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Brain : a Journal of Neurology|March 27, 2016
Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesionsPaola S Denora, Katrien Smets, Federica Zolfanelli, et al.Alzheimer'S Research & Therapy|January 27, 2018
Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one familyAnne Sieben, Sara Van Mossevelde, Eline Wauters, et al.Pediatric Research|July 8, 2009
Lactic acidosis in a newborn with adrenal calcificationsAlexandra Zecic, Joél E Smet, Claudine M De Praeter, et al.Neurobiology of Aging|January 11, 2017
Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patientsFederica Perrone, Hung Phuoc Nguyen, Sara Van Mossevelde, et al.Neurology|April 3, 2016
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutationTobi Van den Bossche, Kristel Sleegers, Elise Cuyvers, et al.Acta Neuropathologica|March 16, 2020
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide exportShaun Martin, Stefanie Smolders, Chris Van den Haute, et al.American Journal of Human Genetics|January 22, 2013
Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegiaElodie Martin, Rebecca Schüle, Katrien Smets, et al.Annals of Clinical and Translational Neurology|January 13, 2017
POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonismLionel Van Maldergem, Arnaud Besse, Boel De Paepe, et al.Orphanet Journal of Rare Diseases|September 11, 2014
Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathiesAnna-Lena Semmler, Sabrina Sacconi, J Elisa Bach, et al.Nature|July 25, 2006
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21Marc Cruts, Ilse Gijselinck, Julie van der Zee, et al.Pageof 11