Why do parents recommend clitoral surgery? Parental perception of the necessity, benefit, and cost of early childhood clitoral surgery for congenital adrenal hyperplasia (CAH)

Autor: Mars Skae, Julie Alderson, Elizabeth Crowne

Publikováno v: International Journal of Impotence Research. 35:56-60

Historically, medical management of Congenital Adrenal Hyperplasia (CAH) in girls typically involved feminising surgery, which meant reducing the size and/or visibility of the enlarged clitoris. This practice may have become less routine but remains

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f00dcfd40076d3407526378735b36bc7
https://doi.org/10.1038/s41443-022-00578-0

1348 Exploring differences in brain perfusion using arterial spin labelling in patients with childhood craniopharyngioma

Autor: Nimra Naeem, Rebecca Elsworth, Kruthika Narayan, Fiona Lithander, Ruth Elson, Tashunka Taylor-Miller, Aileen Wilson, Julian Hamilton-Shield, Elizabeth Crowne, Elanor Hinton

Publikováno v: British Society of Paediatric Endocrinology and Diabetes.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ec00acd80ce8e0a02c6126d72b564637
https://doi.org/10.1136/archdischild-2022-rcpch.460

Novel therapies for childhood cancer and impact on puberty

Autor: Michael C. Stevens, Elizabeth Crowne, Christina Wei

Publikováno v: Current Opinion in Endocrine and Metabolic Research. 14:112-116

Endocrine late effects are common sequelae of the treatment of childhood cancer, and surveillance and management of these are integral to the follow-up of childhood cancer survivors. Cancer treatments are evolving to improve survival and minimize tox

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::24cc61eaa255a1069c8a44d40b7f511d
https://doi.org/10.1016/j.coemr.2020.06.010

Variability in the diagnosis of growth hormone deficiency using dynamic tests. Time for robust pre-test criteria?

Autor: Eva Zilber, Rebecca Cramer, Elizabeth Crowne, Fiona Ryan, Nikolaos Daskas

Publikováno v: Endocrine Abstracts.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4cf64566822ca1e958477ea2f536e661
https://doi.org/10.1530/endoabs.78.oc9.1

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

Autor: Eggermann T., Elbracht M., Kurth I., Juul A., Johannsen T. H., Netchine I., Mastorakos G., Johannsson G., Musholt T. J., Zenker M., Prawitt D., Pereira A. M., Hiort O., Stefan Riedl, Birgit Rami-Merhar, Greisa Vila, Sabina Baumgartner-Parzner, Walter Bonfig, Claudine Heinrichs, Dominique Maiter, Inge Gies, Martine Cools, Kristina Casteels, Albert Beckers, Sabina Zacharieva, Violeta Iotova, Tomislav Jukic, Dario Rahelic, Vassos Neocleous, Leonidas Phylactou, Michal Krsek, Jan Lebl, Claus Gravholt, Anders Juul, Vallo Tillmann, Vallo Volke, Tapani Ebeling, Thierry Brue, Patrice Rodien, Jérôme Bertherat, Christine Poitou Bernert, Philippe Touraine, Philippe Chanson, Michel Polak, Maithe Tauber, Thomas Eggermann, Joachim Spranger, Dagmar Fuhrer, Thomas Danne, Olaf Hiort, Klaus Mohnike, Dirk Prawitt, Markus Luster, Nicole Reisch, Martin Reincke, Julia Rohayem, Martin Fassnacht, Miklós Tóth, Alessandra Cassio, Sonia Toni, Csilla Krausz, Barbara Piccini, Diego Ferone, Gianni Russo, Luca Persani, Annamaria Colao, Mariacarolina Salerno, Marco Boscaro, Carla Scaroni, Ferruccio Santini, Giovanni Ceccarini, Ezio Ghigo, Iveta Dzivite-Krisane, Vita Rovite, Lauma Janozola, Rasa Verkauskiene, Michael Witsch, James Clark, Johannes Romijn, Thera Links, Nienke Biermasz, Sabine Hannema, Bas Havekes, Hedi Claahsen-van der Grinten, Henri Timmers, Robin Peeters, Gerlof Valk, A A Verrijn Stuart, Harm Haak, Eystein Husebye, Jens Bollerslev, Barbara Jarzab, Agnieszka 'Szypowska, João-Filipe Raposo, Dana Craiu, Doina Piciu, Ludmila Kostalova, Jarmila Vojtková, Tadej Battelino, Roque Cardona-Hernandez, Diego Yeste, Sonia Gaztambide, Anna Nordenström, Neil Gittoes, Trevor Cole, Elizabeth Crowne, Faisal Ahmed, Mohammed Didi, Marta Korbonits, Mehul Dattani, Peter Clayton, Justin Davies

Publikováno v: Orphanet Journal of Rare Diseases
Orphanet journal of rare diseases: OJRD 15(1), 144 (2020). doi:10.1186/s13023-020-01420-w
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-16 (2020)
Eggermann, T, Elbracht, M, Kurth, I, Juul, A, Johannsen, T H, Netchine, I, Mastorakos, G, Johannsson, G, Musholt, T J, Zenker, M, Prawitt, D, Pereira, A M, Hiort, O & European Reference Network on Rare Endocrine Conditions (ENDO-ERN 2020, ' Genetic testing in inherited endocrine disorders : joint position paper of the European reference network on rare endocrine conditions (Endo-ERN) ', Orphanet Journal of Rare Diseases, vol. 15, 144 . https://doi.org/10.1186/s13023-020-01420-w

Orphanet journal of rare diseases: OJRD 15(1), 144 (2020). doi:10.1186/s13023-020-01420-w
Published by BioMed Central, London

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21bcdab9c1079b70ef2ccebfd8d9b677