Fertility and pregnancy outcomes in women with nonclassic 21‐hydroxylase deficiency
Carrière, Camille, Nguyen, Lee S., Courtillot, Carine, Tejedor, Isabelle, Chakhtoura, Zeina, Bellanné‐Chantelot, Christine, Tardy, Véronique, Leban, Monique, Touraine, Philippe, Bachelot, Anne
Published in Clinical endocrinology (Oxford) (01.03.2023)
Published in Clinical endocrinology (Oxford) (01.03.2023)
Get full text
Journal Article
Precocious Pubarche: Distinguishing Late-Onset Congenital Adrenal Hyperplasia from Premature Adrenarche
Armengaud, Jean-Baptiste, Charkaluk, Marie-Laure, Trivin, Christine, Tardy, Véronique, Bréart, Gérard, Brauner, Raja, Chalumeau, Martin
Published in The journal of clinical endocrinology and metabolism (01.08.2009)
Published in The journal of clinical endocrinology and metabolism (01.08.2009)
Get full text
Journal Article
New Management Strategy of Pregnancies at Risk of Congenital Adrenal Hyperplasia Using Fetal Sex Determination in Maternal Serum: French Cohort of 258 Cases (2002–2011)
Tardy-Guidollet, Véronique, Menassa, Rita, Costa, Jean-Marc, David, Michel, Bouvattier-Morel, Claire, Baumann, Clarisse, Houang, Muriel, Lorenzini, Françoise, Philip, Nicole, Odent, Sylvie, Guichet, Agnès, Morel, Yves
Published in The journal of clinical endocrinology and metabolism (01.04.2014)
Published in The journal of clinical endocrinology and metabolism (01.04.2014)
Get full text
Journal Article
Secondary amenorrhoea associated with high serum 17-hydroxyprogesterone levels revealing a heterozygous CYP21A2 mutation in a woman with Addison disease
Boscolo, Marina, Bry-Gauillard, Hélène, Tardy, Véronique, Young, Jacques
Published in Clinical endocrinology (Oxford) (01.04.2015)
Published in Clinical endocrinology (Oxford) (01.04.2015)
Get full text
Journal Article
Molecular Genetic Analysis of Tunisian Patients with a Classic Form of 21-Hydroxylase Deficiency: Identification of Four Novel Mutations and High Prevalence of Q318X Mutation
Kharrat, Maher, Tardy, Véronique, M’Rad, Ridha, Maazoul, Faouzi, Jemaa, Lamia Ben, Refaï, Mohamed, Morel, Yves, Chaabouni, Habiba
Published in The journal of clinical endocrinology and metabolism (01.01.2004)
Published in The journal of clinical endocrinology and metabolism (01.01.2004)
Get full text
Journal Article
CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation
Abid, Fatima, Tardy, Véronique, Gaouzi, Ahmed, El hessni, Aboubaker, Morel, Yves, Chabraoui, Layachi
Published in Clinical chemistry and laboratory medicine (01.12.2008)
Published in Clinical chemistry and laboratory medicine (01.12.2008)
Get full text
Journal Article
Adrenal rest tissue in gonads of patients with classical congenital adrenal hyperplasia: Multicenter study of 45 French male patients
Pierre, Peggy, Despert, François, Tranquart, François, Coutant, Régis, Tardy, Véronique, Kerlan, Véronique, Sonnet, Emmanuel, Baron, Sabine, Lorcy, Yannick, Emy, Philippe, Delavierre, Dominique, Monceaux, Françoise, Morel, Yves, Lecomte, Pierre
Published in Annales d'endocrinologie (01.12.2012)
Published in Annales d'endocrinologie (01.12.2012)
Get full text
Journal Article
Evolution of steroids during pregnancy: Maternal, placental and fetal synthesis
Morel, Yves, Roucher, Florence, Plotton, Ingrid, Goursaud, Claire, Tardy, Véronique, Mallet, Delphine
Published in Annales d'endocrinologie (01.06.2016)
Published in Annales d'endocrinologie (01.06.2016)
Get full text
Journal Article
Laparoscopic-assisted vaginal pull-through: A new approach for congenital adrenal hyperplasia patients with high urogenital sinus
Birraux, Jacques, Mouafo, Faustin Tambo, Dahoun, Sophie, Tardy, Veronique, Morel, Yves, Mouriquand, Pierre, Le Coultre, Claude, Mure, Pierre-Yves
Published in African journal of paediatric surgery (01.07.2015)
Published in African journal of paediatric surgery (01.07.2015)
Get full text
Journal Article
Fertility in Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Bidet, Maud, Bellanné-Chantelot, Christine, Galand-Portier, Marie-Béatrice, Golmard, Jean-Louis, Tardy, Véronique, Morel, Yves, Clauin, Séverine, Coussieu, Christiane, Boudou, Philippe, Mowzowicz, Irene, Bachelot, Anne, Touraine, Philippe, Kuttenn, F
Published in The journal of clinical endocrinology and metabolism (01.03.2010)
Published in The journal of clinical endocrinology and metabolism (01.03.2010)
Get full text
Journal Article
Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey
Bouvattier, Claire, Esterle, Laure, Renoult-Pierre, Peggy, de la Perrière, Aude Brac, Illouz, Frederic, Kerlan, Véronique, Pascal-Vigneron, Veronique, Drui, Delphine, Christin-Maitre, Sophie, Galland, Françoise, Brue, Thierry, Reznik, Yves, Schillo, Frank, Pinsard, Denis, Piguel, Xavier, Chabrier, Gérard, Decoudier, Bénédicte, Emy, Philippe, Tauveron, Igor, Raffin-Sanson, Marie-Laure, Bertherat, Jerôme, Kuhn, Jean-Marc, Caron, Philippe, Cartigny, Maryse, Chabre, Olivier, Dewailly, Didier, Morel, Yves, Touraine, Philippe, Tardy-Guidollet, Véronique, Young, Jacques
Published in The journal of clinical endocrinology and metabolism (01.06.2015)
Published in The journal of clinical endocrinology and metabolism (01.06.2015)
Get full text
Journal Article
Clinical and Molecular Characterization of a Cohort of 161 Unrelated Women with Nonclassical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and 330 Family Members
Bidet, Maud, Bellanné-Chantelot, Christine, Galand-Portier, Marie-Béatrice, Tardy, Véronique, Billaud, Line, Laborde, Kathleen, Coussieu, Christiane, Morel, Yves, Vaury, Christelle, Golmard, Jean-Louis, Claustre, Aurélie, Mornet, Etienne, Chakhtoura, Zeina, Mowszowicz, Irene, Bachelot, Anne, Touraine, Philippe, Kuttenn, Frédérique
Published in The journal of clinical endocrinology and metabolism (01.05.2009)
Published in The journal of clinical endocrinology and metabolism (01.05.2009)
Get full text
Journal Article
The experience of diagnosis announcement in rare endocrine diseases: A survey of the French FIRENDO network
Rahabi, Haifa, Givony, Maria, Demaret, Béatrice, Albarel, Frédérique, Aubron, Marie-Reine, Bartès, Beate, Bernard, Lucie, Abdoul, Hendy, Bouazza, Naim, Brun, Philippe, Drui, Delphine, Dujardin, Véronique, Lançon, Catherine, Malivoir, Sabine, Netchine, Irène, Perrotin, Bénédicte, Picard, Virginie, Reynaud, Rachel, Ribeiro, Murielle, Tardy Guidollet, Véronique, Victor, Amélie, Bertherat, Jérôme, Colin, Claudine, Brue, Thierry
Published in Annales d'endocrinologie (01.02.2024)
Published in Annales d'endocrinologie (01.02.2024)
Get full text
Journal Article
Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe
Nowotny, Hanna, Neumann, Uta, Tardy-Guidollet, Véronique, Ahmed, S Faisal, Baronio, Federico, Battelino, Tadej, Bertherat, Jérôme, Blankenstein, Oliver, Bonomi, Marco, Bouvattier, Claire, Brac de la Perrière, Aude, Brucker, Sara, Cappa, Marco, Chanson, Philippe, Claahsen-van der Grinten, Hedi L, Colao, Annamaria, Cools, Martine, Davies, Justin H, Dörr, Helmut-Günther, Fenske, Wiebke K, Ghigo, Ezio, Giordano, Roberta, Gravholt, Claus H, Huebner, Angela, Husebye, Eystein Sverre, Igbokwe, Rebecca, Juul, Anders, Kiefer, Florian W, Léger, Juliane, Menassa, Rita, Meyer, Gesine, Neocleous, Vassos, Phylactou, Leonidas A, Rohayem, Julia, Russo, Gianni, Scaroni, Carla, Touraine, Philippe, Unger, Nicole, Vojtková, Jarmila, Yeste, Diego, Lajic, Svetlana, Reisch, Nicole
Published in European journal of endocrinology (01.05.2022)
Published in European journal of endocrinology (01.05.2022)
Get full text
Journal Article
Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria
Ladjouze, Asmahane, Donaldson, Malcolm, Plotton, Ingrid, Djenane, Nacima, Mohammedi, Kahina, Tardy-Guidollet, Véronique, Mallet, Delphine, Boulesnane, Kamélia, Bouzerar, Zair, Morel, Yves, Roucher-Boulez, Florence
Published in Frontiers in endocrinology (Lausanne) (10.06.2022)
Published in Frontiers in endocrinology (Lausanne) (10.06.2022)
Get full text
Journal Article
Efficiency of neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency in children born in mainland France between 1996 and 2003
Coulm, Bénédicte, Coste, Joel, Tardy, Véronique, Ecosse, Emmanuel, Roussey, Michel, Morel, Yves, Carel, Jean-Claude
Published in Archives of pediatrics & adolescent medicine (01.02.2012)
Published in Archives of pediatrics & adolescent medicine (01.02.2012)
Get more information
Journal Article
Aberrant Splicing Is the Pathogenicity Mechanism of the p.Glu314Lys Variant in CYP11A1 Gene
Goursaud, Claire, Mallet, Delphine, Janin, Alexandre, Menassa, Rita, Tardy-Guidollet, Véronique, Russo, Gianni, Lienhardt-Roussie, Anne, Lecointre, Claudine, Plotton, Ingrid, Morel, Yves, Roucher-Boulez, Florence
Published in Frontiers in endocrinology (Lausanne) (05.09.2018)
Published in Frontiers in endocrinology (Lausanne) (05.09.2018)
Get full text
Journal Article