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als
- Amyotrophic lateral sclerosis (ALS) is a progressive disease that affects motor neurons, which are specialized nerve cells that control muscle movement. These nerve ...
- ... the SOD1 gene have been found to cause amyotrophic lateral sclerosis (ALS), a condition characterized by progressive muscle weakness, a ... dismutase enzyme. About half of all Americans with ALS caused by SOD1 gene mutations have a particular ...
- ... of nerve impulses. MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition At least 20 ... About This Health Condition ALS2_HUMAN ALS2CR6 ALSJ amyotrophic lateral sclerosis 2 (juvenile) IAHSP KIAA1563 PLSJ Tests of ALS2 ...
- ... not show signs and symptoms of the condition. Al-Aqeel Sewairi syndrome Hereditary multicentric osteolysis MONA NAO ... gov MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA PubMed Al Aqeel A, Al Sewairi W, Edress B, Gorlin ...
- Winchester syndrome is a rare inherited disease characterized by a loss of bone tissue (osteolysis), particularly in the hands and feet. Winchester syndrome used ...
- 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- ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...