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R Gitzelmann

Showing results (71-80 of 117) with videos related to

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The Journal of Biological Chemistry|May 5, 1988
Ehlers-Danlos syndrome type IV: a multi-exon deletion in one of the two COL3A1 alleles affecting structure, stability, and processing of type III procollagenA Superti-Furga, E Gugler, R Gitzelmann, et al.
The New England Journal of Medicine|March 29, 1984
Prenatal diagnosis of hereditary tyrosinemiaB Steinmann, R Gitzelmann, E A Kvittingen, et al.
Biochimica Et Biophysica Acta|January 6, 1970
Localization of rabbit intestinal sucrase with ferritin-antibody conjugatesR Gitzelmann, T Bächi, H Binz, et al.
Genomics|August 1, 1993
Complementary DNA sequence and chromosomal mapping of a human proteoglycan-binding cell-adhesion protein (dermatopontin)A Superti-Furga, M Rocchi, B W Schäfer, 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.
Biochemical and Biophysical Research Communications|April 30, 1990
Collagen degradation in I-cells is normalR S Bienkowski, C R Ripley, R Gitzelmann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1995
Early and severe sensory loss in three adult siblings with hexosaminidase A and B deficiency (Sandhoff disease)H Schnorf, R Gitzelmann, N U Bosshard, et al.
European Journal of Pediatrics|July 1, 1985
Fructose-1,6-diphosphatase deficiency: glycerol excretion during fasting testP A Dremsek, M Sacher, W Stögmann, et al.
European Journal of Pediatrics|May 1, 1985
Anomalous eosinophil granulocytes in blood and bone marrow: a diagnostic marker for infantile GM1-gangliosidosis?R Gitzelmann, M A Spycher, S Adank, et al.
Pageof 12

Showing results (71-80 of 117) with videos related to

Sort By:
Pageof 12
The Journal of Biological Chemistry|May 5, 1988
Ehlers-Danlos syndrome type IV: a multi-exon deletion in one of the two COL3A1 alleles affecting structure, stability, and processing of type III procollagenA Superti-Furga, E Gugler, R Gitzelmann, et al.
The New England Journal of Medicine|March 29, 1984
Prenatal diagnosis of hereditary tyrosinemiaB Steinmann, R Gitzelmann, E A Kvittingen, et al.
Biochimica Et Biophysica Acta|January 6, 1970
Localization of rabbit intestinal sucrase with ferritin-antibody conjugatesR Gitzelmann, T Bächi, H Binz, et al.
Genomics|August 1, 1993
Complementary DNA sequence and chromosomal mapping of a human proteoglycan-binding cell-adhesion protein (dermatopontin)A Superti-Furga, M Rocchi, B W Schäfer, 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.
Biochemical and Biophysical Research Communications|April 30, 1990
Collagen degradation in I-cells is normalR S Bienkowski, C R Ripley, R Gitzelmann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1995
Early and severe sensory loss in three adult siblings with hexosaminidase A and B deficiency (Sandhoff disease)H Schnorf, R Gitzelmann, N U Bosshard, et al.
European Journal of Pediatrics|July 1, 1985
Fructose-1,6-diphosphatase deficiency: glycerol excretion during fasting testP A Dremsek, M Sacher, W Stögmann, et al.
European Journal of Pediatrics|May 1, 1985
Anomalous eosinophil granulocytes in blood and bone marrow: a diagnostic marker for infantile GM1-gangliosidosis?R Gitzelmann, M A Spycher, S Adank, et al.
Pageof 12