Showing results (81-90 of 102) with videos related to
Sort By:
Pageof 11
Journal of Medical Genetics|April 14, 2012
Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genesStéphanie Millecamps, Séverine Boillée, Isabelle Le Ber, et al.Journal of the Neurological Sciences|October 22, 2008
Frontal Assessment Battery is a marker of dorsolateral and medial frontal functions: A SPECT study in frontotemporal dementiaEric Guedj, Gilles Allali, Celine Goetz, et al.Cellular and Molecular Life Sciences : CMLS|May 15, 2023
Neurofilament accumulations in amyotrophic lateral sclerosis patients' motor neurons impair axonal initial segment integrityCynthia Lefebvre-Omar, Elise Liu, Carine Dalle, et al.Parkinsonism & Related Disorders|October 10, 2018
Naftazone in advanced Parkinson's disease: An acute L-DOPA challenge randomized controlled trialJean-Christophe Corvol, Franck Durif, Wassilios G Meissner, et al.Journal of Neurology|July 12, 2018
Extrapyramidal deficits in ALS: a combined biomechanical and neuroimaging studyMaryse Feron, Annabelle Couillandre, Eya Mseddi, et al.Annals of Clinical and Translational Neurology|April 25, 2015
Endplate denervation correlates with Nogo-A muscle expression in amyotrophic lateral sclerosis patientsGaëlle Bruneteau, Stéphanie Bauché, Jose Luis Gonzalez de Aguilar, et al.Neurology|June 22, 2018
Longitudinal analysis of impulse control disorders in Parkinson diseaseJean-Christophe Corvol, Fanny Artaud, Florence Cormier-Dequaire, et al.The Lancet. Haematology|December 22, 2015
Methotrexate and temozolomide versus methotrexate, procarbazine, vincristine, and cytarabine for primary CNS lymphoma in an elderly population: an intergroup ANOCEF-GOELAMS randomised phase 2 trialAntonio Omuro, Olivier Chinot, Luc Taillandier, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 14, 2019
Examining the Reserve Hypothesis in Parkinson's Disease: A Longitudinal StudyPei-Chen Lee, Fanny Artaud, Florence Cormier-Dequaire, et al.Human Mutation|April 17, 2007
Progranulin null mutations in both sporadic and familial frontotemporal dementiaIsabelle Le Ber, Julie van der Zee, Didier Hannequin, et al.Pageof 11