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G Hug

Showing results (41-50 of 85) with videos related to

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Laboratory Investigation; a Journal of Technical Methods and Pathology|January 1, 1972
Congenital dyserythropoietic anemia type II. Ultrastructure of erythroid cells and hepatocytesG Hug, K Y Wong, B C Lampkin
The New England Journal of Medicine|October 10, 1974
Letter: Carbamyl phosphate synthetase and ornithine transcarbamylase in liver of Reye's syndromeT Brown, H Brown, L Lansky, et al.
Lancet (London, England)|August 15, 1970
Prenatal detection of Pompe's diseaseH L Nadler, R H Bigley, G Hug
Human Pathology|July 1, 1974
Glycogen storage disease, types I to X: criteria for morphologic diagnosisA J McAdams, G Hug, K E Bove
The New England Journal of Medicine|January 25, 1973
Type II glycogenosis in adultsG Hug, W K Schubert, S W Soukup
Journal of Medical Genetics|October 1, 1984
Antenatal diagnosis of mucopolysaccharidosis type I (Hurler's disease) is not possible by electron microscopy of uncultured amniotic fluid cellsG Hug, S Soukup, G Chuck, et al.
Helvetica Paediatrica Acta|June 1, 1974
[Unusual congenital cholesterol ester storage in the liver]H Wolf, G Hug, R Michaelis, et al.
Human Genetics|January 1, 1980
PiZpratt: a new alpha 1-antitrypsin allele in an American Negro familyG Hug, G Chuck, B Bowles, et al.
Pediatrics|August 1, 1988
Renal calcificationT R Welch, C Restrepo de Rovetto, G Hug
The Journal of Laboratory and Clinical Medicine|July 1, 1974
Liver phosphorylase deficiency in glycogenosis type VI: documentation by biochemical analysis of hepatic biopsy specimensG Hug, G Chuck, L Walling, et al.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
Laboratory Investigation; a Journal of Technical Methods and Pathology|January 1, 1972
Congenital dyserythropoietic anemia type II. Ultrastructure of erythroid cells and hepatocytesG Hug, K Y Wong, B C Lampkin
The New England Journal of Medicine|October 10, 1974
Letter: Carbamyl phosphate synthetase and ornithine transcarbamylase in liver of Reye's syndromeT Brown, H Brown, L Lansky, et al.
Lancet (London, England)|August 15, 1970
Prenatal detection of Pompe's diseaseH L Nadler, R H Bigley, G Hug
Human Pathology|July 1, 1974
Glycogen storage disease, types I to X: criteria for morphologic diagnosisA J McAdams, G Hug, K E Bove
The New England Journal of Medicine|January 25, 1973
Type II glycogenosis in adultsG Hug, W K Schubert, S W Soukup
Journal of Medical Genetics|October 1, 1984
Antenatal diagnosis of mucopolysaccharidosis type I (Hurler's disease) is not possible by electron microscopy of uncultured amniotic fluid cellsG Hug, S Soukup, G Chuck, et al.
Helvetica Paediatrica Acta|June 1, 1974
[Unusual congenital cholesterol ester storage in the liver]H Wolf, G Hug, R Michaelis, et al.
Human Genetics|January 1, 1980
PiZpratt: a new alpha 1-antitrypsin allele in an American Negro familyG Hug, G Chuck, B Bowles, et al.
Pediatrics|August 1, 1988
Renal calcificationT R Welch, C Restrepo de Rovetto, G Hug
The Journal of Laboratory and Clinical Medicine|July 1, 1974
Liver phosphorylase deficiency in glycogenosis type VI: documentation by biochemical analysis of hepatic biopsy specimensG Hug, G Chuck, L Walling, et al.
Pageof 9