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Results 1 - 10 of 24 for Parkinson disease 2
  1. ... disease 7 Genetic Testing Registry: Autosomal recessive juvenile Parkinson disease 2 Genetic Testing Registry: Autosomal recessive Parkinson disease 14 ...
  2. ... leading to tumor formation. AR-JP PARK2 parkin Parkinson disease (autosomal recessive, juvenile) 2, parkin parkinson protein 2, E3 ubiquitin protein ligase ( ...
  3. ... or nerves in the intestinal tract, such as Parkinson's disease, type 2 diabetes, various types of muscular dystrophy, or Kawasaki ...
  4. ... 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): ...
  5. ... 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 ...
  6. ... 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 ...
  7. ... 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 ...
  8. ... 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/ ...
  9. ... in inherited cardiomyopathies: implications for kinase function and disease pathogenesis. J Mol Cell ... syndrome. J Cardiovasc Electrophysiol. 2006 Jul;17( ...
  10. ... 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, ...
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