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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 2
2022
Nowotny, Hanna; Neumann, Uta; Tardy-Guidollet, Veronique; Ahmed, S. Faisal; Baronio, Federico; Battelino, Tadej; Bertherat, Jerome; Blankenstein, Oliver; Bonomi, Marco; Bouvattier, Claire; de la Perriere, Aude Brac; Brucker, Sara; Cappa, Marco; Chanson, Philippe; Claahsen-van der Grinten, Hedi L.; Colao, Annamaria; Cools, Martine; Davies, Justin H.; Dorr, Helmut-Gunther; Fenske, Wiebke K.; Ghigo, Ezio; Giordano, Roberta; Gravholt, Claus H.; Huebner, Angela; Husebye, Eystein Sverre; Igbokwe, Rebecca; Juul, Anders; Kiefer, Florian W.; Leger, Juliane; Menassa, Rita; Meyer, Gesine; Neocleous, Vassos; Phylactou, Leonidas A.; Rohayem, Julia; Russo, Gianni; Scaroni, Carla; Touraine, Philippe; Unger, Nicole; Vojtkova, Jarmila; Yeste, Diego; Lajic, Svetlana und Reisch, Nicole
(2022):
Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe.
In: European Journal of Endocrinology, Bd. 186, Nr. 5:
K17-K24
2017
Khattab, Ahmed; Haider, Shozeb; Kumar, Ameet; Dhawan, Samarth; Alam, Dauood; Romero, Raquel; Burns, James; Li, Di; Estatico, Jessica; Rahi, Simran; Fatima, Saleel; Alzahrani, Ali; Hafez, Mona; Musa, Noha; Azar, Maryam Razzghy; Khaloul, Najoua; Gribaa, Moez; Saad, Ali; Ben Charfeddine, Ilhem; Mendonca, Berenice Bilharinho de; Belgorosky, Alicia; Dumic, Katja; Dumic, Miroslav; Aisenberg, Javier; Kandemir, Nurgun; Alikasifoglu, Ayfer; Ozon, Alev; Gonc, Nazli; Cheng, Tina; Kuhnle-Krahl, Ursula; Cappa, Marco; Holterhus, Paul-Martin; Nour, Munier A.; Pacaud, Daniele; Holtzman, Assaf; Li, Sun; Zaidi, Mone; Yuen, Tony und New, Maria I.
(2017):
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.
In: Proceedings of the National Academy of Sciences of the United States of America, Bd. 114, Nr. 10, E1933-E1940