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Results 1 - 10 of 25 for Parkinson disease 1
  1. Parkinson's disease 
    ... PD Primary parkinsonism Genetic Testing Registry: Autosomal dominant Parkinson disease 1 Genetic Testing Registry: Autosomal dominant Parkinson disease 4 ...
    https://medlineplus.gov/genetics/condition/parkinsons-disease - Genetics
  2. PARK7 gene 
    ... Sleiman PM, Healy DG, Wood NW. Causes of Parkinson's disease: genetics of DJ-1. Cell Tissue Res. 2004 Oct;318(1):185- ... 21. Citation on PubMed da Costa CA. DJ-1: a newcomer in Parkinson's disease pathology. Curr Mol Med. 2007 Nov;7(7): ...
    https://medlineplus.gov/genetics/gene/park7 - Genetics
  3. PRKN gene 
    ... The role of parkin in familial and sporadic Parkinson's disease. Mov Disord. 2010;25 Suppl 1(0 1):S32-9. doi: 10.1002/mds. ... Coelln R, Dawson VL, Dawson TM. Parkin-associated Parkinson's disease. Cell Tissue Res. 2004 Oct;318(1):175-84. doi: 10.1007/s00441-004-0924- ...
    https://medlineplus.gov/genetics/gene/prkn - Genetics
  4. UCHL1 gene 
    ... JL, Revesz T, Goldstein DB, Wood NW. UCHL-1 is not a Parkinson's disease susceptibility gene. Ann Neurol. 2006 Apr;59(4): ... terminal esterase L1 gene (UCHL1) S18Y variant and Parkinson's Disease: a HuGE review and meta-analysis. Am J Epidemiol. 2009 Dec 1;170(11):1344-57. doi: 10.1093/aje/ ...
    https://medlineplus.gov/genetics/gene/uchl1 - Genetics
  5. 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/j.febslet. ...
    https://medlineplus.gov/genetics/gene/snca - Genetics
  6. LRRK2 gene 
    ... This particular mutation has also been reported in 1 to 3 percent of sporadic Parkinson's disease cases, in which there is no family history ... Wood NW. A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet. 2005 Jan 29-Feb ... Citation on PubMed Guo L, Wang W, Chen ...
    https://medlineplus.gov/genetics/gene/lrrk2 - Genetics
  7. PINK1 gene 
    ... 1 Tests of PINK1 PubMed PTEN-INDUCED KINASE 1; PINK1 NCBI Gene ClinVar Abou-Sleiman PM, Muqit MM, Wood NW. Expanding insights of mitochondrial dysfunction in Parkinson's disease. Nat Rev Neurosci. 2006 Mar;7(3):207- ...
    https://medlineplus.gov/genetics/gene/pink1 - Genetics
  8. Wolff-Parkinson-White syndrome 
    ... 300. Citation on PubMed Light PE. Familial Wolff-Parkinson-White Syndrome: a disease of glycogen storage or ion channel dysfunction? J Cardiovasc Electrophysiol. 2006 May;17 Suppl 1:S158-S161. doi: 10.1111/j.1540-8167. ...
    https://medlineplus.gov/.../condition/wolff-parkinson-white-syndrome - Genetics
  9. GBA gene 
    ... Ziegler SG. Multicenter analysis of glucocerebrosidase mutations in Parkinson's ... disorder. Mol Genet Metab. 2004 Sep-Oct;83(1-2):6-15. doi: 10.1016/j.ymgme. ...
    https://medlineplus.gov/genetics/gene/gba - Genetics
  10. Congenital mirror movement disorder 
    ... life in people with neurodegenerative disorders such as Parkinson's disease. Mirror ... prevalence is thought to be less than 1 in 1 million. Researchers suggest that some mildly ...
    https://medlineplus.gov/.../congenital-mirror-movement-disorder - Genetics
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