Recruitment of Patients With Amyotrophic Lateral Sclerosis for Clinical Trials and Epidemiological Studies: Descriptive Study of the National ALS Registry's Research Notification M... von Mehta, Paul, Raymond, Jaime, Han, Moon Kwon, Larson, Theodore, Berry, James D, Paganoni, Sabrina, Mitsumoto, Hiroshi, Bedlack, Richard Stanley, Horton, D Kevin

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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 von Raymond, Jaime, Mehta, Paul, Larson, Ted, Pioro, Erik P., Horton, D. Kevin

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Amyotrophic Lateral Sclerosis Mortality in the United States, 2011–2014 von Larson, Theodore C., Kaye, Wendy, Mehta, Paul, Horton, D. Kevin

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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 von Nelson, Lorene M., Topol, Barbara, Kaye, Wendy, Williamson, David, Horton, D. Kevin, Mehta, Paul, Wagner, Todd

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Preliminary Results of National Amyotrophic Lateral Sclerosis (ALS) Registry Risk Factor Survey Data von Bryan, Leah, Kaye, Wendy, Antao, Vinicius, Mehta, Paul, Muravov, Oleg, Horton, D Kevin

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The National Amyotrophic Lateral Sclerosis (ALS) Registry von Antao, Vinicius C, Horton, D Kevin

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Impact of the National Amyotrophic Lateral Sclerosis Registry: Analysis of Registry‐funded Research von Rechtman, Lindsay, Brenner, Stephan, Wright, Marcienne, Ritsick, Maggie, Rahman, Farhana, Han, Moon, Raymond, Jaime, Larson, Theodore, Horton, D. Kevin, Mehta, Paul

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Threat of Secondary Chemical Contamination of Emergency Departments and Personnel: An Uncommon but Recurrent Problem von Larson, Theodore C., Orr, Maureen F., Auf der Heide, Erik, Wu, Jennifer, Mukhopadhyay, Sutapa, Kevin Horton, D.

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Risk factors for amyotrophic lateral sclerosis: A regional United States case‐control study von Andrew, Angeline S., Bradley, Walter G., Peipert, Daniel, Butt, Tanya, Amoako, Kwadwo, Pioro, Erik P., Tandan, Rup, Novak, John, Quick, Adam, Pugar, K. Doug, Sawlani, Komal, Katirji, Bashar, Hayes, Todd A., Cazzolli, Pamela, Gui, Jiang, Mehta, Paul, Horton, D. Kevin, Stommel, Elijah W.

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Evaluation of the Completeness of ALS Case Ascertainment in the US National ALS Registry: Application of the Capture-Recapture Method von Nelson, Lorene M., Topol, Barbara, Kaye, Wendy, Raymond, Jaime, Horton, D. Kevin, Mehta, Paul, Wagner, Todd

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Quantifying a Nonnotifiable Disease in the United States: The National Amyotrophic Lateral Sclerosis Registry Model von Horton, D. Kevin, Mehta, Paul, Antao, Vinicius C

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Comparison of Demographics: National Amyotrophic Lateral Sclerosis Registry and Clinical Trials Data von Han, Moon, Raymond, Jaime, Larson, Theodore C, Mehta, Paul, Horton, D Kevin

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Correction to: Comparison of Demographics: National Amyotrophic Lateral Sclerosis Registry and Clinical Trials Data von Han, Moon, Raymond, Jaime, Larson, Theodore C, Mehta, Paul, Horton, D Kevin

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Qualitative Data Collection 1-Year Post Disaster Provided Insight Into Unique Concerns of Affected Community Residents During Long-Term Recovery – Illinois, July 2022 von DeJonge, Peter, Sekkarie, Ahlia, Martell, Sandra, Patrick, Sarah, Caudill, Motria, Horton, D. Kevin, Orr, Maureen F., Konkle, Stacey

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Racial Disparities in the Diagnosis and Prognosis of ALS Patients in the United States von Raymond, Jaime, Nair, Theresa, Gwathmey, Kelly Graham, Larson, Theodore, Horton, D Kevin, Mehta, Paul

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Workshop summary: Potential usefulness and feasibility of a US National Mesothelioma Registry von Cummings, Kristin J., Becich, Michael J., Blackley, David J., Deapen, Dennis, Harrison, Robert, Hassan, Raffit, Henley, S. Jane, Hesdorffer, Mary, Horton, D. Kevin, Mazurek, Jacek M., Pass, Harvey I., Taioli, Emanuela, Wu, Xiao‐Cheng, Zauderer, Marjorie G., Weissman, David N.

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Analysis of Biospecimen Demand and Utilization of Samples from the National Amyotrophic Lateral Sclerosis Biorepository von Bledsoe, Marianna J., Rechtman, Lindsay, Wagner, Laurie, Mehta, Paul, Horton, D. Kevin, Kaye, Wendy E.

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The Incidence of Amyotrophic Lateral Sclerosis in Ohio 2016–2018: The Ohio Population-Based ALS Registry von Andrew, Angeline S., Pioro, Erik P., Li, Meifang, Shi, Xun, Gui, Jiang, Stommel, Elijah W., Butt, Tanya H., Peipert, Daniel, Henegan, Patricia, Tischbein, Maeve, Cazzolli, Pamela, Novak, John, Quick, Adam, Pugar, K. Doug, Sawlani, Komal, Katirji, Bashar, Hayes, Todd A., Horton, D. Kevin, Mehta, Paul, Bradley, Walter G.

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The National ALS Registry: A recruitment tool for research von Malek, Angela M., Stickler, David E., Antao, Vinicius C., Horton, D. Kevin

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Integrating a Biorepository Into the National Amyotrophic Lateral Sclerosis Registry von Horton, D Kevin, Kaye, Wendy, Wagner, Laurie

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