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Journal Abstract Search
352 related items for PubMed ID: 19076426
1. A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease. Khusnutdinova E, Gilyazova I, Ruiz-Pesini E, Derbeneva O, Khusainova R, Khidiyatova I, Magzhanov R, Wallace DC. Ann N Y Acad Sci; 2008 Dec; 1147():1-20. PubMed ID: 19076426 [Abstract] [Full Text] [Related]
11. Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family. Swerdlow RH, Parks JK, Davis JN, Cassarino DS, Trimmer PA, Currie LJ, Dougherty J, Bridges WS, Bennett JP, Wooten GF, Parker WD. Ann Neurol; 1998 Dec 08; 44(6):873-81. PubMed ID: 9851431 [Abstract] [Full Text] [Related]
12. Mitochondrial DNA polymorphisms associated with longevity in a Finnish population. Niemi AK, Hervonen A, Hurme M, Karhunen PJ, Jylhä M, Majamaa K. Hum Genet; 2003 Jan 08; 112(1):29-33. PubMed ID: 12483296 [Abstract] [Full Text] [Related]
13. Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease. Luoma PT, Eerola J, Ahola S, Hakonen AH, Hellström O, Kivistö KT, Tienari PJ, Suomalainen A. Neurology; 2007 Sep 11; 69(11):1152-9. PubMed ID: 17846414 [Abstract] [Full Text] [Related]
14. Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? Mancuso M, Conforti FL, Rocchi A, Tessitore A, Muglia M, Tedeschi G, Panza D, Monsurrò M, Sola P, Mandrioli J, Choub A, DelCorona A, Manca ML, Mazzei R, Sprovieri T, Filosto M, Salviati A, Valentino P, Bono F, Caracciolo M, Simone IL, La Bella V, Majorana G, Siciliano G, Murri L, Quattrone A. Neurosci Lett; 2004 Nov 23; 371(2-3):158-62. PubMed ID: 15519748 [Abstract] [Full Text] [Related]