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Assessment of Chemical Exposures Program: Toolkit Advances and Recent Investigations

Journal of environmental health, 2023-11, Vol.86 (4), p.36-44

2023

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Potential Environmental Factors in Amyotrophic Lateral Sclerosis

Neurologic clinics, 2015-11, Vol.33 (4), p.877-888

2015

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Recruitment of Patients With Amyotrophic Lateral Sclerosis for Clinical Trials and Epidemiological Studies: Descriptive Study of the National ALS Registry's Research Notification Mechanism

Journal of medical Internet research, 2021-12, Vol.23 (12), p.e28021-e28021

2021

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Incidence of amyotrophic lateral sclerosis in the United States, 2014-2016

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2022-07, Vol.23 (5-6), p.378-382

2022

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Reproductive History and Age of Onset for Women Diagnosed with Amyotrophic Lateral Sclerosis: Data from the National ALS Registry: 2010–2018

Neuroepidemiology, 2021-09, Vol.55 (5), p.416-424

2021

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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

Neuroepidemiology, 2018-01, Vol.51 (3-4), p.149-157

2018

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Amyotrophic Lateral Sclerosis Mortality in the United States, 2011–2014

Neuroepidemiology, 2018-01, Vol.51 (1-2), p.96-103

2018

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Preliminary Results of National Amyotrophic Lateral Sclerosis (ALS) Registry Risk Factor Survey Data

PloS one, 2016-04, Vol.11 (4), p.e0153683

2016

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Keratinous biomarker of mercury exposure associated with amyotrophic lateral sclerosis risk in a nationwide U.S. study

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2020-07, Vol.21 (5-6), p.420-427

2020

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The National Amyotrophic Lateral Sclerosis (ALS) Registry

Journal of environmental health, 2012-07, Vol.75 (1), p.28-30

2012

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Impact of the National Amyotrophic Lateral Sclerosis Registry: Analysis of Registry‐funded Research

Annals of clinical and translational neurology, 2022-11, Vol.9 (11), p.1692-1701

2022

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What do you think caused your ALS? An analysis of the CDC national amyotrophic lateral sclerosis patient registry qualitative risk factor data using artificial intelligence and qualitative methodology

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-05, Vol.25 (5-6), p.1-624

2024

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A brief report on juvenile amyotrophic lateral sclerosis cases in the United States National ALS Registry: 2010-2018

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-02, Vol.25 (1-2), p.211-213

2024

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Survival and epidemiology of amyotrophic lateral sclerosis (ALS) cases in the Chicago and Detroit metropolitan cohort: incident cases 2009-2011 and survival through 2018

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2023-04, Vol.24 (3-4), p.203-211

2023

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Comparing Amyotrophic lateral sclerosis (ALS) patient characteristics from the National ALS Registry and the Massachusetts ALS Registry, data through 2015

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2023-10, Vol.24 (7-8), p.1-694

2023

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Prevalence of amyotrophic lateral sclerosis in the United States using established and novel methodologies, 2017

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2023-02, Vol.24 (1-2), p.108-116

2023

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Prevalence of amyotrophic lateral sclerosis in the United States, 2018

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2023-08, Vol.24 (7-8), p.702-708

2023

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Risk factors for amyotrophic lateral sclerosis: A regional United States case‐control study

Muscle & nerve, 2021-01, Vol.63 (1), p.52-59

2021

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Prevalence of ALS in all 50 states in the United States, data from the National ALS Registry, 2011-2018

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-06, p.1-7

2024

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Racial and ethnic differences among amyotrophic lateral sclerosis cases in the United States

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2015-03, Vol.16 (1-2), p.65-71

2015

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Evaluation of the Completeness of ALS Case Ascertainment in the US National ALS Registry: Application of the Capture-Recapture Method

Neuroepidemiology, 2022-04, Vol.56 (2), p.104-114

2022

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Quantifying a nonnotifiable disease in the United States: the National Amyotrophic Lateral Sclerosis Registry model

JAMA : the journal of the American Medical Association, 2014-09, Vol.312 (11), p.1097

2014

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Comparison of Demographics: National Amyotrophic Lateral Sclerosis Registry and Clinical Trials Data

Journal of racial and ethnic health disparities, 2024-07

2024

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Correction to: Comparison of Demographics: National Amyotrophic Lateral Sclerosis Registry and Clinical Trials Data

Journal of racial and ethnic health disparities, 2024-07

2024

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Racial Disparities in the Diagnosis and Prognosis of ALS Patients in the United States

Journal of racial and ethnic health disparities, 2024-07

2024

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Assessment of Chemical Exposures Program: Toolkit Advances and Recent Investigations

Potential Environmental Factors in Amyotrophic Lateral Sclerosis

Recruitment of Patients With Amyotrophic Lateral Sclerosis for Clinical Trials and Epidemiological Studies: Descriptive Study of the National ALS Registry's Research Notification Mechanism

Incidence of amyotrophic lateral sclerosis in the United States, 2014-2016

Reproductive History and Age of Onset for Women Diagnosed with Amyotrophic Lateral Sclerosis: Data from the National ALS Registry: 2010–2018

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

Amyotrophic Lateral Sclerosis Mortality in the United States, 2011–2014

Preliminary Results of National Amyotrophic Lateral Sclerosis (ALS) Registry Risk Factor Survey Data

Keratinous biomarker of mercury exposure associated with amyotrophic lateral sclerosis risk in a nationwide U.S. study

The National Amyotrophic Lateral Sclerosis (ALS) Registry

Impact of the National Amyotrophic Lateral Sclerosis Registry: Analysis of Registry‐funded Research

What do you think caused your ALS? An analysis of the CDC national amyotrophic lateral sclerosis patient registry qualitative risk factor data using artificial intelligence and qualitative methodology

A brief report on juvenile amyotrophic lateral sclerosis cases in the United States National ALS Registry: 2010-2018

Survival and epidemiology of amyotrophic lateral sclerosis (ALS) cases in the Chicago and Detroit metropolitan cohort: incident cases 2009-2011 and survival through 2018

Comparing Amyotrophic lateral sclerosis (ALS) patient characteristics from the National ALS Registry and the Massachusetts ALS Registry, data through 2015

Prevalence of amyotrophic lateral sclerosis in the United States using established and novel methodologies, 2017

Prevalence of amyotrophic lateral sclerosis in the United States, 2018

Risk factors for amyotrophic lateral sclerosis: A regional United States case‐control study

Prevalence of ALS in all 50 states in the United States, data from the National ALS Registry, 2011-2018

Racial and ethnic differences among amyotrophic lateral sclerosis cases in the United States

Evaluation of the Completeness of ALS Case Ascertainment in the US National ALS Registry: Application of the Capture-Recapture Method

Quantifying a nonnotifiable disease in the United States: the National Amyotrophic Lateral Sclerosis Registry model

Comparison of Demographics: National Amyotrophic Lateral Sclerosis Registry and Clinical Trials Data

Correction to: Comparison of Demographics: National Amyotrophic Lateral Sclerosis Registry and Clinical Trials Data

Racial Disparities in the Diagnosis and Prognosis of ALS Patients in the United States

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