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E Tournier-Lasserve

Showing results (31-40 of 123) with videos related to

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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.
Journal of Autoimmunity|October 10, 2001
A dinucleotide repeat polymorphism at the poly(ADP-ribose) polymerase gene is not associated with predisposition to type 1 diabetes in French CaucasiansO Delrieu, D Dubois-Laforgue, J Timsit, 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.
Journal of Neuroimmunology|June 1, 1995
In vivo clonal expression of T lymphocytes specific for an immunodominant N-terminal myelin basic protein epitope in healthy individualsA Shanmugam, C Copie-Bergman, S Caillat, et al.
Neurology|April 1, 1991
MS and HTLV-IO Gout, E Tournier-Lasserve, O Lyon-Caen, et al.
Archives of Neurology|February 15, 2001
Missense CACNA1A mutation causing episodic ataxia type 2C Denier, A Ducros, A Durr, et al.
Stroke|November 1, 1994
Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASILM M Ruchoux, H Chabriat, M G Bousser, et al.
Genes & Development|February 1, 1989
The Hox-1.3 homeo box protein is a sequence-specific DNA-binding phosphoproteinW F Odenwald, J Garbern, H Arnheiter, 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.
Pageof 13

Showing results (31-40 of 123) with videos related to

Sort By:
Pageof 13
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.
Journal of Autoimmunity|October 10, 2001
A dinucleotide repeat polymorphism at the poly(ADP-ribose) polymerase gene is not associated with predisposition to type 1 diabetes in French CaucasiansO Delrieu, D Dubois-Laforgue, J Timsit, 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.
Journal of Neuroimmunology|June 1, 1995
In vivo clonal expression of T lymphocytes specific for an immunodominant N-terminal myelin basic protein epitope in healthy individualsA Shanmugam, C Copie-Bergman, S Caillat, et al.
Neurology|April 1, 1991
MS and HTLV-IO Gout, E Tournier-Lasserve, O Lyon-Caen, et al.
Archives of Neurology|February 15, 2001
Missense CACNA1A mutation causing episodic ataxia type 2C Denier, A Ducros, A Durr, et al.
Stroke|November 1, 1994
Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASILM M Ruchoux, H Chabriat, M G Bousser, et al.
Genes & Development|February 1, 1989
The Hox-1.3 homeo box protein is a sequence-specific DNA-binding phosphoproteinW F Odenwald, J Garbern, H Arnheiter, 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.
Pageof 13