Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sabine, Hannema"'
Autor:
Lisette van Alewijk, Kirsten Davidse, Karlijn Pellikaan, Judith van Eck, Anita C S Hokken-Koelega, Theo C J Sas, Sabine Hannema, Aart J van der Lely, Laura C G de Graaff
Publikováno v:
Endocrine Connections, Vol 10, Iss 4, Pp 432-446 (2021)
Objective: Adolescents and young adults (AYA) with common endocrine disorders show a high dropout (up to 50%) after the transfer from paediatric to adult endocrinology. Little is known about transition readiness in rare endocrine conditions (rEC). Th
Externí odkaz:
https://doaj.org/article/3257f955ba6d42a2bc3de921cba3e0e2
Autor:
Martine Cools, Sabine Hannema
Publikováno v:
Endocrinology ISBN: 9783030189013
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10e23cf64c0c7121ccc3d2e38e3c284e
https://doi.org/10.1007/978-3-030-18901-3_1-1
https://doi.org/10.1007/978-3-030-18901-3_1-1
Autor:
Neil Lawrence, Irina Bacila, Jeremy Dawson, Jillian Bryce, Salma R. Ali, Erica L. T. van den Akker, Tânia A. S. S. Bachega, Federico Baronio, Niels H. Birkebæk, Walter Bonfig, Hedi C. van der Grinten, Eduardo C. Costa, Liat de Vries, Heba Elsedfy, Ayla Güven, Sabine Hannema, Violeta Iotova, Hetty J. van der Kamp, María Clemente, Corina R. Lichiardopol, Tatjana Milenkovic, Uta Neumann, Ana Nordenström, Şukran Poyrazoğlu, Ursina Probst‐Scheidegger, Luisa De Sanctis, Rieko Tadokoro‐Cuccaro, Ajay Thankamony, Ana Vieites, Zehra Yavaş, Syed Faisal Ahmed, Nils Krone
Publikováno v:
Clinical Endocrinology. Wiley-Blackwell
Lawrence, N, Bacila, I, Dawson, J, Bryce, J, Ali, S R, van den Akker, E L T, Bachega, T A S S, Baronio, F, Birkebæk, N H, Bonfig, W, van der Grinten, H C, Costa, E C, de Vries, L, Elsedfy, H, Güven, A, Hannema, S, Iotova, V, van der Kamp, H J, Clemente, M, Lichiardopol, C R, Milenkovic, T, Neumann, U, Nordenström, A, Poyrazoğlu, Ş, Probst-Scheidegger, U, De Sanctis, L, Tadokoro-Cuccaro, R, Thankamony, A, Vieites, A, Yavaş, Z, Faisal Ahmed, S & Krone, N 2022, ' Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry ', Clinical Endocrinology, vol. 97, no. 5, pp. 551-561 . https://doi.org/10.1111/cen.14796
Clinical Endocrinology, 97(5), 551-561. Wiley-Blackwell Publishing Ltd
Lawrence, N, Bacila, I, Dawson, J, Bryce, J, Ali, S R, van den Akker, E L T, Bachega, T N A S S, Baronio, F, Birkebæk, N H, Bonfig, W, van der Grinten, H C, Costa, E C, de Vries, L, Elsedfy, H, Güven, A, Hannema, S, Iotova, V, van der Kamp, H J, León, M C, Lichiardopol, C R, Milenkovic, T, Neumann, U, Nordenström, A, Poyrazoğlu, Ş, Probst-Scheidegger, U, de Sanctis, L, Tadokoro-Cuccaro, R, Thankamony, A, Vieites, A, Yavaş, Z, Faisal Ahmed, S & Krone, N 2022, ' Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry ', Clinical Endocrinology, vol. 97, no. 5, pp. 551-561 . https://doi.org/10.1111/cen.14796
Scientia
Clinical Endocrinology, 97(5), 551-561. Wiley-Blackwell
Lawrence, N, Bacila, I, Dawson, J, Bryce, J, Ali, S R, van den Akker, E L T, Bachega, T A S S, Baronio, F, Birkebæk, N H, Bonfig, W, van der Grinten, H C, Costa, E C, de Vries, L, Elsedfy, H, Güven, A, Hannema, S, Iotova, V, van der Kamp, H J, Clemente, M, Lichiardopol, C R, Milenkovic, T, Neumann, U, Nordenström, A, Poyrazoğlu, Ş, Probst-Scheidegger, U, De Sanctis, L, Tadokoro-Cuccaro, R, Thankamony, A, Vieites, A, Yavaş, Z, Faisal Ahmed, S & Krone, N 2022, ' Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry ', Clinical Endocrinology, vol. 97, no. 5, pp. 551-561 . https://doi.org/10.1111/cen.14796
Clinical Endocrinology, 97(5), 551-561. Wiley-Blackwell Publishing Ltd
Lawrence, N, Bacila, I, Dawson, J, Bryce, J, Ali, S R, van den Akker, E L T, Bachega, T N A S S, Baronio, F, Birkebæk, N H, Bonfig, W, van der Grinten, H C, Costa, E C, de Vries, L, Elsedfy, H, Güven, A, Hannema, S, Iotova, V, van der Kamp, H J, León, M C, Lichiardopol, C R, Milenkovic, T, Neumann, U, Nordenström, A, Poyrazoğlu, Ş, Probst-Scheidegger, U, de Sanctis, L, Tadokoro-Cuccaro, R, Thankamony, A, Vieites, A, Yavaş, Z, Faisal Ahmed, S & Krone, N 2022, ' Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry ', Clinical Endocrinology, vol. 97, no. 5, pp. 551-561 . https://doi.org/10.1111/cen.14796
Scientia
Clinical Endocrinology, 97(5), 551-561. Wiley-Blackwell
Funder: European Society for Paediatric Endocrinology Research Unit
OBJECTIVE: Congenital adrenal hyperplasia (CAH) requires exogenous steroid replacement. Treatment is commonly monitored by measuring 17-OH progesterone (17OHP) and androstenedio
OBJECTIVE: Congenital adrenal hyperplasia (CAH) requires exogenous steroid replacement. Treatment is commonly monitored by measuring 17-OH progesterone (17OHP) and androstenedio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af9b36d82eac4a4fadb9fe4277d9926c
https://doi.org/10.1111/cen.14796
https://doi.org/10.1111/cen.14796
Autor:
Sabine Hannema
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b344ba0738108d2e065d397d6d250e87
https://doi.org/10.1530/endoabs.78.emm2.1
https://doi.org/10.1530/endoabs.78.emm2.1
Autor:
Neil Lawrence, Irina Bacila, Jeremy Dawson, Jillian Bryce, den Akker Erica van, Sanchez Bachega Tania Aparecida Sartori, Federico Baronio, Niels Holtum Birkebaek, Walter Bonfig, Hedi Claahsen, Costa Eduardo Correa, Liat Devries, Heba Elsedfy, Ayla Guven, Sabine Hannema, Violeta Iotova, der Kamp Hetty J van, Leon Maria Clemente, Corina Raducanu Lichiardopol, Tatjana Milenkovic, Uta Neumann, Ana Nordenstrom, Sukran Poyrazoglu, Ursina Probst-Scheidegger, Sanctis Luisa De, Ajay Thankamony, Ana Vieites, Zehra Yavas, Faisal Ahmed, Nils Krone
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::210e45559df77547a238968e3aa17863
https://doi.org/10.1530/endoabs.78.p1
https://doi.org/10.1530/endoabs.78.p1
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
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
Published by BioMed Central, London
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21bcdab9c1079b70ef2ccebfd8d9b677
Autor:
Sabine Hannema
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 106:e2852-e2852
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e9b343c041f328c5b0184afcc2bef62
https://doi.org/10.1210/clinem/dgab315
https://doi.org/10.1210/clinem/dgab315
Autor:
Isabelle, van der Meulen1 (AUTHOR), Anna, van der Miesen1 (AUTHOR), Sabine, Hannema1 (AUTHOR), Annelou, de Vries1 (AUTHOR)
Publikováno v:
Journal of Sexual Medicine. 2023 Supplement, Vol. 20, p1-1. 1p.