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Brain : a Journal of Neurology|December 20, 2024
C21ORF2 mutations point towards primary cilia dysfunction in amyotrophic lateral sclerosisMathias De Decker, Pavol Zelina, Thomas G Moens, 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|September 11, 2009
Randomized sequential trial of valproic acid in amyotrophic lateral sclerosisSanne Piepers, Jan H Veldink, Sonja W de Jong, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 3, 2023
UNC13A in amyotrophic lateral sclerosis: from genetic association to therapeutic targetSean W Willemse, Peter Harley, Ruben P A van Eijk, et al.
Brain : a Journal of Neurology|September 12, 2012
Genotype-phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohortKoen L I van Gassen, Charlotte D C C van der Heijden, Susanne T de Bot, et al.
Neurology|July 27, 2018
The multistep hypothesis of ALS revisited: The role of genetic mutationsAdriano Chiò, Letizia Mazzini, Sandra D'Alfonso, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 27, 2023
Epidemiological and clinical profile of amyotrophic lateral sclerosis in Ethiopia: a 5-year multicenter retrospective studyDereje Melka, Hanna Demisse, Hanna Assefa, 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.
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