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Revue Neurologique|June 30, 2021
Measles Sclerosing Subacute PanEncephalitis (SSPE), an intriguing and ever-present disease: Data, assumptions and new perspectivesP Lebon, A Gelot, S-Y Zhang, et al.Revue Neurologique|July 13, 2021
Electro-clinical presentation of hereditary transthyretin related amyloidosis when presenting as a polyneuropathy of unknown origin in northern FranceJ-B Davion, P Bocquillon, F Cassim, et al.Revue Neurologique|May 22, 2022
Loss of bone mineral density in hemiplegic patients after stroke: Prospective single-center studyP Potin, Y Degboé, G Couture, et al.Revue Neurologique|January 1, 1986
[Marchiafava-Bignami disease with favorable development]T Delangre, D Hannequin, E Clavier, et al.Revue Neurologique|May 14, 2022
Rasmussen's encephalitis: Early diagnostic criteria in childrenN Villeneuve, A Lépine, N Girard, et al.Revue Neurologique|July 24, 2021
Lafora disease: Current biology and therapeutic approachesS Mitra, E Gumusgoz, B A MinassianRevue Neurologique|October 11, 2017
Cerebral amyloid angiopathy-related cognitive impairment: The search for a specific neuropsychological patternM Planton, N Raposo, J-F Albucher, et al.Revue Neurologique|January 1, 1986
[Complete human Klüver-Bucy syndrome after encephalitis caused by herpes simplex type 2]S Bakchine, F Chain, F LhermitteRevue Neurologique|January 1, 1986
[Congenital oculomotor apraxia with corpus callosum agenesis and subtentorial atrophy]M Vercelletto-Friol, F Lavenant, J H Bricout, et al.Revue Neurologique|January 1, 1986
[Prolonged absence states in aged patients without epileptic antecedents]C Bourrat, P Garde, M Boucher, et al.Pageof 566