Resultats de la cerca - Elisabeth Tournier‐Lasserve

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  1. 1
    Summary of the proceedings of the First International Workshop on CADASIL. Paris, May 19-21, 1993.

    Summary of the proceedings of the First International Workshop on CADASIL. Paris, May 19-21, 1993. per M G Bousser, Elisabeth Tournier‐Lasserve

    Publicat 1994
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  2. 2
    The Control of Vascular Integrity by Endothelial Cell Junctions: Molecular Basis and Pathological Implications

    The Control of Vascular Integrity by Endothelial Cell Junctions: Molecular Basis and Pathological Implications per Elisabetta Dejana, Elisabeth Tournier‐Lasserve, Brant M. Weinstein

    Publicat 2009
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  3. 3
    Moyamoya disease and syndromes: from genetics to clinical management

    Moyamoya disease and syndromes: from genetics to clinical management per Manoëlle Kossorotoff, Elisabeth Tournier‐Lasserve, Dominique Hervé, Stéphanie Guey

    Publicat 2015
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  4. 4
    Recent insights into cerebral cavernous malformations: the molecular genetics of CCM

    Recent insights into cerebral cavernous malformations: the molecular genetics of CCM per Florence Riant, Françoise Bergametti, Xavier Ayrignac, Gwénola Boulday, Elisabeth Tournier‐Lasserve

    Publicat 2010
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  5. 5
    Pathogenic Mutations Associated with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Differently Affect Jagged1 Binding and Notch3 Activity via the RBP/JK Signaling Pathway

    Pathogenic Mutations Associated with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Differently Affect Jagged1 Binding and Notch3 Activi... per Anne Joutel, Marie Monet, Valérie Domenga, Florence Riant, Elisabeth Tournier‐Lasserve

    Publicat 2004
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  6. 6
    Impaired Cerebral Vasoreactivity in a Transgenic Mouse Model of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Arteriopathy

    Impaired Cerebral Vasoreactivity in a Transgenic Mouse Model of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Arteriopathy per Pierre Lacombe, Charleen Oligo, Valérie Domenga, Elisabeth Tournier‐Lasserve, Anne Joutel

    Publicat 2005
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  7. 7
    Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.

    Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy. per Elisabeth Tournier‐Lasserve, M T Iba-Zizen, Nicolás Romero, M G Bousser

    Publicat 1991
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  8. 8
    Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study.

    Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study. per Magalie Baudrimont, Frédéric Dubas, Anne Joutel, Elisabeth Tournier‐Lasserve, Marie‐Germaine Bousser

    Publicat 1993
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  9. 9
    The Hox-1.3 homeo box protein is a sequence-specific DNA-binding phosphoprotein.

    The Hox-1.3 homeo box protein is a sequence-specific DNA-binding phosphoprotein. per Ward F. Odenwald, James Garbern, Heinz Arnheiter, Elisabeth Tournier‐Lasserve, Robert A. Lazzarini

    Publicat 1989
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  10. 10
    Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL.

    Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL. per M M Ruchoux, Hugues Chabriat, M G Bousser, M. Baudrimont, Elisabeth Tournier‐Lasserve

    Publicat 1994
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  11. 11
    <i>COL4A1</i> Mutation in a Patient With Sporadic, Recurrent Intracerebral Hemorrhage

    <i>COL4A1</i> Mutation in a Patient With Sporadic, Recurrent Intracerebral Hemorrhage per Katayoun Vahedi, Nathalie Kubis, Monique Boukobza, Minh Arnoult, Pascale Massin, Elisabeth Tournier‐Lasserve, Marie‐Germaine Bousser

    Publicat 2007
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  12. 12
    Transgenic Mice Expressing Mutant Notch3 Develop Vascular Alterations Characteristic of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

    Transgenic Mice Expressing Mutant Notch3 Develop Vascular Alterations Characteristic of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy per M M Ruchoux, Valérie Domenga, Peggy Brulin, Jacqueline Maciazek, Sylvie Limol, Elisabeth Tournier‐Lasserve, Anne Joutel

    Publicat 2003
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  13. 13
    Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations

    Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations per Florence Riant, Christian Denier, Pierre Labauge, Michaelle Cécillon, Jacqueline Maciazek, Anne Joutel, Sophie Laberge, Elisabeth Tournier‐Lasserve

    Publicat 2002
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  14. 14
    Cerebral Cavernous Malformation-1 Protein Controls DLL4-Notch3 Signaling Between the Endothelium and Pericytes

    Cerebral Cavernous Malformation-1 Protein Controls DLL4-Notch3 Signaling Between the Endothelium and Pericytes per Gerald Bastian Schulz, Elfriede Wieland, Joycelyn Wüstehube‐Lausch, Gwénola Boulday, Iris Moll, Elisabeth Tournier‐Lasserve, Andreas Fischer

    Publicat 2015
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  15. 15
    Impaired Vascular Mechanotransduction in a Transgenic Mouse Model of CADASIL Arteriopathy

    Impaired Vascular Mechanotransduction in a Transgenic Mouse Model of CADASIL Arteriopathy per Caroline Dubroca, Pierre Lacombe, Valérie Domenga, Jacqueline Maciazek, Bernard Lévy, Elisabeth Tournier‐Lasserve, Anne Joutel, Daniel Henrion

    Publicat 2004
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  16. 16
    The Genetic Basis of Moyamoya Disease

    The Genetic Basis of Moyamoya Disease per Robert Mertens, Mariona Graupera, Holger Gerhardt, Anna Bersano, Elisabeth Tournier‐Lasserve, Martin A. Mensah, Stefan Mundlos, Peter Vajkoczy

    Publicat 2021
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  17. 17
    Familial Lupus Erythematosus

    Familial Lupus Erythematosus per Marc Michel, Catherine Johanet, Olivier Meyer, C. Francès, Frederick Wittke, Catherine Michel, S. Arfi, Elisabeth Tournier‐Lasserve, Jean-Charles Piette

    Publicat 2001
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  18. 18
    Tissue-specific conditional<i>CCM2</i>knockout mice establish the essential role of endothelial CCM2 in angiogenesis: implications for human cerebral cavernous malformations

    Tissue-specific conditional<i>CCM2</i>knockout mice establish the essential role of endothelial CCM2 in angiogenesis: implications for human cerebral cavernous malformations per Gwénola Boulday, Anne Blécon, Nathalie Petit, Fabrice Chareyre, Luis A. García, Michiko Niwa‐Kawakita, Marco Giovannini, Elisabeth Tournier‐Lasserve

    Publicat 2009
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  19. 19
    Cognitive impairment in children with <i><scp>CACNA</scp>1A</i> mutations

    Cognitive impairment in children with <i><scp>CACNA</scp>1A</i> mutations per Véronique Humbertclaude, Florence Riant, Benjamin Krams, Zimmermann Valérie, Nicolas Nagot, D. Annequin, Bernard Échenne, Elisabeth Tournier‐Lasserve, Agathe Roubertie

    Publicat 2019
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  20. 20
    The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients

    The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients per Anne Joutel, F. Andreux, Swann Gaulis, Valérie Domenga, Michaelle Cécillon, Nicole Battail, Nadia Piga, Françoise Chapon, Catherine Godfrain, Elisabeth Tournier‐Lasserve

    Publicat 2000
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