V
Véronique Baudouin
Researcher at University of Paris
Publications - 114
Citations - 3972
Véronique Baudouin is an academic researcher from University of Paris. The author has contributed to research in topics: Transplantation & Medicine. The author has an hindex of 30, co-authored 98 publications receiving 3344 citations. Previous affiliations of Véronique Baudouin include Necker-Enfants Malades Hospital & French Institute of Health and Medical Research.
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Journal ArticleDOI
Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
Mathieu Lemaire,Véronique Frémeaux-Bacchi,Franz Schaefer,Murim Choi,Wai Ho Tang,Moglie Le Quintrec,Fadi Fakhouri,Sophie Taque,François Nobili,Frank Martinez,Weizhen Ji,John D. Overton,Shrikant Mane,Gudrun Nürnberg,Janine Altmüller,Holger Thiele,Denis Morin,Georges Deschênes,Véronique Baudouin,Brigitte Llanas,Laure Collard,Mohammed Abdul Majid,Eva Simkova,Peter Nürnberg,Nathalie Rioux-Leclerc,Gilbert W. Moeckel,Marie Claire Gubler,John Hwa,Chantal Loirat,Richard P. Lifton +29 more
TL;DR: Using exome sequencing, it is inferred that loss of DGKE function results in a prothrombotic state, identifying a new mechanism of pathologic thrombosis and kidney failure and have immediate implications for treating individuals with aHUS.
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Rituximab treatment for severe steroid- or cyclosporine-dependent nephrotic syndrome: a multicentric series of 22 cases.
Vincent Guigonis,Aymeric Dallocchio,Véronique Baudouin,Maud Dehennault,Caroline Hachon-Le Camus,Mickael Afanetti,Jaap W. Groothoff,Brigitte Llanas,Patrick Niaudet,Hubert Nivet,Natacha Raynaud,Sophie Taque,Pierre Ronco,François Bouissou +13 more
TL;DR: RTX was effective in all patients when administered during a proteinuria-free period in association with other IS agents, and when relapses occurred, they were always associated with an increase in CD19 cell count.
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Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature.
Tracy A Briggs,Gillian I. Rice,Sarah B. Daly,Jill E. Urquhart,Hannah Gornall,Brigitte Bader-Meunier,Kannan Baskar,Shankar Baskar,Véronique Baudouin,Michael W. Beresford,Graeme C.M. Black,Rebecca J. Dearman,Francis de Zegher,Emily S. Foster,Camille Francès,Alison R. Hayman,Emma Hilton,Chantal Job-Deslandre,M. L. Kulkarni,Martine Le Merrer,Agnès Linglart,Simon C. Lovell,Kathrin Maurer,Lucile Musset,Vincent Navarro,Capucine Picard,Capucine Picard,Capucine Picard,Anne Puel,Anne Puel,Frédéric Rieux-Laucat,Frédéric Rieux-Laucat,Chaim M. Roifman,Sabine Scholl-Bürgi,Nigel Smith,Marcin Szynkiewicz,Alice E. Wiedeman,Alice E. Wiedeman,Carine Wouters,Leo A. H. Zeef,Jean-Laurent Casanova,Jean-Laurent Casanova,Jean-Laurent Casanova,Keith B. Elkon,Keith B. Elkon,Anthony J. Janckila,Pierre Lebon,Yanick J. Crow +47 more
TL;DR: Findings reveal a previously unrecognized link between tartrate-resistant acid phosphatase activity and interferon metabolism and highlight the importance of type Iinterferon in the genesis of autoimmunity.
Journal ArticleDOI
Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations.
Isabelle Perrault,Sophie Saunier,Sylvain Hanein,Emilie Filhol,Albane A. Bizet,Felicity Collins,Mustafa A. Salih,Sylvie Gerber,Nathalie Delphin,Karine Bigot,Christophe Orssaud,Eduardo Silva,Véronique Baudouin,Machteld M. Oud,Nora Shannon,Martine Le Merrer,Olivier Roche,Christine Pietrement,Jamal Goumid,Clarisse Baumann,Christine Bole-Feysot,Patrick Nitschke,Mohammed Zahrate,Philip L. Beales,Heleen H. Arts,Arnold Munnich,Josseline Kaplan,Corinne Antignac,Valérie Cormier-Daire,Jean-Michel Rozet +29 more
TL;DR: Ciliary abundance and localization of anterograde IFTs were altered in fibroblasts of affected individuals, a result that supports the pivotal role of IFT140 in proper development and function of ciliated cells.
Journal ArticleDOI
Human complement factor H deficiency associated with hemolytic uremic syndrome.
Nathalie Rougier,Michel D. Kazatchkine,Jean-Philippe Rougier,Véronique Frémeaux-Bacchi,Jacques Blouin,Georges Deschênes,Bernard Soto,Véronique Baudouin,Brigitte Pautard,Willem Proesmans,Elisabeth Weiss,Laurence Weiss +11 more
TL;DR: Observations suggest a role for FH and/or FH receptors in the pathogenesis of idiopathic HUS, the only complement deficiency associated with HUS.