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Results 1 - 7 of 7 for Parkinson disease 17
  1. ... Ziegler SG. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N Engl J Med. 2009 Oct 22;361(17):1651-61. doi: 10.1056/NEJMoa0901281. Citation on ...
  2. ... Rocca WA, Maraganore DM. UCHL1 is associated with Parkinson's disease: a case-unaffected sibling and case-unrelated control study. Neurosci Lett. 2005 Jun 10-17;381(1-2):131-4. doi: 10.1016/ ...
  3. ... Farrer MJ, Taylor JP, Gallo KA. LRRK2 in Parkinson's disease: protein domains and functional insights. Trends Neurosci. 2006 May;29(5):286-93. doi: 10.1016/j.tins.2006.03.006. Epub 2006 Apr 17. Citation on PubMed Ozelius LJ, Senthil G, Saunders- ...
  4. ... neurodegenerative diseases. Curr Top Dev Biol. 2004;60:17-54. doi: 10.1016/S0070-2153(04)60002-0. Citation on PubMed Nuytemans K, Theuns J, Cruts M, Van Broeckhoven C. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, ...
  5. ... in inherited cardiomyopathies: implications for kinase function and disease ... J Cardiovasc Electrophysiol. 2006 Jul;17(7):724-32. doi: 10.1111/j.1540- ...
  6. ... Zeng T, Glover JN, Vanderhyden B, Zhao C, Parkinson CA, Jimenez-Linan M, Bowtell DD, Mes-Masson ... mutations. Hum Mol Genet. 2011 Sep 1;20(17):3376-85. doi: 10.1093/hmg/ddr244. Epub ...
  7. ... 10.1159/000094771. Citation on PubMed Skibinski G, Parkinson NJ, Brown JM, Chakrabarti L, Lloyd SL, Hummerich ... in vitro. Hum Mol Genet. 2008 Jan 15;17(2):313-22. doi: 10.1093/hmg/ddm309. ...