Atypical Familial Amyotrophic Lateral Sclerosis with Slowly Progressing Lower Extremities-predominant Late-onset Muscular Weakness and Atrophy

OBJECTIVE: Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disease characterized by the progressive loss of the upper and lower motor neurons that progresses to paralysis of almost all skeletal muscles of the extremities, bulbar, and respiratory system. Although most ALS case...

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Detalhes bibliográficos
Publicado no:Intern Med
Main Authors: Togawa, Jumpei, Ohi, Takekazu, Yuan, Jun-Hui, Takashima, Hiroshi, Furuya, Hirokazu, Takechi, Shinji, Fujitake, Junko, Hayashi, Saki, Ishiura, Hiroyuki, Naruse, Hiroya, Mitsui, Jun, Tsuji, Shoji
Formato: Artigo
Idioma:Inglês
Publicado em: The Japanese Society of Internal Medicine 2019
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6663526/
https://ncbi.nlm.nih.gov/pubmed/31257275
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2169/internalmedicine.2222-18
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