Publications by authors named "Turkan Patiroglu"

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Clinical spectrum of primary hemophagocytic lymphohistiocytosis: experience of reference centers in Central and Southeast Anatolia.
Şefika Akyol, Ebru Yılmaz, Hüseyin Tokgöz, Kamuran Karaman, Esra Pekpak

Ann Hematol· January 2025

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Retrospective analysis of hemophilia B in Turkey: identifying main characteristics and treatment options.
Bülent Zülfikar, Başak Koç, Fahri Şahin, Hatice İlgen Şaşmaz, Kaan Kavaklı

Res Pract Thromb Haemost· October 2024

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Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.
Veysel Gök, Göksel Leblebisatan, Dilek Gürlek Gökçebay, Salih Güler, Muhammet Ensar Doğan

Br J Haematol· July 2024

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Neurological Complications in Children With Cancer: Experience From a Single Center in Türkiye.
Leyla Kara, Ekrem Unal, Huseyin Per, Sefer Kumandas, Mehmet Canpolat, Turkan Patiroglu

J Clin Pract Res· March 2024

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Correction to: A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature.
Anna-Lisa Lanz, Serife Erdem, Alper Ozcan, Gulay Ceylaner, Murat Cansever, Turkan Patiroglu

J Clin Immunol· January 2024

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A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature.
Anna-Lisa Lanz, Serife Erdem, Alper Ozcan, Gulay Ceylaner, Murat Cansever, Turkan Patiroglu

J Clin Immunol· December 2023

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Neonatal Lymphopenia Screening Is Important for Early Diagnosis of Severe Combined Immunodeficiency.
Aykut Poyraz, Murat Cansever, Ipek Muderris, Turkan Patiroglu

Am J Perinatol· May 2023

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Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment.
Veysel Gök, Şerife Erdem, Yeşim Haliloğlu, Atıl Bişgin, Serkan Belkaya

Genes Immun· February 2023

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Evaluation of primary care physicians' approaches to hemophilia and bleeding disorders: a questionnaire survey.
Bahadir M Samur, Tuğba G Samur, Fatma-Ekin Çiflikli, Alper Özcan, Veysel Gök, Turkan Patiroglu

Blood Coagul Fibrinolysis· October 2022

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Social exclusion and behavior problems in adolescents with cancer and healthy counterparts.
Yağmur Sezer Efe, Harun Özbey, Nuray Caner, Emine Erdem, Emine Gül Kuzucu

J Pediatr Nurs· July 2022

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Serum levels of soluble HLA-G correlate with disease activity in pediatric patients with Crohn's disease.
Murat Cansever, Mehmet Akif Göktaş, Duran Arslan, Türkan Patiroğlu

Saudi J Gastroenterol· May 2022

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A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia.
Serdar Goktas, Zehra B Azizoglu, Daniel Petersheim, Merve Erdogan, Hatice Eke Gungor, Turkan Patiroglu

J Pediatr Hematol Oncol· January 2022

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Therapeutic effects of vitamin D and IL-22 on methotrexate-induced mucositis in mice.
Ebru Yilmaz, Zehra Busra Azizoglu, Kubra Aslan, Serife Erdem, Yesim Haliloglu, Turkan Patiroglu

Anticancer Drugs· January 2022

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Genetic Analysis of a Cohort of 275 Patients with Hyper-IgE Syndromes and/or Chronic Mucocutaneous Candidiasis.
Natalie Frede, Jessica Rojas-Restrepo, Andrés Caballero Garcia de Oteyza, Mary Buchta, Katrin Hübscher, Turkan Patiroglu

J Clin Immunol· November 2021

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Long-Term Follow-Up of Patients with a Diagnosis of Posterior Reversible Encephalopathy Syndrome.
Mehmet Canpolat, Gül Demet Kaya Özçora, Hakan Poyrazoğlu, Huseyin Per, Abdulhakim Çoşkun

Turk Arch Pediatr· November 2021

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Congenital afibrinogenemia in a 4-year-old girl complicated with acute lymphoblastic leukemia.
Alper Özcan, Bahadır Samur, Şefika Akyol, Necdet Arda Erdoğmuş, Türkan Patıroğlu

Turk J Pediatr· August 2021

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Type 1 Plasminogen Deficiency With Pulmonary Involvement: Novel Treatment and Novel Mutation.
Melih Hangul, Ahmet B Tuzuner, Ido Somekh, Christoph Klein, Turkan Patiroglu

J Pediatr Hematol Oncol· May 2021

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Refractory and Fatal Presentation of Severe Autoimmune Hemolytic Anemia in a Child With the DNASE1L3 Mutation Complicated With an Additional DOCK8 Variant.
Aysenur Paç Kisaarslan, Maximilam Witzel, Ekrem Unal, Meino Rohlfs, Başaknur Akyildiz, Turkan Patiroglu

J Pediatr Hematol Oncol· April 2021

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Common Variable Immunodeficiency, Autoimmune Hemolytic Anemia, and Pancytopenia Associated With a Defect in IKAROS.
Ebru Yilmaz, Hye S Kuehn, Eda Odakir, Julie E Niemela, Alper Ozcan, Turkan Patiroglu

J Pediatr Hematol Oncol· April 2021

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A rare cause of vomiting in an adolescent: gastric Burkitt`s lymphoma.
Derya Altay, Alper Özcan, Ekrem Ünal, Kemal Deniz, Keramettin Uğur Özkan

Turk J Pediatr· July 2020

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Role of a second transplantation for children with acute leukemia following posttransplantation relapse: a study by the Turkish Bone Marrow Transplantation Study Group.
Volkan Hazar, Gülsün Tezcan Karasu, Vedat Uygun, Namık Özbek, Musa Karakükçü

Leuk Lymphoma· June 2020

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Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells.
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, Ulrich Pannicke, Marcel Stern

Nat Commun· April 2020

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Vena cava superior syndrome in the children with mediastinal tumors: Single-center experience.
Alper Ozcan, Ekrem Unal, Musa Karakukcu, Abdulhakim Coskun, Mehmet Akif Ozdemir, Turkan Patiroglu

North Clin Istanb· April 2020

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Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells.
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, Ulrich Pannicke, Marcel Stern

Nat Commun· February 2020

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Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease.
Juan C Ravell, Mami Matsuda-Lennikov, Samuel D Chauvin, Juan Zou, Matthew Biancalana, Turkan Patiroglu

J Clin Invest· January 2020

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