Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Teoman Akcay"'
Autor:
Meltem Weger, Benjamin D. Weger, Benjamin Görling, Gernot Poschet, Melek Yildiz, Rüdiger Hell, Burkhard Luy, Teoman Akcay, Tülay Güran, Thomas Dickmeis, Ferenc Müller, Nils Krone
Publikováno v:
EBioMedicine, Vol 36, Iss , Pp 376-389 (2018)
Background: Deficient glucocorticoid biosynthesis leading to adrenal insufficiency is life-threatening and is associated with significant co-morbidities. The affected pathways underlying the pathophysiology of co-morbidities due to glucocorticoid def
Externí odkaz:
https://doaj.org/article/ae10baa3647d4ebc93656935ff620747
Autor:
Hasan Serdar Kıhtır, Teoman Akcay
Publikováno v:
Bagcilar Medical Bulletin. 5:24-27
Objective: Premature thelarche is defined as breast enlargement in females (younger than eight years) without other signs of secondary gender character development. Although it is common in the first two years of life, it can be seen in any age group
Publikováno v:
Biomedical Reports
The determination of the genetic profiles of successful athletes and the effects of these genetic parameters on athletic performance is gaining increasing interest. The majority of studies assessing the genetics of athletes usually analyse the most w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d83861cf34e378ab87e02f0f87061118
https://hdl.handle.net/11424/243030
https://hdl.handle.net/11424/243030
Humans spend one-third of their lives sleeping. Alteration of quality and duration of sleep can affect health. The importance of sleep has shown that total sleep loss is fatal. Sleep begins at the molecular and cellular levels, but it is also sensiti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::998583e13de529307c4893e517f6ba3f
https://doi.org/10.1016/b978-0-12-816658-1.00005-3
https://doi.org/10.1016/b978-0-12-816658-1.00005-3
Autor:
Deldar Morad Abdulah, Teoman Akcay, Tatiane dos Santos Andrade, Kostas Archontogeorgis, Peter M. Baptista Jardin, Jeff Boissoneault, Jeremy C. Borniger, Nicole P. Bowles, Heráclito Barbosa Carvalho, Naricha Chirakalwasan, Flávia Campos Corgosinho, Ashley F. Curtis, Megan J. Dailey, Ana Raimunda Dâmaso, Avelino A. De Leon, Marco Túlio de Mello, Esra Dogru Huzmeli, Jennifer Chinomso Ehiri, Mengyu Fan, Augusto César Ferreira De Moraes, Lindsey Freeman, Joaquín S. Galindo Muñoz, Daniel G. Glaze, Ozden Gokcek, Murat Guntel, Ilana S. Hairston, Erin C. Hanlon, Juan José Hernández Morante, Maria Izquierdo-Pulido, Peter G. Jacobs, Tejas V. Joshi, Deniz Kirac, Marco Luppi, António Macedo, Megan M. Mahoney, Frederico Moraes Cardoso Marques, Giselle de Martin Truzzi, Füsun Mayda Domaç, Christina S. McCrae, Andrew W. McHill, Arnaud Metlaine, Mary Beth Miller, Yoriyuki Nakamura, Marcus Vinicius Nascimento-Ferreira, Evangelia Nena, Natalie Nevárez, Esra Okuyucu, Olakunle J. Onaolapo, Adejoke Y. Onaolapo, Parth J. Parekh, Amee A. Patel, Amanda J. Piper, Guillermo Plaza, Arcady A. Putilov, Lu Qi, Ravi Reddy, Sirimon Reutrakul, Rodrigo Rodrigues, Fernando Morgadinho Santos Coelho, Akiyoshi Shimura, Maria João Soares, Maria Fernanda Soares Naufel, Marie-Pierre St-Onge, Paschalis Steiropoulos, David Thivel, Francisco Leonardo Torres-Leal, Cambras Trinitat, Robin M. Tucker, Korkut Ulucan, Keiko Unno, Boran Urfali, Senem Urfali, Xuewen Wang, Chia-Lun Yang, Shinobu Yasuo, María Fernanda Zerón-Rugerio, Faris M. Zuraikat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1353126438c5e05a61950da8db290d7
https://doi.org/10.1016/b978-0-12-816658-1.01002-4
https://doi.org/10.1016/b978-0-12-816658-1.01002-4
Autor:
Hasan Önal, Abdurrahman Akgun, Teoman Akcay, Melek Yildiz, Sian Ellard, Elisa De Franco, Banu Kucukemre Aydin, Beyza Belde Dogan
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 31:345-348
Background: As KATP channel mutations are the most common cause of neonatal diabetes mellitus (NDM) and patients with these mutations can be treated with oral sulfonylureas, empiric therapy is a common practice for NDM patients. Case presentation: A
Autor:
Safiye Giran Örtekin, Mustafa Kemal Adali, Selin Üstün Bezgin, Teoman Akcay, Taliye Çakabay, Murat Koçyiğit, Melek Yildiz, Güven Özkaya
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: Otitis media with effusion (OME) is a condition in which fluid is retained in the middle ear cavity. The association between endocrine disorders and OME has not yet been determined. This study aimed to investigate the presence of OME in ch
Autor:
Bon Chu Chung, Goncagül Haklar, Serap Turan, Cengiz Kara, Jamala Mamadova, Tulay Guran, Melek Yildiz, Ahmet Anık, Eda Celebi Bitkin, Jen-Chieh Lin, Zeynep Atay, Teoman Akcay, Gönül Çatlı, Birgül Kirel, Hasan Önal, Azad Akbarzade, Onder Sirikci, Abdullah Bereket, Mehmet Keskin, Karl-Heinz Storbeck, Ayla Guven, Gülay Can Yılmaz, Tugba Baris, Filiz Tutunculer, Lise Barnard
Publikováno v:
The Journal of clinical endocrinology and metabolism. 105(3)
Context The clinical effects of classical 3β-hydroxysteroid dehydrogenase 2 (3βHSD2) deficiency are insufficiently defined due to a limited number of published cases. Objective To evaluate an integrated steroid metabolome and the short- and long-te
Autor:
Tulay Guran, Ilknur Arslanoglu, Ala Üstyol, Sukran Poyrazoglu, Derya Karaman Aksakal, Songül Karadeniz, Nurcan Cebeci, Olcay Evliyaoğlu, Halim Issever, Nihal Memioglu, Ahmet Uçar, Serap Semiz, Firdevs Bas, Didem Bezen, Feyza Darendeliler, Erdal Adal, Gül Yeşiltepe Mutlu, Hasan Önal, Saygin Abali, Abdurrahman Akgun, Serpil Bas, Nese Akcan, Sevil Sarikaya, Gulcan Seymen Karabulut, Ayla Güven, Ömer Tarım, Elif Sagsak, Melek Yildiz, Esra Deniz Papatya Cakir, Havva Nur Peltek, Bahar Ozcabi, Teoman Akcay, Aysegul Yuksel, Şükrü Hatun, Zeynep Atay, Hüseyin Anıl Korkmaz, Mehmet Azizoğlu, Oya Ercan, Pinar Isguven, Aydilek Dağdeviren, Abdullah Bereket, Filiz Tutunculer, Erdal Eren, Semih Bolu, Serap Turan, Tolga Özgen, Filiz Mine Çizmecioğlu, Emine Dilek, Yaşar Cesur, Heves Kırmızıbekmez, Metin Yildiz, Zehra Yavas Abali, Rüveyde Bundak, Cigdem Binay, Fatma Dursun
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
ABALI, SAYGIN/0000-0001-6552-2801; Turan, Serap/0000-0002-5172-5402; Hatun, Sukru/0000-0003-1633-9570; Akgun, Abdurrahman/0000-0002-2917-2469; yesiltepe mutlu, gul/0000-0003-3919-7763; Ozgen, Ilker Tolga/0000-0001-6592-9652 WOS: 000451667000006 PubMe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65aab0f3d06236cbc7acf777c68a0d8b
https://hdl.handle.net/11443/2827
https://hdl.handle.net/11443/2827
Autor:
Benjamin Görling, Gernot Poschet, Ferenc Müller, Benjamin D. Weger, Meltem Weger, Melek Yildiz, Teoman Akcay, Burkhard Luy, Nils Krone, Tulay Guran, Thomas Dickmeis, Rüdiger Hell
Publikováno v:
EBioMedicine, 36, 376–389
EBioMedicine
EBioMedicine
Background: Deficient glucocorticoid biosynthesis leading to adrenal insufficiency is life-threatening and is associated with significant co-morbidities. The affected pathways underlying the pathophysiology of co-morbidities due to glucocorticoid def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5910cd9651bf426ce8e186c37cfafcc8
https://publikationen.bibliothek.kit.edu/1000087323/19216469
https://publikationen.bibliothek.kit.edu/1000087323/19216469