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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6663526/
https://www.ncbi.nlm.nih.gov/pubmed/31257275
http://dx.doi.org/10.2169/internalmedicine.2222-18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6663526/
https://www.ncbi.nlm.nih.gov/pubmed/31257275
http://dx.doi.org/10.2169/internalmedicine.2222-18

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