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European Journal of Pharmacology|April 4, 1994
Selective enhancement by cyclosporin A of collagen expression by mesangial cells 'in culture'G M Ghiggeri, P Altieri, R Oleggini, et al.Kidney International|October 1, 1987
Characterization of cationic albumin in minimal change nephropathyG M Ghiggeri, F Ginevri, G Candiano, 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.Pediatrics|August 3, 2001
Case report: liver glycogen synthase deficiency--a cause of ketotic hypoglycemiaS L Rutledge, J Atchison, N U Bosshard, et al.European Journal of Pediatrics|August 1, 1998
Persistence of the intestinal defect in abetalipoproteinaemia after liver transplantationC P Braegger, D C Belli, G Mentha, et al.European Journal of Pediatrics|October 1, 1989
Hyperprolinaemia type I and white matter disease: coincidence or causal relationship?M Steinlin, E Boltshauser, B Steinmann, et al.Journal of Craniofacial Genetics and Developmental Biology|July 1, 1996
Mild dental findings associated with severe osteogenesis imperfecta due to a point mutation in the alpha 2(I) collagen gene demonstrate different expression of the genetic defect in bone and teethH U Luder, H van Waes, M Raghunath, et al.Pageof 31