Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Antonio Balsamo"'
Autor:
Daniel Konrad, Aneta Gawlik, Rajni Sharma, Olcay Evliyaoğlu, Dejun Li, Marek Niedziela, Jeremy W. Tomlinson, Farida Jennane, Nils Krone, Sukran Poyrazoglu, Evgenia Globa, S Faisal Ahmed, Angela K Lucas-Herald, Inas Mazen, Liat de Vries, Andreas Kyriakou, Katherine Lachlan, Wiebke Arlt, Renata Markosyan, Antonia Brooke, Olaf Hiort, Gil Guerra Júnior, Ruth Krone, Colin Johnston, Gloria Hermann, Antonio Balsamo, Corina Lichiardopol, Hedi L Claahsen-van der Grinten, Vandana Jain, Vilhelm Mladenov, Nataliya Zelinska, Naomi Weintrob, Markus Bettendorf, Simone Fica, Ieuan A. Hughes, Laura Audí, Lidka Lisa, Klaus Mohnike, Mona Ellaithi, Paul-Martin Holterhus, Lavinia Nedelea, Mars Skaeil, Rodolfo Rey, Violeta Iotova, Hannema Se, Silvano Bertelloni, Rieko Tadokoro-Cuccaro, Feyza Darendeliler, Jillian Bryce, Lloyd J.W. Tack, Tulay Guran, Odile Gaisl, Justin H Davies, Martine Cools, Anna Nordenström, Federico Baronio, Marie Lindhardt Ljubicic, Ayla Güven
Publikováno v:
European Journal of Endocrinology, 184, 6, pp. 791-801
Lucas-Herald, A K, Bryce, J, Kyriakou, A, Ljubicic, M L, Arlt, W, Audí, L, Balsamo, A, Baronio, F, Bertelloni, S, Bettendorf, M, Brooke, A, Claahsen-van der Grinten, H L, Davies, J, Hermann, G, de Vries, L, Hughes, I A, Tadokoro-Cuccaro, R, Darendeliler, F, Poyrazoglu, S, Ellaithi, M, Evliyaoglu, O, Fica, S, Stejereanu, L, Gawlik, A, Globa, E, Zelinska, N, Guran, T, Güven, A, Hannema, S, Hiort, O, Holterhus, P-M, Iotova, V, Mladenov, V, Jain, V, Sharma, R, Jennane, F, Johnston, C, Guerra-Junior, G, Konrad, D, Gaisl, O, Krone, N P, Krone, R, Lachlan, K, Li, D, Lichiardopol, C, Lisá, L, Markosyan, R L, Mazen, I, Mohnike, K, Niedziela, M, Nordenstrom, A, Rey, R A, Skae, M, Tack, L J, Tomlinson, J W, Weintrob, N, Cools, M & Ahmed, S F 2021, ' Gonadectomy In Conditions Affecting Sex Development-A Registry-Based Cohort Study ', European Journal of Endocrinology, vol. 184, no. 6, pp. 791-801 . https://doi.org/10.1530/EJE-20-1058
European Journal of Endocrinology, 184, 791-801
European Journal of Endocrinology, 184(6), 791-801. BioScientifica Ltd.
EUROPEAN JOURNAL OF ENDOCRINOLOGY
European Journal of Endocrinology, 184(6), 791-801. Bioscientifica Ltd
Lucas-Herald, A K, Bryce, J, Kyriakou, A, Ljubicic, M L, Arlt, W, Audí, L, Balsamo, A, Baronio, F, Bertelloni, S, Bettendorf, M, Brooke, A, Claahsen-van der Grinten, H L, Davies, J, Hermann, G, de Vries, L, Hughes, I A, Tadokoro-Cuccaro, R, Darendeliler, F, Poyrazoglu, S, Ellaithi, M, Evliyaoglu, O, Fica, S, Stejereanu, L, Gawlik, A, Globa, E, Zelinska, N, Guran, T, Güven, A, Hannema, S, Hiort, O, Holterhus, P-M, Iotova, V, Mladenov, V, Jain, V, Sharma, R, Jennane, F, Johnston, C, Guerra-Junior, G, Konrad, D, Gaisl, O, Krone, N P, Krone, R, Lachlan, K, Li, D, Lichiardopol, C, Lisá, L, Markosyan, R L, Mazen, I, Mohnike, K, Niedziela, M, Nordenstrom, A, Rey, R A, Skae, M, Tack, L J, Tomlinson, J W, Weintrob, N, Cools, M & Ahmed, S F 2021, ' Gonadectomy In Conditions Affecting Sex Development-A Registry-Based Cohort Study ', European Journal of Endocrinology, vol. 184, no. 6, pp. 791-801 . https://doi.org/10.1530/EJE-20-1058
European Journal of Endocrinology, 184, 791-801
European Journal of Endocrinology, 184(6), 791-801. BioScientifica Ltd.
EUROPEAN JOURNAL OF ENDOCRINOLOGY
European Journal of Endocrinology, 184(6), 791-801. Bioscientifica Ltd
Objectives To determine trends in clinical practice for individuals with DSD requiring gonadectomy. Design Retrospective cohort study. Methods Information regarding age at gonadectomy according to diagnosis; reported sex; time of presentation to spec
Publikováno v:
Endocrinology and Diabetes ISBN: 9783030906832
Endocrinology and Diabetes ISBN: 9781461486831
Endocrinology and Diabetes ISBN: 9781461486831
Hirsutism is the medical term that refers to the presence of excessive terminal (coarse) hair in androgen-sensitive areas of the female body (upper lip, chin, chest, back, abdomen, arms, and thighs). Virilization is more extensive than hirsutism with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d23324c84568edf6de8d18c31f778a4
https://doi.org/10.1007/978-3-030-90684-9_12
https://doi.org/10.1007/978-3-030-90684-9_12
Autor:
Camila D.Almeida Mgnani Silva, Débora de Paula Michelatto, Ana Letícia Gori Lusa, Soara Menabo, Leif Karlsson, Bengt Persson, Svetlana Lajic, Linus J. Östberg, Lilia Baldazzi, Gil Guerra-Júnior, Sofia Helena Valente de Lemos-Marini, Antonio Balsamo, Michela Barbaro, Maricilda Palandi de Mello, Nella Augusta Greggio
Publikováno v:
Clinical Biochemistry. 73:50-56
Objective Congenital adrenal hyperplasia (CAH) is an inborn error of metabolism and a common disorder of sex development where >90% of all cases are due to 21-hydroxylase deficiency. Novel and rare pathogenic variants account for 5% of all clinical c
Autor:
Salma R Ali, Ruth Krone, Vivien Thornton-Jones, Feyza Darendeliler, Mirela C Miranda, Violeta Iotova, Tulay Guran, Jillian Bryce, Nils Krone, S Faisal Ahmed, Walter Bonfig, Antonio Balsamo, Amalia Cannuccia, Claire E Higham, Richard J. Ross, Wiebke Arlt, Andrea M. Isidori, Jeremy W. Tomlinson, Ayla Güven, Tania A. S. S. Bachega, Federico Baronio, Márta Korbonits, Berenice B. Mendonca, Riccardo Pofi, Liat de Vries, Alessandro Prete, Andrea Lenzi
Context No consensus exists for optimization of mineralocorticoid therapy in patients with primary adrenal insufficiency. Objective To explore the relationship between mineralocorticoid (MC) replacement dose, plasma renin concentration (PRC), and cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffe3c8e6390e94e14a7fff9c06d34542
http://hdl.handle.net/11573/1347830
http://hdl.handle.net/11573/1347830
Autor:
Carla Bizzarri, Rita Ortolano, Silvia Einaudi, Mariangela Chiarito, Tommaso Aversa, Mariacarolina Salerno, Federico Baronio, Laura Guazzarotti, Angela Alibrandi, Maria Felicia Faienza, Domenico Corica, Donatella Capalbo, Barbara Baldini Ferroli, Enrica Abrigo, Malgorzata Wasniewska, Anna Grandone, Antonio Balsamo, Antonietta Spinuzza, Gianni Russo, Letteria Morabito
Background: Children with nonclassical congenital adrenal hyperplasia (NCCAH) often present increased growth velocity secondary to elevation of adrenal androgens that accelerates bone maturation and might compromise adult height (AH). Objective: The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::757b4b6d64728e5d253ec60d3fd3a87d
http://hdl.handle.net/11588/828454
http://hdl.handle.net/11588/828454
Autor:
Naomi Weintrob, Birgit Köhler, Sabine E. Hannema, Paul Martin Holterhus, Justin H Davies, Martine Cools, Angela K Lucas-Herald, Anna Nordenström, Antonio Balsamo, Christa E. Flück, Gilvydas Verkauskas, Otilia Marginean, Annemarie A. Verrijn Stuart, Laura Audí, Guy T'Sjoen, Mona Ellaithi, Lloyd J.W. Tack, Ellen Maris, Nils Krone, S Faisal Ahmed, Kirsten B. Kluivers, Leendert H. J. Looijenga, Stefan Riedl, Amy B. Wisniewski, Violeta Iotova, Katja P. Wolffenbuttel, Olcay Evliyaoğlu
Publikováno v:
Hormone research in pædiatrics, 90(4), 236. S. Karger AG
Hormone Research in Paediatrics, 90, 236-246
Tack, L J W, Maris, E, Looijenga, L H J, Hannema, S E, Audi, L, Köhler, B, Holterhus, P M, Riedl, S, Wisniewski, A, Flück, C E, Davies, J H, T'Sjoen, G, Lucas-Herald, A K, Evliyaoglu, O, Krone, N, Iotova, V, Marginean, O, Balsamo, A, Verkauskas, G, Weintrob, N, Ellaithi, M, Nordenström, A, Verrijn Stuart, A, Kluivers, K B, Wolffenbuttel, K P, Ahmed, S F & Cools, M 2019, ' Management of gonads in adults with androgen insensitivity : An international survey ', Hormone Research in Paediatrics, vol. 90, no. 4, pp. 236-246 . https://doi.org/10.1159/000493645
Hormone Research in Paediatrics, 90, 4, pp. 236-246
Hormone Research in Paediatrics, 90(4), 236-246. Karger
Hormone Research in Paediatrics, 90(4), 236-246
Hormone Research in Paediatrics, 90, 236-246
Tack, L J W, Maris, E, Looijenga, L H J, Hannema, S E, Audi, L, Köhler, B, Holterhus, P M, Riedl, S, Wisniewski, A, Flück, C E, Davies, J H, T'Sjoen, G, Lucas-Herald, A K, Evliyaoglu, O, Krone, N, Iotova, V, Marginean, O, Balsamo, A, Verkauskas, G, Weintrob, N, Ellaithi, M, Nordenström, A, Verrijn Stuart, A, Kluivers, K B, Wolffenbuttel, K P, Ahmed, S F & Cools, M 2019, ' Management of gonads in adults with androgen insensitivity : An international survey ', Hormone Research in Paediatrics, vol. 90, no. 4, pp. 236-246 . https://doi.org/10.1159/000493645
Hormone Research in Paediatrics, 90, 4, pp. 236-246
Hormone Research in Paediatrics, 90(4), 236-246. Karger
Hormone Research in Paediatrics, 90(4), 236-246
Background: Complete and partial androgen insensitivity syndrome (CAIS, PAIS) are associated with an increased risk of gonadal germ cell cancer (GGCC). Recent guidelines recommend gonadectomy in women with CAIS in late adolescence. Nevertheless, many
Autor:
Saverio Scianguetta, Marco Cappa, Silverio Perrotta, Lorenzo Iughetti, Mariacarolina Salerno, Natascia Di Iorgi, Roberto Salerno, Milena Brugnara, Sabrina Corbetta, Mohamad Maghnie, Domenico Roberti, Antonio Balsamo, Paolo Cavarzere, Sarah Cipriani, Elena Passeri, Rossella Gaudino, Flavia Napoli, Giuseppa Patti, Lucia Martini, Maddalena Casale, Alessandro Peri, Alberto Di Mascio
Publikováno v:
European journal of endocrinology. 181(3)
Background Autosomal dominant neurohypophyseal diabetes insipidus (adNDI) is caused by arginine vasopressin (AVP) deficiency resulting from mutations in the AVP-NPII gene encoding the AVP preprohormone. Aim To describe the clinical and molecular feat
Autor:
L. de Sanctis, Daniele Tessaris, E. P. Lanati, Marco Cappa, Stefano Mora, M. L. Brandi, N. Di Iorgi, C Eller Vainicher, Giampiero I. Baroncelli, Mohamad Maghnie, Alessandra Cassio, Antonio Balsamo, Giovanna Weber, Francesco Emma, Iacopo Chiodini, M. L. Bianchi, A. D’Ausilio, Federico Baronio, Franco Antoniazzi
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-7 (2019)
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-7 (2019)
Background X-linked hypophosphatemic rickets (XLH) is the first cause of inherited hypophosphatemia and is caused by mutation in the PHEX gene, resulting in excessive expression of the phosphaturic factor FGF23. Symptoms are mainly related to rickets
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e91f755da533f88f51d7ffe05a89231
http://hdl.handle.net/11562/997803
http://hdl.handle.net/11562/997803
Autor:
Giovanna Weber, Lorenzo Iughetti, Barbara Predieri, Graziano Grugni, Maurizio Delvecchio, Giulia Vivi, Alessandro Salvatoni, Antonio Balsamo, Malgorzata Wasniewska, Nella Augusta Greggio, Antonino Crinò, Luigi Gargantini, Uros Hladnik, L. Ragusa, Andrea Corrias, Alba Pilotta
Background Prader-Willi syndrome (PWS) is a genetic disorder due to loss of expression of paternally transcribed genes of the imprinted region of chromosome 15q11-13. PWS is characterized by peculiar signs and symptoms and many endocrine abnormalitie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ff305fada9966a7891dd2fcfaa84fa3
http://www.reference-global.com/loi/jpem
http://www.reference-global.com/loi/jpem
Autor:
Marta Berra, Martine Cools, Antonio Balsamo, Olaf Hiort, Angela K Lucas-Herald, Rita Bertalan, Zofia Kolesinska
Publikováno v:
Orphanet Journal of Rare Diseases
ORPHANET JOURNAL OF RARE DISEASES
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-8 (2018)
ORPHANET JOURNAL OF RARE DISEASES
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-8 (2018)
Background The Differences of Sex Development network (DSDnet) aims to establish interactive relationships between clinicians, scientists, support groups and people with a difference of sex development (DSD) to improve the overall care for people aff