Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Busra, Gurpinar Tosun"'
Autor:
Serap Turan, Steven Mumm, Ceren Alavanda, Betul Sare Kaygusuz, Busra Gurpinar Tosun, Ahmet Arman, Margaret Huskey, Tulay Guran, Shenghui Duan, Abdullah Bereket, Michael P. Whyte
Publikováno v:
JBMR Plus, Vol 6, Iss 8, Pp n/a-n/a (2022)
ABSTRACT Dysosteosclerosis (DSS), the term coined in 1968 for ultrarare dysplasia of the skeleton featuring platyspondyly with focal appendicular osteosclerosis, has become generic by encompassing the genetic heterogeneity recently reported for this
Externí odkaz:
https://doaj.org/article/8154fb917ffb49d3850c595ac9649403
Autor:
Tarik Kirkgoz, Tulay Guran, Didem Helvacioglu, Tuba Seven Menevse, Mehmet Eltan, Serap Turan, Sare Betul Kaygusuz, Busra Gurpinar Tosun, Abdullah Bereket, Zehra Yavas Abali
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 14:10-16
To evaluate the efficacy of degludec/aspart (IDegAsp) insulin co-formulation in children and adolescents with poorly controlled type 1 diabetes (T1DM).Patients with poorly controlled T1DM on basal-bolus insulin regimes and having compliance problems
Autor:
Ambika P. Ashraf, Farahnak Assadi, Thomas M. Barber, Filippo Ceccato, Stuti Fernandes, Cornelius J. Fernandesz, Maria Fleseriu, Rousseau Gama, David S. Geller, Iuri Martin Goemann, Guido Grassi, Tulay Guran, Fahmy W.F. Hanna, Nakysa Hooman, Pieter Jansen, Felix Jebasingh, Márta Korbonits, Ana Luiza Maia, Franco Mantero, Mojgan Mazaheri, Gabriela Mihai, Matthew A. Nazari, Dominic Oduro-Donkor, Katherine Ordidge, Karel Pacak, Joseph M. Pappachan, Ondřej Petrák, Oskar Ragnarsson, Anju Sahdev, Anna Sanders, Ute I. Scholl, Gino Seravalle, Fatemeh Ghane Sharbaf, Michael Stowasser, Constantine A. Stratakis, Naomi Szwarcbard, Nihal Thomas, Irene Tizianel, Duncan J. Topliss, Busra Gurpinar Tosun, Badhma Valaiyapathi, Elena V. Varlamov, Giacomo Voltan, Martin Wolley, Tomáš Zelinka
Publikováno v:
Endocrine Hypertension ISBN: 9780323961202
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d95b4fa36590a54b213c914f605d1b4
https://doi.org/10.1016/b978-0-323-96120-2.01002-5
https://doi.org/10.1016/b978-0-323-96120-2.01002-5
Autor:
Esra Arslan Ates, Mehmet Eltan, Bahadir Sahin, Busra Gurpinar Tosun, Tuba Seven Menevse, Bilgen Bilge Geckinli, Andy Greenfield, Serap Turan, Abdullah Bereket, Tulay Guran
Background The human INHA gene encodes the inhibin subunit alpha protein, which is common to both inhibin A and B. The functional importance of inhibins in male sex development, sexual function, and reproduction remain largely unknown. Objective We r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71a73cd30156b0a2ab39c81fd219367f
https://hdl.handle.net/11424/287187
https://hdl.handle.net/11424/287187
Autor:
Tuba Seven Menevse, Yasemin Kendir Demirkol, Busra Gurpinar Tosun, Elvan Bayramoglu, Melek Yildiz, Sezer Acar, Seda Erisen Karaca, Zerrin Orbak, Asan Onder, Elif Sobu, Ahmet Anık, Zeynep Atay, Fuat Bugrul, Ayse Derya Bulus, Korcan Demir, Durmus Dogan, Hamdi Cihan Emeksiz, Heves Kirmizibekmez, Nurhan Ozcan Murat, Akan Yaman, Serap Turan, Abdullah Bereket, Tulay Guran
Context There is a significant challenge of attributing specific diagnoses to patients with primary adrenal insufficiency of unknown etiology other than congenital adrenal hyperplasia (non-CAH PAI). Specific diagnoses per se may guide personalized tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66161d52b4c8c93bac44addb72e3c563
https://hdl.handle.net/20.500.12511/9391
https://hdl.handle.net/20.500.12511/9391
Autor:
Gül Yeşiltepe Mutlu, Serap Turan, Tulay Guran, Özlem Nalbantoğlu, Agharza Aghayev, Esra Döğer, Atilla Cayir, Jamala Mammadova, Busra Gurpinar Tosun, Mehmet Nuri Ozbek, Sare Betul Kaygusuz, Elvan Bayramoğlu, Yasemin Kendir Demirkol, Tuba Seven Menevse, Abdullah Bereket, Selda Ayça Altıncık
Background Aldosterone synthase deficiency (ASD) caused by mutations in the CYP11B2 gene is characterized by isolated mineralocorticoid deficiency. Data are scarce regarding clinical and biochemical outcomes of the disease in the follow-up. Objective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36655e21d589de55133f1035a4f501dc
https://avesis.gazi.edu.tr/publication/details/f1b667a3-29be-4b4f-a085-a8f5b4324f10/oai
https://avesis.gazi.edu.tr/publication/details/f1b667a3-29be-4b4f-a085-a8f5b4324f10/oai
Autor:
Michelle Simon, Matthew Mackenzie, Sare Betul Kaygusuz, Zehra Yavas Abali, Busra Gurpinar Tosun, Hatice Kocak Eker, Nihal Hatipoglu, Sukran Poyrazoglu, Didem Helvacioglu, Mehmet Eltan, Firdevs Bas, Gozde Yesil, Gul Direk, Tuba Seven Menevse, Abdullah Bereket, Andy Greenfield, Lydia Teboul, Dilek Çiçek, Tulay Guran, Richard Reeves, Serap Turan, Nick Warr, Feyza Darendeliler
Publikováno v:
European Journal of Endocrinology
Context Homozygous and heterozygous variants in PPP2R3C are associated with syndromic 46,XY complete gonadal dysgenesis (Myo-Ectodermo-Gonadal Dysgenesis (MEGD) syndrome), and impaired spermatogenesis, respectively. This study expands the role of PPP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fa57bd6bd3a6729eeb372c3600715ed
https://avesis.kayseri.edu.tr/publication/details/58cbde97-66b0-4e72-970c-81619c50e2ea/oai
https://avesis.kayseri.edu.tr/publication/details/58cbde97-66b0-4e72-970c-81619c50e2ea/oai
Autor:
Busra, Gurpinar Tosun, Ahsen, Karagozlu Akgul, Eda, Almus, Sadik, Abidoglu, Serap, Turan, Abdullah, Bereket, Tulay, Guran
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology.
Clitoromegaly usually develops due to hyperandrogenism. There are few cases of clitoromegaly described without clinical and biochemical hyperandrogenism. Clitoromegaly due to clitoral priapism and clitoral priapism after appendectomy have not been re