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E Tournier

Showing results (51-60 of 155) with videos related to

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Human Mutation|January 11, 2000
Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene with a high G-C contentJ L Escary, M Cécillon, J Maciazek, et al.
Neurology|June 1, 1995
Monozygotic twins discordant for familial hemiplegic migraineA Ducros, A Joutel, P Labauge, et al.
Radiology|January 22, 2000
Familial form of intracranial cavernous angioma: MR imaging findings in 51 families. French Society of NeurosurgeryL Brunereau, P Labauge, E Tournier-Lasserve, et al.
Thrombosis and Haemostasis|January 4, 1998
Lack of association between thrombosis in primary antiphospholipid syndrome and the recently described thrombophilic 3'-untranslated prothrombin gene polymorphismS Bentolila, L Ripoll, L Drouet, et al.
Annales De Dermatologie Et De Venereologie|March 18, 2026
Gamma secretase inhibitor nirogacestat and secondary hidradenitis suppurativa: An expected on-target effectM D'Agostino, N Gerard, L Coquard, et al.
Neurology|August 25, 2010
Acute urinary retention due to a novel collagen COL4A1 mutationT Rouaud, P Labauge, E Tournier Lasserve, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 26, 2016
Immunohistochemical staining for diagnosis of cutaneous mastocytosisN Kirsten, E Tournier, B Lepage, et al.
Journal of the Neurological Sciences|February 23, 2015
Occurrence of multiple Cerebral Cavernous Malformations in a patient with Neurofibromatosis type 1K Rerat, F Parker, G Nasser, et al.
Eye (London, England)|December 19, 2006
Familial central retinal vein occlusionJ-F Girmens, S Scheer, E Héron, et al.
Neurology|October 17, 2007
Clinical and brain MRI follow-up study of a family with COL4A1 mutationK Vahedi, M Boukobza, P Massin, et al.
Pageof 16

Showing results (51-60 of 155) with videos related to

Sort By:
Pageof 16
Human Mutation|January 11, 2000
Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene with a high G-C contentJ L Escary, M Cécillon, J Maciazek, et al.
Neurology|June 1, 1995
Monozygotic twins discordant for familial hemiplegic migraineA Ducros, A Joutel, P Labauge, et al.
Radiology|January 22, 2000
Familial form of intracranial cavernous angioma: MR imaging findings in 51 families. French Society of NeurosurgeryL Brunereau, P Labauge, E Tournier-Lasserve, et al.
Thrombosis and Haemostasis|January 4, 1998
Lack of association between thrombosis in primary antiphospholipid syndrome and the recently described thrombophilic 3'-untranslated prothrombin gene polymorphismS Bentolila, L Ripoll, L Drouet, et al.
Annales De Dermatologie Et De Venereologie|March 18, 2026
Gamma secretase inhibitor nirogacestat and secondary hidradenitis suppurativa: An expected on-target effectM D'Agostino, N Gerard, L Coquard, et al.
Neurology|August 25, 2010
Acute urinary retention due to a novel collagen COL4A1 mutationT Rouaud, P Labauge, E Tournier Lasserve, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 26, 2016
Immunohistochemical staining for diagnosis of cutaneous mastocytosisN Kirsten, E Tournier, B Lepage, et al.
Journal of the Neurological Sciences|February 23, 2015
Occurrence of multiple Cerebral Cavernous Malformations in a patient with Neurofibromatosis type 1K Rerat, F Parker, G Nasser, et al.
Eye (London, England)|December 19, 2006
Familial central retinal vein occlusionJ-F Girmens, S Scheer, E Héron, et al.
Neurology|October 17, 2007
Clinical and brain MRI follow-up study of a family with COL4A1 mutationK Vahedi, M Boukobza, P Massin, et al.
Pageof 16