Publications by authors named "Umran Caliskan"

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Innovative design and comprehensive characterization of a valine-enhanced lipid nanoparticle-coated mRNA vaccine targeting the SARS-CoV-2 S-RBD antigen.
Tugce Duran, Naci Cine, Mehmet Ali Karaselek, Nadir Gul, Serkan Kuccukturk

Sci Rep· September 2025

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Acute promyelocytic leukemia presenting as isolated femoral granulocytic sarcoma.
Ayşe Şimşek, Hüseyin Tokgöz, Ümran Çalışkan

Turk J Pediatr· February 2025

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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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Central Nervous System Fungal Infections in Children With Leukemia and Undergoing Hematopoietic Stem Cell Transplantation: A Retrospective Multicenter Study.
Serap Karaman, Rejin Kebudi, Hande Kizilocak, Zeynep Karakas, Bengu Demirag, Umran Caliskan

J Pediatr Hematol Oncol· November 2022

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Pulmonary Embolism in Childhood: A Multicenter Experience from Turkey.
Melih Hangül, Mehmet Köse, Sevgi Pekcan, Ümran Çalışkan, Hüseyin Tokgöz

Balkan Med J· September 2022

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Impact of the HEAD-US Scoring System for Observing the Protective Effect of Prophylaxis in Hemophilia Patients: A Prospective, Multicenter, Observational Study.
Kaan Kavaklı, Süha Süreyya Özbek, Ali Bülent Antmen, Fahri Şahin, Şevkiye Selin Aytaç

Turk J Haematol· June 2021

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Traumatic hyphema in a patient with severe hemophilia A: Clinical features and management.
Selman Belviranli, Ahmet Ozkagnici, Huseyin Tokgoz, Gulfidan Bitirgen, Umran Caliskan

Eur J Ophthalmol· March 2021

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Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.
Deniz Yılmaz Karapınar, Türkan Patıroğlu, Ayşe Metin, Ümran Çalışkan, Tiraje Celkan

Pediatr Blood Cancer· October 2019

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Deferasirox in children with transfusion-dependent thalassemia or sickle cell anemia: A large cohort real-life experience from Turkey (REACH-THEM).
Bulent Antmen, Zeynep Karakaş, Mehmet Akif Yeşilipek, Osman Alphan Küpesiz, İlgen Şaşmaz

Eur J Haematol· February 2019

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Glanzmann Thrombasthenia in a Newborn with Heterozygous Factor V Leiden and Heterozygous MTHFR C677T Gene Mutations.
Nazli Dilay Gultekin, Fatma Hilal Yilmaz, Huseyin Tokgoz, Nuriye Tarakci, Umran Caliskan

Indian Pediatr· February 2019

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Coexistence of Kasabach-Merritt Syndrome and placental chorioangioma in a premature infant.
N Dilay Gültekin, F Hilal Yilmaz, H Altunhan, S Findik, H Tokgöz

J Neonatal Perinatal Med· December 2018

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Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of Sixty-five Patients.
Özlem Tüfekçi, Ülker Koçak, Zühre Kaya, İdil Yenicesu, Canan Albayrak

Turk J Haematol· March 2018

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A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention.
Yeşim Aydınok, Yeşim Oymak, Berna Atabay, Gönül Aydoğan, Akif Yeşilipek

Turk J Haematol· March 2018

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Three Novel Calreticulin Mutations in Two Turkish Patients.
Veysel Sabri Hançer, Hüseyin Tokgöz, Serkan Güvenç, Ümran Çalışkan, Murat Büyükdoğan

Turk J Haematol· December 2017

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Infectious diseases, autoimmunity and midline defect in a patient with a novel bi-allelic mutation in IL12RB1 gene.
Bahar Göktürk, İsmail Reisli, Ümran Çalışkan, Carmen Oleaga-Quintas, Caroline Deswarte

Turk J Pediatr· June 2017

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Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome Patients.
Samuel C C Chiang, Stephanie M Wood, Bianca Tesi, Himmet Haluk Akar, Waleed Al-Herz, Umran Caliskan

Front Immunol· April 2017

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Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency.
Buket Dönmez-Demir, Tiraje Celkan, Nazan Sarper, Gülhis Deda, Elif İnce

Blood Coagul Fibrinolysis· September 2016

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Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann's thrombasthenia.
Huseyin Tokgoz, Didem Torun Ozkan, Umran Caliskan, Nejat Akar

Platelets· June 2016

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Essential thrombocythemia with Mpl W515 K mutation in a child presenting with Budd-Chiari syndrome.
Huseyin Tokgoz, Umran Caliskan, Hasan Ali Yüksekkaya, Reyhan Kucukkaya

Platelets· June 2016

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Isotypic analysis of antibodies against activated Factor VII in patients with Factor VII deficiency using the x-MAP technology.
Caroline Pfeiffer, Eve Mathieu-Dupas, Pauline Logghe, Géraldine Lissalde-Lavigne, Julien Balicchi, Umran Caliskan

Thromb Res· May 2016

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Ophthalmic manifestations in recently diagnosed childhood leukemia.
Gulfidan Bitirgen, Selman Belviranli, Umran Caliskan, Huseyin Tokgoz, Ahmet Ozkagnici

Eur J Ophthalmol· April 2016

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Effects of Prednisolone, L-Asparaginase, Gemfibrozil, and Combinations of These Elements on Mice Lipid Profile, Liver, and Pancreas.
Dogan Kose, Nuriye Tarakci, Zeliha Esin Celik, Husamettin Vatansev, Emine Ayca Cimbek, Umran Caliskan

J Pediatr Hematol Oncol· January 2016

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Pilomatrixoma in childhood.
Dogan Kose, Ilhan Ciftci, Ismail Harmankaya, Serdar Ugras, Umran Caliskan

J Cancer Res Ther· June 2015

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