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Neurology
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June 1, 1988
Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10
N Bresolin, L Bet, A Binda, et al.
Journal of the Neurological Sciences
|
May 1, 1994
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy
N Checcarelli, A Prelle, M Moggio, et al.
Neurology
|
October 1, 1987
Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features
D Biral, E Damiani, E Scarpini, et al.
Human Mutation
|
November 21, 2002
Molecular characterisation of GSD III subjects and identification of six novel mutations in AGL
S Lucchiari, M A Donati, R Parini, et al.
Journal of Neurology
|
December 1, 1991
The natural history and results of surgery in 50 cases of syringomyelia
C Mariani, M G Cislaghi, S Barbieri, et al.
Neuroscience Letters
|
October 29, 1993
Myelin protein transcripts increase in experimental diabetic neuropathy
A M Conti, M L Malosio, E Scarpini, et al.
Brain : a Journal of Neurology
|
January 29, 2000
Synergistic effect of beta-amyloid protein and interferon gamma on nitric oxide production by C2C12 muscle cells
P Baron, D Galimberti, L Meda, et al.
Journal of Neurology
|
February 1, 1995
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility
I Moroni, E F Gonano, G P Comi, et al.
Journal of the Neurological Sciences
|
May 1, 1994
Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile
A Fassati, A Bordoni, P Amboni, et al.
Applied Neurophysiology
|
January 1, 1988
Primary cultures of human caudate nucleus
V Silani, G Pezzoli, E Motti, et al.
Page
of 24
Search research articles
Search
Showing results (151-160 of 234) with videos related to
Sort By:
Page
of 24
Neurology
|
June 1, 1988
Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10
N Bresolin, L Bet, A Binda, et al.
Journal of the Neurological Sciences
|
May 1, 1994
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy
N Checcarelli, A Prelle, M Moggio, et al.
Neurology
|
October 1, 1987
Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features
D Biral, E Damiani, E Scarpini, et al.
Human Mutation
|
November 21, 2002
Molecular characterisation of GSD III subjects and identification of six novel mutations in AGL
S Lucchiari, M A Donati, R Parini, et al.
Journal of Neurology
|
December 1, 1991
The natural history and results of surgery in 50 cases of syringomyelia
C Mariani, M G Cislaghi, S Barbieri, et al.
Neuroscience Letters
|
October 29, 1993
Myelin protein transcripts increase in experimental diabetic neuropathy
A M Conti, M L Malosio, E Scarpini, et al.
Brain : a Journal of Neurology
|
January 29, 2000
Synergistic effect of beta-amyloid protein and interferon gamma on nitric oxide production by C2C12 muscle cells
P Baron, D Galimberti, L Meda, et al.
Journal of Neurology
|
February 1, 1995
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility
I Moroni, E F Gonano, G P Comi, et al.
Journal of the Neurological Sciences
|
May 1, 1994
Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile
A Fassati, A Bordoni, P Amboni, et al.
Applied Neurophysiology
|
January 1, 1988
Primary cultures of human caudate nucleus
V Silani, G Pezzoli, E Motti, et al.
Page
of 24