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509 results

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Page 1
Mitochondria and degenerative disorders.
Orth M, Schapira AH. Orth M, et al. Am J Med Genet. 2001 Spring;106(1):27-36. doi: 10.1002/ajmg.1425. Am J Med Genet. 2001. PMID: 11579422 Review.
Mitochondrial involvement in Parkinson's disease.
Orth M, Schapira AH. Orth M, et al. Neurochem Int. 2002 May;40(6):533-41. doi: 10.1016/s0197-0186(01)00124-3. Neurochem Int. 2002. PMID: 11850110 Review. No abstract available.
Models of Parkinson's disease.
Orth M, Tabrizi SJ. Orth M, et al. Mov Disord. 2003 Jul;18(7):729-37. doi: 10.1002/mds.10447. Mov Disord. 2003. PMID: 12815651 Review.
Discrepancies in reporting the CAG repeat lengths for Huntington's disease.
Quarrell OW, Handley O, O'Donovan K, Dumoulin C, Ramos-Arroyo M, Biunno I, Bauer P, Kline M, Landwehrmeyer GB; European Huntington’s Disease Network. Quarrell OW, et al. Eur J Hum Genet. 2012 Jan;20(1):20-6. doi: 10.1038/ejhg.2011.136. Epub 2011 Aug 3. Eur J Hum Genet. 2012. PMID: 21811303 Free PMC article.
The neuroanatomy of subthreshold depressive symptoms in Huntington's disease: a combined diffusion tensor imaging (DTI) and voxel-based morphometry (VBM) study.
Sprengelmeyer R, Orth M, Müller HP, Wolf RC, Grön G, Depping MS, Kassubek J, Justo D, Rees EM, Haider S, Cole JH, Hobbs NZ, Roos RA, Dürr A, Tabrizi SJ, Süssmuth SD, Landwehrmeyer GB. Sprengelmeyer R, et al. Among authors: orth m. Psychol Med. 2014 Jul;44(9):1867-78. doi: 10.1017/S003329171300247X. Epub 2013 Oct 7. Psychol Med. 2014. PMID: 24093462
509 results