Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Elif SAG"'
Autor:
Murat Cakir, Elif Sag, Burcu Guven, Ulas Emre Akbulut, Fatma Issi, Alper Han Cebi, Thomas Müller, Denise Aldrian, Andreas R. Janecke
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 6, Pp 612-619 (2021)
Background: Congenital diarrheal disorders (CDDs) are a rare group of enteropathies that typically present in the early few months of life and pose a diagnostic challenge. We aimed to analyze the clinical findings and outcome of infants with CDDs and
Externí odkaz:
https://doaj.org/article/4f1f67007e0342319775497790907672
Autor:
Elif Sag, Aysenur Bahadir, Mustafa Imamoglu, Sefa Sag, Gokce Pinar Reis, Erol Erduran, Murat Cakir
Publikováno v:
Clinical and Experimental Pediatrics, Vol 63, Iss 11, Pp 447-450 (2020)
Background Esophageal stricture (ES) is an uncommon clinic entity in pediatrics that may be congenital or acquired in childhood. Acquired noncaustic ES is very rare, and clinical features of affected patients are unknown. Purpose We aimed to evaluate
Externí odkaz:
https://doaj.org/article/d8c70dbfc9ff45abab53dc8214668234
Autor:
Guven Burcu, Emanuele Bellacchio, Elif Sag, Alper Han Cebi, Ismail Saygin, Aysenur Bahadir, Guldal Yilmaz, Marialuisa Corbeddu, Murat Cakir, Francesco Callea
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 14, p 5139 (2020)
Particular fibrinogen γ chain mutations occurring in the γ-module induce changes that hamper γ-γ dimerization and provoke intracellular aggregation of the mutant fibrinogen, defective export and plasma deficiency. The hepatic storage predisposes
Externí odkaz:
https://doaj.org/article/09b5966f361e4129b031e7ac1eaeb771
Autor:
Murat Cakir, Erol Erduran, Elif Sag Turkmen, Yuksel Aliyazicioglu, Gokce Pinar Reis, Umit Cobanoglu, Selim Demir
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 21, Iss 5, Pp 300-305 (2015)
Background/Aim: We aimed to analyze serum hepcidin level in children with chronic liver disease (CLD) and its relationship with serum cytokines level, liver function tests, hepatic iron content, and liver fibrosis. Patients and Methods: The study inc
Externí odkaz:
https://doaj.org/article/d28372ab9e614e16a979aac7f99534c4
Autor:
Zeynep Şıklar, Elif Özsu, Sirmen Kızılcan Çetin, Samim Özen, Filiz Çizmecioğlu-jones, Hanife Gül Balkı, Zehra Aycan, Damla Gökşen, Fatih Kilci, Sema Nilay Abseyi, Ummahan Tercan, Gözde Gürpınar, Şükran Poyrazoğlu, Feyza Darendeliler, Korcan Demir, Özge Besci, İlker Tolga Özgen, Semra Bahar Akın, Zümrüt Kocabey Sütçü, Emel Hatun Aykaç Kaplan, Emine Çamtosun, İsmail Dündar, Elif Sağsak, Hüseyin Anıl Korkmaz, Ahmet Anık, Gül Yeşiltepe Mutlu, Bahar Özcabı, Ahmet Uçar, Aydilek Dağdeviren Çakır, Beray Selver Eklioğlu, Birgül Kırel, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 16, Iss 3, Pp 288-296 (2024)
INTRODUCTION: Craniopharyngiomas (CPG) have complex treatment challenges due to their proximity to vital structures, surgical and radiotherapeutic complexities, and the tendency for recurrence. The aim of this study was to identify the prevalence of
Externí odkaz:
https://doaj.org/article/6b8a9e21a0b84e9e8ec5bc2a07ecc15e
Autor:
Elif Özsu, Semra Çetinkaya, Semih Bolu, Nihal Hatipoğlu, Şenay Savaş Erdeve, Olcay Evliyaoğlu, Firdevs Baş, Atilla Çayır, İsmail Dündar, Emine Demet Akbaş, Seyid Ahmet Uçaktürk, Merih Berberoğlu, Zeynep Şıklar, Şervan Özalkak, Nursel Muratoğlu Şahin, Melikşah Keskin, Ülkü Gül Şiraz, Hande Turan, Ayşe Pınar Öztürk, Eda Mengen, Elif Sağsak, Fatma Dursun, Nesibe Akyürek, Sevinç Odabaşı Güneş, Zehra Aycan
Publikováno v:
JCRPE, Vol 16, Iss 3, Pp 297-305 (2024)
INTRODUCTION: Maturity onset diabetes of the young (MODY) occurs due to mutations in genes involved in pancreatic beta cell function and insulin secretion, has heterogeneous clinical and laboratory features, and account for 1-5% of all diabetes cases
Externí odkaz:
https://doaj.org/article/eb7e190aaeb24a0bb6a30c654ca0303b
Autor:
Yakup Arslan, Süleyman Caner Karahan, Hatice Sonay Yalçın Cömert, Elif Sag, Emine Esra Öztürk, Murat Çakır
Publikováno v:
Journal of Academic Research in Medicine. 11:90-96
Publikováno v:
Acta Reumatológica Portuguesa, Vol 2021, Iss 2, Pp 134-139 (2021)
Introduction: Generalized joint hypermobility is a clinical feature that is associated with excessive joint laxity, which can occur alone or with various inherited disorders. The term of benign joint hypermobility or joint hypermobility is used when
Publikováno v:
Irish Journal of Medical Science (1971 -). 191:739-744
The present study assesses the diagnostic significance of low ferritin levels in gastrointestinal diseases by evaluating the endoscopic findings of patients with low ferritin levels without anemia. The study included patients aged 0–18 years who un
Autor:
Erol Erduran, Elif Sag, Aysenur Bahadir, Sefa Sag, Mustafa İmamoğlu, Gokce Pinar Reis, Murat Cakir
Publikováno v:
Clinical and Experimental Pediatrics, Vol 63, Iss 11, Pp 447-450 (2020)
Clinical and Experimental Pediatrics
Clinical and Experimental Pediatrics
Background: Esophageal stricture (ES) is an uncommon clinic entity in pediatrics that may be congenital or acquired in childhood. Acquired noncaustic ES is very rare, and clinical features of affected patients are unknown.Purpose: We aimed to evaluat