Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Genevieve Fourcade"'
Autor:
Lavinia Tatu, Xavier Ayrignac, Nicolas Gaillard, Sylvain Lehmann, Mahmoud Charif, Eric Thouvenot, Yassine Boukriche, Souhayla Azakri, Anne Wacongne, Laurent Collombier, Genevieve Fourcade, Dimitri Renard, Laura Chiper, Erick Mercier
Publikováno v:
Journal of Alzheimer's Disease
Journal of Alzheimer's Disease, IOS Press, 2018, pp.1-9. ⟨10.3233/JAD-180269⟩
Journal of Alzheimer's Disease, IOS Press, 2018, pp.1-9. ⟨10.3233/JAD-180269⟩
BACKGROUND Cerebral amyloid angiopathy (CAA) can be associated with primary vasculitis of small/medium-sized leptomeningeal and cortical arteries, called CAA-related inflammation (CAA-ri). OBJECTIVE To compare hemorrhagic and diffusion-weighted imagi
Autor:
Eric Thouvenot, Yassine Boukriche, Nicolas Menjot de Champfleur, Audrey Gabelle, Caroline Arquizan, Claire Duflos, Genevieve Fourcade, Nicolas Raposo, Anne Wacongne, Alain Viguier, Anne Ducros, Laura Chiper, Dimitri Renard, Pierre Labauge, Fabrice Bonneville, Sylvain Lehmann, Mahmoud Charif, Thibaut Allou, Xavier Ayrignac, Sarah Coulette
Publikováno v:
Cerebrovascular Diseases
Cerebrovascular Diseases, Karger, 2019, 48 (1-2), pp.38-44. ⟨10.1159/000502832⟩
Cerebrovascular Diseases, Karger, 2019, 48 (1-2), pp.38-44. ⟨10.1159/000502832⟩
Objective: To describe the clinico-radiological features and long-term prognosis in patients with cerebral amyloid angiopathy-related inflammation (CAA-ri). Methods: Twenty-eight CAA-ri patients were recruited retrospectively from 6 neurological cent
Autor:
Anne Le Floch, Dimitri Renard, Souhayla Azakri, Xavier Ayrignac, Sylvain Lehmann, Cecilia Marelli, Christophe Hirtz, Eric Thouvenot, Anne Wacongne, Mahmoud Charif, Stephane Bouly, Audrey Gabelle, Caroline Arquizan, Genevieve Fourcade
Publikováno v:
Journal of Alzheimer's Disease
Journal of Alzheimer's Disease, IOS Press, 2016, 50 (3), pp.759-764. ⟨10.3233/JAD-150621⟩
Journal of Alzheimer's Disease, IOS Press, 2016, 50 (3), pp.759-764. ⟨10.3233/JAD-150621⟩
BACKGROUND Decreased cerebrospinal fluid (CSF) amyloid-β 1-40 (Aβ40) and amyloid-β 1-42 (Aβ42) and increased total and phosphorylated tau (t-tau, p-tau) concentrations have been described in cerebral amyloid angiopathy (CAA). OBJECTIVE Our aim wa
Publikováno v:
Revue Neurologique. 167:522-525
Resume Introduction La « paralysie du samedi soir » touche de maniere exceptionnelle le plexus brachial. Observation Un jeune homme presenta un deficit sensitivo-moteur du membre superieur droit au reveil. L’electroneuromyogramme, en faveur d’u
Publikováno v:
Pratique Neurologique - FMC. 1:205-207
Autor:
Dimitri, Renard, Laurent, Collombier, Giovanni, Castelnovo, Genevieve, Fourcade, Pierre-Olivier, Kotzki, Pierre, LaBauge
Publikováno v:
Acta neurologica Belgica. 111(4)
FDG-PET in ALS most typically demonstrates a primary (and sometimes also supplementary) motor cortex hypometabolism, often associated with more diffuse cortical hypometabolism involving mostly the dorsolateral prefrontal cortex, the medial and latera
Autor:
Dimitri, Renard, Laurent, Collombier, Giovanni, Castelnovo, Genevieve, Fourcade, Charles, Debrigode, Pierre, Labauge
Publikováno v:
Acta neurologica Belgica. 110(1)
Brain FDG-PET after radiation therapy is classically used to differentiate between tumor recurrence and radiation-related tumor necrosis. Little is known about FDG-PET in patients with radiation-induced leukoencephalopathy without radiological aspect
Autor:
Patrice Bourgeois, Amandine Boyer, Didier Bessis, Dimitri Renard, Didier Milhaud, Vera Esteves-Vieira, Patrice Roll, Nicolas Lévy, Genevieve Fourcade, Annachiara De Sandre-Giovannoli
Publikováno v:
Stroke
Stroke, American Heart Association, 2009, 40 (2), ⟨10.1161/STROKEAHA.108.531780⟩
Stroke, 2009, 40 (2), ⟨10.1161/STROKEAHA.108.531780⟩
Stroke, American Heart Association, 2009, 40 (2), ⟨10.1161/STROKEAHA.108.531780⟩
Stroke, 2009, 40 (2), ⟨10.1161/STROKEAHA.108.531780⟩
Background and Purpose— Laminopathies arise through mutations in genes encoding Lamin A/C ( LMNA ) or associated proteins. They cause 4 different groups of disorders with diverse severity and often overlapping features: diseases of striated muscle
Publikováno v:
Neurology. 84:e194-e194
We present 2 patients with genetically proven symptomatic fragile X-associated tremor ataxia syndrome (FXTAS), one 62-year-old man with progressive action tremor and one 74-year-old man with progressive ataxia, showing typical middle cerebellar pedun