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Results 1 - 10 of 47 for Amyotrophic lateral sclerosis type 4
  1. Charcot-Marie-Tooth disease 
    ... the nerve impulse. People with CMT2 may develop amyotrophic lateral ... myelin and axons. Type 4 (CMT4) is distinguished from the other types by ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  2. Degenerative Nerve Diseases (National Library of Medicine)  
    ... is unknown. Degenerative nerve diseases include: Alzheimer's ... no cure. Treatments may help improve symptoms, relieve pain, and increase mobility.
    https://medlineplus.gov/degenerativenervediseases.html - Health Topics
  3. Amyotrophic lateral sclerosis 
    ... SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8 AMYOTROPHIC ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  4. FUS gene 
    ... in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science. 2009 Feb 27;323(5918):1208- ...
    https://medlineplus.gov/genetics/gene/fus - Genetics
  5. Distal myopathy 2 
    ... pharyngeal weakness with distal myopathy Genetic Testing Registry: Amyotrophic lateral sclerosis type 21 Vocal cord and pharyngeal distal myopathy National ...
    https://medlineplus.gov/genetics/condition/distal-myopathy-2 - Genetics
  6. Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Living With ... Neuromuscular Disorders ... Muscular Dystrophy Association ... PDF ... muscular dystrophy; exercise with a disability; neuromuscular ...
    https://www.mda.org/.../files/MDA_Quest_Excercise_Package_2009.pdf - External Health Links
  7. C9orf72 gene 
    ... the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. Lancet Neurol. 2012 Apr;11(4):323-30. doi: 10.1016/S1474-4422(12) ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  8. SETX gene 
    ... of damaged DNA. MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition At least 125 mutations in the SETX gene have been found to cause ataxia with oculomotor apraxia type 2. This condition is characterized by difficulty coordinating ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
  9. SOD1 gene 
    ... j.bbadis.2006.03.008. Epub 2006 Apr 4. Citation on PubMed ... lateral sclerosis genetics: novel SOD1 and FUS variants. Neurobiol Aging. ...
    https://medlineplus.gov/genetics/gene/sod1 - Genetics
  10. Genetics and Neuromuscular Disease (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Genetics ... Neuromuscular Disorders ... Muscular Dystrophy Association ... PDF
    https://www.mda.org/sites/default/files/2021/07/Genetics-and-NMD.pdf - External Health Links
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