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Results 1 - 10 of 25 for Amyotrophic lateral sclerosis type 11
  1. 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
  2. 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. doi: 10.1007/s00415-012-6521- ...
    https://medlineplus.gov/genetics/gene/c19orf12 - Genetics
  3. Amyotrophic lateral sclerosis 
    ... SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10 AMYOTROPHIC LATERAL SCLEROSIS 11; ALS11 AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE; ALS16 AMYOTROPHIC ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  4. 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
  5. SETX gene 
    ... PJ. Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis. Nat Rev Neurol. 2011 Nov;7(11):616-30. doi: 10.1038/nrneurol.2011.152. ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
  6. 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. ...
    https://medlineplus.gov/genetics/gene/sod1 - Genetics
  7. Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Living With ... Neuromuscular Disorders ... muscular dystrophy; exercise with a disability; neuromuscular disease; adapted exercise; accesible ...
    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( ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  9. SMN1 gene 
    ... quickly broken down. ... a wide range of severity. There are many types of spinal muscular atrophy that differ in age ...
    https://medlineplus.gov/genetics/gene/smn1 - Genetics
  10. DCTN1 gene 
    ... how this mutation causes distal hereditary motor neuronopathy type VIIB. ... amyotrophic lateral sclerosis (ALS). This disorder occurs in mid- to late ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
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