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R Gitzelmann

Showing results (11-20 of 117) with videos related to

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Der Orthopade|January 1, 1984
[Collagen in connective tissue: from glue to molecular structure]B Steinmann, R Gitzelmann
Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Beiheft|January 1, 1976
[Fructose and sorbitol in infusion solutions are not always harmless]B Steinmann, R Gitzelmann
Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|January 1, 1973
Fluorescent spot screening test for galactosemia: increased sensitivityR Gitzelmann, I Schneller
Helvetica Paediatrica Acta|September 1, 1981
The diagnosis of hereditary fructose intoleranceB Steinmann, R Gitzelmann
Helvetica Paediatrica Acta|January 1, 1979
Strychnine treatment attempted in newborn twins with severe nonketotic hyperglycinemiaB Steinmann, R Gitzelmann
Enzyme|January 1, 1984
Galactosemia: how does long-term treatment change the outcome?R Gitzelmann, B Steinmann
European Journal of Pediatrics|December 1, 1986
Infant dumping syndrome: reversal of symptoms by feeding uncooked starchR Gitzelmann, J Hirsig
The Journal of Pediatrics|August 1, 1977
Screening for congenital hypothyroidismR Illig, R Gitzelmann
Der Orthopade|January 1, 1984
[Hereditary diseases with joint laxity]B Steinmann, R Gitzelmann
Helvetica Paediatrica Acta|December 1, 1973
Uridine diphosphate galactose 4-epimerase deficiency. II. Clinical follow-up, biochemical studies and family investigationR Gitzelmann, B Steinmann
Pageof 12

Showing results (11-20 of 117) with videos related to

Sort By:
Pageof 12
Der Orthopade|January 1, 1984
[Collagen in connective tissue: from glue to molecular structure]B Steinmann, R Gitzelmann
Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Beiheft|January 1, 1976
[Fructose and sorbitol in infusion solutions are not always harmless]B Steinmann, R Gitzelmann
Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|January 1, 1973
Fluorescent spot screening test for galactosemia: increased sensitivityR Gitzelmann, I Schneller
Helvetica Paediatrica Acta|September 1, 1981
The diagnosis of hereditary fructose intoleranceB Steinmann, R Gitzelmann
Helvetica Paediatrica Acta|January 1, 1979
Strychnine treatment attempted in newborn twins with severe nonketotic hyperglycinemiaB Steinmann, R Gitzelmann
Enzyme|January 1, 1984
Galactosemia: how does long-term treatment change the outcome?R Gitzelmann, B Steinmann
European Journal of Pediatrics|December 1, 1986
Infant dumping syndrome: reversal of symptoms by feeding uncooked starchR Gitzelmann, J Hirsig
The Journal of Pediatrics|August 1, 1977
Screening for congenital hypothyroidismR Illig, R Gitzelmann
Der Orthopade|January 1, 1984
[Hereditary diseases with joint laxity]B Steinmann, R Gitzelmann
Helvetica Paediatrica Acta|December 1, 1973
Uridine diphosphate galactose 4-epimerase deficiency. II. Clinical follow-up, biochemical studies and family investigationR Gitzelmann, B Steinmann
Pageof 12