Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Maşallah BARAN"'
Autor:
Maşallah Baran, Tülay Kılıçaslan Ayna, Melek Pehlivan, Betül Aksoy, Aslı Özkızılcık Koçyiğit, Yeliz Çağan Appak, Aslı Eldem, Bumin Nuri Dündar, Mustafa Soyöz, İbrahim Pirim
Publikováno v:
Journal of Pediatric Research, Vol 11, Iss 1, Pp 25-29 (2024)
Aim: The goal of this study was to investigate the expression levels of microRNAs (miRNAs) (miR-196b, miR-10a, miR-31-5p, and miR-338-3p) which regulate the genes involved in the proliferation and function of cells functioning in the inflammatory pro
Externí odkaz:
https://doaj.org/article/b864e61feb7a489a98fb37137bb71dc1
Publikováno v:
Forbes Tıp Dergisi, Vol 4, Iss 3, Pp 272-283 (2023)
Objective: The aim of this study was to determine the nutritional status of children and adolescents with inflammatory bowel disease (IBD) in remission and to evaluate their adherence to the Mediterranean diet. Methods: The study was conducted with 4
Externí odkaz:
https://doaj.org/article/0aaff1fd77c046daa8a5387acc085878
Autor:
Selen Güler, Betül Aksoy, M. Onur Öztan, Yeliz Ç. Appak, Sinem Kahveci Çelik, Şenay Onbaşı Karabağ, Gökhan Köylüoğlu, Maşallah Baran
Publikováno v:
The Turkish Journal of Gastroenterology, Vol 34, Iss 9, Pp 968-974 (2023)
Externí odkaz:
https://doaj.org/article/8f498db5ed3c4309829bca3dd4b7ec45
Autor:
Tülay Demircan, Yeliz Çağan Appak, Maşallah Baran, Betül Aksoy, Barış Güven, Nazmi Narin, Cem Karadeniz
Publikováno v:
Journal of Pediatric Research, Vol 8, Iss 1, Pp 7-13 (2021)
Aim:Cardiac abnormalities associated with celiac disease (CD) have been reported. However, changes in electrocardiographic (ECG) parameters in children with CD have not been previously evaluated in the literature. In this study, we aimed to evaluate
Externí odkaz:
https://doaj.org/article/b742773264d54ca08ddcb82ab1312f8f
Autor:
Maşallah Baran, Yeliz Çağan Appak, Fatma Demet Arslan, Dudu Solakoğlu Kahraman, Miray Karakoyun, İnanç Karakoyun, Büşra Emir, Gülden Diniz
Publikováno v:
Journal of Pediatric Research, Vol 7, Iss 3, Pp 185-191 (2020)
Aim:In this study, the correlation of faecal calprotectin (FC) levels with endoscopic and histopathological findings was evaluated in children who underwent upper gastrointestinal system (UGIS) endoscopy.Materials and Methods:The patients aged 4-18 y
Externí odkaz:
https://doaj.org/article/76ea66339f1c4d518901c4074a0c5578
Autor:
Dilek Yılmaz-Ciftdoğan, Ahu Kara-Aksay, Gülcan Erbaş, Ümit Başak Sarkış, Eda Karadağ-Oncel, Ayşe Berna Anıl, Maşallah Baran, Halil Er, Nisel Yılmaz
Publikováno v:
Microbiology Spectrum, Vol 9, Iss 2 (2021)
ABSTRACT The aims of the study were to describe Candida species in children with candidemia, to determine the changing epidemiology of candidemia over time in our tertiary care hospital, and to examine the demographic and clinical characteristics of
Externí odkaz:
https://doaj.org/article/a476628a1c274050a47d81cc6dcc5924
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 4, Pp 259-265 (2019)
Aim:This study aims to evaluate the sleep quality and the quality of life (QoL) of adolescents with chronic gastritis, and determine the related factors.Materials and Methods:This study included patients who were diagnosed with chronic gastritis both
Externí odkaz:
https://doaj.org/article/2282218d79b0422da0c35e94bba6732b
Publikováno v:
São Paulo Medical Journal, Iss 0 (2018)
ABSTRACT CONTEXT: Rapunzel syndrome is a rare form of gastric trichobezoar that develops through outstretching of the bezoar from the stomach to the intestine. CASE REPORT: A 12-year-old girl who had been diagnosed with celiac disease six years earli
Externí odkaz:
https://doaj.org/article/3d64da33aee248b7b1ea6cd50403426c
Publikováno v:
Pediatric Nephrology. 37:1033-1039
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddb734d25f5fdf79c8c62fb0ce281b9d
https://doi.org/10.1007/s00467-021-05363-7
https://doi.org/10.1007/s00467-021-05363-7
Publikováno v:
Turkish archives of pediatrics. 57(3)
Gilbert syndrome (GS) is a disease characterized by mildly elevated indirect serum bilirubin levels due to mutation in the promoter of the UGT1A1 gene, which causes a decrease in uridine diphosphate glucuronyltransferase enzyme activity. Gilbert synd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a27708e50df9b40fef7ad502495b164
https://pubmed.ncbi.nlm.nih.gov/35781232
https://pubmed.ncbi.nlm.nih.gov/35781232