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C Denier

Showing results (41-50 of 67) with videos related to

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Neurology|May 2, 2007
Adult-onset vanishing white matter leukoencephalopathy presenting as psychosisC Denier, A Orgibet, F Roffi, et al.
Revue Neurologique|August 15, 2025
Transthyretin variant cerebral amyloid angiopathy fulfilling the modified Boston criteria: Retrospective data from the Bicêtre hospital cohortJ-B Brunet de Courssou, L Gorza, M Babin, et al.
Revue Neurologique|September 16, 2019
Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature reviewO Osman, P Labrune, P Reiner, et al.
Neurology|February 11, 2000
Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A geneH Chabriat, K Vahedi, C A Clark, et al.
Cerebrovascular Diseases (Basel, Switzerland)|January 12, 2016
Thrombolysis in Stroke Patients with Isolated AphasiaC Denier, O Chassin, C Vandendries, et al.
Journal Francais D'Ophtalmologie|September 9, 2017
Fundus autofluorescence in retinal artery occlusion: A more precise diagnosisJ-L Bacquet, M Sarov-Rivière, C Denier, et al.
Neurology|November 4, 2000
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophyK Vahedi, C Denier, A Ducros, et al.
The New England Journal of Medicine|July 7, 2001
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channelA Ducros, C Denier, A Joutel, et al.
Journal Francais D'Ophtalmologie|November 14, 2015
[Bilateral chronic ischemic retinopathy: A case report]F El Asri, J-M Giraud, H El Chehab, et al.
Revue Neurologique|April 7, 2015
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 geneA Bisserbe, G Tertian, C Buffet, et al.
Pageof 7

Showing results (41-50 of 67) with videos related to

Sort By:
Pageof 7
Neurology|May 2, 2007
Adult-onset vanishing white matter leukoencephalopathy presenting as psychosisC Denier, A Orgibet, F Roffi, et al.
Revue Neurologique|August 15, 2025
Transthyretin variant cerebral amyloid angiopathy fulfilling the modified Boston criteria: Retrospective data from the Bicêtre hospital cohortJ-B Brunet de Courssou, L Gorza, M Babin, et al.
Revue Neurologique|September 16, 2019
Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature reviewO Osman, P Labrune, P Reiner, et al.
Neurology|February 11, 2000
Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A geneH Chabriat, K Vahedi, C A Clark, et al.
Cerebrovascular Diseases (Basel, Switzerland)|January 12, 2016
Thrombolysis in Stroke Patients with Isolated AphasiaC Denier, O Chassin, C Vandendries, et al.
Journal Francais D'Ophtalmologie|September 9, 2017
Fundus autofluorescence in retinal artery occlusion: A more precise diagnosisJ-L Bacquet, M Sarov-Rivière, C Denier, et al.
Neurology|November 4, 2000
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophyK Vahedi, C Denier, A Ducros, et al.
The New England Journal of Medicine|July 7, 2001
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channelA Ducros, C Denier, A Joutel, et al.
Journal Francais D'Ophtalmologie|November 14, 2015
[Bilateral chronic ischemic retinopathy: A case report]F El Asri, J-M Giraud, H El Chehab, et al.
Revue Neurologique|April 7, 2015
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 geneA Bisserbe, G Tertian, C Buffet, et al.
Pageof 7