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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.European Journal of Pediatrics|November 11, 1998
Fanconi-Bickel syndrome--the original patient and his natural history, historical steps leading to the primary defect, and a review of the literatureR Santer, R Schneppenheim, D Suter, et al.Pediatric Research|April 1, 1976
Hydantoin-5-propionic aciduria in folic acid nondependent formiminoglutamic aciduria observed in two siblingsA Niederwieser, A Matasović, B Steinmann, et al.Cardiology|January 21, 2000
Early-onset familial dilatation of the ascending aortaM Beghetti, B Steinmann, D Didier, et al.Pageof 25