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E Tournier

Showing results (81-90 of 155) with videos related to

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The Journal of Rheumatology|June 1, 1995
Primary antiphospholipid syndrome is not associated with activated protein C resistance caused by factor V Arg 506 -->Gln mutationV Biousse, J C Piette, C Frances, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1995
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss familyH H Jung, C Bassetti, E Tournier-Lasserve, et al.
Translational Stroke Research|September 16, 2021
The Genetic Basis of Moyamoya DiseaseR Mertens, M Graupera, H Gerhardt, et al.
Cerebrovascular Diseases (Basel, Switzerland)|April 21, 1998
Cognitive alterations in non-demented CADASIL patientsH Taillia, H Chabriat, A Kurtz, et al.
La Revue De Medecine Interne|July 11, 2015
[Asthenia and chronic joint pain in a 73-year-old woman]G Moulis, C Luxembourger, E Tournier, et al.
Annales De Dermatologie Et De Venereologie|January 22, 2021
Aggressive locoregional behavior of cutaneous squamous cell carcinoma during ruxolitinib useM Sauvage, S Tavitian, V Sibaud, et al.
Annales De Dermatologie Et De Venereologie|September 16, 2018
[Familial chilblain lupus: Four cases spanning three generations]A-S Beltoise, C Audouin-Pajot, P Lucas, et al.
Revue Neurologique|September 16, 2019
Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature reviewO Osman, P Labrune, P Reiner, et al.
Lancet (London, England)|July 4, 1987
HTLV-I, brain abnormalities on magnetic resonance imaging, and relation with multiple sclerosisE Tournier-Lasserve, O Gout, A Gessain, et al.
Lancet (London, England)|December 6, 1980
Deficit of suppressor T cells in active multiple sclerosisM A Bach, F Phan-Dinh-Tuy, E Tournier, et al.
Pageof 16

Showing results (81-90 of 155) with videos related to

Sort By:
Pageof 16
The Journal of Rheumatology|June 1, 1995
Primary antiphospholipid syndrome is not associated with activated protein C resistance caused by factor V Arg 506 -->Gln mutationV Biousse, J C Piette, C Frances, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1995
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss familyH H Jung, C Bassetti, E Tournier-Lasserve, et al.
Translational Stroke Research|September 16, 2021
The Genetic Basis of Moyamoya DiseaseR Mertens, M Graupera, H Gerhardt, et al.
Cerebrovascular Diseases (Basel, Switzerland)|April 21, 1998
Cognitive alterations in non-demented CADASIL patientsH Taillia, H Chabriat, A Kurtz, et al.
La Revue De Medecine Interne|July 11, 2015
[Asthenia and chronic joint pain in a 73-year-old woman]G Moulis, C Luxembourger, E Tournier, et al.
Annales De Dermatologie Et De Venereologie|January 22, 2021
Aggressive locoregional behavior of cutaneous squamous cell carcinoma during ruxolitinib useM Sauvage, S Tavitian, V Sibaud, et al.
Annales De Dermatologie Et De Venereologie|September 16, 2018
[Familial chilblain lupus: Four cases spanning three generations]A-S Beltoise, C Audouin-Pajot, P Lucas, et al.
Revue Neurologique|September 16, 2019
Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature reviewO Osman, P Labrune, P Reiner, et al.
Lancet (London, England)|July 4, 1987
HTLV-I, brain abnormalities on magnetic resonance imaging, and relation with multiple sclerosisE Tournier-Lasserve, O Gout, A Gessain, et al.
Lancet (London, England)|December 6, 1980
Deficit of suppressor T cells in active multiple sclerosisM A Bach, F Phan-Dinh-Tuy, E Tournier, et al.
Pageof 16