Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Sinan Sarı"'
Publikováno v:
Turkish Archives of Pediatrics, Vol 59, Iss 3, Pp 283-289 (2024)
Objective: Early diagnosis of biliary atresia (BA) and the timing of Kasai hepatic portoenterostomy are associated with improved survival rates of the native liver. Acholic stool is a major and earliest sign of BA. We evaluated the awareness and reco
Externí odkaz:
https://doaj.org/article/1aacb79b60cd44769b8cac8420ec4e3c
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
Autor:
Ozgun Karakus, Ahmet Sinan Sarı
Publikováno v:
Journal of Orthopaedic Surgery, Vol 28 (2020)
Purpose: The aim of this study was to determine the time points during a total knee arthroplasty operation when there is the greatest possibility of tearing a surgical glove and thus the stage of the operation at which there is the greatest risk of i
Externí odkaz:
https://doaj.org/article/fecc15ee6b3f43f4aa8168f69e878ab8
Publikováno v:
Experimental and Clinical Transplantation. 20:76-80
Progressive familial intrahepatic cholestasis is a heterogeneous group of genetic disorders characterized by disrupted bile homeostasis. Patients with this disease typically present with cholestasis and pruritus early in life and often progress to en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe98fb6f75587ec522ab146fd623e15b
https://doi.org/10.6002/ect.pediatricsymp2022.o26
https://doi.org/10.6002/ect.pediatricsymp2022.o26
Autor:
Aslı İnci, Gonca Kılıç Yıldırım, Filiz Başak Cengiz Ergin, Sinan Sarı, Ödül Eğritaş Gürkan, İlyas Okur, Gürsel Biberoğlu, Ayşegül Bükülmez, Fatih Süheyl Ezgü, Buket Dalgıç, Leyla Tümer
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 35:451-462
Objectives To reveal the different clinical presentations of liver glycogen storage disease type IX (GSD IX), which is a clinically and genetically heterogeneous type of glycogenosis. Methods The data from the electronic hospital records of 25 patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fa2388813005e884289e78f9aaefb2a
https://doi.org/10.1515/jpem-2021-0278
https://doi.org/10.1515/jpem-2021-0278
Autor:
Demet, Teker Düztaş, Sinan, Sarı, Ödül, Eğritaş Gürkan, Gülsüm, Kayhan, Aydın, Dalgıç, Buket, Dalgıç
Publikováno v:
Experimental and Clinical Transplantation. 20:115-117
Ciliopathies are a heterogeneous group of diseases that are observed after deterioration of the ciliary structures on the cell surface that facilitate communication with the environment. Both liver and kidney involvement are frequently observed in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::912b38642ee7b9d75cba6db4acf63827
https://doi.org/10.6002/ect.pediatricsymp2022.o37
https://doi.org/10.6002/ect.pediatricsymp2022.o37
Autor:
Hacer İlbilge, Ertoy Karagöl, Dilek, Yapar, Ödül, Eğritaş Gürkan, Sinan, Sarı, Mustafa Necmi, İlhan, Buket, Dalgıç, Arzu, Bakırtaş, Gazi University Pediatric Eosinophilic Gastrointestinal, Diseases Working Group
Publikováno v:
Turk J Gastroenterol
Background/aims There has been no valid and reliable Turkish scale that measures symptoms in children with eosinohilic esophagitis (EoE). The aim of the study is test the validity and reliability of Turkish version of Pediatric Eosinophilic Esophagit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce70d7d3aa750a320643675a71726a53
https://pubmed.ncbi.nlm.nih.gov/34231483
https://pubmed.ncbi.nlm.nih.gov/34231483
Autor:
Zarife, Kuloglu, Funda, Çetin, Nafiye, Urgancı, Zerrin, Önal, Sinan, Sarı, Hasan, Yüksekkaya, Gönül, Çaltepe, Günsel, Kutluk, Ebru, Dumlupinar, Aylin, Yücel
Publikováno v:
European journal of clinical nutrition. 76(9)
We analyzed the nationwide pediatric inflammatory bowel disease (PIBD) registry (1998-2016), to evaluate the nutritional status at the time of diagnosis.Nine types of nutritional status by the combination of weight-for-length (2 years)/body mass inde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c342b7630a014c1a8a54e1079826da4
https://pubmed.ncbi.nlm.nih.gov/35173290
https://pubmed.ncbi.nlm.nih.gov/35173290
Autor:
ahmet sinan sarı
Publikováno v:
The Anatolian Journal of Family Medicine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff3ea1a86f3584ad0971d874d08eb69a
https://doi.org/10.5505/anatoljfm.2021.92005
https://doi.org/10.5505/anatoljfm.2021.92005
Publikováno v:
Ağrı - The Journal of The Turkish Society of Algology.
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare syndrome characterized by a lack of sensitivity to pain due to congenital sensory and autonomic neuropathies, anhidrosis, an inability to regulate body temperature, growth retardation,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06384cd60ef55c8b84fc90f33315a93d
https://doi.org/10.14744/agri.2019.91297
https://doi.org/10.14744/agri.2019.91297