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Mitochondrial respiratory chain disorders I: mitochondrial DNA defects.
Leonard JV, Schapira AH. Leonard JV, et al. Among authors: schapira ah. Lancet. 2000 Jan 22;355(9200):299-304. doi: 10.1016/s0140-6736(99)05225-3. Lancet. 2000. PMID: 10675086 Review.
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease.
Smith CA, Gough AC, Leigh PN, Summers BA, Harding AE, Maraganore DM, Sturman SG, Schapira AH, Williams AC, et al. Smith CA, et al. Among authors: schapira ah. Lancet. 1992 Jun 6;339(8806):1375-7. doi: 10.1016/0140-6736(92)91196-f. Lancet. 1992. PMID: 1350805
Mitochondrial function in neurodegeneration and ageing.
Schapira AH, Cooper JM. Schapira AH, et al. Mutat Res. 1992 Sep;275(3-6):133-43. doi: 10.1016/0921-8734(92)90018-k. Mutat Res. 1992. PMID: 1383756 Review.
Analyses of mitochondrial respiratory chain function and mitochondrial DNA deletion in human skeletal muscle: effect of ageing.
Cooper JM, Mann VM, Schapira AH. Cooper JM, et al. Among authors: schapira ah. J Neurol Sci. 1992 Nov;113(1):91-8. doi: 10.1016/0022-510x(92)90270-u. J Neurol Sci. 1992. PMID: 1469460
Platelet mitochondrial function in Parkinson's disease. The Royal Kings and Queens Parkinson Disease Research Group.
Krige D, Carroll MT, Cooper JM, Marsden CD, Schapira AH. Krige D, et al. Among authors: schapira ah. Ann Neurol. 1992 Dec;32(6):782-8. doi: 10.1002/ana.410320612. Ann Neurol. 1992. PMID: 1471869
Mitochondrial function in Parkinson's disease. The Royal Kings and Queens Parkinson's Disease Research Group.
Schapira AH, Mann VM, Cooper JM, Krige D, Jenner PJ, Marsden CD. Schapira AH, et al. Ann Neurol. 1992;32 Suppl:S116-24. doi: 10.1002/ana.410320720. Ann Neurol. 1992. PMID: 1510369 Review.
Quantitation of a mitochondrial DNA deletion in Parkinson's disease.
Mann VM, Cooper JM, Schapira AH. Mann VM, et al. Among authors: schapira ah. FEBS Lett. 1992 Mar 16;299(3):218-22. doi: 10.1016/0014-5793(92)80118-z. FEBS Lett. 1992. PMID: 1544498
Brain, skeletal muscle and platelet homogenate mitochondrial function in Parkinson's disease.
Mann VM, Cooper JM, Krige D, Daniel SE, Schapira AH, Marsden CD. Mann VM, et al. Among authors: schapira ah. Brain. 1992 Apr;115 ( Pt 2):333-42. doi: 10.1093/brain/115.2.333. Brain. 1992. PMID: 1606472
Human mitochondrial complex I dysfunction.
Cooper JM, Mann VM, Krige D, Schapira AH. Cooper JM, et al. Among authors: schapira ah. Biochim Biophys Acta. 1992 Jul 17;1101(2):198-203. doi: 10.1016/s0005-2728(05)80019-2. Biochim Biophys Acta. 1992. PMID: 1633185 Review.
The molecular pathology of human respiratory chain defects.
Morgan-Hughes JA, Cooper JM, Schapira AH, Sweeny M, Holt IJ, Harding AE, Clark JB. Morgan-Hughes JA, et al. Among authors: schapira ah. Rev Neurol (Paris). 1991;147(6-7):450-4. Rev Neurol (Paris). 1991. PMID: 1962049 Review.
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