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Results 1 - 9 of 9 for Parkinson disease 9
  1. Parkinson's disease 
    ... nrg1831. Citation on PubMed Gasser T. Genetics of Parkinson's disease. Curr Opin Neurol. 2005 Aug;18(4):363-9. doi: 10.1097/01.wco.0000170951.08924.3d. ...
    https://medlineplus.gov/genetics/condition/parkinsons-disease - Genetics
  2. 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
  3. Infantile neuroaxonal dystrophy 
    ... as the more common Alzheimer's disease and Parkinson's disease, also are associated with changes in brain iron ... iron accumulation, PLA2G6-related Seitelberger disease Seitelberger's disease ... with infantile neuroaxonal dystrophy but not dystonia-parkinsonism. PLoS One. 2010 Sep 23;5(9):e12897. doi: 10.1371/journal.pone.0012897. Citation ...
    https://medlineplus.gov/.../infantile-neuroaxonal-dystrophy - Genetics
  4. Restless legs syndrome 
    ... disease, diabetes mellitus, multiple sclerosis, rheumatoid arthritis, and Parkinson's disease. People with low iron levels associated with a ...
    https://medlineplus.gov/genetics/condition/restless-legs-syndrome - Genetics
  5. Intestinal pseudo-obstruction 
    ... or nerves in the intestinal tract, such as Parkinson's disease, type 2 diabetes, various types of muscular dystrophy, ...
    https://medlineplus.gov/.../condition/intestinal-pseudo-obstruction - Genetics
  6. Congenital mirror movement disorder 
    ... 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
  7. 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 ... J Am Acad Nurse Pract. 2004 Sep;16(9):378-83. doi: 10.1111/j.1745-7599.2004.tb00387.x. Citation on PubMed
    https://medlineplus.gov/.../condition/wolff-parkinson-white-syndrome - Genetics
  8. Multiple system atrophy 
    ... PubMed ... system atrophy. PLoS One. 2009 Sep 22;4(9):e7114. doi: 10.1371/journal.pone.0007114. Citation ...
    https://medlineplus.gov/genetics/condition/multiple-system-atrophy - Genetics
  9. CHMP2B-related frontotemporal dementia 
    ... gov/books/NBK1199/ Citation on PubMed Skibinski G, Parkinson NJ, Brown JM, Chakrabarti L, Lloyd SL, Hummerich ...
    https://medlineplus.gov/.../chmp2b-related-frontotemporal-dementia - Genetics