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Revue Neurologique
|
January 1, 1991
The molecular pathology of human respiratory chain defects
J A Morgan-Hughes, J M Cooper, A H Schapira, et al.
Journal of Neurochemistry
|
December 1, 1990
Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease
A H Schapira, V M Mann, J M Cooper, et al.
Journal of the Neurological Sciences
|
January 1, 1997
Raised serum nitrate and nitrite levels in patients with multiple sclerosis
G Giovannoni, S J Heales, N C Silver, et al.
Lancet (London, England)
|
March 5, 1988
Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency
A H Schapira, J M Cooper, J A Morgan-Hughes, et al.
Perfusion
|
February 19, 2014
The impact of cerebral embolization during infant cardiac surgery on neurodevelopmental outcomes at intermediate follow-up
R J Naik, J B Wagner, D Chowdhury, et al.
Journal of the Neurological Sciences
|
January 1, 1992
Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathy
S R Hammans, M G Sweeney, I J Holt, et al.
Biochimica Et Biophysica Acta
|
May 24, 1995
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype
J A Morgan-Hughes, M G Sweeney, J M Cooper, et al.
Biochemical Society Transactions
|
August 1, 1997
Nitric oxide, energy metabolism and neurological disease
S J Heales, J E Barker, V C Stewart, et al.
NMR in Biomedicine
|
December 1, 1994
Identification of ethanolamine in rat and gerbil brain tissue extracts by NMR spectroscopy
S C Smart, G B Fox, K L Allen, et al.
Journal of the Neurological Sciences
|
February 1, 1988
An animal model of mitochondrial myopathy: a biochemical and physiological investigation of rats treated in vivo with the NADH-CoQ reductase inhibitor, diphenyleneiodonium
J M Cooper, R K Petty, D J Hayes, et al.
Page
of 28
Search research articles
Search
Showing results (261-270 of 271) with videos related to
Sort By:
Page
of 28
Revue Neurologique
|
January 1, 1991
The molecular pathology of human respiratory chain defects
J A Morgan-Hughes, J M Cooper, A H Schapira, et al.
Journal of Neurochemistry
|
December 1, 1990
Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease
A H Schapira, V M Mann, J M Cooper, et al.
Journal of the Neurological Sciences
|
January 1, 1997
Raised serum nitrate and nitrite levels in patients with multiple sclerosis
G Giovannoni, S J Heales, N C Silver, et al.
Lancet (London, England)
|
March 5, 1988
Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency
A H Schapira, J M Cooper, J A Morgan-Hughes, et al.
Perfusion
|
February 19, 2014
The impact of cerebral embolization during infant cardiac surgery on neurodevelopmental outcomes at intermediate follow-up
R J Naik, J B Wagner, D Chowdhury, et al.
Journal of the Neurological Sciences
|
January 1, 1992
Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathy
S R Hammans, M G Sweeney, I J Holt, et al.
Biochimica Et Biophysica Acta
|
May 24, 1995
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype
J A Morgan-Hughes, M G Sweeney, J M Cooper, et al.
Biochemical Society Transactions
|
August 1, 1997
Nitric oxide, energy metabolism and neurological disease
S J Heales, J E Barker, V C Stewart, et al.
NMR in Biomedicine
|
December 1, 1994
Identification of ethanolamine in rat and gerbil brain tissue extracts by NMR spectroscopy
S C Smart, G B Fox, K L Allen, et al.
Journal of the Neurological Sciences
|
February 1, 1988
An animal model of mitochondrial myopathy: a biochemical and physiological investigation of rats treated in vivo with the NADH-CoQ reductase inhibitor, diphenyleneiodonium
J M Cooper, R K Petty, D J Hayes, et al.
Page
of 28