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Schweizerische Medizinische Wochenschrift
|
January 26, 1974
[Congenital dyserythropoietic anemia type II. Biochemical and electron microscopic studies]
P Kerkhoven, G Hug, H R Marti
The Journal of Pediatrics
|
March 1, 1971
Sporadic hypoglycemia: abnormal epinephrine response to the ketogenic diet or to insulin
H Koffler, W K Schubert, G Hug
American Journal of Human Genetics
|
July 1, 1970
Liver glycogenosis and phosphorylase kinase deficiency
G Hug, W K Schubert, G Chuck
The New England Journal of Medicine
|
December 26, 1991
Lethal neonatal multiorgan deficiency of carnitine palmitoyltransferase II
G Hug, K E Bove, S Soukup
Biochemical and Biophysical Research Communications
|
August 24, 1970
Loss of cyclic 3'5'-AMP dependent kinase and reduction of phosphorylase kinase in skeletal muscle of a girl with deactivated phosphorylase and glycogenosis of liver and muscle
G Hug, W K Schubert, G Chuck
The New England Journal of Medicine
|
April 19, 1984
Rapid prenatal diagnosis of glycogen-storage disease type II by electron microscopy of uncultured amniotic-fluid cells
G Hug, S Soukup, M Ryan, et al.
Forensic Science International
|
February 1, 1986
Phosphoenolpyruvate carboxykinase activity in human liver
C A McGraw, G F Vawter, G Hug
Schweizerische Rundschau Fur Medizin Praxis = Revue Suisse De Medecine Praxis
|
April 6, 1976
[The variable pattern of gluten induced enteropathy (sprue nostras, idiopathic sprue) (author's transl)]
W Kreyenbühl, B Hammer, G Hug, et al.
The Journal of Pediatrics
|
June 1, 1970
Chronic lactic acidosis of infancy
H L Greene, W K Schubert, G Hug
Blood
|
January 1, 1972
Congenital dyserythropoietic anemia type II: ultrastructural and radioautographic studies of blood and bone marrow
K Y Wong, G Hug, B C Lampkin
Page
of 9
Search research articles
Search
Showing results (31-40 of 85) with videos related to
Sort By:
Page
of 9
Schweizerische Medizinische Wochenschrift
|
January 26, 1974
[Congenital dyserythropoietic anemia type II. Biochemical and electron microscopic studies]
P Kerkhoven, G Hug, H R Marti
The Journal of Pediatrics
|
March 1, 1971
Sporadic hypoglycemia: abnormal epinephrine response to the ketogenic diet or to insulin
H Koffler, W K Schubert, G Hug
American Journal of Human Genetics
|
July 1, 1970
Liver glycogenosis and phosphorylase kinase deficiency
G Hug, W K Schubert, G Chuck
The New England Journal of Medicine
|
December 26, 1991
Lethal neonatal multiorgan deficiency of carnitine palmitoyltransferase II
G Hug, K E Bove, S Soukup
Biochemical and Biophysical Research Communications
|
August 24, 1970
Loss of cyclic 3'5'-AMP dependent kinase and reduction of phosphorylase kinase in skeletal muscle of a girl with deactivated phosphorylase and glycogenosis of liver and muscle
G Hug, W K Schubert, G Chuck
The New England Journal of Medicine
|
April 19, 1984
Rapid prenatal diagnosis of glycogen-storage disease type II by electron microscopy of uncultured amniotic-fluid cells
G Hug, S Soukup, M Ryan, et al.
Forensic Science International
|
February 1, 1986
Phosphoenolpyruvate carboxykinase activity in human liver
C A McGraw, G F Vawter, G Hug
Schweizerische Rundschau Fur Medizin Praxis = Revue Suisse De Medecine Praxis
|
April 6, 1976
[The variable pattern of gluten induced enteropathy (sprue nostras, idiopathic sprue) (author's transl)]
W Kreyenbühl, B Hammer, G Hug, et al.
The Journal of Pediatrics
|
June 1, 1970
Chronic lactic acidosis of infancy
H L Greene, W K Schubert, G Hug
Blood
|
January 1, 1972
Congenital dyserythropoietic anemia type II: ultrastructural and radioautographic studies of blood and bone marrow
K Y Wong, G Hug, B C Lampkin
Page
of 9