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Neurology
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May 2, 2007
Adult-onset vanishing white matter leukoencephalopathy presenting as psychosis
C 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 cohort
J-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 review
O Osman, P Labrune, P Reiner, et al.
Neurology
|
February 11, 2000
Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene
H Chabriat, K Vahedi, C A Clark, et al.
Cerebrovascular Diseases (Basel, Switzerland)
|
January 12, 2016
Thrombolysis in Stroke Patients with Isolated Aphasia
C Denier, O Chassin, C Vandendries, et al.
Journal Francais D'Ophtalmologie
|
September 9, 2017
Fundus autofluorescence in retinal artery occlusion: A more precise diagnosis
J-L Bacquet, M Sarov-Rivière, C Denier, et al.
Neurology
|
November 4, 2000
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy
K 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 channel
A 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 gene
A Bisserbe, G Tertian, C Buffet, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 67) with videos related to
Sort By:
Page
of 7
Neurology
|
May 2, 2007
Adult-onset vanishing white matter leukoencephalopathy presenting as psychosis
C 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 cohort
J-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 review
O Osman, P Labrune, P Reiner, et al.
Neurology
|
February 11, 2000
Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene
H Chabriat, K Vahedi, C A Clark, et al.
Cerebrovascular Diseases (Basel, Switzerland)
|
January 12, 2016
Thrombolysis in Stroke Patients with Isolated Aphasia
C Denier, O Chassin, C Vandendries, et al.
Journal Francais D'Ophtalmologie
|
September 9, 2017
Fundus autofluorescence in retinal artery occlusion: A more precise diagnosis
J-L Bacquet, M Sarov-Rivière, C Denier, et al.
Neurology
|
November 4, 2000
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy
K 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 channel
A 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 gene
A Bisserbe, G Tertian, C Buffet, et al.
Page
of 7