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G Hug

Showing results (81-90 of 85) with videos related to

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The New England Journal of Medicine|October 11, 1984
Increased serum hexosaminidase in a woman pregnant with a fetus affected by mucolipidosis II (I-cell disease)G Hug, K E Bove, S Soukup, et al.
The New England Journal of Medicine|April 15, 1976
Transiently reduced activity of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of children with Reye's syndromeT Brown, G Hug, L Lansky, et al.
Journal of Pediatric Surgery|July 1, 1995
Weanling and adult rats differ in fatty acid and carnitine metabolism during sepsisD N Linz, V F Garcia, G Arya, et al.
Klinische Wochenschrift|June 16, 1980
[Prenatal diagnosis of alpha-1-antitrypsin phenotype. Case record and prognosis in severe alpha-antitrypsin deficiency Pi ZZ (author's transl)]S L Roth, K Havemann, G A Martini, et al.
European Journal of Pediatrics|December 22, 1999
Liver transplantation for glycogen storage disease types I, III, and IVD Matern, T E Starzl, W Arnaout, et al.
Pageof 9

Showing results (81-90 of 85) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 85 results.
The New England Journal of Medicine|October 11, 1984
Increased serum hexosaminidase in a woman pregnant with a fetus affected by mucolipidosis II (I-cell disease)G Hug, K E Bove, S Soukup, et al.
The New England Journal of Medicine|April 15, 1976
Transiently reduced activity of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of children with Reye's syndromeT Brown, G Hug, L Lansky, et al.
Journal of Pediatric Surgery|July 1, 1995
Weanling and adult rats differ in fatty acid and carnitine metabolism during sepsisD N Linz, V F Garcia, G Arya, et al.
Klinische Wochenschrift|June 16, 1980
[Prenatal diagnosis of alpha-1-antitrypsin phenotype. Case record and prognosis in severe alpha-antitrypsin deficiency Pi ZZ (author's transl)]S L Roth, K Havemann, G A Martini, et al.
European Journal of Pediatrics|December 22, 1999
Liver transplantation for glycogen storage disease types I, III, and IVD Matern, T E Starzl, W Arnaout, et al.
Pageof 9