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Neurology|October 27, 2015
Brain morphologic changes in asymptomatic C9orf72 repeat expansion carriersRenée Walhout, Ruben Schmidt, Henk-Jan Westeneng, et al.Annals of Neurology|May 1, 2016
Autoantibody pathogenicity in a multifocal motor neuropathy induced pluripotent stem cell-derived modelOliver Harschnitz, Leonard H van den Berg, Lill Eva Johansen, et al.Nature Communications|March 22, 2017
Genetic correlation between amyotrophic lateral sclerosis and schizophreniaRussell L McLaughlin, Dick Schijven, Wouter van Rheenen, et al.Plos One|June 26, 2018
Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker studyWouter van Rheenen, Frank P Diekstra, Oliver Harschnitz, et al.Neurobiology of Aging|November 29, 2011
UNC13A is a modifier of survival in amyotrophic lateral sclerosisFrank P Diekstra, Paul W J van Vught, Wouter van Rheenen, et al.Human Molecular Genetics|May 31, 2012
Evidence for an oligogenic basis of amyotrophic lateral sclerosisMarka van Blitterswijk, Michael A van Es, Eric A M Hennekam, et al.Human Molecular Genetics|March 2, 2012
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosisHylke M Blauw, Wouter van Rheenen, Max Koppers, et al.Annals of Neurology|October 24, 2024
Recessive Variants in PIGG Cause a Motor Neuropathy with Variable Conduction Block, Childhood Tremor, and Febrile Seizures: Expanding the PhenotypeChristopher J Record, Antoinette O'Connor, Nienke E Verbeek, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 3, 2023
<i>UNC13A</i> in amyotrophic lateral sclerosis: from genetic association to therapeutic targetSean W Willemse, Peter Harley, Ruben P A van Eijk, et al.Neurology|July 31, 2012
Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseasesWouter van Rheenen, Marka van Blitterswijk, Mark H B Huisman, et al.Pageof 8