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P Labauge

Showing results (101-110 of 142) with videos related to

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Annals of Neurology|May 1, 1997
Allelic heterogeneity of Mediterranean myoclonus and the cystatin B geneP Labauge, R Ouazzani, A M'Rabet, et al.
Neuro-Chirurgie|May 18, 2007
[Natural history of intramedullary cavernomas. Results of the French Multicentric Study]F Parker, J-P Lejeune, S Bouly, et al.
La Revue De Medecine Interne|October 9, 2004
[Resurgence of syphilis: a prospective study at an University Hospital, Nimes]J P Lavigne, I Rouanet, E Gleize, et al.
European Journal of Neurology|July 14, 2012
Novel SPG10 mutation associated with dysautonomia, spinal cord atrophy, and skin biopsy abnormalityN Collongues, C Depienne, N Boehm, et al.
European Journal of Neurology|August 19, 2020
Acute retinal arterial ischaemia: silent brain infarcts prevalence and short-term recurrenceX Ayrignac, C Zagroun, A Coget, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 28, 1999
Spanish families with cavernous angiomas do not share the Hispano-American CCM1 haplotypeH H Jung, P Labauge, S Laberge, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical|April 28, 2022
The socioeconomic impact of multiple sclerosis in France: Results from the PETALS studyA Bouleau, C Dulong, C A Schwerer, et al.
Nature Genetics|October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomasS Laberge-le Couteulx, H H Jung, P Labauge, et al.
Neurology|March 27, 2002
Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME)P Labauge, L O Amer, M Simonetta-Moreau, et al.
Journal of Neurology|February 17, 2015
A novel autosomal dominant leukodystrophy with specific MRI patternA Corlobé, F Taithe, P Clavelou, et al.
Pageof 15

Showing results (101-110 of 142) with videos related to

Sort By:
Pageof 15
Annals of Neurology|May 1, 1997
Allelic heterogeneity of Mediterranean myoclonus and the cystatin B geneP Labauge, R Ouazzani, A M'Rabet, et al.
Neuro-Chirurgie|May 18, 2007
[Natural history of intramedullary cavernomas. Results of the French Multicentric Study]F Parker, J-P Lejeune, S Bouly, et al.
La Revue De Medecine Interne|October 9, 2004
[Resurgence of syphilis: a prospective study at an University Hospital, Nimes]J P Lavigne, I Rouanet, E Gleize, et al.
European Journal of Neurology|July 14, 2012
Novel SPG10 mutation associated with dysautonomia, spinal cord atrophy, and skin biopsy abnormalityN Collongues, C Depienne, N Boehm, et al.
European Journal of Neurology|August 19, 2020
Acute retinal arterial ischaemia: silent brain infarcts prevalence and short-term recurrenceX Ayrignac, C Zagroun, A Coget, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 28, 1999
Spanish families with cavernous angiomas do not share the Hispano-American CCM1 haplotypeH H Jung, P Labauge, S Laberge, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical|April 28, 2022
The socioeconomic impact of multiple sclerosis in France: Results from the PETALS studyA Bouleau, C Dulong, C A Schwerer, et al.
Nature Genetics|October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomasS Laberge-le Couteulx, H H Jung, P Labauge, et al.
Neurology|March 27, 2002
Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME)P Labauge, L O Amer, M Simonetta-Moreau, et al.
Journal of Neurology|February 17, 2015
A novel autosomal dominant leukodystrophy with specific MRI patternA Corlobé, F Taithe, P Clavelou, et al.
Pageof 15