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I M Burr

Showing results (61-70 of 70) with videos related to

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Urology|June 1, 1980
True hermaphroditism: a rational appraoch to diagnosis and treatmentV Braren, A Slonim, J J Warner, et al.
Nucleic Acids Research|June 25, 1992
Multiple mRNA species generated by alternate polyadenylation from the rat manganese superoxide dismutase geneJ Hurt, J L Hsu, W C Dougall, et al.
Diabetologia|June 1, 1970
Metabolic state, pancreatic insulin content and B-cell morphology of normoglycemie spiny mice (Acomys cahirinus): indications for an impairment of insulin secretionW Stauffacher, L Orci, M Amherdt, et al.
The American Journal of Medicine|June 1, 1982
Cholesterol reduction by a high-glucose diet in a patient with homozygous familial hypercholesterolemia. A preliminary reportP W Stacpoole, L L Swift, H L Greene, et al.
The Journal of Clinical Investigation|November 1, 1981
Elevated cholesterol and bile acid synthesis in an adult patient with homozygous familial hypercholesterolemia. Reduction by a high glucose dietP W Stacpoole, S M Grundy, L L Swift, et al.
Endocrinology|February 1, 1971
Insulin of spiny mice (Acomys cahirinus)--partial characterization and evidence for two insulinsL Balant, I M Burr, W Stauffacher, et al.
Human Genetics|January 1, 1982
Ovarian development in 46,XY gonadal dysgenesisM H Russell, S S Wachtel, B W Davis, et al.
The Journal of Pediatrics|October 1, 1981
Dietary-dependent carnitine deficiency as a cause of nonketotic hypoglycemia in an infantA E Slonim, P R Borum, K Tanaka, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1987
P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasiaK J Matteson, J A Phillips, W L Miller, et al.
The Journal of Clinical Investigation|August 1, 1978
ATP depletion, a possible role in the pathogenesis of hyperuricemia in glycogen storage disease type IH L Greene, F A Wilson, P Hefferan, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Urology|June 1, 1980
True hermaphroditism: a rational appraoch to diagnosis and treatmentV Braren, A Slonim, J J Warner, et al.
Nucleic Acids Research|June 25, 1992
Multiple mRNA species generated by alternate polyadenylation from the rat manganese superoxide dismutase geneJ Hurt, J L Hsu, W C Dougall, et al.
Diabetologia|June 1, 1970
Metabolic state, pancreatic insulin content and B-cell morphology of normoglycemie spiny mice (Acomys cahirinus): indications for an impairment of insulin secretionW Stauffacher, L Orci, M Amherdt, et al.
The American Journal of Medicine|June 1, 1982
Cholesterol reduction by a high-glucose diet in a patient with homozygous familial hypercholesterolemia. A preliminary reportP W Stacpoole, L L Swift, H L Greene, et al.
The Journal of Clinical Investigation|November 1, 1981
Elevated cholesterol and bile acid synthesis in an adult patient with homozygous familial hypercholesterolemia. Reduction by a high glucose dietP W Stacpoole, S M Grundy, L L Swift, et al.
Endocrinology|February 1, 1971
Insulin of spiny mice (Acomys cahirinus)--partial characterization and evidence for two insulinsL Balant, I M Burr, W Stauffacher, et al.
Human Genetics|January 1, 1982
Ovarian development in 46,XY gonadal dysgenesisM H Russell, S S Wachtel, B W Davis, et al.
The Journal of Pediatrics|October 1, 1981
Dietary-dependent carnitine deficiency as a cause of nonketotic hypoglycemia in an infantA E Slonim, P R Borum, K Tanaka, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1987
P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasiaK J Matteson, J A Phillips, W L Miller, et al.
The Journal of Clinical Investigation|August 1, 1978
ATP depletion, a possible role in the pathogenesis of hyperuricemia in glycogen storage disease type IH L Greene, F A Wilson, P Hefferan, et al.
Pageof 7