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Annals of Neurology
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March 1, 1978
Studies of fragmented sarcoplasmic reticulum from human skeletal muscle
A Scarpa, S DiMauro, E Bonilla, et al.
Brain Pathology (Zurich, Switzerland)
|
April 1, 1995
Myoclonic epilepsy with ragged-red fibers (MERRF): an immunohistochemical study of the brain
M Sparaco, E A Schon, S DiMauro, et al.
Journal of Neuropathology and Experimental Neurology
|
January 1, 1993
Neuropathology of mitochondrial encephalomyopathies due to mitochondrial DNA defects
M Sparaco, E Bonilla, S DiMauro, et al.
The Journal of Biological Chemistry
|
November 15, 1988
Isolation of a cDNA encoding the B isozyme of human phosphoglycerate mutase (PGAM) and characterization of the PGAM gene family
S Sakoda, S Shanske, S DiMauro, et al.
Transactions of the American Neurological Association
|
January 1, 1977
McArdle disease: the mysterious appearance of phosphorylase activity in cells that ought to lack the genetic program. A fetal isoenzyme?
S DiMauro, S Arnold, A Miranda, et al.
Neurology
|
July 1, 1997
Heterogeneous clinical presentation of the mtDNA NARP/T8993G mutation
F M Santorelli, K Tanji, S Shanske, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
Biochemistry and molecular genetics of human glycogenoses: an overview
S DiMauro, S Tsujino, S Shanske, et al.
Seminars in Neurology
|
October 20, 2001
Diseases of oxidative phosphorylation due to mtDNA mutations
S DiMauro, A L Andreu, O Musumeci, et al.
Journal of Ultrastructure Research
|
June 1, 1975
Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondria
E 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 muscle
S DiMauro, W Trojaborg, P Gambetti, et al.
Page
of 43
Search research articles
Search
Showing results (81-90 of 421) with videos related to
Sort By:
Page
of 43
Annals of Neurology
|
March 1, 1978
Studies of fragmented sarcoplasmic reticulum from human skeletal muscle
A Scarpa, S DiMauro, E Bonilla, et al.
Brain Pathology (Zurich, Switzerland)
|
April 1, 1995
Myoclonic epilepsy with ragged-red fibers (MERRF): an immunohistochemical study of the brain
M Sparaco, E A Schon, S DiMauro, et al.
Journal of Neuropathology and Experimental Neurology
|
January 1, 1993
Neuropathology of mitochondrial encephalomyopathies due to mitochondrial DNA defects
M Sparaco, E Bonilla, S DiMauro, et al.
The Journal of Biological Chemistry
|
November 15, 1988
Isolation of a cDNA encoding the B isozyme of human phosphoglycerate mutase (PGAM) and characterization of the PGAM gene family
S Sakoda, S Shanske, S DiMauro, et al.
Transactions of the American Neurological Association
|
January 1, 1977
McArdle disease: the mysterious appearance of phosphorylase activity in cells that ought to lack the genetic program. A fetal isoenzyme?
S DiMauro, S Arnold, A Miranda, et al.
Neurology
|
July 1, 1997
Heterogeneous clinical presentation of the mtDNA NARP/T8993G mutation
F M Santorelli, K Tanji, S Shanske, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
Biochemistry and molecular genetics of human glycogenoses: an overview
S DiMauro, S Tsujino, S Shanske, et al.
Seminars in Neurology
|
October 20, 2001
Diseases of oxidative phosphorylation due to mtDNA mutations
S DiMauro, A L Andreu, O Musumeci, et al.
Journal of Ultrastructure Research
|
June 1, 1975
Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondria
E 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 muscle
S DiMauro, W Trojaborg, P Gambetti, et al.
Page
of 43