Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Aysel, Ünlüsoy Aksu"'
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
Autor:
Selim DERECİ, Fatih DURAN, Salim NESELİOGLU, Burcu HIDIMOGLU, Duygu İSKENDER MAZMAN, Aysel ÜNLÜSOY AKSU, Arzu Meltem DEMİR, Özcan EREL, Samil HİZLİ
Publikováno v:
Turkish Journal of Pediatric Disease. :1-6
Objective: Pediatric ulcerative colitis (PUC) is an inflammatory disease. PUC pathogenesis is associated with an imbalance between reactive oxygen species and antioxidant activity which creates oxidative stress. Native thiol (NT) level is antioxidant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df648857a5d4cbbccf7dbfd7ffd53363
https://doi.org/10.12956/tchd.1260388
https://doi.org/10.12956/tchd.1260388
Autor:
Duygu İskender Mazman, Aslınur Özkaya Parlakay, Selim Dereci, Samil Hizli, Gülin Hizal, Arzu Meltem Demir, Fisun Kirca, Aysel Ünlüsoy Aksu, Burcu Berberoğlu Ateş, Bekir Yalcin, Bedia Dinc
Publikováno v:
Turkish Journal of Pediatric Disease. :1-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a6ab01b04af94008b49ae199bb1431e
https://doi.org/10.12956/tchd.889841
https://doi.org/10.12956/tchd.889841
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 3, Pp 991-998 (2019)
Amac: Bu calismada; a kut pankreatit, akut tekrarlayan pankreatit ve kronik pankreatit tanisi ile izlenen cocuklarin klinik, laboratuvar ve etyolojik farkliliklarinin degerlendirilmesi amaclanmistir. Gerec ve Yontem: Ocak 2009 - Eylul 2018 tarihleri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a7310e2d73d1170cdad6b333edc0af5
https://doi.org/10.17826/cumj.511605
https://doi.org/10.17826/cumj.511605
Autor:
Subhash K. Das, Dhanpat Jain, Carol Nelson-Williams, Richard P. Lifton, Gülseren Evirgen Şahin, Aysel Ünlüsoy Aksu, Silvia Vilarinho, Ferda Özbay Hoşnut
Publikováno v:
Hepatology Communications. 3:471-477
Undiagnosed liver disease remains an unmet medical need in pediatric hepatology, including children with high gamma-glutamyltransferase (GGT) cholestasis. Here, we report whole-exome sequencing of germline DNA from 2 unrelated children, both offsprin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76f150f3bb5dc995975f714a869483d4
https://doi.org/10.1002/hep4.1320
https://doi.org/10.1002/hep4.1320
Autor:
Fatma Tuba Eminoğlu, Engin Kose, Aysel Ünlüsoy Aksu, Ceyda Tuna Kırsaçlıoğlu, Neslihan Doğulu, Aydan Kansu, Zarife Kuloğlu
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 34(10)
Objectives Deoxyguanosine kinase (DGUOK) deficiency is one of the leading causes of the mitochondrial DNA-depletion syndromes (MDDS) associated with hepatocerebral involvement. Herein, we present four cases of DGUOK deficiency to emphasize the clinic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::969a74790afee1d66b3e57eba47b5aea
https://pubmed.ncbi.nlm.nih.gov/34167177
https://pubmed.ncbi.nlm.nih.gov/34167177
Autor:
S Ünal, J Koeglmeier, M Meissl, H Ayyıldız Civan, J Melek, T Siahanidou, A M Demir, Patrick Gerner, J H Montoya, Duba H-C., Denise Aldrian, A Koutroumpa, Sahar Mansour, Michael W. Hess, Murat Cakir, Georg F. Vogel, Thomas Müller, J Hornova, T K Frey, Aysel Ünlüsoy Aksu, Y Rachman, Ekkehard Sturm, Andreas R. Janecke, G Düker, M Miqdady, Lukas A. Huber, R Lima, Frank M. Ruemmele, Carsten Posovszky, J Hertecant, Holm H. Uhlig, E Ramos Boluda, Stefan Wirth, Raffi Lev-Tzion, C Deppisch, R Lanzersdorfer, Merit M. Tabbers, Simone Kathemann, Yaron Avitzur
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 481, p 481 (2021)
Journal of clinical medicine, 10(3):481, 1-15. Multidisciplinary Digital Publishing Institute (MDPI)
Journal of Clinical Medicine
Volume 10
Issue 3
Journal of clinical medicine, 10(3):481, 1-15. Multidisciplinary Digital Publishing Institute (MDPI)
Journal of Clinical Medicine
Volume 10
Issue 3
Myosin Vb (MYO5B) is a motor protein that facilitates protein trafficking and recycling in polarized cells by RAB11- and RAB8-dependent mechanisms. Biallelic MYO5B mutations are identified in the majority of patients with microvillus inclusion diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a378cf582516dca7504ff713f219f8f
https://www.mdpi.com/2077-0383/10/3/481
https://www.mdpi.com/2077-0383/10/3/481
Autor:
Dhanpat Jain, Gülseren Evirgen Şahin, Kaela Drzewiecki, Joseph Brancale, Elif Karakoc-Aydiner, Buket Dalgic, Helen C. Su, Richard P. Lifton, Kadakkal Radhakrishnan, David E. Kleiner, Aysel Ünlüsoy Aksu, Jungmin Choi, Sinan Sari, Silvia Vilarinho, Junhui Zhang, Ahmet Ozen, Michael A. Leney-Greene, Safa Baris, Kasper Hoebe, Michael J. Lenardo, Michael Schmalz, João Pereira
Publikováno v:
The Journal of Experimental Medicine
Genomic analysis of families with unexplained portal hypertension reveals GIMAP5 as a critical regulator of liver sinusoidal endothelial cells and hepatic vascular homeostasis. This study identifies a novel genetic cause of portal hypertension and pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c100dc488efddb47698bd3eb60b26cfa
https://pubmed.ncbi.nlm.nih.gov/33956074
https://pubmed.ncbi.nlm.nih.gov/33956074
Autor:
Arzu Meltem Demir, Burcu Bereberoğlu Ateş, Gülin Hizal, Aysel Ünlüsoy Aksu, Fatih Duran, Selim Dereci, Samil Hizli
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 73:e107
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd42f027500de53a5b4fa80f4aceedf4
https://doi.org/10.1097/mpg.0000000000003224
https://doi.org/10.1097/mpg.0000000000003224