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E Tournier-Lasserve

Showing results (21-30 of 123) with videos related to

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European Journal of Human Genetics : EJHG|June 3, 1999
Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas familiesS Laberge, P Labauge, E Maréchal, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1996
Prevalence of serum antibodies to hepatitis C virus is not increased in patients with multiple sclerosisO Heinzlef, E Roullet, C Johanet, et al.
Lancet (London, England)|December 24, 1998
Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Société Française de NeurochirurgieP Labauge, S Laberge, L Brunereau, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 30, 2009
Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhoodP Bertholon, S Chabrier, F Riant, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 21, 2009
Frequency and phenotypes of cutaneous vascular malformations in a consecutive series of 417 patients with familial cerebral cavernous malformationsJ Sirvente, O Enjolras, M Wassef, et al.
Journal of Neurology|March 16, 2012
Presymptomatic genetic testing in CADASILS Reyes, A Kurtz, D Hervé, et al.
La Revue De Medecine Interne|November 25, 1998
[Immunogenetic bases of systemic lupus erythematosus in humans]M Michel, O Meyer, C Françès, et al.
American Journal of Medical Genetics|November 11, 1996
An additional monogenic disorder that masquerades as multiple sclerosisK Vahedi, E Tournier-Lasserve, K Vahedi, et al.
Stroke|January 1, 1993
Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological studyM Baudrimont, F Dubas, A Joutel, et al.
Stroke|October 1, 1991
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathyE Tournier-Lasserve, M T Iba-Zizen, N Romero, et al.
Pageof 13

Showing results (21-30 of 123) with videos related to

Sort By:
Pageof 13
European Journal of Human Genetics : EJHG|June 3, 1999
Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas familiesS Laberge, P Labauge, E Maréchal, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1996
Prevalence of serum antibodies to hepatitis C virus is not increased in patients with multiple sclerosisO Heinzlef, E Roullet, C Johanet, et al.
Lancet (London, England)|December 24, 1998
Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Société Française de NeurochirurgieP Labauge, S Laberge, L Brunereau, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 30, 2009
Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhoodP Bertholon, S Chabrier, F Riant, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 21, 2009
Frequency and phenotypes of cutaneous vascular malformations in a consecutive series of 417 patients with familial cerebral cavernous malformationsJ Sirvente, O Enjolras, M Wassef, et al.
Journal of Neurology|March 16, 2012
Presymptomatic genetic testing in CADASILS Reyes, A Kurtz, D Hervé, et al.
La Revue De Medecine Interne|November 25, 1998
[Immunogenetic bases of systemic lupus erythematosus in humans]M Michel, O Meyer, C Françès, et al.
American Journal of Medical Genetics|November 11, 1996
An additional monogenic disorder that masquerades as multiple sclerosisK Vahedi, E Tournier-Lasserve, K Vahedi, et al.
Stroke|January 1, 1993
Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological studyM Baudrimont, F Dubas, A Joutel, et al.
Stroke|October 1, 1991
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathyE Tournier-Lasserve, M T Iba-Zizen, N Romero, et al.
Pageof 13