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S Shanske

Showing results (1-10 of 141) with videos related to

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Brain Pathology (Zurich, Switzerland)|April 1, 1992
Mitochondrial encephalomyopathies: defects of nuclear DNAS Shanske
Current Opinion in Rheumatology|February 12, 1998
Diagnosis of the mitochondrial encephalomyopathiesS Shanske, S DiMauro
Journal of the Neurological Sciences|April 1, 1981
Late-onset acid maltase deficiency. Biochemical studies of leukocytesS Shanske, S Dimauro
Annals of the New York Academy of Sciences|January 1, 1991
Mitochondrial inheritance of acquired deafnessM Gold, I Rapin, S Shanske
The New England Journal of Medicine|July 22, 1993
Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, S DiMauro
Muscle & Nerve|March 1, 1986
Targeting of lysosomal enzymes: N-acetylglucosamine-1-phosphotransferase during muscle developmentH Den, S Shanske, S DiMauro
Experimental Neurology|June 1, 1984
Multiple neutral maltase activities in normal and acid maltase-deficient human muscleS Shanske, N Bresolin, S DiMauro
Muscle & Nerve. Supplement|January 1, 1995
Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiencyS Tsujino, S Shanske, S DiMauro
Archives of Pediatrics & Adolescent Medicine|November 29, 2001
The other human genomeA L Shanske, S Shanske, S DiMauro
Muscle & Nerve. Supplement|January 1, 1995
The molecular genetic basis of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, I Nonaka, et al.
Pageof 15

Showing results (1-10 of 141) with videos related to

Sort By:
Pageof 15
Brain Pathology (Zurich, Switzerland)|April 1, 1992
Mitochondrial encephalomyopathies: defects of nuclear DNAS Shanske
Current Opinion in Rheumatology|February 12, 1998
Diagnosis of the mitochondrial encephalomyopathiesS Shanske, S DiMauro
Journal of the Neurological Sciences|April 1, 1981
Late-onset acid maltase deficiency. Biochemical studies of leukocytesS Shanske, S Dimauro
Annals of the New York Academy of Sciences|January 1, 1991
Mitochondrial inheritance of acquired deafnessM Gold, I Rapin, S Shanske
The New England Journal of Medicine|July 22, 1993
Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, S DiMauro
Muscle & Nerve|March 1, 1986
Targeting of lysosomal enzymes: N-acetylglucosamine-1-phosphotransferase during muscle developmentH Den, S Shanske, S DiMauro
Experimental Neurology|June 1, 1984
Multiple neutral maltase activities in normal and acid maltase-deficient human muscleS Shanske, N Bresolin, S DiMauro
Muscle & Nerve. Supplement|January 1, 1995
Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiencyS Tsujino, S Shanske, S DiMauro
Archives of Pediatrics & Adolescent Medicine|November 29, 2001
The other human genomeA L Shanske, S Shanske, S DiMauro
Muscle & Nerve. Supplement|January 1, 1995
The molecular genetic basis of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, I Nonaka, et al.
Pageof 15