Schapira AH - Search Results

1

Chaperone-mediated autophagy markers in Parkinson disease brains.

Alvarez-Erviti L, Rodriguez-Oroz MC, Cooper JM, Caballero C, Ferrer I, Obeso JA, Schapira AH. Alvarez-Erviti L, et al. Among authors: schapira ah. Arch Neurol. 2010 Dec;67(12):1464-72. doi: 10.1001/archneurol.2010.198. Epub 2010 Aug 9. Arch Neurol. 2010. PMID: 20697033

2

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.

3

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

4

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

5

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.

6

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 Free article.

7

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

8

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.

9

Irreversible inhibition of mitochondrial complex I by 1-methyl-4-phenylpyridinium: evidence for free radical involvement.

Cleeter MW, Cooper JM, Schapira AH. Cleeter MW, et al. Among authors: schapira ah. J Neurochem. 1992 Feb;58(2):786-9. doi: 10.1111/j.1471-4159.1992.tb09789.x. J Neurochem. 1992. PMID: 1729421

10

Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease.

Schapira AH, Mann VM, Cooper JM, Dexter D, Daniel SE, Jenner P, Clark JB, Marsden CD. Schapira AH, et al. J Neurochem. 1990 Dec;55(6):2142-5. doi: 10.1111/j.1471-4159.1990.tb05809.x. J Neurochem. 1990. PMID: 2121905

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