Carregant...

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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Intern Med
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: The Japanese Society of Internal Medicine 2019
Matèries:
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!