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S Shanske

Showing results (21-30 of 141) with videos related to

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Archives of Neurology|April 1, 1985
Immunocytochemical analysis of normal and acid maltase-deficient muscle culturesA F Miranda, S Shanske, A P Hays, et al.
Pediatric Research|October 1, 1981
Mucolipidosis II (I-cell disease): studies of muscle biopsy and muscle culturesS Shanske, A F Miranda, A S Penn, et al.
Muscle & Nerve. Supplement|January 1, 1995
Molecular genetic studies in muscle phosphoglycerate mutase (PGAM-M) deficiencyS Tsujino, S Shanske, S Sakoda, et al.
Human Mutation|January 1, 1995
Two novel missense mutations (E654K, L396P) in Caucasian patients with myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, A Martinuzzi, et al.
Muscle & Nerve|September 1, 1984
Phosphoglycerate kinase deficiency myopathy: biochemical and immunological studies of the mutant enzymeN Bresolin, A Miranda, H W Chang, et al.
Pediatric Research|August 29, 2000
A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathyA L Andreu, N Checcarelli, S Iwata, et al.
Annals of Neurology|September 1, 1995
A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosisD Thyagarajan, S Shanske, M Vazquez-Memije, et al.
Muscle & Nerve|September 1, 1996
Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the Italian kindredA Toscano, S Tsujino, G Vita, et al.
Annals of Neurology|December 1, 1988
McArdle's disease: biochemical and molecular genetic studiesS Servidei, S Shanske, M Zeviani, et al.
The Journal of Biological Chemistry|October 25, 1987
Isolation of a cDNA encoding the muscle-specific subunit of human phosphoglycerate mutaseS Shanske, S Sakoda, M A Hermodson, et al.
Pageof 15

Showing results (21-30 of 141) with videos related to

Sort By:
Pageof 15
Archives of Neurology|April 1, 1985
Immunocytochemical analysis of normal and acid maltase-deficient muscle culturesA F Miranda, S Shanske, A P Hays, et al.
Pediatric Research|October 1, 1981
Mucolipidosis II (I-cell disease): studies of muscle biopsy and muscle culturesS Shanske, A F Miranda, A S Penn, et al.
Muscle & Nerve. Supplement|January 1, 1995
Molecular genetic studies in muscle phosphoglycerate mutase (PGAM-M) deficiencyS Tsujino, S Shanske, S Sakoda, et al.
Human Mutation|January 1, 1995
Two novel missense mutations (E654K, L396P) in Caucasian patients with myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, A Martinuzzi, et al.
Muscle & Nerve|September 1, 1984
Phosphoglycerate kinase deficiency myopathy: biochemical and immunological studies of the mutant enzymeN Bresolin, A Miranda, H W Chang, et al.
Pediatric Research|August 29, 2000
A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathyA L Andreu, N Checcarelli, S Iwata, et al.
Annals of Neurology|September 1, 1995
A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosisD Thyagarajan, S Shanske, M Vazquez-Memije, et al.
Muscle & Nerve|September 1, 1996
Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the Italian kindredA Toscano, S Tsujino, G Vita, et al.
Annals of Neurology|December 1, 1988
McArdle's disease: biochemical and molecular genetic studiesS Servidei, S Shanske, M Zeviani, et al.
The Journal of Biological Chemistry|October 25, 1987
Isolation of a cDNA encoding the muscle-specific subunit of human phosphoglycerate mutaseS Shanske, S Sakoda, M A Hermodson, et al.
Pageof 15