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Medical Physics|May 1, 1992
Verification data for electron beam dose algorithmsA S Shiu, S Tung, K R Hogstrom, et al.Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.Neuromuscular Disorders : NMD|December 24, 2019
Congenital fiber type disproportion caused by TPM3 mutation: A report of two atypical casesCristiane Araújo Martins Moreno, Eduardo de Paula Estephan, Alan Fappi, et al.Research Square|January 10, 2024
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.BMC Genomics|July 2, 2024
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 8, 2020
Primary lateral sclerosis: consensus diagnostic criteriaMartin R Turner, Richard J Barohn, Philippe Corcia, et al.Annals of Neurology|December 15, 2015
MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signsObaid M Albulym, Marina L Kennerson, Matthew B Harms, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 4, 2025
A VAPB (P56S) mutation in a Dutch patient with familial motor neuron disease: a case reportSean W Willemse, Koen C Demaegd, Ruben P A Van Eijk, et al.JAMA Neurology|February 19, 2014
TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosisJanet Cady, Erica D Koval, Bruno A Benitez, et al.Proceedings of the National Academy of Sciences of the United States of America|November 20, 2013
RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementiaTao Zu, Yuanjing Liu, Monica Bañez-Coronel, et al.Pageof 14