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Annals of Emergency Medicine|February 1, 1989
Thermal stability of prehospital medicationsT D Valenzuela, E A Criss, W M Hammargren, et al.Annals of Neurology|December 1, 1989
Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNAI J Holt, A E Harding, J M Cooper, et al.Brain Research|September 5, 1998
Increased inducible nitric oxide synthase protein but limited nitric oxide formation occurs in astrocytes of the hph-1 (tetrahydrobiopterin deficient) mouseJ E Barker, H M Strangward, M P Brand, et al.Revue Neurologique|January 1, 1991
The molecular pathology of human respiratory chain defectsJ 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 diseaseA 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 sclerosisG 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 deficiencyA 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-upR 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 myopathyS 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 phenotypeJ A Morgan-Hughes, M G Sweeney, J M Cooper, et al.Pageof 27