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Journal of Neurology, Neurosurgery, and Psychiatry|September 6, 2015
Factors related to caregiver strain in ALS: a longitudinal studyHuub Creemers, Sandra de Morée, Jan H Veldink, et al.Stroke|June 25, 2021
Role of Rare Genetic Variants Found in Families With Intracranial Aneurysms in the General Dutch and UK PopulationMark K Bakker, Roos A Ettema, Maxime Klostermann, et al.Neurobiology of Aging|May 16, 2020
Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsyDick Schijven, Remi Stevelink, Mark McCormack, et al.Journal of Neurology|November 24, 2011
Associated autoimmune diseases in patients with multifocal motor neuropathy and their family membersElisabeth A Cats, Anne Suzanne Bertens, Jan H Veldink, et al.European Journal of Human Genetics : EJHG|March 1, 2022
Genome-wide linkage analysis combined with genome sequencing in large families with intracranial aneurysmsMark K Bakker, Suze Cobyte, Frederic A M Hennekam, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 25, 2007
Validity of the Dutch version of the Amyotrophic Lateral Sclerosis Assessment Questionnaire, ALSAQ-40, ALSAQ-5Maud Maessen, Marcel W Post, Rianne Maillé, et al.Plos One|September 14, 2011
Impaired structural motor connectome in amyotrophic lateral sclerosisEsther Verstraete, Jan H Veldink, Rene C W Mandl, et al.European Journal of Neurology|October 25, 2023
Analysis of aneurysmal subarachnoid hemorrhage as a multistep processYnte M Ruigrok, Gabriel J E Rinkel, Han-Sol Chang, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 4, 2011
Structural MRI reveals cortical thinning in amyotrophic lateral sclerosisEsther Verstraete, Jan H Veldink, Jeroen Hendrikse, et al.BMC Genomics|September 7, 2012
Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific mannerSimone de Jong, Iouri Chepelev, Esther Janson, et al.Pageof 28