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R Gitzelmann

Showing results (41-50 of 117) with videos related to

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FEBS Letters|October 12, 1981
Intracellular degradation of newly synthesized collagen is conformation-dependentB Steinmann, V H Rao, R Gitzelmann
European Journal of Clinical Investigation|April 1, 1974
Galactose metabolism in a patient with hereditary galactokinase deficiencyR Gitzelmann, H J Wells, S Segal
Helvetica Paediatrica Acta|December 1, 1971
Infantile lactic acidosis due to hereditary fructose 1,6-diphosphatase deficiencyK Baerlocher, R Gitzelmann, R Nüssli, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1975
Reversal of UDP-galactose 4-epimerase deficiency of human leukocytes in cultureB Mitchell, E Haigis, B Steinmann, et al.
Archives of Disease in Childhood|July 1, 1977
Hepatic glycogen synthetase deficiency. Definition of syndrome from metabolic and enzyme studies on a 9-year-old girlA Aynsley-Green, D H Williamson, R Gitzelmann
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1976
[Lysosomal storage diseases: possibilities of the clinical-biochemical diagnostics (author's transl)]U N Wiesmann, M A Spycher, R Gitzelmann
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1976
[Lysosomal storage diseases: possibilities of the ultrastructural diagnosis (author's transl)]M A Spycher, R Gitzelmann, U N Wiesmann
Human Genetics|January 28, 1999
A mutation (IVS8+0.6kbdelTC) creating a new donor splice site activates a cryptic exon in an Alu-element in intron 8 of the human beta-glucuronidase geneR Vervoort, R Gitzelmann, W Lissens, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 15, 1977
Blood cell glycogen synthetase activities in hepatic glycogen synthetase deficiencyR Gitzelmann, A Aynsley-Green, D H Williamson
Helvetica Paediatrica Acta|May 1, 1975
Catalytically inactive sucrase antigen of rabbit small intestine: the enzyme precursorR Dubs, R Gitzelmann, B Steinmann, et al.
Pageof 12

Showing results (41-50 of 117) with videos related to

Sort By:
Pageof 12
FEBS Letters|October 12, 1981
Intracellular degradation of newly synthesized collagen is conformation-dependentB Steinmann, V H Rao, R Gitzelmann
European Journal of Clinical Investigation|April 1, 1974
Galactose metabolism in a patient with hereditary galactokinase deficiencyR Gitzelmann, H J Wells, S Segal
Helvetica Paediatrica Acta|December 1, 1971
Infantile lactic acidosis due to hereditary fructose 1,6-diphosphatase deficiencyK Baerlocher, R Gitzelmann, R Nüssli, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1975
Reversal of UDP-galactose 4-epimerase deficiency of human leukocytes in cultureB Mitchell, E Haigis, B Steinmann, et al.
Archives of Disease in Childhood|July 1, 1977
Hepatic glycogen synthetase deficiency. Definition of syndrome from metabolic and enzyme studies on a 9-year-old girlA Aynsley-Green, D H Williamson, R Gitzelmann
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1976
[Lysosomal storage diseases: possibilities of the clinical-biochemical diagnostics (author's transl)]U N Wiesmann, M A Spycher, R Gitzelmann
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1976
[Lysosomal storage diseases: possibilities of the ultrastructural diagnosis (author's transl)]M A Spycher, R Gitzelmann, U N Wiesmann
Human Genetics|January 28, 1999
A mutation (IVS8+0.6kbdelTC) creating a new donor splice site activates a cryptic exon in an Alu-element in intron 8 of the human beta-glucuronidase geneR Vervoort, R Gitzelmann, W Lissens, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 15, 1977
Blood cell glycogen synthetase activities in hepatic glycogen synthetase deficiencyR Gitzelmann, A Aynsley-Green, D H Williamson
Helvetica Paediatrica Acta|May 1, 1975
Catalytically inactive sucrase antigen of rabbit small intestine: the enzyme precursorR Dubs, R Gitzelmann, B Steinmann, et al.
Pageof 12