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Archives of Neurology|February 10, 2010
FUS mutations in familial amyotrophic lateral sclerosis in the NetherlandsEwout J N Groen, Michael A van Es, Paul W J van Vught, et al.
Neurology|October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2J C de Greef, R J L F Lemmers, P Camaño, et al.
Annals of Neurology|September 5, 2018
Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History StudyRianne J M Goselink, Tim H A Schreuder, Nens van Alfen, et al.
Neurocase|April 21, 2021
The bvFTD phenocopy syndrome: a case study supported by repeated MRI, [18F]FDG-PET and pathological assessmentMarie-Paule E van Engelen, Annemieke J M Rozemuller, Hülya Ulugut Erkoyun, et al.
Journal of Neuromuscular Diseases|September 6, 2024
A Likely Pathogenic variant in the KBTBD13 Gene: A Case Series of Three Patients with Nemaline Myopathy Type 6Esmee S B van Kleef, Karlijn Bouman, Joery P F Molenaar, et al.
Familial Cancer|January 5, 2019
TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohortJ J Bakhuizen, F B Hogervorst, M E Velthuizen, et al.
Frontiers in Aging Neuroscience|May 24, 2024
The pursuit for markers of disease progression in behavioral variant frontotemporal dementia: a scoping review to optimize outcome measures for clinical trialsJay L P Fieldhouse, Dirk N van Paassen, Marie-Paule E van Engelen, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|February 26, 2026
Autonomic dysfunction and hypothalamic atrophy in frontotemporal dementia and primary psychiatric disordersYannick S S Timar, Marie-Paule Emilie van Engelen, Vikram Venkatraghavan, et al.
Neurology|December 30, 2004
Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositisU A Badrising, G M Th Schreuder, M J Giphart, et al.
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