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Results 31 - 40 of 652 for als
  1. Brain Facts: Glossary (Society for Neuroscience)  
    Brain Diseases/Reference Desk ... Brain Diseases ... Society for Neuroscience
    https://www.brainfacts.org/Glossary - External Health Links
  2. Understanding ALS | NIH MedlinePlus Magazine 
    Amyotrophic lateral sclerosis ... Amyotrophic Lateral Sclerosis Understanding ALS ALS—short for amyotrophic lateral sclerosis—is a rare but serious disease that attacks nerve cells in the brain and ...
    https://magazine.medlineplus.gov/multimedia/understanding-als - MedlinePlus Magazine
  3. Winchester syndrome 
    Winchester syndrome is a rare inherited disease characterized by a loss of bone tissue (osteolysis), particularly in the hands and feet. Winchester syndrome used ...
    https://medlineplus.gov/genetics/condition/winchester-syndrome - Genetics
  4. Primary localized cutaneous amyloidosis 
    Primary localized cutaneous amyloidosis (PLCA) is a condition in which clumps of abnormal proteins called amyloids build up in the skin, specifically in the wave- ...
    https://medlineplus.gov/.../primary-localized-cutaneous-amyloidosis - Genetics
  5. C9orf72 gene 
    ... the C9orf72 gene have been found to cause amyotrophic lateral sclerosis (ALS), a condition characterized by progressive muscle weakness, a ... is repeated too many times, it can cause ALS. This type of mutation is called a hexanucleotide ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  6. SLC19A3 gene 
    ... Alfadhel M, Almuntashri M, Jadah RH, Bashiri FA, Al Rifai MT, Al Shalaan H, Al Balwi M, Al Rumayan A, Eyaid W, Al-Twaijri W. Biotin-responsive basal ganglia disease should ...
    https://medlineplus.gov/genetics/gene/slc19a3 - Genetics
  7. Biotin-thiamine-responsive basal ganglia disease 
    ... Alfadhel M, Almuntashri M, Jadah RH, Bashiri FA, Al Rifai MT, Al Shalaan H, Al Balwi M, Al Rumayan A, Eyaid W, Al-Twaijri W. Biotin-responsive basal ganglia disease should ...
    https://medlineplus.gov/...thiamine-responsive-basal-ganglia-disease - Genetics
  8. IRAK-4 deficiency 
    ... Good NK, Miller R, Takada H, Hara T, Al-Hajjar S, Al-Ghonaium A, Speert D, Sanlaville D, Li X, ... Elbim C, Hitchcock R, Lammas D, Davies G, Al-Ghonaium A, Al-Rayes H, Al-Jumaah S, ...
    https://medlineplus.gov/genetics/condition/irak-4-deficiency - Genetics
  9. TARDBP gene 
    ... the TARDBP gene have been found to cause amyotrophic lateral sclerosis (ALS), a condition characterized by progressive muscle weakness, a ... muscle movement (motor neurons) in some people with ALS. It is unclear whether TDP-43 protein aggregates ...
    https://medlineplus.gov/genetics/gene/tardbp - Genetics
  10. FUS gene 
    ... the FUS gene have been found to cause amyotrophic lateral sclerosis (ALS), a condition characterized by progressive muscle weakness, a ... muscle movement (motor neurons) in some people with ALS. It is unclear if protein aggregates cause the ...
    https://medlineplus.gov/genetics/gene/fus - Genetics
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