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Anzahl der Publikationen: 7
Zeitschriftenartikel
Franik, Sebastian; Fleischer, Kathrin; Kortmann, Barbara; Stikkelbroeck, Nike M.; D'Hauwers, Kathleen; Bouvattier, Claire; Slowikowska-Hilczer, Jolanta; Grunenwald, Solange; Grift, Tim van de; Cartault, Audrey; Richter-Unruh, Annette; Reisch, Nicole; Thyen, Ute; IntHout, Joanna und Claahsen-van der Grinten, Hedi L.
(2022):
The impact of Klinefelter syndrome on socioeconomic status: a multicenter study.
In: Endocrine Connections, Bd. 11, Nr. 7, e220010
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
Verhees, Myrthe J. M.; Engels, Manon; Span, Paul N.; Sweep, Fred C. G. J.; Herwaarden, Antonius E. van; Falhammar, Henrik; Nordenstroem, Anna; Webb, Emma A.; Richter-Unruh, Annette; Bouvattier, Claire; Perriere, Aude Brac de la; Arlt, Wiebke; Reisch, Nicole; Koehler, Birgit; Rapp, Marion; Stikkelbroeck, Nike M. M. L.; Roeleveld, Nel und Claahsen-van der Grinten, Hedi L.
(19. März 2021):
Quality of Life in Men With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
In: Frontiers in Endocrinology, Bd. 12, 626646
[PDF, 749kB]
Claahsen-van der Grinten, Hedi L.; Speiser, Phyllis W.; Ahmed, S. Faisal; Arlt, Wiebke; Auchus, Richard J.; Falhammar, Henrik; Fluck, Christa E.; Guasti, Leonardo; Huebner, Angela; Kortmann, Barbara B. M.; Krone, Nils; Merke, Deborah P.; Miller, Walter L.; Nordenstrom, Anna; Reisch, Nicole; Sandberg, David E.; Stikkelbroeck, Nike M. M. L.; Touraine, Philippe; Utari, Agustini; Wudy, Stefan A. und White, Perrin C.
(2021):
Y Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
In: Endocrine Reviews, Bd. 43, Nr. 1: S. 91-159
Claahsen-van der Grinten, Hedi L.; Stikkelbroeck, Nike; Falhammar, Henrik und Reisch, Nicole
(2021):
MANAGEMENT OF ENDOCRINE DISEASE Gonadal dysfunction in congenital adrenal hyperplasia.
In: European Journal of Endocrinology, Bd. 184, Nr. 2:
R85-R97
Gehrmann, Katharina; Engels, Manon; Bennecke, Elena; Bouvattier, Claire; Falhammar, Henrik; Kreukels, Baudewijntje P. C.; Nordenstrom, Anna; Reisch, Nicole; Gehrmann, Nicole; Stikkelbroeck, Nike L.; Quinkler, Marcus und Claahsen-van der Grinten, Hedi L.
(2019):
Sexuality in Males With Congenital Adrenal Hyperplasia Resulting From 21-Hydroxylase Deficiency.
In: Journal of the Endocrine Society, Bd. 3, Nr. 8: S. 1445-1456
Noordman, Iris D.; van der Velden, Janielle A. E. M.; Timmers, Henri J. L. M.; Pienkowski, Catherine; Köhler, Birgit; Kempers, Marlies; Reisch, Nicole; Richter-Unruh, Annette; Arlt, Wiebke; Nordenstrom, Anna; Webb, Emma A.; Roeleveld, Nel und Claahsen-van der Grinten, Hedi L.
(2019):
Karyotype - Phenotype Associations in Patients with Turner Syndrome.
In: Pediatric Endocrinology Reviews Per, Bd. 16, Nr. 4: S. 431-440