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Muscle & Nerve
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May 1, 1994
Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophy
M Moggio, A Prelle, G Fagiolari, et al.
Annals of Neurology
|
July 1, 1990
Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies
M Zeviani, C Gellera, M Pannacci, et al.
Journal of Neurology
|
February 1, 1992
Dystrophin deficiency in a case of congenital myopathy
A Prelle, R Medori, M Moggio, et al.
Journal of the Neurological Sciences
|
May 1, 1990
Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues
C Ponzetto, N Bresolin, A Bordoni, et al.
Neurology
|
August 1, 1991
Dystrophin deficiency in young girls with sporadic myopathy and normal karyotype
C Minetti, H W Chang, R Medori, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 13, 2006
Diffusion anisotropy of the cervical cord is strictly associated with disability in amyotrophic lateral sclerosis
P Valsasina, F Agosta, B Benedetti, et al.
Journal of the Neurological Sciences
|
July 1, 1993
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis
A Prelle, M Moggio, N Checcarelli, et al.
Journal of Neurology
|
September 1, 1995
Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic study
C Mariotti, G Uziel, F Carrara, et al.
Annals of the New York Academy of Sciences
|
January 1, 1986
Cytochrome oxidase deficiency: clinical and biochemical heterogeneity
S DiMauro, M Zeviani, S Servidei, et al.
Advances in Neurology
|
January 1, 1988
Biochemical and molecular aspects of cytochrome C oxidase deficiency
S DiMauro, M Zeviani, S Servidei, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 84) with videos related to
Sort By:
Page
of 9
Muscle & Nerve
|
May 1, 1994
Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophy
M Moggio, A Prelle, G Fagiolari, et al.
Annals of Neurology
|
July 1, 1990
Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies
M Zeviani, C Gellera, M Pannacci, et al.
Journal of Neurology
|
February 1, 1992
Dystrophin deficiency in a case of congenital myopathy
A Prelle, R Medori, M Moggio, et al.
Journal of the Neurological Sciences
|
May 1, 1990
Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues
C Ponzetto, N Bresolin, A Bordoni, et al.
Neurology
|
August 1, 1991
Dystrophin deficiency in young girls with sporadic myopathy and normal karyotype
C Minetti, H W Chang, R Medori, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 13, 2006
Diffusion anisotropy of the cervical cord is strictly associated with disability in amyotrophic lateral sclerosis
P Valsasina, F Agosta, B Benedetti, et al.
Journal of the Neurological Sciences
|
July 1, 1993
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis
A Prelle, M Moggio, N Checcarelli, et al.
Journal of Neurology
|
September 1, 1995
Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic study
C Mariotti, G Uziel, F Carrara, et al.
Annals of the New York Academy of Sciences
|
January 1, 1986
Cytochrome oxidase deficiency: clinical and biochemical heterogeneity
S DiMauro, M Zeviani, S Servidei, et al.
Advances in Neurology
|
January 1, 1988
Biochemical and molecular aspects of cytochrome C oxidase deficiency
S DiMauro, M Zeviani, S Servidei, et al.
Page
of 9