Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Buket Dalgiç"'
Autor:
Ödül Eğribaş Gürkan, Hakan Öztürk, Cem Kaya, Neslihan Gürcan Kaya, Neslihan Ekşi Bozbulut, Ayşe Can, Kamercan Ceylan, Aysel Ünlüsoy Aksu, Demet Teker Düztaş, Sinan Sarı, Buket Dalgıç, Alparslan Kapısız, Demet Coşkun, Gökcen emmez, Gözde İnan, İsmail Akdulum, Hasan Kutlu Pampal, Nuray Camgoz Eryılmaz, Selin Erel, Volkan Şıvgın, Ercan Yıldırım, Okan Ermiş, İrfan Güngör, Gülay Kip, Nurdan Bedirli, Berrin Işık, İbrahim Onur Özen, Yusuf Hakan Çavuşoğlu, Ramazan Karabulut, Zafer Türkyılmaz, Kaan Sönmez
Publikováno v:
The Turkish Journal of Gastroenterology, Vol 35, Iss 3, Pp 255-261 (2024)
Background/Aims: Gastric outlet obstruction (GOO) is a rare condition in childhood, with the exception of infantile hypertrophic pyloric stenosis (IHPS). However, no classification exists from a pediatric gastroenterologist’s perspective. Materi
Externí odkaz:
https://doaj.org/article/5449add8de5843c5bc86c94133a0f4af
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 3, Pp 991-998 (2019)
Amaç: Bu çalışmada; akut pankreatit, akut tekrarlayan pankreatit ve kronik pankreatit tanısı ile izlenen çocukların klinik, laboratuvar ve etiyolojik farklılıklarının değerlendirilmesi amaçlanmıştır.Gereç ve Yöntem: Ocak 2009 - Eyl
Externí odkaz:
https://doaj.org/article/2d09a4ce26dc42f28b616abc41db897c
Publikováno v:
Arquivos de Gastroenterologia, Iss 0 (2017)
ABSTRACT BACKGROUND: As being the first bacteria determined to be carcinogenic, Helicobacter pylori (H. pylori) is a pathogen localized in the stomach in more than half of the world population. Some earlier studies have found a relation between tissu
Externí odkaz:
https://doaj.org/article/9cb8f3a9ac3a443b9fb034fbde51e5f1
Autor:
Fatma Derya Bulut, Neslihan Ekşi Bozbulut, Özge Özalp, Buket Dalgiç, Neslihan Önenli Mungan, Habibe Koç Uçar, Gürsel Biberoğlu
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 35:681-685
Objectives Niemann–Pick disease type C (NPC) is a lysosomal storage disease due to impaired intracellular lipid trafficking caused by biallelic pathogenic variants in NPC1 or NPC2 genes. NPC is classified according to the age of onset of neurologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13b99e46a0b3b6ac29e30655406c739c
https://doi.org/10.1515/jpem-2021-0580
https://doi.org/10.1515/jpem-2021-0580
Autor:
Demet Teker Düztaş, Sinan Sari, Ödül Eğritaş Gürkan, Mustafa Hakan Sözen, Buket Dalgiç, Aydın Dalgiç
Publikováno v:
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation. 20(Suppl 3)
Progressive familial intrahepatic cholestasis is a heterogeneous group of autosomal recessive disorders, and liver transplant is the only curative treatment. A biliary diversion operation for disruption of enterohepatic circulation in patients with p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ad1f0bfcd380427112420527364877e
https://pubmed.ncbi.nlm.nih.gov/35570607
https://pubmed.ncbi.nlm.nih.gov/35570607
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:
Richard J. Thompson, Reha Artan, Ulrich Baumann, Pier Luigi Calvo, Piotr Czubkowski, Buket Dalgic, Lorenzo D’Antiga, Angelo Di Giorgio, Özlem Durmaz, Emmanuel Gonzalès, Tassos Grammatikopoulos, Girish Gupte, Winita Hardikar, Roderick H.J. Houwen, Binita M. Kamath, Saul J. Karpen, Florence Lacaille, Alain Lachaux, Elke Lainka, Kathleen M. Loomes, Cara L. Mack, Jan P. Mattsson, Patrick McKiernan, Quanhong Ni, Hasan Özen, Sanjay R. Rajwal, Bertrand Roquelaure, Eyal Shteyer, Etienne Sokal, Ronald J. Sokol, Nisreen Soufi, Ekkehard Sturm, Mary Elizabeth Tessier, Wendy L. van der Woerd, Henkjan J. Verkade, Jennifer M. Vittorio, Terese Wallefors, Natalie Warholic, Qifeng Yu, Patrick Horn, Lise Kjems
Publikováno v:
JHEP Reports, Vol 5, Iss 8, Pp 100782- (2023)
Background & Aims: PEDFIC 2, an ongoing, open-label, 72-week study, evaluates odevixibat, an ileal bile acid transporter inhibitor, in patients with progressive familial intrahepatic cholestasis. Methods: PEDFIC 2 enrolled and dosed 69 patients acros
Externí odkaz:
https://doaj.org/article/943aa785601b46a586443dc2851475ff
Autor:
Aydan Kansu, Nafiye Urganci, Aysegul Bukulmez, Gunsel Kutluk, Didem Gulcu Taskin, Lutfiye Sahin Keskin, Mahir Igde, Lutfi Molon, Yasar Dogan, Bulent Enis Sekerel, Mutlu Yuksek, Ilknur Bostanci, Nelgin Gerenli, Esra Polat, Buket Dalgic, Hasret Ayyildiz, Merve Usta, Ahmet Basturk, Ozlem Yuce Kirmemis, Ceyda Tuna Kirsaclioglu, Hacer Fulya Gulerman, Aysugul Alptekin Sarioglu, Simge Erdogan
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
ObjectiveTo evaluate growth, tolerance and safety outcomes with use of an extensively hydrolyzed casein-based formula (eHCF) in infants with cow’s milk protein allergy (CMPA).MethodsA total of 226 infants (mean ± SD age: 106.5 ± 39.5 days, 52.7%
Externí odkaz:
https://doaj.org/article/caa99cc52f06419883b5e8f15c3d4e19
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
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