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DiMauro

Showing results (211-220 of 1,071) with videos related to

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Journal of Child Neurology|February 25, 2003
Mitochondrial disordersSalvatore DiMauro, Antoni L Andreu, Darryl C De Vivo
Muscle & Nerve. Supplement|January 1, 1995
Biochemistry and molecular genetics of human glycogenoses: an overviewS DiMauro, S Tsujino, S Shanske, et al.
Seminars in Neurology|October 20, 2001
Diseases of oxidative phosphorylation due to mtDNA mutationsS DiMauro, A L Andreu, O Musumeci, et al.
Brain : a Journal of Neurology|June 1, 1980
A distinct form of adult polyglucosan body disease with massive involvement of central and peripheral neuronal processes and astrocytes: a report of four cases and a review of the occurrence of polyglucosan bodies in other conditions such as Lafora's disease and normal ageingY Robitaille, S Carpenter, G Karpati, et al.
Journal of Ultrastructure Research|June 1, 1975
Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondriaE Bonilla, D L Schotland, S DiMauro, et al.
Archives of Biochemistry and Biophysics|May 1, 1971
Binding of enzymes of glycogen metabolism to glycogen in skeletal muscleS DiMauro, W Trojaborg, P Gambetti, et al.
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.
Pageof 108

Showing results (211-220 of 1,071) with videos related to

Sort By:
Pageof 108
Journal of Child Neurology|February 25, 2003
Mitochondrial disordersSalvatore DiMauro, Antoni L Andreu, Darryl C De Vivo
Muscle & Nerve. Supplement|January 1, 1995
Biochemistry and molecular genetics of human glycogenoses: an overviewS DiMauro, S Tsujino, S Shanske, et al.
Seminars in Neurology|October 20, 2001
Diseases of oxidative phosphorylation due to mtDNA mutationsS DiMauro, A L Andreu, O Musumeci, et al.
Brain : a Journal of Neurology|June 1, 1980
A distinct form of adult polyglucosan body disease with massive involvement of central and peripheral neuronal processes and astrocytes: a report of four cases and a review of the occurrence of polyglucosan bodies in other conditions such as Lafora's disease and normal ageingY Robitaille, S Carpenter, G Karpati, et al.
Journal of Ultrastructure Research|June 1, 1975
Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondriaE Bonilla, D L Schotland, S DiMauro, et al.
Archives of Biochemistry and Biophysics|May 1, 1971
Binding of enzymes of glycogen metabolism to glycogen in skeletal muscleS DiMauro, W Trojaborg, P Gambetti, et al.
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.
Pageof 108