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E Tournier

Showing results (141-150 of 155) with videos related to

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Journal of the European Academy of Dermatology and Venereology : JEADV|April 23, 2019
Frequency of isolated cutaneous involvement in adult mastocytosis: a cohort studyM Fradet, M Negretto, E Tournier, et al.
Molecular Syndromology|June 27, 2013
CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple MeningiomasF Riant, F Bergametti, H-D Fournier, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|January 16, 2016
Bone marrow tryptase as a possible diagnostic criterion for adult systemic mastocytosisC Bulai Livideanu, P A Apoil, B Lepage, et al.
Journal of Neurology|April 23, 2020
Heritable and non-heritable uncommon causes of strokeA Bersano, M Kraemer, A Burlina, et al.
Journal of Neurology|June 20, 2020
Correction to: Heritable and non-heritable uncommon causes of strokeA Bersano, M Kraemer, A Burlina, et al.
American Journal of Human Genetics|November 16, 2004
Mutations within the programmed cell death 10 gene cause cerebral cavernous malformationsF Bergametti, C Denier, P Labauge, et al.
American Journal of Human Genetics|January 23, 1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxiaA Ducros, C Denier, A Joutel, et al.
Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.
Nature|October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiaA Joutel, C Corpechot, A Ducros, et al.
Neurology|June 17, 1999
High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2C Denier, A Ducros, K Vahedi, et al.
Pageof 16

Showing results (141-150 of 155) with videos related to

Sort By:
Pageof 16
Journal of the European Academy of Dermatology and Venereology : JEADV|April 23, 2019
Frequency of isolated cutaneous involvement in adult mastocytosis: a cohort studyM Fradet, M Negretto, E Tournier, et al.
Molecular Syndromology|June 27, 2013
CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple MeningiomasF Riant, F Bergametti, H-D Fournier, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|January 16, 2016
Bone marrow tryptase as a possible diagnostic criterion for adult systemic mastocytosisC Bulai Livideanu, P A Apoil, B Lepage, et al.
Journal of Neurology|April 23, 2020
Heritable and non-heritable uncommon causes of strokeA Bersano, M Kraemer, A Burlina, et al.
Journal of Neurology|June 20, 2020
Correction to: Heritable and non-heritable uncommon causes of strokeA Bersano, M Kraemer, A Burlina, et al.
American Journal of Human Genetics|November 16, 2004
Mutations within the programmed cell death 10 gene cause cerebral cavernous malformationsF Bergametti, C Denier, P Labauge, et al.
American Journal of Human Genetics|January 23, 1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxiaA Ducros, C Denier, A Joutel, et al.
Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.
Nature|October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiaA Joutel, C Corpechot, A Ducros, et al.
Neurology|June 17, 1999
High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2C Denier, A Ducros, K Vahedi, et al.
Pageof 16