Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 19 for Parkinsonism
  1. ... 1 gene associated with autosomal recessive early-onset parkinsonism. Science. 2003 Jan 10;299(5604):256-9. ...
  2. ... a rare movement disorder called rapid-onset dystonia parkinsonism. This disorder is characterized by the abrupt appearance ... abnormalities seen in people with rapid-onset dystonia parkinsonism. More About This Health Condition Variants in the ...
  3. ... been identified in people with X-linked dystonia-parkinsonism. This condition affects movement and has been found ... abnormalities characteristic of the disease.X-linked dystonia-parkinsonism may also be related to an extra segment ...
  4. ... have been found to cause frontotemporal dementia with parkinsonism-17 (FTDP-17). Some of these mutations change ... Wszolek ZK; Reisensburg Working Group for Tauopathies With Parkinsonism. Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological ...
  5. ... cause atypical neuroaxonal dystrophy and PLA2G6-related dystonia-parkinsonism, which are conditions in which deterioration of neurological ... evident until the teenage years.PLA2G6-related dystonia-parkinsonism is also caused by PLA2G6 gene mutations and ...
  6. ... PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability. Proc Natl ... Hattori N. Novel PINK1 mutations in early-onset parkinsonism. Ann Neurol. 2004 Sep;56(3):424-7. ...
  7. ... are also associated with Parkinson's disease and parkinsonism, which are similar disorders that affect movement. Characteristic ... increased risk of developing Parkinson's disease or parkinsonism.Symptoms of Parkinson's disease and parkinsonism result ...
  8. ... a cell surface-localized manganese efflux transporter, and parkinsonism-causing mutations block its intracellular trafficking and efflux ... Warrenburg BP, Bonifati V. Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver ...
  9. ... R, Weiner WJ. Synucleinopathies from bench to bedside. Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S24- ... K, Patel N, Kalia LV. alpha-Synuclein and Parkinsonism: Updates and Future Perspectives. Curr Neurol Neurosci Rep. ...
  10. ... U. Missense dopamine transporter mutations associate with adult parkinsonism and ADHD. J Clin Invest. 2014 Jul;124( ... encoding the dopamine transporter are associated with infantile parkinsonism-dystonia. J Clin Invest. 2009 Jun;119(6): ...
previous · 1 · 2 · next