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Parkinson disease 2
- ... disease 7 Genetic Testing Registry: Autosomal recessive juvenile Parkinson disease 2 Genetic Testing Registry: Autosomal recessive Parkinson disease 14 ...
- ... leading to tumor formation. AR-JP PARK2 parkin Parkinson disease (autosomal recessive, juvenile) 2, parkin parkinson protein 2, E3 ubiquitin protein ligase ( ...
- ... or nerves in the intestinal tract, such as Parkinson's disease, type 2 diabetes, various types of muscular dystrophy, or Kawasaki ...
- ... MR. The role of leucine-rich repeat kinase 2 (LRRK2) in Parkinson's disease. Nat Rev Neurosci. 2010 Dec;11(12):791- ... Wang W, Chen SG. Leucine-rich repeat kinase 2: relevance to Parkinson's disease. Int J Biochem Cell Biol. 2006;38(9): ...
- ... the UCHL1 gene may increase the risk of Parkinson's disease. This mutation has been reported in two siblings with the disease. The mutation replaces the ...
- ... been found to increase the risk of developing Parkinson's disease, although they do not appear to be a direct cause of the disease.Researchers have described two types of alterations of the SNCA gene in ...
- ... people with Danon disease is called the Wolff-Parkinson-White syndrome pattern.Skeletal myopathy occurs in most people with Danon disease who have one Y chromosome and in some affected individuals with two X chromosomes. The weakness typically occurs in the ...
- ... the glucocerebrosidase gene are associated with early-onset Parkinson disease. ... J Inherit Metab Dis. 2001;24 Suppl 2:106-21; discussion 87-8. doi: 10.1023/ ...
- ... in inherited cardiomyopathies: implications for kinase function and disease pathogenesis. J Mol Cell ... syndrome. J Cardiovasc Electrophysiol. 2006 Jul;17( ...
- ... 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, ...