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E Tournier

Showing results (121-130 of 155) with videos related to

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Journal of the European Academy of Dermatology and Venereology : JEADV|September 12, 2014
Acquired perforating dermatosis associated with sorafenib therapyM Severino-Freire, V Sibaud, E Tournier, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 7, 2020
Langerhans cell histiocytosis associated with chronic myelomonocytic leukaemia both harbouring the same BRAF V600E mutation: efficacy of vemurafenibM P Konstantinou, P Lucas, C Uthurriague, et al.
Neurology|June 20, 1998
SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia onlyJ K Mellies, T Bäumer, J A Müller, et al.
Revue Neurologique|April 7, 2015
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 geneA Bisserbe, G Tertian, C Buffet, et al.
The American Journal of Medicine|May 12, 2000
The R131 low-affinity allele of the Fc gamma RIIA receptor is associated with systemic lupus erythematosus but not with other autoimmune diseases in French CaucasiansM Michel, J C Piette, E Roullet, et al.
Neurology|April 1, 2009
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutationsK Vahedi, C Depienne, D Le Fort, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 28, 1999
Spanish families with cavernous angiomas do not share the Hispano-American CCM1 haplotypeH H Jung, P Labauge, S Laberge, et al.
Annals of Neurology|December 24, 1997
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneityA Ducros, A Joutel, K Vahedi, et al.
Nature Genetics|October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomasS Laberge-le Couteulx, H H Jung, P Labauge, et al.
Lancet (London, England)|December 6, 1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patientsA Joutel, K Vahedi, C Corpechot, et al.
Pageof 16

Showing results (121-130 of 155) with videos related to

Sort By:
Pageof 16
Journal of the European Academy of Dermatology and Venereology : JEADV|September 12, 2014
Acquired perforating dermatosis associated with sorafenib therapyM Severino-Freire, V Sibaud, E Tournier, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 7, 2020
Langerhans cell histiocytosis associated with chronic myelomonocytic leukaemia both harbouring the same BRAF V600E mutation: efficacy of vemurafenibM P Konstantinou, P Lucas, C Uthurriague, et al.
Neurology|June 20, 1998
SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia onlyJ K Mellies, T Bäumer, J A Müller, et al.
Revue Neurologique|April 7, 2015
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 geneA Bisserbe, G Tertian, C Buffet, et al.
The American Journal of Medicine|May 12, 2000
The R131 low-affinity allele of the Fc gamma RIIA receptor is associated with systemic lupus erythematosus but not with other autoimmune diseases in French CaucasiansM Michel, J C Piette, E Roullet, et al.
Neurology|April 1, 2009
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutationsK Vahedi, C Depienne, D Le Fort, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 28, 1999
Spanish families with cavernous angiomas do not share the Hispano-American CCM1 haplotypeH H Jung, P Labauge, S Laberge, et al.
Annals of Neurology|December 24, 1997
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneityA Ducros, A Joutel, K Vahedi, et al.
Nature Genetics|October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomasS Laberge-le Couteulx, H H Jung, P Labauge, et al.
Lancet (London, England)|December 6, 1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patientsA Joutel, K Vahedi, C Corpechot, et al.
Pageof 16