Publications by authors named "Gulseren Sahin"

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Chronic Hepatitis B In Children: Case Series From A Tertiary Paediatric Hospital.
Fazilcan Zirek, Ferda Ozbay Hosnut, Gulseren Sahin, Saliha Senel

Klin Padiatr· July 2025

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Non-syndromic Congenital Sodium Diarrhea: A Novel Mutation in the SLC9A3 Gene.
Ferda Ozbay Hosnut, Gulseren Sahin, Bulent Uyanik, Serdar Ceylaner, Meltem Akcaboy

Klin Padiatr· January 2025

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Cholecystectomy in children: indications, clinical, laboratory and histopathological findings and cost analysis.
Aysel Ünlüsoy Aksu, Nebiyye Genel, Gülseren Şahin, Ferda Özbay Hoşnut, Ayşegül Tok

Turk J Pediatr· October 2024

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Author Correction: GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway.
Ann Y Park, Michael Leney-Greene, Matthew Lynberg, Justin Q Gabrielski, Xijin Xu

Nat Immunol· April 2024

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GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway.
Ann Y Park, Michael Leney-Greene, Matthew Lynberg, Justin Q Gabrielski, Xijin Xu

Nat Immunol· February 2024

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Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption.
Ferda Ö Hoşnut, Andreas R Janecke, Gülseren Şahin, Georg F Vogel, Naz G Lafcı

Genes (Basel)· June 2023

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Congenital Rare Diseases Causing Persistent Diarrhea in the Newborn: A Single Center Experience.
Ferda Özbay Hoşnut, Gulseren Evirgen Sahin, Ahmet Ozyazıcı, Asburce Olgac, Aysel Unlusoy Aksu

Z Geburtshilfe Neonatol· October 2022

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Sirolimus treatment of a PTEN hamartoma tumor syndrome presenting with melena.
Gülseren Evirgen Şahin, Ferda Özbay Hoşnut, Şule Yeşil, Naz Güleray Lafcı, Aylin Ege Gül

Turk J Pediatr· September 2022

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Coats Plus syndrome: a diagnostic and therapeutic challenge in pediatric gastrointestinal hemorrhage.
Ferda Özbay Hoşnut, Gülseren Şahin, Meltem Akçaboy

Turk J Pediatr· May 2022

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OCT Evaluation of Retinal Parameters in Pediatric Gastritis Patients with Helicobacter Pylori.
Mehmet Fatih Kocamaz, Gulseren Sahin, Ferda Ozbay Hosnut, Nesibe Gokce Kocamaz, Pinar Altiaylik Ozer

Beyoglu Eye J· December 2021

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Hypergonadotrophic hypogonadism in a patient with transaldolase deficiency: novel mutation in the pentose phosphate pathway.
Naz Guleray Lafcı, Fatma Kurt Colak, Gulseren Sahin, Merve Sakar, Semra Çetinkaya

Hormones (Athens)· September 2021

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Homozygous missense VPS16 variant is associated with a novel disease, resembling mucopolysaccharidosis-plus syndrome in two siblings.
Yılmaz Yıldız, Can Koşukcu, Damla Aygün, Meltem Akçaboy, Fatma Zehra Öztek Çelebi

Clin Genet· September 2021

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When Pancreatitis Stinks: A Rare Cause of Acute Recurrent Pancreatitis in a Child.
Yilmaz Yildiz, Gülseren Şahin, Ferda Özbay Hoşnut

Pancreas· January 2020

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Assessment of Corneal and Lens Density in Children With Celiac Disease.
Serdar Ozates, Sibel Doguizi, Ferda Ozbay Hosnut, Gulseren Sahin, Mehmet Ali Sekeroglu

J Pediatr Ophthalmol Strabismus· November 2019

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Assessment of corneal and lens clarity in children with Wilson disease.
Sibel Doğuizi, Serdar Özateş, Ferda Özbay Hoşnut, Gülseren Evirgen Şahin, Mehmet Ali Şekeroğlu

J AAPOS· June 2019

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The Frequency of Lysosomal Acid Lipase Deficiency in Children With Unexplained Liver Disease.
Zarife Kuloglu, Aydan Kansu, Suna Selbuz, Ayhan G Kalaycı, Gülseren Şahin

J Pediatr Gastroenterol Nutr· March 2019

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Recurrent hepatic failure and status epilepticus: an uncommon presentation of hyperargininemia.
Husniye Yucel, Çiğdem Seher Kasapkara, Meltem Akcaboy, Erhan Aksoy, Gülseren Evirgen Sahin

Metab Brain Dis· October 2018

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Antral gastritis caused by Helicobacter pylori infection in the pediatric age group is associated with increased mesenteric lymph node dimension observed by ultrasonography.
Emin Cakmakci, Gulseren Evirgen Sahin, Ferda Ozbay Hosnut, Hasibe Gokce Cinar, Berna Ucan

Quant Imaging Med Surg· December 2015

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Inflammatory myofibroblastic tumor of the colon with an unusual presentation of intestinal intussusception.
Yeliz Çağan Appak, Gülseren Evirgen Sahin, Semin Ayhan, Can Taneli, Erhun Kasırga

European J Pediatr Surg Rep· June 2014

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Diagnostic yield of upper gastrointestinal endoscopy in the evaluation of iron deficiency anemia in older children and adolescents.
Huseyin Gulen, Erhun Kasirga, Sule Aslan Yildirim, Sebnem Kader, Gulseren Sahin

Pediatr Hematol Oncol· November 2011

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A Case of Henoch-Schönlein Purpura with P369S Mutation in MEFV Gene.
Pelin Ertan, Gökhan Tekin, Gülseren Evirgen Sahin, Erhun Kasırga, Fatma Taneli

Iran J Pediatr· June 2011

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[Jeune syndrome (asphyxiating thoracic dystrophy): a case report].
Sit Uçar, Pelin Zorlu, Gülseren Sahin, Miraç Yildirim, Esma Uşak

Tuberk Toraks· March 2010

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