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Neuroimage. Clinical|December 8, 2018
The spinal and cerebral profile of adult spinal-muscular atrophy: A multimodal imaging studyGiorgia Querin, Mohamed-Mounir El Mendili, Timothée Lenglet, et al.
Plos One|September 9, 2016
Correction: Bee Venom for the Treatment of Parkinson Disease - A Randomized Controlled Clinical TrialAndreas Hartmann, Julia Muellner, Niklaus Meier, et al.
Plos One|July 13, 2016
Bee Venom for the Treatment of Parkinson Disease - A Randomized Controlled Clinical TrialAndreas Hartmann, Julia Müllner, Niklaus Meier, et al.
Journal of Medical Genetics|June 26, 2010
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlationsStéphanie Millecamps, François Salachas, Cécile Cazeneuve, et al.
Human Mutation|March 9, 2007
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementiaJulie van der Zee, Isabelle Le Ber, Sebastian Maurer-Stroh, et al.
Brain : a Journal of Neurology|October 31, 2006
Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementiaIsabelle Le Ber, Eric Guedj, Audrey Gabelle, et al.
Brain : a Journal of Neurology|February 5, 2008
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic studyIsabelle Le Ber, Agnès Camuzat, Didier Hannequin, et al.
Journal of Alzheimer'S Disease : JAD|December 21, 2012
C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testingIsabelle Le Ber, Agnès Camuzat, Lena Guillot-Noel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 17, 2018
Suggestive association between OPRM1 and impulse control disorders in Parkinson's diseaseFlorence Cormier-Dequaire, Samir Bekadar, Mathieu Anheim, et al.
Brain : a Journal of Neurology|August 28, 2024
Dysregulation of muscle cholesterol transport in amyotrophic lateral sclerosisDelphine Sapaly, Flore Cheguillaume, Laure Weill, et al.
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