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Enzyme
|
January 1, 1992
Essential fructosuria: increased levels of fructose 3-phosphate in erythrocytes
A Petersen, B Steinmann, R Gitzelmann
Nutrition and Metabolism
|
January 1, 1975
[Hereditary disorders of fructose metabolism. Loading tests with fructose, sorbitol and dihydroxyacetone]
B Steinmann, K Baerlocher, R Gitzelmann
Monatsschrift Fur Kinderheilkunde
|
May 1, 1973
[Hereditary defects of fructose and galactose metabolism]
R Gitzelmann, K Baerlocher, A Prader
Helvetica Paediatrica Acta
|
January 1, 1979
Skin and bone lesions (dermato-osteolathyrism), possible side effects of D-penicillamine treatment, in a boy with cystinuria
B Steinmann, A Otten, R Gitzelmann
The New England Journal of Medicine
|
October 16, 1975
Letter: Intestinal sucrase-isomaltase
R Gitzelmann, R Dubs, B Steinmann
Gynecologic and Obstetric Investigation
|
January 1, 1981
A newly recognized cause of low urinary estriol in pregnancy: multiple sulfatase deficiency of the fetus
B Steinmann, D Mieth, R Gitzelmann
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 9, 1983
Hepatic glycogen synthetase deficiency not expressed in cultured skin fibroblasts
R Gitzelmann, B Steinmann, A Aynsley-Green
European Journal of Pediatrics
|
September 20, 1997
Hypergalactosaemia in a newborn: self-limiting intrahepatic portosystemic venous shunt
R Gitzelmann, I Forster, U V Willi
European Journal of Cell Biology
|
May 1, 1984
Presence and absence of the microsomal beta-glucuronidase in mice correlates with differences in the processing of the lysosomal enzyme
P Beltramini-Guarini, R Gitzelmann, K Pfister
Helvetica Paediatrica Acta
|
January 1, 1971
[Phenylketonuria and hyperphenylalaninemia]
S Rampini, R Gitzelmann, H C Curtius
Page
of 12
Search research articles
Search
Showing results (31-40 of 117) with videos related to
Sort By:
Page
of 12
Enzyme
|
January 1, 1992
Essential fructosuria: increased levels of fructose 3-phosphate in erythrocytes
A Petersen, B Steinmann, R Gitzelmann
Nutrition and Metabolism
|
January 1, 1975
[Hereditary disorders of fructose metabolism. Loading tests with fructose, sorbitol and dihydroxyacetone]
B Steinmann, K Baerlocher, R Gitzelmann
Monatsschrift Fur Kinderheilkunde
|
May 1, 1973
[Hereditary defects of fructose and galactose metabolism]
R Gitzelmann, K Baerlocher, A Prader
Helvetica Paediatrica Acta
|
January 1, 1979
Skin and bone lesions (dermato-osteolathyrism), possible side effects of D-penicillamine treatment, in a boy with cystinuria
B Steinmann, A Otten, R Gitzelmann
The New England Journal of Medicine
|
October 16, 1975
Letter: Intestinal sucrase-isomaltase
R Gitzelmann, R Dubs, B Steinmann
Gynecologic and Obstetric Investigation
|
January 1, 1981
A newly recognized cause of low urinary estriol in pregnancy: multiple sulfatase deficiency of the fetus
B Steinmann, D Mieth, R Gitzelmann
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 9, 1983
Hepatic glycogen synthetase deficiency not expressed in cultured skin fibroblasts
R Gitzelmann, B Steinmann, A Aynsley-Green
European Journal of Pediatrics
|
September 20, 1997
Hypergalactosaemia in a newborn: self-limiting intrahepatic portosystemic venous shunt
R Gitzelmann, I Forster, U V Willi
European Journal of Cell Biology
|
May 1, 1984
Presence and absence of the microsomal beta-glucuronidase in mice correlates with differences in the processing of the lysosomal enzyme
P Beltramini-Guarini, R Gitzelmann, K Pfister
Helvetica Paediatrica Acta
|
January 1, 1971
[Phenylketonuria and hyperphenylalaninemia]
S Rampini, R Gitzelmann, H C Curtius
Page
of 12