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Neuromuscular Disorders : NMD|January 27, 2009
Peripheral neuropathy and 46XY gonadal dysgenesis: a heterogeneous entityJonathan Baets, Ines Dierick, Chantal Ceuterick-de Groote, et al.Genome Research|July 22, 2025
Genotype imputation from low-coverage data for medical and population genetic analysesSimone Andrea Biagini, Sara Becelaere, Mio Aerden, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 23, 2025
Basic Science and PathogenesisCeleste Laureyssen, Fahri Küçükali, Jasper Van Dongen, et al.Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|September 29, 2019
TSPO Versus P2X7 as a Target for Neuroinflammation: An In Vitro and In Vivo StudyDonatienne Van Weehaeghe, Evelien Van Schoor, Joke De Vocht, et al.Annals of Clinical and Translational Neurology|September 14, 2019
Serum neurofilament heavy chains as early marker of motor neuron degenerationMaxim De Schaepdryver, Janne Goossens, Steffi De Meyer, et al.Neuroimage. Clinical|July 13, 2020
Non-invasive characterization of amyotrophic lateral sclerosis in a hTDP-43A315T mouse model: A PET-MR studyAkila Weerasekera, Melissa Crabbé, Sandra O Tomé, et al.Acta Neuropathologica Communications|September 18, 2023
A toxic gain-of-function mechanism in C9orf72 ALS impairs the autophagy-lysosome pathway in neuronsJimmy Beckers, Arun Kumar Tharkeshwar, Laura Fumagalli, et al.Seminars in Arthritis and Rheumatism|April 8, 2021
Detection of multiple myositis-specific autoantibodies in unique patients with idiopathic inflammatory myopathy: A single centre-experience and literature review: Systematic reviewNele Van Horebeek, Jean-Baptiste Vulsteke, Xavier Bossuyt, et al.Acta Neuropathologica|July 22, 2022
Increased pyroptosis activation in white matter microglia is associated with neuronal loss in ALS motor cortexEvelien Van Schoor, Simona Ospitalieri, Sebastiaan Moonen, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 5, 2018
Multicenter validation of [18F]-FDG PET and support-vector machine discriminant analysis in automatically classifying patients with amyotrophic lateral sclerosis versus controlsLudovic D'hulst, Donatienne Van Weehaeghe, Adriano Chiò, et al.Pageof 37