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Results 1 - 10 of 31 for Parkinson disease
  1. Parkinson's disease 
    Parkinson's disease is a progressive disorder of the nervous system. The disorder affects several regions of the brain, especially an area called the substantia ...
    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 ... Cruts M, Van Broeckhoven C. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, ...
    https://medlineplus.gov/genetics/gene/park7 - Genetics
  3. PINK1 gene 
    ... 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, ...
    https://medlineplus.gov/genetics/gene/pink1 - Genetics
  4. PRKN gene 
    ... leading to tumor formation. AR-JP PARK2 parkin Parkinson disease (autosomal recessive, juvenile) 2, parkin parkinson protein 2, ... K, Chiba T, Tanaka K, Suzuki T. Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase. ...
    https://medlineplus.gov/genetics/gene/prkn - Genetics
  5. GBA1 gene 
    ... the glucocerebrosidase gene are associated with early-onset Parkinson disease. Neurology. 2007 Sep 18;69(12):1270-7. ... Sidransky E. The role of glucocerebrosidase mutations in Parkinson disease and Lewy body disorders. Curr Neurol Neurosci Rep. ...
    https://medlineplus.gov/genetics/gene/gba1 - Genetics
  6. LRRK2 gene 
    ... Cookson MR. Role of LRRK2 kinase dysfunction in Parkinson disease. Expert Rev Mol Med. 2011 Jun 13;13: ...
    https://medlineplus.gov/genetics/gene/lrrk2 - Genetics
  7. SNCA gene 
    ... Cruts M, Van Broeckhoven C. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, ... transporter: a possible role in the pathogenesis of Parkinson's disease. FEBS Lett. 2004 May 7;565(1-3): ...
    https://medlineplus.gov/genetics/gene/snca - Genetics
  8. UCHL1 gene 
    ... UCHL1 gene may reduce the risk of developing Parkinson's disease, a condition characterized by progressive problems with movement ... having the S18Y polymorphism may help protect against Parkinson's disease, particularly in young adults. However, other studies have ...
    https://medlineplus.gov/genetics/gene/uchl1 - Genetics
  9. Essential tremor 
    ... from other disorders or known causes, such as Parkinson's disease or head trauma. Essential tremor usually occurs alone, ... than average risk of developing neurological conditions including Parkinson's disease or sensory problems such as hearing loss, especially ...
    https://medlineplus.gov/genetics/condition/essential-tremor - Genetics
  10. Tyrosine hydroxylase deficiency 
    ... symptoms may resemble those seen in people with Parkinson disease: stiffness of the muscles in the arms and ...
    https://medlineplus.gov/.../tyrosine-hydroxylase-deficiency - Genetics
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