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Results 1 - 10 of 25 for Parkinson disease 4
  1. Parkinson's disease 
    ... Parkinson disease 1 Genetic Testing Registry: Autosomal dominant Parkinson disease 4 Genetic Testing Registry: Autosomal dominant Parkinson disease 8 ...
    https://medlineplus.gov/genetics/condition/parkinsons-disease - Genetics
  2. LRRK2 gene 
    ... frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. Lancet. 2005 Jan 29-Feb 4;365(9457):412-5. doi: 10.1016/S0140- ... Wood NW. A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet. 2005 Jan 29-Feb 4;365(9457):415-6. doi: 10.1016/S0140- ...
    https://medlineplus.gov/genetics/gene/lrrk2 - Genetics
  3. UCHL1 gene 
    ... DB, Wood NW. UCHL-1 is not a Parkinson's disease susceptibility gene. Ann Neurol. 2006 Apr;59(4):627-33. doi: 10.1002/ana.20757. Citation ... WA; UCHL1 Global Genetics Consortium. UCHL1 is a Parkinson's disease susceptibility gene. Ann Neurol. 2004 Apr;55(4):512-21. doi: 10.1002/ana.20017. Erratum ...
    https://medlineplus.gov/genetics/gene/uchl1 - Genetics
  4. GBA gene 
    ... Baruch R. Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews. N Engl J Med. 2004 Nov 4;351(19):1972-7. doi: 10.1056/NEJMoa033277. ...
    https://medlineplus.gov/genetics/gene/gba - Genetics
  5. PRKN gene 
    ... Coelln R, Dawson VL, Dawson TM. Parkin-associated Parkinson's disease. Cell Tissue Res. 2004 Oct;318(1):175-84. doi: 10.1007/s00441-004-0924-4. Epub 2004 Jul 30. Citation on PubMed
    https://medlineplus.gov/genetics/gene/prkn - Genetics
  6. Wolff-Parkinson-White syndrome 
    ... N Engl J Med 2002 Jan 24;346(4):300. Citation on PubMed Light PE. Familial Wolff-Parkinson-White Syndrome: a disease of glycogen storage or ion channel dysfunction? J ...
    https://medlineplus.gov/.../condition/wolff-parkinson-white-syndrome - Genetics
  7. SNCA gene 
    ... balance and movement, are a characteristic feature of Parkinson's disease. More About This Health Condition ... Bonini NM, Giasson BI. Snaring the function of alpha-synuclein. Cell. 2005 Nov 4;123(3):359-61. doi: 10.1016/j. ...
    https://medlineplus.gov/genetics/gene/snca - Genetics
  8. PINK1 gene 
    ... 20251. Erratum In: Ann Neurol. 2004 Oct;56(4):603. Citation on PubMed Ibanez P, Lesage S, Lohmann E, Thobois S, De Michele G, Borg M, Agid Y, Durr A, Brice A; French Parkinson's Disease Genetics Study Group. Mutational analysis of the PINK1 ...
    https://medlineplus.gov/genetics/gene/pink1 - Genetics
  9. 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
  10. 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
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