Cargando…
Survival and Cause of Death among a Cohort of Confirmed Amyotrophic Lateral Sclerosis Cases
INTRODUCTION: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder. Estimates of survival from disease onset range from 20 to 48 months and have been generated using clinical populations or death records alone. METHODS: Data on a cohort of ALS cases diagnosed between 2009–...
Autores principales: | Paulukonis, Susan T., Roberts, Eric M., Valle, Jhaqueline P., Collins, Natalie N., English, Paul B., Kaye, Wendy E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501568/ https://www.ncbi.nlm.nih.gov/pubmed/26172548 http://dx.doi.org/10.1371/journal.pone.0131965 |
Ejemplares similares
-
Epidemiology and surveillance of amyotrophic lateral sclerosis in two large metropolitan areas in California
por: Valle, Jhaqueline, et al.
Publicado: (2015) -
Concurrent use of hydroxyurea and deferasirox in Californians with sickle cell disease
por: Wong, Trisha E., et al.
Publicado: (2021) -
Amyotrophic lateral sclerosis surveillance in Baltimore and Philadelphia
por: Jordan, Heather, et al.
Publicado: (2015) -
Sickle cell disease among Latinx in California
por: Valle, Jhaqueline, et al.
Publicado: (2022) -
Evaluating the cerebral correlates of survival in amyotrophic lateral sclerosis
por: Ishaque, Abdullah, et al.
Publicado: (2018)