Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Filiz Tutunculer"'
Autor:
Hümeyra Yaşar Köstek, Fatma Özgüç Çömlek, Hakan Gürkan, Emine Neşe Özkayın, Filiz Tütüncüler Kökenli
Publikováno v:
JCRPE, Vol 16, Iss 2, Pp 205-210 (2024)
Maturity onset diabetes of the young (MODY) is characterized by noninsulin-dependent diabetes diagnosed before the age of 25 years with an autosomal dominant inheritance. Rare mutations in the hepatocyte nuclear factor-1-beta (HNF1B) gene produce a s
Externí odkaz:
https://doaj.org/article/c1227e0d45644e6eae677ca4321ea148
Autor:
Eylem Kiral, Birgul Kirel, Merve Havan, Mehmet Keskin, Murat Karaoglan, Ahmet Yildirim, Murat Kangin, Mehmet Nur Talay, Tuba Urun, Umit Altug, Selman Kesici, Erennur Tufan, Ebru Kacmaz, Gurkan Bozan, Ebru Azapagasi, Mutlu Uysal Yazici, Zeynelabidin Ozturk, Osman Yesilbas, Gulay Karaguzel, Gulay Kaya, Ulkem Barlas, Muhterem Duyu, Merve Boyraz, Esra Sevketoglu, Nihal Akcay, Suna Hancili, Ayla Guven, Oǧuz Dursun, Nazan Ulgen Tekerek, Gokçen Ozcifci, Pinar Yazici, Eda Turanli, Tanil Kendirli, Fevzi Kahveci, Ayse Filiz Yetimakman, Agop Citak, Guntulu Şik, Ibrahim Bingol, Fatih Aygun, Cansu Durak, Resul Yilmaz, Fuat Bugrul, Yusuf Sari, Hakan Tekguç, Hatice Albayrak, Nazik Yener, Hasan Agin, Ekin Soydan, Dincer Yildizdas, Semine Ozdemir Dilek, Nilufer Yalindag, Feyza Incekoy-Girgin, Nuri Alacakir, Filiz Tutunculer, Mehmet Ozgur Arslanaoglu, Can Aydin, Muzaffer Bilgin, Enver Simsek, Ener Cagri Dinleyici
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
IntroductionThere have been some significant changes regarding healthcare utilization during the COVID-19 pandemic. Majority of the reports about the impact of the COVID-19 pandemic on diabetes care are from the first wave of the pandemic. We aim to
Externí odkaz:
https://doaj.org/article/046df642da5243edba23ad456734b874
Akademický článek
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Akademický článek
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Akademický článek
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Publikováno v:
Oxford Medical Case Reports
Leydig cell aplasia/hypoplasia is an autosomal recessive condition. In its complete form, these patients are 46XY but are cryptorchid and phenotypically female. Most cases reported in literature presented with in adolescence with pubertal delay. We r
Autor:
Olcay Evliyaoğlu, Orhun Cig Taskin, Mehmet Nuri Ozbek, Beyza Eliuz Tipici, Gül Yeşiltepe Mutlu, Ömer Faruk Beşer, Firdevs Bas, Alev Keser, Mukadder Ayşe Selimoğlu, Zarife Kuloğu, Serra Muradoğlu, Aysun Bideci, Şükrü Hatun, Feyza Darendeliler, Nuray Uslu Kızılkan, Damla Gökşen, Yasar Dogan, Sema Aydogdu, Deniz Ertem, Tugba Koca, Zehra Aycan, Şenay Savaş Erdeve, Tuğba Gökçe, Buket Dalgic, Filiz Tutunculer
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
It is well-known that in children with type 1 diabetes (T1D), the frequency of Celiac disease (CD) is increased due to mechanisms which are not fully elucidated but include autoimmune injury as well as shared genetic predisposition. Although histopat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09b2f0c999b2037773583237698e9194
https://hdl.handle.net/11424/238588
https://hdl.handle.net/11424/238588
Publikováno v:
INTERNATIONAL JOURNAL OF ENDOCRINOLOGY (Ukraine); Том 16, № 1 (2020); 76-79
Международный эндокринологический журнал-Mìžnarodnij endokrinologìčnij žurnal; Том 16, № 1 (2020); 76-79
Міжнародний ендокринологічний журнал-Mìžnarodnij endokrinologìčnij žurnal; Том 16, № 1 (2020); 76-79
Международный эндокринологический журнал-Mìžnarodnij endokrinologìčnij žurnal; Том 16, № 1 (2020); 76-79
Міжнародний ендокринологічний журнал-Mìžnarodnij endokrinologìčnij žurnal; Том 16, № 1 (2020); 76-79
Insulin-induced oedema is a rare complication of insulin therapy and occurs shortly after the initiation of intensive insulin therapy in patients with newly diagnosed type 1 diabetes mellitus (DM) or in patients with poorly controlled type 2 DM follo
Publikováno v:
Volume: 42, Issue: 3 325-333
Osmangazi Tıp Dergisi
Osmangazi Tıp Dergisi
TipI Diabetes Mellitus çocukluk çağının ciddi komplikasyonlar ile seyreden kronikmetabolik hastalıklarından biridir. Bu çalışmanın amacı Tip I DiabetesMellituslu çocuklarda erken dönemde santral sinir sistemi tutulumunun uyarılmışpot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29d99a86338a35ef4f7c4db4b1782c20
https://app.trdizin.gov.tr/makale/TkRBME1UUTNOdz09
https://app.trdizin.gov.tr/makale/TkRBME1UUTNOdz09
Publikováno v:
Türk Pediatri Arşivi. 53:120-123
Benign transient hyperphosphatasemia is characterized by a significant increase in alkaline phosphatase levels, which is detected incidentally in infancy and children without underlying bone and liver disease. This condition is a biochemical disorder