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Results 1 - 10 of 18 for Dystonia 33
  1. Deep Brain Stimulation (DBS) for the Treatment of Parkinson's Disease and other Movement Disorders From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Parkinson's Disease/Statistics and Research ... Parkinson's Disease ... Movement Disorders/Statistics and Research ... Movement Disorders ... National Institute of Neurological ...
    https://www.ninds.nih.gov/...ns-disease-and-other-movement-disorders - National Institutes of Health
  2. Pantothenate kinase-associated neurodegeneration 
    ... Engl J Med. 2003 Jan 2;348(1):33-40. doi: 10.1056/NEJMoa020817. Citation on PubMed ...
    https://medlineplus.gov/...enate-kinase-associated-neurodegeneration - Genetics
  3. Botulinum toxin injection - larynx 
    ... quality. It is not a cure for laryngeal dystonia, but can help ease the symptoms. In most ... procedure if you have been diagnosed with laryngeal dystonia . BTX injections are the most common treatment for ...
    https://medlineplus.gov/ency/article/007637.htm - Medical Encyclopedia
  4. TAF1 gene 
    ... RETRACTED: TAF1 activates transcription by phosphorylation of serine 33 in histone H2B. Science. 2004 May 14;304( ... the TAF1 gene is associated with X-linked dystonia-parkinsonism. Am J Hum Genet. 2007 Mar;80( ...
    https://medlineplus.gov/genetics/gene/taf1 - Genetics
  5. Familial paroxysmal kinesigenic dyskinesia 
    ... analyses of 163 patients. Mov Disord. 2018 Mar;33(3):459-467. doi: 10.1002/mds.27274. ...
    https://medlineplus.gov/...amilial-paroxysmal-kinesigenic-dyskinesia - Genetics
  6. GLUT1 deficiency syndrome 
    ... Eur J Endocrinol. 2004 May;150(5):627-33. doi: 10.1530/eje.0.1500627. Citation on ...
    https://medlineplus.gov/genetics/condition/glut1-deficiency-syndrome - Genetics
  7. ARX gene 
    ... dystonicus. Neurology. 2007 Jul 31;69(5):427-33. doi: 10.1212/01.wnl.0000266594.16202.c1. ...
    https://medlineplus.gov/genetics/gene/arx - Genetics
  8. Spinocerebellar ataxia type 2 
    ... times without causing any health problems. Individuals with 33 or more CAG repeats in the ATXN2 gene develop signs and symptoms of SCA2. People with 33 to 34 repeats tend to first experience signs ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  9. Ataxia with oculomotor apraxia 
    ... ataxia and oculomotor apraxia. Hum Mutat. 2012 Feb;33(2):351-4. doi: 10.1002/humu.21650. ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  10. MT-ND6 gene 
    ... 43. doi: 10.1002/1096-8628(20010122)98:33.0.co;2-o. Citation on PubMed Fauser ...
    https://medlineplus.gov/genetics/gene/mt-nd6 - Genetics
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