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E Tournier

Showing results (71-80 of 155) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|April 24, 2002
Anticardiolipin antibodies in patients with multiple sclerosis do not represent a subgroup of patients according to clinical, familial, and biological characteristicsO Heinzlef, B Weill, C Johanet, et al.
Annals of Neurology|March 15, 2000
De novo mutation in the Notch3 gene causing CADASILA Joutel, D D Dodick, J E Parisi, et al.
European Journal of Immunology|June 1, 1991
T cell response to myelin basic protein epitopes in multiple sclerosis patients and healthy subjectsR Liblau, E Tournier-Lasserve, J Maciazek, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 4, 2016
Tumour lysis syndrome: an unexpected adverse event associated with ipilimumabM Masson Regnault, J Ofaiche, S Boulinguez, et al.
Annales De Dermatologie Et De Venereologie|February 4, 2022
Skin manifestations of hypereosinophilic syndrome are polymorphous and difficult to treat: A retrospective cohort studyG Salomon, M Severino, E Casassa, et al.
Annals of Neurology|February 16, 1999
An association between autosomal dominant cerebral cavernomas and a distinctive hyperkeratotic cutaneous vascular malformation in 4 familiesP Labauge, O Enjolras, J J Bonerandi, et al.
Clinical Genetics|November 21, 2013
Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformationsF Riant, S Odent, M Cecillon, et al.
Methodsx|July 8, 2015
Modification of a commercial DNA extraction kit for safe and rapid recovery of DNA and RNA simultaneously from soil, without the use of harmful solventsE Tournier, L Amenc, A L Pablo, et al.
The British Journal of Dermatology|December 24, 2017
Efficacy of anti-programmed cell death-1 immunotherapy for skin carcinomas and melanoma metastases in a patient with xeroderma pigmentosumG Salomon, A Maza, S Boulinguez, et al.
Journal of Neurology|May 18, 2001
Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?J Julien, C Denier, X Ferrer, et al.
Pageof 16

Showing results (71-80 of 155) with videos related to

Sort By:
Pageof 16
Journal of Neurology, Neurosurgery, and Psychiatry|April 24, 2002
Anticardiolipin antibodies in patients with multiple sclerosis do not represent a subgroup of patients according to clinical, familial, and biological characteristicsO Heinzlef, B Weill, C Johanet, et al.
Annals of Neurology|March 15, 2000
De novo mutation in the Notch3 gene causing CADASILA Joutel, D D Dodick, J E Parisi, et al.
European Journal of Immunology|June 1, 1991
T cell response to myelin basic protein epitopes in multiple sclerosis patients and healthy subjectsR Liblau, E Tournier-Lasserve, J Maciazek, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 4, 2016
Tumour lysis syndrome: an unexpected adverse event associated with ipilimumabM Masson Regnault, J Ofaiche, S Boulinguez, et al.
Annales De Dermatologie Et De Venereologie|February 4, 2022
Skin manifestations of hypereosinophilic syndrome are polymorphous and difficult to treat: A retrospective cohort studyG Salomon, M Severino, E Casassa, et al.
Annals of Neurology|February 16, 1999
An association between autosomal dominant cerebral cavernomas and a distinctive hyperkeratotic cutaneous vascular malformation in 4 familiesP Labauge, O Enjolras, J J Bonerandi, et al.
Clinical Genetics|November 21, 2013
Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformationsF Riant, S Odent, M Cecillon, et al.
Methodsx|July 8, 2015
Modification of a commercial DNA extraction kit for safe and rapid recovery of DNA and RNA simultaneously from soil, without the use of harmful solventsE Tournier, L Amenc, A L Pablo, et al.
The British Journal of Dermatology|December 24, 2017
Efficacy of anti-programmed cell death-1 immunotherapy for skin carcinomas and melanoma metastases in a patient with xeroderma pigmentosumG Salomon, A Maza, S Boulinguez, et al.
Journal of Neurology|May 18, 2001
Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?J Julien, C Denier, X Ferrer, et al.
Pageof 16