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Cyril Amouroux

multdisciplinary paediatrics department

10H-index
54Paper Count
284Citation Count
Published Papers 11
Publication Date
RAS/MAPK pathway modulation with simvastatin in children with Noonan syndrome: a multicentre, randomised, double-blind, placebo-controlled phase 3 trial
err2026-08-11
err0
errOAAI
errThomas Edouard; Yline Capri; Alain Verloes; Cyril Amouroux; Marie Bournez; Patricia Bretones; Régis Coutant; Muriel Houang; Jessica Amsellem Jager; Marc de Kerdanet; Didier Lacombe; Christine Lefevre; Irène Netchine; Marc Nicolino; Patricia Pigeon Kherchiche; Rachel Reynaud; Massimiliano Rossi; Aurélie Berot; Julien Van Gils; Marjolaine Willems
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French national diagnosis and care protocol (PNDS) for infantile idiopathic hypercalcemia (IIH)
err2026-07-17
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errOAAI
errCyril Amouroux; Valérie Porquet-Bordes; Elodie Adler; Yoan Le Goff; Justine Bacchetta; Jean Philippe Bertocchio; Gilles Cambonie; Marie Courbebaisse; Odile Dicky; Thomas Edouard; Barbara Girerd; Vincent Guigonis; Fairouz Halitim; Pascal Houiller; Agnès Linglart; Emeline Marquant; Denis Morin; Jean Pierre Salles; Anya Rothenbuhler
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Genetic Heterogeneity Underlying Familial Short Stature
err2025-12-09
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errOAAI
errMargot Comel; Mouna Barat-Houari; Fanny Alkar; Cyril Amouroux; Olivier Prodhomme; Nathalie Ruiz; Sophie Rondeau; Constance F. Wells; Yves-Marie Pers; David Geneviève; Marjolaine Willems
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Expanding the molecular spectrum of aggrecanopathies: exploring 24 patients with ACAN significant variants
err2025-09-23
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PREAI
errMelek Trigui; Nathalie Pallares-Ruiz; David Geneviève; Cyril Amouroux; Thomas Edouard; Sabine Sigaudy; Marjolaine Willems; Mouna Barat-Houari
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Adult height improved over decades in patients with X-linked hypophosphatemia: a cohort study
err2023-10-13
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PREAI
errBoros, Emese; Ertl, Diana-Alexandra; Berkenou, Jugurtha; Audrain, Christelle; Lecoq, Anne Lise; Kamenicky, Peter; Briot, Karine; Amouroux, Cyril; Zhukouskaya, Volha; Gueorguieva, Iva; Mignot, Brigitte; Girerd, Barbara; Bordes, Valerie Porquet; Salles, Jean Pierre; Edouard, Thomas; Coutant, Regis; Bacchetta, Justine; Linglart, Agnes; Rothenbuhler, Anya
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A novel TBX19 gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical origin
err2023-02-15
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errOAAI
errCharnay, Theo; Mougel, Gregory; Amouroux, Cyril; Gueorguieva, Iva; Joubert, Florence; Pertuit, Morgane; Reynaud, Rachel; Barlier, Anne; Brue, Thierry; Saveanu, Alexandru
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Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric population
err2021-02-01
err15
errOAAI
errEl Allali, Yasmine; Hermetet, Coralie; Bacchetta, Justine; Amouroux, Cyril; Rothenbuhler, Anya; Porquet-Bordes, Valerie; Champigny, Marie-Alexandrine; Baron, Sabine; Barat, Pascal; Bony-Trifunovic, Helene; Bourdet, Karine; Busiah, Kanetee; Cartigny-Maciejewski, Maryse; Compain, Florence; Coutant, Regis; Amsellem-Jager, Jessica; De Kerdanet, Marc; Magontier, Nathalie; Mignot, Brigitte; Richard, Odile; Rossignol, Sylvie; Soskin, Sylvie; Berot, Aurelie; Naud-Saudreau, Catherine; Salles, Jean-Pierre; Linglart, Agnes; Edouard, Thomas; Lienhardt-Roussie, Anne
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Should We Really Screen for Genital Variants Before Birth?
err2019-08-01
err0
errOAAI
errKalfa, Nicolas; Amouroux, Cyril; Fuchs, Florent; Paris, Francoise
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Prenatal imaging of genital defects: clinical spectrum and predictive factors for severe forms
err2019-03-18
err13
errOAAI
errFuchs, Florent; Borrego, Paula; Amouroux, Cyril; Antoine, Benoit; Ollivier, Margot; Faure, Jean-Michel; Lopez, Christophe; Forgues, Dominique; Faure, Alice; Merrot, Thierry; Boulot, Pierre; Jeandel, Claire; Philibert, Pascal; Gaspari, Laura; Sultan, Charles; Paris, Francoise; Kalfa, Nicolas
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Late surgical correction of hypospadias increases the risk of complications: a series of 501 consecutive patients
err2017-02-01
err23
errOAAI
errGarnier, Sarah; Maillet, Olivier; Cereda, Barbara; Ollivier, Margot; Jeandel, Clement; Broussous, Sylvie; Lopez, Christophe; Paris, Francoise; Philibert, Pascal; Amouroux, Cyril; Jeandel, Claire; Coffy, Amandine; Gaspari, Laura; Daures, Jean Pierre; Sultan, Charles; Kalfa, Nicolas
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Duplication 8q12: confirmation of a novel recognizable phenotype with duane retraction syndrome and developmental delay
err2012-01-18
err18
errOAAI
errAmouroux, Cyril; Vincent, Marie; Blanchet, Patricia; Puechberty, Jacques; Schneider, Anouck; Chaze, Anne Marie; Girard, Manon; Tournaire, Magali; Jorgensen, Christian; Morin, Denis; Sarda, Pierre; Lefort, Genevieve; Genevieve, David
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