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S Dimauro

Showing results (91-100 of 421) with videos related to

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Annals of Neurology|January 1, 1978
McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzymeS DiMauro, S Arnold, A Miranda, et al.
Journal of Child Neurology|March 1, 2000
HyperCKemia as the only sign of McArdle's disease in a childC Bruno, E Bertini, F M Santorelli, et al.
Neurology|August 1, 1996
Diagnosis of McArdle's disease by molecular genetic analysis of bloodM el-Schahawi, S Tsujino, S Shanske, et al.
Biochimica Et Biophysica Acta|December 10, 1992
Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCRS Simonetti, X Chen, S DiMauro, et al.
Human Mutation|January 1, 1994
An A-to-C substitution involving the translation initiation codon in a patient with myophosphorylase deficiency (McArdle's disease)S Tsujino, L A Rubin, S Shanske, et al.
Epilepsy Research. Supplement|January 1, 1991
Epilepsy in mitochondrial encephalomyopathiesS DiMauro, E Ricci, M Hirano, et al.
The Journal of Pediatrics|July 1, 1988
Fatal infantile cardiopathy caused by phosphorylase b kinase deficiencyS Servidei, L A Metlay, J Chodosh, et al.
Neurologic Clinics|February 1, 1989
Mitochondrial diseasesM Zeviani, E Bonilla, D C DeVivo, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy, other ocular myopathies, and progressive external ophthalmoplegiaL P Rowland, M Hirano, S DiMauro, et al.
Advances in Neurology|October 9, 1999
Mitochondrial genes for generalized epilepsiesS DiMauro, R Kulikova, K Tanji, et al.
Pageof 43

Showing results (91-100 of 421) with videos related to

Sort By:
Pageof 43
Annals of Neurology|January 1, 1978
McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzymeS DiMauro, S Arnold, A Miranda, et al.
Journal of Child Neurology|March 1, 2000
HyperCKemia as the only sign of McArdle's disease in a childC Bruno, E Bertini, F M Santorelli, et al.
Neurology|August 1, 1996
Diagnosis of McArdle's disease by molecular genetic analysis of bloodM el-Schahawi, S Tsujino, S Shanske, et al.
Biochimica Et Biophysica Acta|December 10, 1992
Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCRS Simonetti, X Chen, S DiMauro, et al.
Human Mutation|January 1, 1994
An A-to-C substitution involving the translation initiation codon in a patient with myophosphorylase deficiency (McArdle's disease)S Tsujino, L A Rubin, S Shanske, et al.
Epilepsy Research. Supplement|January 1, 1991
Epilepsy in mitochondrial encephalomyopathiesS DiMauro, E Ricci, M Hirano, et al.
The Journal of Pediatrics|July 1, 1988
Fatal infantile cardiopathy caused by phosphorylase b kinase deficiencyS Servidei, L A Metlay, J Chodosh, et al.
Neurologic Clinics|February 1, 1989
Mitochondrial diseasesM Zeviani, E Bonilla, D C DeVivo, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy, other ocular myopathies, and progressive external ophthalmoplegiaL P Rowland, M Hirano, S DiMauro, et al.
Advances in Neurology|October 9, 1999
Mitochondrial genes for generalized epilepsiesS DiMauro, R Kulikova, K Tanji, et al.
Pageof 43