Showing results (11-20 of 157) with videos related to
Sort By:
Pageof 16
Journal of Neurosurgery|July 12, 2003
Treatment of anterior communicating artery aneurysms: complementary aspects of microsurgical and endovascular proceduresFrançois Proust, Bertrand Debono, Didier Hannequin, et al.Journal of Alzheimer'S Disease : JAD|August 17, 2013
Amyloid-related imaging abnormalities in AβPP duplication carriersLudivine Chamard, David Wallon, Alexa Pijoff, et al.Plos One|January 26, 2012
Visual agnosia and posterior cerebral artery infarcts: an anatomical-clinical studyOlivier Martinaud, Dorothée Pouliquen, Emmanuel Gérardin, et al.Journal of Neurosurgery|November 3, 2009
Alleviation of off-period dystonia in Parkinson disease by a microlesion following subthalamic implantationStéphane Derrey, Romain Lefaucheur, Nathalie Chastan, et al.Archives of Clinical Neuropsychology : the Official Journal of the National Academy of Neuropsychologists|July 20, 2014
Agnosia for mirror stimuli: a new case report with a small parietal lesionOlivier Martinaud, Nicolas Mirlink, Sandrine Bioux, et al.American Journal of Medical Genetics. Part A|March 18, 2011
Juvenile Huntington disease in an 18-month-old boy revealed by global developmental delay and reduced cerebellar volumeGaël Nicolas, Didier Devys, Alice Goldenberg, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2009
Microsubthalamotomy effect at day 3: screening for determinantsDavid Maltête, Nathalie Chastan, Stéphane Derrey, et al.Cognitive Neuropsychology|November 2, 2010
Right ventral frontal hypometabolism and abnormal sense of self in a case of disproportionate retrograde amnesiaPascale Piolino, Didier Hannequin, Beatrice Desgranges, et al.Journal of Neurosurgery|October 16, 2012
Validation of the superior interhemispheric approach for tuberculum sellae meningioma: clinical articleSophie Curey, Stéphane Derrey, Pierre Hannequin, et al.Muscle & Nerve|November 1, 2005
Cardiac conduction alterations in a French family with amyloidosis of the Finnish type with the p.Asp187Tyr mutation in the GSN geneNathalie Chastan, Stéphanie Baert-Desurmont, Pascale Saugier-Veber, et al.Pageof 16