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Results 1 - 10 of 21 for Parkinson disease 7
  1. Parkinson's disease 
    ... 6 Genetic Testing Registry: Autosomal recessive early-onset Parkinson disease 7 Genetic Testing Registry: Autosomal recessive juvenile Parkinson disease ...
    https://medlineplus.gov/genetics/condition/parkinsons-disease - Genetics
  2. PARK7 gene 
    ... This Health Condition DJ-1 DJ1 PARK7_HUMAN Parkinson disease (autosomal recessive, early onset) 7 parkinson protein 7 Tests of PARK7 PubMed ONCOGENE ... da Costa CA. DJ-1: a newcomer in Parkinson's disease pathology. Curr Mol Med. 2007 Nov;7(7):650-7. doi: 10.2174/156652407782564426. Citation ...
    https://medlineplus.gov/genetics/gene/park7 - Genetics
  3. LRRK2 gene 
    ... a common LRRK2 gene mutation in 3 to 7 percent of familial Parkinson's disease cases. This mutation replaces the amino acid glycine ... of leucine-rich repeat kinase 2 (LRRK2) in Parkinson's disease. Nat Rev Neurosci. 2010 Dec;11(12):791-7. doi: 10.1038/nrn2935. Epub 2010 Nov 19. ...
    https://medlineplus.gov/genetics/gene/lrrk2 - Genetics
  4. SNCA gene 
    ... transporter: a possible role in the pathogenesis of Parkinson's disease. FEBS Lett. 2004 May 7;565(1-3):1-5. doi: 10.1016/ ...
    https://medlineplus.gov/genetics/gene/snca - Genetics
  5. PINK1 gene 
    ... Wood NW. Expanding insights of mitochondrial dysfunction in Parkinson's disease. Nat Rev Neurosci. 2006 Mar;7(3):207-19. doi: 10.1038/nrn1868. Citation ...
    https://medlineplus.gov/genetics/gene/pink1 - Genetics
  6. GBA gene 
    ... the glucocerebrosidase gene are associated with early-onset Parkinson disease. Neurology. 2007 Sep 18;69(12):1270-7. doi: 10.1212/01.wnl.0000276989.17578.02. ...
    https://medlineplus.gov/genetics/gene/gba - Genetics
  7. PRKN gene 
    ... Wood NW. Expanding insights of mitochondrial dysfunction in Parkinson's disease. Nat Rev Neurosci. 2006 Mar;7(3):207-19. doi: 10.1038/nrn1868. Citation ...
    https://medlineplus.gov/genetics/gene/prkn - Genetics
  8. UCHL1 gene 
    ... enzymatic activities that affect alpha-synuclein degradation and Parkinson's disease susceptibility. Cell. 2002 Oct 18;111(2):209-18. doi: 10.1016/s0092-8674(02)01012-7. Citation on PubMed Maraganore DM, Lesnick TG, Elbaz ...
    https://medlineplus.gov/genetics/gene/uchl1 - Genetics
  9. Congenital mirror movement disorder 
    ... of young children and typically disappear before age 7. They can also develop later in life in people with neurodegenerative disorders such as Parkinson's disease. Mirror movements may also be present in certain ...
    https://medlineplus.gov/.../congenital-mirror-movement-disorder - Genetics
  10. PRKAG2 gene 
    ... maintaining the heart's normal rhythm. ... cardiomyopathy, a form of heart disease that enlarges and weakens the heart (cardiac) muscle. ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
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