in Ehlers-Danlos syndrome type IVA Superti-Furga, B Saesseli, B Steinmann, et al.
Pediatric Research|February 1, 1987
The renal handling of carnitine in patients with selective tubulopathy and with Fanconi syndromeB Steinmann, C Bachmann, J P Colombo, et al.
Human Genetics|May 1, 1989
Molecular defects of type III procollagen in Ehlers-Danlos syndrome type IVA Superti-Furga, B Steinmann, F Ramirez, et al.
Pediatric Research|October 1, 1994
Changes of liver metabolite concentrations in adults with disorders of fructose metabolism after intravenous fructose by 31P magnetic resonance spectroscopyP Boesiger, R Buchli, D Meier, et al.
Pediatric Research|March 1, 1984
Short communication. Glycogenosis Ib: neutrophil microbicidal defects due to impaired hexose monophosphate shuntR Seger, B Steinmann, L Tiefenauer, et al.
Aktuelle Gerontologie|August 1, 1977
[Analysis of gait in hemiplegics (author's transl)]M Löffel-Wagner, H U Debrunner, B Steinmann, et al.
Biochemical and Biophysical Research Communications|April 30, 1990
Collagen degradation in I-cells is normalR S Bienkowski, C R Ripley, R Gitzelmann, et al.
Pageof 24

Showing results (111-120 of 238) with videos related to

Sort By:
Pageof 24
Biochemical and Biophysical Research Communications|August 19, 1974
Antibody activation of mutant human fructosediphosphate aldolase B in liver extracts of patients with hereditary fructose intoleranceR Gitzelmann, B Steinmann, C Bally, et al.
Human Genetics|January 1, 1993
Decreased extracellular deposition of fibrillin and decorin in neonatal Marfan syndrome fibroblastsM Raghunath, A Superti-Furga, M Godfrey, et al.
Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 1, 1988
[Brittle cornea syndrome: a hereditary disease of connective tissue with spontaneous corneal perforation]U Steinhorst, A Kohlschütter, B Steinmann, et al.
International Journal of Microcirculation, Clinical and Experimental|August 1, 1992
Microangiopathy in Ehlers-Danlos syndrome type IVA Superti-Furga, B Saesseli, B Steinmann, et al.
Pediatric Research|February 1, 1987
The renal handling of carnitine in patients with selective tubulopathy and with Fanconi syndromeB Steinmann, C Bachmann, J P Colombo, et al.
Human Genetics|May 1, 1989
Molecular defects of type III procollagen in Ehlers-Danlos syndrome type IVA Superti-Furga, B Steinmann, F Ramirez, et al.
Pediatric Research|October 1, 1994
Changes of liver metabolite concentrations in adults with disorders of fructose metabolism after intravenous fructose by 31P magnetic resonance spectroscopyP Boesiger, R Buchli, D Meier, et al.
Pediatric Research|March 1, 1984
Short communication. Glycogenosis Ib: neutrophil microbicidal defects due to impaired hexose monophosphate shuntR Seger, B Steinmann, L Tiefenauer, et al.
Aktuelle Gerontologie|August 1, 1977
[Analysis of gait in hemiplegics (author's transl)]M Löffel-Wagner, H U Debrunner, B Steinmann, et al.
Biochemical and Biophysical Research Communications|April 30, 1990
Collagen degradation in I-cells is normalR S Bienkowski, C R Ripley, R Gitzelmann, et al.
Pageof 24