Zobrazeno 1 - 10
of 133
pro vyhledávání: '"Mukadder Ayşe SELİMOĞLU"'
Publikováno v:
The Korean Journal of Gastroenterology, Vol 63, Iss 1, Pp 17-22 (2024)
Background/Aims: Solitary rectal ulcer syndrome (SRUS) can be overlooked, diagnosed late, or misdiagnosed, particularly in childhood. This study reviewed the 13-year experience of the authors’ institution to increase clinicians' awareness of SRUS i
Externí odkaz:
https://doaj.org/article/755358112c1e402c97eb747c632fb764
Autor:
Fatih ÖZDENER, İlknur KILIÇ, Coşkun SAF, Tuğba DEMİRCAN BİLEN, Dicle ÇELİK, Nurdan URAŞ, Doruk GÜL, Gamze DEMİREL, Hayrettin TEMEL, Dilek ÇOBAN, ENVER MAHIR GÜLCAN, Alihan SÜRSAL, Vildan ERTEKİN, Mukadder Ayşe SELİMOĞLU
Publikováno v:
Forbes Tıp Dergisi, Vol 4, Iss 3, Pp 336-345 (2023)
Objective: Formula milk aims to mimic breast milk or can serve as a complementary diet, thus reducing the risk of developing nutritional deficiencies. In this study, we evaluated the factors affecting compliance with the use of prebiotic formula milk
Externí odkaz:
https://doaj.org/article/29f920c7bd97491c8d1551fcefe4717b
Publikováno v:
JCRPE, Vol 15, Iss 1, Pp 62-68 (2023)
INTRODUCTION: It has been reported that bone mineral density (BMD) is decreased in children with Celiac disease (CD) compared to their healthy peers. The aim of this study was to reveal possible risk factors for low BMD in Turkish children newly diag
Externí odkaz:
https://doaj.org/article/e153a41bafdf41c280c7e3a4bf48ab88
Publikováno v:
JCRPE, Vol 14, Iss 4, Pp 409-414 (2022)
INTRODUCTION: A close relationship has been suggested between Celiac disease (CD) and glandular autoimmunity. The aim of this study was to determine the predictive factors for autoimmune glandular disease (AGD) in children with CD. METHODS: The stud
Externí odkaz:
https://doaj.org/article/485cfeee11d743f98d4ef1463e6a3a72
Autor:
Aydan Kansu, Zarife Kuloglu, Gökhan Tümgör, Didem Gülcü Taşkın, Buket Dalgıç, Gönül Çaltepe, Kaan Demirören, Güzide Doğan, Ceyda Tuna Kırsaçlıoğlu, Duran Arslan, İshak Abdurrahman Işık, Hülya Demir, Özlem Bekem, Yasin Şahin, Nevzat Aykut Bayrak, Mukadder Ayşe Selimoğlu, Sibel Yavuz, İbrahim Ethem Taşkaya, Derya Altay, the VICTORIA Study Group, Ayşegül Bükülmez, Arzu Meltem Demir, Yavuz Tokgöz, Zarife Kuloğlu, Hasret Ayyıldız, Günsel Kutluk, Meryem Keçeli Başaran, Oya Balcı Sezer, Tanju Başarır Özkan, Taner Özgür, Gonca Handan Üstündağ, Eda Somuncu, Ali İşlek, Ferda Özbay Hoşnut, Gülseren Evirgen Şahin, Yaşar Doğan, Uğur Deveci, Kamercan Ceylan, Ahmet Baştürk, Necati Balamtekin, Melike Arslan, Hayriye Hızarcıoğlu Gülşen, Atakan Comba, İlknur Varol, Sebahat Çam, Eylem Sevinç, Erkan Doğan, Murat Çakır, Burcu Güven, Suna Selbuz, Hacer Fulya Gülerman, Zeynep Arslan, Ayşen Uncuoğlu, Neslihan Gürcan Kaya, Deniz Ertem, Engin Tutar, Burcu Volkan, Yusuf Usta, Asuman Nur Karhan, Halil Kocamaz, Tuğba Gürsoy Koca, Fatih Ünal, Birol Öztürk, Cansu Altuntaş, Halil Haldun Emiroğlu, Meltem Gümüş, Mustafa Akçam, Yeliz Çağan Appak, Betül Aksoy, Elif Sağ, Ulaş Emre Akbulut, Cahit Barış Erdur, Nafiye Urgancı, Ayşe Merve Usta, Coşkun Çeltik, Nelgin Gerenli
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionElevated transaminases and/or creatine phosphokinase can indicate underlying muscle disease. Therefore, this study aims to determine the frequency of Duchenne muscular dystrophy/Becker muscular dystrophy (DMD/BMD) in male children and Pom
Externí odkaz:
https://doaj.org/article/017a5b24b62a45e585ae24595455e694
Autor:
Şükrü Hatun, Buket Dalgıç, Damla Gökşen, Sema Aydogdu, Şenay Savaş Erdeve, Zarife Kuloğlu, Yaşar Doğan, Zehra Aycan, Gül Yeşiltepe Mutlu, Nuray Uslu Kızılkan, Alev Keser, Ömer Faruk Beşer, Mehmet Nuri Özbek, Aysun Bideci, Deniz Ertem, Olcay Evliyaoğlu, Beyza Eliuz Tipici, Tuğba Gökçe, Serra Muradoğlu, Orhun Çığ Taşkın, Tuğba Koca, Filiz Tütüncüler, Firdevs Baş, Feyza Darendeliler, Mukadder Ayşe Selimoğlu
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 1-9 (2022)
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://doaj.org/article/ebf94e0f56414df49390df3e2ddb8cd4
Autor:
Kürşad Aydın, Buket Dalgıç, Aydan Kansu, Hasan Özen, Mukadder Ayşe Selimoğlu, Hasan Tekgül, Bülent Ünay, Aysel Yüce
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
This review by a panel of pediatric gastroenterology-hepatology-nutrition and pediatric neurology experts aimed to address the significance of mid-upper arm circumference (MUAC) assessment in diagnosis of pediatric malnutrition. Specifically, the pot
Externí odkaz:
https://doaj.org/article/1898da980b2043c684f6706a754f34c8
Publikováno v:
Balkan Medical Journal, Vol 35, Iss 6, Pp 442-444 (2018)
Externí odkaz:
https://doaj.org/article/498a4af5e6d44360b2efb23f1751b567
Publikováno v:
São Paulo Medical Journal, Vol 136, Iss 4, Pp 304-309
ABSTRACT BACKGROUND: Wilson’s disease (WD) may present with different manifestations: from an asymptomatic state to liver cirrhosis. Here, we aimed to evaluate clinical presentations and laboratory findings and prognoses among WD cases. DESIGN AND
Externí odkaz:
https://doaj.org/article/3cb149a9390a4bf1991cbea20d7de262
Publikováno v:
Arab Journal of Gastroenterology. 22:310-315
Background and study aims Progressive familial intrahepatic cholestasis (PFIC) is an autosomal recessively inherited disease that causes intrahepatic-hepatocellular cholestasis. PFIC constitutes approximately 10–15% of cholestatic liver diseases in