Resultados da busca - Sophie Dupuis‐Girod

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  1. 1
    Hereditary hemorrhagic telangiectasia: from molecular biology to patient care

    Hereditary hemorrhagic telangiectasia: from molecular biology to patient care por Sophie Dupuis‐Girod, Sabine Bailly, Henri Plauchu

    Publicado em 2010
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  2. 2
    The Lung in Hereditary Hemorrhagic Telangiectasia

    The Lung in Hereditary Hemorrhagic Telangiectasia por Sophie Dupuis‐Girod, Vincent Cottin, Claire L. Shovlin

    Publicado em 2017
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  3. 3
    Immunological abnormalities associated with hereditary haemorrhagic telangiectasia

    Immunological abnormalities associated with hereditary haemorrhagic telangiectasia por A Guilhem, Christophe Malcus, B. Clarivet, Henri Plauchu, Sophie Dupuis‐Girod

    Publicado em 2013
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  4. 4
    Future treatments for hereditary hemorrhagic telangiectasia

    Future treatments for hereditary hemorrhagic telangiectasia por F. Robert, Agnès Desroches‐Castan, Sabine Bailly, Sophie Dupuis‐Girod, Jean‐Jacques Feige

    Publicado em 2020
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  5. 5
    Hereditary hemorrhagic telangiectasia: from signaling insights to therapeutic advances

    Hereditary hemorrhagic telangiectasia: from signaling insights to therapeutic advances por Tala Al Tabosh, Mohammad Al Tarrass, Laura Tourvieilhe, A Guilhem, Sophie Dupuis‐Girod, Sabine Bailly

    Publicado em 2024
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  6. 6
    Bone Morphogenetic Protein-9 Is a Circulating Vascular Quiescence Factor

    Bone Morphogenetic Protein-9 Is a Circulating Vascular Quiescence Factor por Laurent David, Christine Mallet, Michelle Kéramidas, Noël Lamandé, Jean‐Marie Gasc, Sophie Dupuis‐Girod, Henri Plauchu, Jean‐Jacques Feige, Sabine Bailly

    Publicado em 2008
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  7. 7
    Long-term outcome of patients with hereditary hemorrhagic telangiectasia and severe hepatic involvement after orthotopic liver transplantation: A single-center study

    Long-term outcome of patients with hereditary hemorrhagic telangiectasia and severe hepatic involvement after orthotopic liver transplantation: A single-center study por Sophie Dupuis‐Girod, Anne-Laure Chesnais, Isabelle Ginon, Jérôme Dumortier, Jean‐Christophe Saurin, Gérard Finet, Évelyne Decullier, Denis Marion, Henri Plauchu, Olivier Boillot

    Publicado em 2010
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  8. 8
    European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT)

    European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT) por Claire L. Shovlin, Elisabetta Buscarini, Anette Drøhse Kjeldsen, Hans Jurgen Mager, Carlo Sabbà, Freya Droege, Urban W. Geisthoff, Sara Ugolini, Sophie Dupuis‐Girod

    Publicado em 2018
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  9. 9
    Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia

    Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia por Elisabetta Buscarini, Luisa M. Botella, Urban W. Geisthoff, Anette Drøhse Kjeldsen, Hans Jurgen Mager, Fabio Pagella, Patrizia Suppressa, Roberto Zarrabeitia, Sophie Dupuis‐Girod, Claire L. Shovlin

    Publicado em 2019
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  10. 10
    Differential susceptibility of adenovirus clinical isolates to cidofovir and ribavirin is not related to species alone

    Differential susceptibility of adenovirus clinical isolates to cidofovir and ribavirin is not related to species alone por Florence Morfin, Sophie Dupuis‐Girod, Émilie Frobert, Stéphanie Mundweiler, D Carrington, Petr Sedláček, Marc Bierings, Petr Cetkovský, Aloys C.M. Kroes, Maarten JD van Tol, D Thouvenot

    Publicado em 2009
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  11. 11
    <i>In Vitro</i> Susceptibility of Adenovirus to Antiviral Drugs is Species-Dependent

    <i>In Vitro</i> Susceptibility of Adenovirus to Antiviral Drugs is Species-Dependent por Florence Morfin, Sophie Dupuis‐Girod, Stéphanie Mundweiler, Delphine Falcon, D Carrington, Petr Sedláček, Marc Bierings, Petr Cetkovský, Aloys C.M. Kroes, Maarten JD van Tol, D Thouvenot

    Publicado em 2005
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  12. 12
    ELLIPSE Study

    ELLIPSE Study por Sophie Dupuis‐Girod, A. Ambrun, Évelyne Decullier, Géraldine Samson, Adeline Roux, Anne‐Emmanuelle Fargeton, Catherine Rioufol, Vérane Schwiertz, F. Disant, François Chapuis, Yves Donazzolo, Gilles Paintaud, Patrick Edery, Frédéric Faure

    Publicado em 2014
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  13. 13
    Treatment of the Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome (IPEX) by Allogeneic Bone Marrow Transplantation

    Treatment of the Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome (IPEX) by Allogeneic Bone Marrow Transplantation por Olivier Baud, Olivier Goulet, Danielle Canioni, Françoise Le Deist, Isabelle Radford, D Rieu, Sophie Dupuis‐Girod, Nadine Cerf‐Bensussan, Marina Cavazzana, Nicole Brousse, Alain Fischer, Christine Rivet, Christine Bodemer, Robert S. Wildin, Jean‐Laurent Casanova

    Publicado em 2001
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  14. 14
    Intra-venous bevacizumab in hereditary hemorrhagic telangiectasia (HHT): A retrospective study of 46 patients

    Intra-venous bevacizumab in hereditary hemorrhagic telangiectasia (HHT): A retrospective study of 46 patients por A Guilhem, Anne‐Emmanuelle Fargeton, Anne-Claire Simon, P. Duffau, Jean‐Robert Harlé, Christian Lavigne, Marie‐France Carette, O Blétry, P. Kaminsky, V. Leguy, Nathalie Lerolle, Dominique Roux, M. Lambert, Thierry Chinet, Delphine Bonnet, Sophie Dupuis‐Girod, Sophie Rivière

    Publicado em 2017
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  15. 15
    Effect of Bevacizumab Nasal Spray on Epistaxis Duration in Hereditary Hemorrhagic Telangectasia

    Effect of Bevacizumab Nasal Spray on Epistaxis Duration in Hereditary Hemorrhagic Telangectasia por Sophie Dupuis‐Girod, A. Ambrun, Évelyne Decullier, Anne‐Emmanuelle Fargeton, Adeline Roux, Valentine Bréant, Bettina Colombet, Sophie Rivière, C. Cartier, Pascal Lacombe, Thierry Chinet, Sandra Blivet, J.-H. Blondel, Brigitte Gilbert‐Dussardier, Xavier Dufour, Justin Michel, Jean‐Robert Harlé, P. Dessi, Frédéric Faure

    Publicado em 2016
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  16. 16
    A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency

    A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency por Gilles Courtois, Asma Smahi, Janine Reichenbach, Rainer Döffinger, Caterina Cancrini, Marion Bonnet, Anne Puel, Christine Chable-Bessia, Shoji Yamaoka, Jacqueline Feinberg, Sophie Dupuis‐Girod, Christine Bodemer, Susanna Livadiotti, Francesco Novelli, Paolo Rossi, Alain Fischer, Alain Israël, Arnold Munnich, Françoise Le Deist, Jean‐Laurent Casanova

    Publicado em 2003
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  17. 17
    Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD)

    Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD) por Pauline Arnaud, Nadine Hanna, Louise Benarroch, Mélodie Aubart, Laurence Bal, Patrice Bouvagnet, Tiffany Busa, Yves Dulac, Sophie Dupuis‐Girod, Thomas Édouard, Laurence Faivre, Laurent Gouya, Didier Lacombe, Maud Langeois, Bruno Leheup, Olivier Milleron, Sophie Naudion, Sylvie Odent, Maria Tchitchinadze, Jacques Ropers, Guillaume Jondeau, Cathérine Boileau

    Publicado em 2019
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  18. 18
    Genetic variants of <i>Adam17</i> differentially regulate TGFβ signaling to modify vascular pathology in mice and humans

    Genetic variants of <i>Adam17</i> differentially regulate TGFβ signaling to modify vascular pathology in mice and humans por Kyoko Kawasaki, Julia Freimuth, Dominique S. Meyer, Marie M. Lee, Akiko Tochimoto-Okamoto, Michael Benzinou, Frederic F. Clermont, Gloria Wu, Ritu Roy, Tom G.W. Letteboer, Johannes Kristian Ploos van Amstel, Sophie Giraud, Sophie Dupuis‐Girod, Gaëtan Lesca, Cornelius J.J. Westermann, Robert J. Coffey, Rosemary J. Akhurst

    Publicado em 2014
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  19. 19
    MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections

    MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections por Mathieu Barbier, Marie Sylvie Gross, Mélodie Aubart, Nadine Hanna, Ketty Kessler, Dong Guo, Laurent Tosolini, Benoît Ho‐Tin‐Noé, Ellen S. Regalado, Mathilde Varret, Marianne Abifadel, Olivier Milleron, Sylvie Odent, Sophie Dupuis‐Girod, Laurence Faivre, Thomas Édouard, Yves Dulac, Tiffany Busa, Laurent Gouya, Dianna M. Milewicz, Guillaume Jondeau, Cathérine Boileau

    Publicado em 2014
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  20. 20
    Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia

    Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia por Claire L. Shovlin, Carolyn M. Millar, Freya Droege, Anette Drøhse Kjeldsen, Guido Manfredi, Patrizia Suppressa, Sara Ugolini, Nicole Coote, Annette Dam Fialla, Urban W. Geisthoff, Gennaro M. Lenato, Hans-Jurgen Mager, Fabio Pagella, Martijn C. Post, Carlo Sabbà, Ulrich Sure, Pernille Mathiesen Tørring, Sophie Dupuis‐Girod, Elisabetta Buscarini

    Publicado em 2019
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