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Parkinson disease 6
- ... 8 Genetic Testing Registry: Autosomal recessive early-onset Parkinson disease 6 Genetic Testing Registry: Autosomal recessive early-onset Parkinson ... disease 17 Parkinson disease 2, autosomal recessive juvenile Parkinson disease 6, autosomal recessive early-onset National Organization for Rare ...
- ... The role of pathogenic DJ-1 mutations in Parkinson's disease. Ann Neurol. 2003 Sep;54(3):283-6. doi: 10.1002/ana.10675. Citation on PubMed ... Sleiman PM, Healy DG, Wood NW. Causes of Parkinson's disease: genetics of DJ-1. Cell Tissue Res. ... Epub 2004 Jun 26. Citation on PubMed Bonifati ...
- ... Wood NW. A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet. 2005 Jan 29-Feb 4;365(9457):415-6. doi: 10.1016/S0140-6736(05)17830-1. ... JJ. The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: ... evidence. Hum Genet. 2007 Feb;120(6):857-63. doi: 10.1007/s00439-006-0268- ...
- ... WA; UCHL1 Global Genetics Consortium. UCHL1 is a Parkinson's disease susceptibility gene. Ann Neurol. 2004 Apr;55(4):512-21. doi: 10.1002/ana.20017. Erratum In: Ann Neurol. 2004 Jun;55(6):899. Toda, Taksushi [corrected to Toda, Tatsushi]. Citation ...
- ... CA, McKenna WJ. Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history. J Am Coll Cardiol. 2005 Mar 15;45(6):922-30. doi: 10.1016/j.jacc.2004. ...
- ... Ziegler SG. Multicenter analysis of glucocerebrosidase mutations in Parkinson's ... Mol Genet Metab. 2004 Sep-Oct;83(1-2):6-15. doi: 10.1016/j.ymgme.2004.08. ...
- ... Hilker R, Kramer PL, Klein C. Lewy body Parkinson's disease in a large pedigree with ... leprae. Semin Immunol. 2006 Dec;18(6):404-10. doi: 10.1016/j.smim.2006. ...
- ... 1 antitrypsin deficiency Celiac disease Familial ... disease Lactose intolerance Cheek dimples Eye color ...
- ... backgrounds. More About This Health Condition At ... of Parkinson's disease (described below) such as rigidity of limbs, tremors, ...
- ... and autophagy in mitochondrial quality control: implications for Parkinson disease. Hum Mol Genet. 2010 Apr 15;19(R1): ... Cruts M, Van Broeckhoven C. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, ...