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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 8, 2021
Genotype-phenotype correlations of <i>KIF5A</i> stalk domain variantsEva M J de Boer, Wouter van Rheenen, H Stephan Goedee, et al.
Neuromuscular Disorders : NMD|May 31, 2022
Distal spinal muscular atrophy featured by predominant calf muscle involvement in VRK1 associated disease - Case series and reviewKoen Demaegd, Eva H Brilstra, Jessica E Hoogendijk, et al.
Neurobiology of Aging|November 13, 2012
Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3Max Koppers, Ewout J N Groen, Paul W J van Vught, et al.
Neurobiology of Aging|April 18, 2012
CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosisEwout J N Groen, Wouter van Rheenen, Max Koppers, et al.
Neurobiology of Aging|August 11, 2012
VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patientMarka van Blitterswijk, Michael A van Es, Max Koppers, et al.
Neurobiology of Aging|June 9, 2012
UBQLN2 in familial amyotrophic lateral sclerosis in The NetherlandsPerry T C van Doormaal, Wouter van Rheenen, Marka van Blitterswijk, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 20, 2023
Assessment of risk of ALS conferred by the GGGGCC hexanucleotide repeat expansion in <i>C9orf72</i> among first-degree relatives of patients with ALS carrying the repeat expansionIris F Van Wijk, Ruben P A Van Eijk, Loes Van Boxmeer, et al.
Journal of Neurology|February 8, 2017
No association between gluten sensitivity and amyotrophic lateral sclerosisAnne E Visser, Raha Pazoki, Sara L Pulit, et al.
Neurology|May 29, 2026
Diagnostic Revision From Primary Lateral Sclerosis to Amyotrophic Lateral Sclerosis: A Cohort StudyEva M J de Boer, Sean W Willemse, Jan H Veldink, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 4, 2025
A <i>VAPB</i> (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.
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