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E Tournier

Showing results (31-40 of 155) with videos related to

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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.
Journal of Chromatography. B, Biomedical Sciences and Applications|March 18, 1999
Purification of immunoglobulins G by protein A/G affinity membrane chromatographyO P Dancette, J L Taboureau, E Tournier, 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.
The American Journal of Hospice & Palliative Care|June 11, 2004
Hospice referral decisions: the role of physiciansBrenda S Sanders, Tracy L Burkett, George E Dickinson, et al.
Stroke|October 1, 1991
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathyE Tournier-Lasserve, M T Iba-Zizen, N Romero, 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.
Neurology|September 15, 2010
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraineF Riant, A Ducros, C Ploton, et al.
Molecular and Cellular Biology|May 1, 1989
Remarkable intron and exon sequence conservation in human and mouse homeobox Hox 1.3 genesE Tournier-Lasserve, W F Odenwald, J Garbern, et al.
Pageof 16

Showing results (31-40 of 155) with videos related to

Sort By:
Pageof 16
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.
Journal of Chromatography. B, Biomedical Sciences and Applications|March 18, 1999
Purification of immunoglobulins G by protein A/G affinity membrane chromatographyO P Dancette, J L Taboureau, E Tournier, 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.
The American Journal of Hospice & Palliative Care|June 11, 2004
Hospice referral decisions: the role of physiciansBrenda S Sanders, Tracy L Burkett, George E Dickinson, et al.
Stroke|October 1, 1991
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathyE Tournier-Lasserve, M T Iba-Zizen, N Romero, 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.
Neurology|September 15, 2010
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraineF Riant, A Ducros, C Ploton, et al.
Molecular and Cellular Biology|May 1, 1989
Remarkable intron and exon sequence conservation in human and mouse homeobox Hox 1.3 genesE Tournier-Lasserve, W F Odenwald, J Garbern, et al.
Pageof 16