Cargando…
Evaluating the completeness of the national ALS registry, United States
Our objective was to evaluate the completeness of the United States National ALS Registry (Registry). We compared persons with ALS who were passively identified by the Registry with those actively identified in the State and Metropolitan Area ALS Surveillance project. Cases in the two projects were...
Autores principales: | KAYE, WENDY E., WAGNER, LAURIE, WU, RUOMING, MEHTA, PAUL |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815913/ https://www.ncbi.nlm.nih.gov/pubmed/29020837 http://dx.doi.org/10.1080/21678421.2017.1384021 |
Ejemplares similares
-
Preliminary Results of National Amyotrophic Lateral Sclerosis (ALS) Registry Risk Factor Survey Data
por: Bryan, Leah, et al.
Publicado: (2016) -
Prevalence of Amyotrophic Lateral Sclerosis — United States, 2014
por: Mehta, Paul, et al.
Publicado: (2018) -
Estimation of the Prevalence of Amyotrophic Lateral Sclerosis in the
United States Using National Administrative Healthcare Data from 2002 to 2004
and Capture-Recapture Methodology
por: Nelson, Lorene M., et al.
Publicado: (2018) -
State and metropolitan area-based amyotrophic lateral sclerosis (ALS) surveillance
por: Wagner, Laurie, et al.
Publicado: (2016) -
Recruitment of population-based controls for ALS cases from the National ALS Registry
por: BEAR, TODD M., et al.
Publicado: (2021)