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Results 1 - 10 of 29 for Amyotrophic lateral sclerosis type 12
  1. C19orf12 gene 
    ... to have a condition called hereditary spastic paraplegia type 43. More About This Health Condition ... with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis. J Neurol. 2012 Nov;259(11):2434-9. ...
    https://medlineplus.gov/genetics/gene/c19orf12 - Genetics
  2. Amyotrophic lateral sclerosis 
    ... 11; ALS11 AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE; ALS16 AMYOTROPHIC LATERAL SCLEROSIS 12 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS12 AMYOTROPHIC LATERAL ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  3. Distal myopathy 2 
    ... pharyngeal weakness with distal myopathy Genetic Testing Registry: Amyotrophic lateral sclerosis type 21 Distal myopathy with vocal cord weakness Disease ...
    https://medlineplus.gov/genetics/condition/distal-myopathy-2 - 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. SOD1 gene 
    ... and misfolding of Cu,Zn superoxide dismutase in amyotrophic lateral sclerosis. Biochim Biophys Acta. 2006 Nov-Dec;1762(11-12):1025-37. doi: 10.1016/j.bbadis.2006. ...
    https://medlineplus.gov/genetics/gene/sod1 - Genetics
  6. Metals: In Sickness and in Health From the National Institutes of Health (National Institute of General Medical Sciences)  
    Minerals/Related Issues ... Minerals ... National Institute of General Medical Sciences ... From the National Institutes of Health
    https://www.nigms.nih.gov/.../metals-in-sickness-and-in-health.aspx - External Health Links
  7. Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDF  
    muscular dystrophy; exercise with a disability; neuromuscular disease; adapted exercise; accesible sports equipment; power wheelchair; power soccer ... Neuromuscular ...
    https://www.mda.org/.../files/MDA_Quest_Excercise_Package_2009.pdf - External Health Links
  8. 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)70043-1. Epub 2012 Mar 9. Citation on ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  9. 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
  10. Charcot-Marie-Tooth disease 
    ... the nerve impulse. People with CMT2 may develop amyotrophic lateral sclerosis ... as intermediate type, the nerve impulses are both slowed and reduced ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
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