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Results 1 - 10 of 27 for Amyotrophic lateral sclerosis type 19
  1. C19orf12 gene 
    ... to have a condition called hereditary spastic paraplegia type 43. More About This Health Condition ... TB. C19orf12 mutations in neurodegeneration 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. Curing the Epilepsies: The Promise of Research From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Epilepsy/Statistics and Research ... Epilepsy ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Request free mailed ...
    https://www.ninds.nih.gov/.../curing-epilepsies-promise-research - External Health Links
  3. Amyotrophic lateral sclerosis 
    ... SCLEROSIS 12 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS12 AMYOTROPHIC LATERAL SCLEROSIS 19; ALS19 FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  4. 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
  5. 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
  6. 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
  7. Pregnancy and Childbirth with Neuromuscular Disease (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Women ... Neuromuscular Disorders ... Muscular Dystrophy Association ... PDF
    https://www.mda.org/.../Quest17-3_Pregnancy_Series_revised_0.pdf - External Health Links
  8. SOD1 gene 
    ... regulate oxidative stress resistance. Nat Commun. 2014 Mar 19;5:3446. doi: 10.1038/ncomms4446. Citation on PubMed or Free article on PubMed Central Valentine JS, Doucette PA, Zittin Potter S. Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis. Annu Rev Biochem. 2005;74:563-93. doi: ...
    https://medlineplus.gov/genetics/gene/sod1 - Genetics
  9. SPG11 gene 
    ... cause the signs and symptoms of spastic paraplegia type 11 by interfering with the protein's ... This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/spg11 - Genetics
  10. Focus on Stem Cell Research From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Image ... Stem Cells/Statistics and Research ... Stem Cells ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health
    https://www.ninds.nih.gov/.../focus-stem-cell-research - External Health Links
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