Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Secil Özışık"'
Autor:
Dilek Yazıcı, Mehmet Mahir Fersahoğlu, Tuba Fersahoğlu, Nuriye Esen Bulut, Hüseyin Çiğiltepe, Özgen Çeler, SEDA Sancak, Cem Sulu, Emre Durcan, Serdar Şahin, Özge Polat Korkmaz, Sıla Hidayet Bozdoğan Polat, Eren Taskin, Ceren İşeri, Evren Gürsoy, Meral Küçük Yetgin, Tuğba Kaya, Feyza Özdemir, Naime Mestanoğlu İstanbullu, Sinem Kıyıcı, Serkan Öztürk, Kağan Güngör, Bülent Can, Mehmet Sargın, Zeynep Tabak, Sevda Averi, Aysun Nazlı, Yeliz Polat, Feray Akbas, Sakin Tekin, Ömercan Topaloğlu, Ebru Boz Uzaldı, Safiye Çatalçam, Taner Bayraktaroğlu, Bedia Fulya Çalıkoğlu, Vefa Nasifova, Özlem Soyluk Selçukbiricik, Kubilay Karşıdağ, Havva Sezer, Secil Özışık, Hande Bulut, Bahar Bekdemir, Oğuzhan Deyneli, Ceyda Dinçer, Dilek Gogas Yavuz, Hasan Ilkova, Volkan Demirhan Yumuk
Publikováno v:
Obesity Facts (2022)
Introduction: The COVID-19 pandemic led to a lockdown period. Confinement periods have been related to unhealthy lifestyle behaviors. Our study aimed to determine weight change, changes in eating and exercise habits, the presence of depression and an
Externí odkaz:
https://doaj.org/article/a4acbdc7495c41c189bf30ce4c8ee27f
Autor:
Canan Altay, Mustafa Seçil, Tevfik Demir, Tahir Atik, Gülçin Akıncı, Nilüfer Özdemir Kutbay, Ela Keskin Temeloğlu, Ilgın Yıldırım Şimşir, Seçil Özışık, Leyla Demir, Erdal Eren, Emine Burçin Tuna, Hasibe Aytaç, Hüseyin Onay, Barış Akıncı
Publikováno v:
Diagnostic and Interventional Radiology, Vol 23, Iss 6, Pp 428-434 (2017)
PURPOSE:We aimed to investigate residual adipose tissue with whole-body magnetic resonance imaging to differentiate between subtypes of lipodystrophy.METHODS:A total of 32 patients (12 with congenital generalized lipodystrophy [CGL], 1 with acquired
Externí odkaz:
https://doaj.org/article/adbbce66f92d49a799c6f28d2f31de48
Autor:
Sezer Acar, Huda A BinEssa, Korcan Demir, Roua A Al-Rijjal, Minjing Zou, Gönül Çatli, Ahmet Anık, Anwar F Al-Enezi, Seçil Özışık, Manar S A Al-Faham, Ayhan Abacı, Bumin Dündar, Walaa E Kattan, Maysoon Alsagob, Salih Kavukçu, Hamdi E Tamimi, Brian F Meyer, Ece Böber, Yufei Shi
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0193388 (2018)
Hereditary hypophosphatemia is a group of rare renal phosphate wasting disorders. The diagnosis is based on clinical, radiological, and biochemical features, and may require genetic testing to be confirmed.Clinical features and mutation spectrum were
Externí odkaz:
https://doaj.org/article/10b254c616884e3f832371affc2506e0