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Parkinson disease 5
- ... frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. Lancet. 2005 Jan 29-Feb 4;365(9457):412-5. doi: 10.1016/S0140-6736(05)17829-5. ...
- ... transporter: a possible role in the pathogenesis of Parkinson's disease. FEBS Lett. 2004 May 7;565(1-3):1-5. doi: 10.1016/j.febslet.2004.03.063. ...
- ... K, Chiba T, Tanaka K, Suzuki T. Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase. Nat Genet. 2000 Jul;25(3):302-5. doi: 10.1038/77060. Citation on PubMed Veeriah ...
- ... gene mutation is a true risk factor for Parkinson's disease, because it has been identified in only one family. More About This Health Condition MSY1 neuron cytoplastic protein 9.5 PARK5 PGP9.5 ubiquitin carboxyl-terminal esterase L1 ( ...
- ... in inherited cardiomyopathies: implications for kinase function and disease pathogenesis. J Mol Cell ... syndrome. J Cardiovasc Electrophysiol. 2006 Jul;17( ...
- ... doi: 10.1093/hmg/ddi377. Epub 2005 Oct 5. Citation on PubMed Valente ... Parkinson's disease caused by mutations in PINK1. Science. 2004 May ...
- ... with lewy bodies. Arch Neurol. 2009 May;66(5):578-83. doi: ... with early-onset Parkinson disease. Neurology. 2007 Sep 18;69(12):1270-7. ...
- ... This Health Condition DJ-1 DJ1 PARK7_HUMAN Parkinson disease (autosomal recessive, early onset) 7 parkinson protein 7 ... Cruts M, Van Broeckhoven C. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, ...
- ... as the more common Alzheimer's disease and Parkinson's disease, also are associated with changes in brain iron ...
- ... attention and mood; and movement problems characteristic of Parkinson's disease such as rigidity of limbs, tremors, and impaired ... of numerous clinical conditions including HSV-1 corneal disease. Exp Eye Res. 2007 May;84(5):801-11. doi: 10.1016/j.exer.2006. ...