A
Arnaud Murat
Researcher at Hotel Dieu Hospital
Publications - 61
Citations - 6610
Arnaud Murat is an academic researcher from Hotel Dieu Hospital. The author has contributed to research in topics: Multiple endocrine neoplasia & Germline mutation. The author has an hindex of 41, co-authored 61 publications receiving 6188 citations. Previous affiliations of Arnaud Murat include University of Nantes & Texas A&M University.
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Journal ArticleDOI
Genetic Testing in Pheochromocytoma or Functional Paraganglioma
Laurence Amar,Jérôme Bertherat,Eric Baudin,Christiane Ajzenberg,Brigitte Bressac-de Paillerets,Olivier Chabre,Bernard Chamontin,Brigitte Delemer,Sophie Giraud,Arnaud Murat,Patricia Niccoli-Sire,Stéphane Richard,Vincent Rohmer,Jean-Louis Sadoul,Laurence Strompf,Martin Schlumberger,Xavier Bertagna,Pierre-François Plouin,Xavier Jeunemaitre,Anne-Paule Gimenez-Roqueplo +19 more
TL;DR: Genetic testing oriented by family/sporadic presentation should be proposed to all patients with pheo or functional pgl to allow the confirmation of suspected inherited disease as well as the diagnosis of unexpected inherited disease.
Journal ArticleDOI
Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.
Catherine Dodé,Luis Augusto Teixeira,Jacqueline Levilliers,Corinne Fouveaut,Philippe Bouchard,Marie Laure Kottler,James Lespinasse,Anne Lienhardt-Roussie,Michèle Mathieu,Alexandre Moerman,Graeme Morgan,Arnaud Murat,Jean Edmont Toublanc,Slawomir Wolczynski,Marc Delpech,Christine Petit,Jacques Young,J.-P. Hardelin +17 more
TL;DR: Findings reveal that insufficient prokineticin-signaling through PROKR2 leads to abnormal development of the olfactory system and reproductive axis in man and shed new light on the complex genetic transmission of Kallmann syndrome.
Journal ArticleDOI
Pituitary disease in MEN type 1 (MEN1): data from the France-Belgium MEN1 multicenter study.
Bruno Vergès,Françoise Boureille,Pierre Goudet,Arnaud Murat,Albert Beckers,Geneviève Sassolas,Patrick Cougard,Béatrice Chambe,Corinne Montvernay,Alain Calender +9 more
TL;DR: Pituitary adenomas occur in 42% of the cases and are characterized by a larger size and a more aggressive presentation than without MEN1, and are significantly more frequent in women than in men.
Journal ArticleDOI
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
Nelly Burnichon,Nelly Burnichon,Vincent Rohmer,Laurence Amar,Laurence Amar,Philippe Herman,Sophie Leboulleux,Vincent Darrouzet,Patricia Niccoli,Dominique Gaillard,Gérard Chabrier,Frédéric Chabolle,Isabelle Coupier,Philippe Thieblot,P. Lecomte,Jérôme Bertherat,N. Wion-Barbot,Arnaud Murat,Annabelle Venisse,Pierre-François Plouin,Pierre-François Plouin,Xavier Jeunemaitre,Xavier Jeunemaitre,Anne-Paule Gimenez-Roqueplo,Anne-Paule Gimenez-Roqueplo +24 more
TL;DR: SDH genetic testing, including tests for large genomic deletions, is indicated in all patients with head and neck and/or thoracic-abdominal or pelvic paraganglioma and can be targeted according to clinical criteria.
Journal ArticleDOI
Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study
Adrian Daly,Maria A. Tichomirowa,Patrick Petrossians,Elina Heliövaara,Marie Lise Jaffrain-Rea,Anne Barlier,Luciana Ansaneli Naves,Tapani Ebeling,Auli Karhu,Antti Raappana,Laure Cazabat,Ernesto De Menis,Carmen Fajardo Montañana,Gérald Raverot,Robert J. Weil,Timo Sane,Dominique Maiter,Sebastian J C M M Neggers,Maria Yaneva,AntoineAntoine Tabarin,Elisa Verrua,Eija Eloranta,Arnaud Murat,Outi Vierimaa,Pasi I. Salmela,Philippe Emy,Rodrigo A. Toledo,Maria Isabel Sabaté,Chiara Villa,Chiara Villa,Marc Popelier,Roberto Salvatori,Juliet Jennings,Ángel Ferrández Longás,José Ignacio Labarta Aizpún,Marianthi Georgitsi,Ralf Paschke,Cristina L. Ronchi,Matti Välimäki,Carola Saloranta,Wouter W. de Herder,Renato Cozzi,Mirtha Guitelman,Flavia Magri,Maria Stefania Lagonigro,Georges Halaby,Vinciane Corman,Marie-Thérèse Hagelstein,Jean-Francis Vanbellinghen,Gustavo Barcelos Barra,Anne-Paule Gimenez-Roqueplo,Fergus J. Cameron,Françoise Borson-Chazot,Ian M. Holdaway,Sergio P. A. Toledo,Günter K. Stalla,Anna Spada,Sabina Zacharieva,Jérôme Bertherat,Thierry Brue,Vincent Bours,Philippe Chanson,Lauri A. Aaltonen,Albert Beckers +63 more
TL;DR: Prisposition for aggressive disease in young patients, often in a familial setting, suggests that earlier diagnosis of AIPmut pituitary adenomas may have clinical utility.