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S Alamowitch

Showing results (21-30 of 34) with videos related to

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Genomics|December 1, 1996
A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical regionA Joutel, A Ducros, S Alamowitch, et al.
Revue Neurologique|July 3, 2016
Posterior reversible encephalopathy syndrome (PRES) and hypomagnesemia: A frequent association?A Chardain, V Mesnage, S Alamowitch, et al.
Revue Des Maladies Respiratoires|April 16, 2023
[Hereditary hemorrhagic telangiectasia]A Parrot, M Barral, X Amiot, et al.
Revue Neurologique|November 5, 2025
Transient ischemic attack care pathways in stroke units: Findings from a French nationwide surveyD Sablot, S Rivas Lamelo, P Renou, et al.
Presse Medicale (Paris, France : 1983)|October 19, 2002
[Prophylactic prescription of low-molecular-weight heparin in the non-surgical setting: impact of recommendations]J P Fagot, A Flahault, M Fodil, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|February 13, 2023
Preventive treatment of unruptured intracranial aneurysms in adult patients with sickle cell anemia: A cohort studyA Dimancea, S Mattioni, A Nouet, et al.
International Journal of Clinical Practice|October 17, 2009
Aseptic meningitis and ischaemic stroke in Fabry diseaseO Lidove, M-P Chauveheid, C Caillaud, et al.
European Journal of Neurology|January 31, 2020
Should posterior cerebral artery occlusions be recanalized? Insights from the Trevo RegistryF Clarençon, F Baronnet, E Shotar, et al.
Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.
Nature|October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiaA Joutel, C Corpechot, A Ducros, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Genomics|December 1, 1996
A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical regionA Joutel, A Ducros, S Alamowitch, et al.
Revue Neurologique|July 3, 2016
Posterior reversible encephalopathy syndrome (PRES) and hypomagnesemia: A frequent association?A Chardain, V Mesnage, S Alamowitch, et al.
Revue Des Maladies Respiratoires|April 16, 2023
[Hereditary hemorrhagic telangiectasia]A Parrot, M Barral, X Amiot, et al.
Revue Neurologique|November 5, 2025
Transient ischemic attack care pathways in stroke units: Findings from a French nationwide surveyD Sablot, S Rivas Lamelo, P Renou, et al.
Presse Medicale (Paris, France : 1983)|October 19, 2002
[Prophylactic prescription of low-molecular-weight heparin in the non-surgical setting: impact of recommendations]J P Fagot, A Flahault, M Fodil, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|February 13, 2023
Preventive treatment of unruptured intracranial aneurysms in adult patients with sickle cell anemia: A cohort studyA Dimancea, S Mattioni, A Nouet, et al.
International Journal of Clinical Practice|October 17, 2009
Aseptic meningitis and ischaemic stroke in Fabry diseaseO Lidove, M-P Chauveheid, C Caillaud, et al.
European Journal of Neurology|January 31, 2020
Should posterior cerebral artery occlusions be recanalized? Insights from the Trevo RegistryF Clarençon, F Baronnet, E Shotar, et al.
Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.
Nature|October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiaA Joutel, C Corpechot, A Ducros, et al.
Pageof 4