Search Results - "Özdemir, Gül Nihal"

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    Gaucher Disease for Hematologists by Özdemir, Gül Nihal, Gündüz, Eren

    Published in Turkish journal of haematology (01-06-2022)
    “…Gaucher disease (GD) is a rare hereditary lysosomal storage disease that arises due to deficiency of glucocerebrosidase. Early diagnosis is very important for…”
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    Journal Article
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    Gaucher Disease for Hematologists by Özdemir, Gül Nihal, Gündüz, Eren

    Published in Turkish journal of haematology (2022)
    “…Gaucher disease (GD) is a rare hereditary lysosomal storage disease that arises due to deficiency of glucocerebrosidase. Early diagnosis is very important for…”
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    Journal Article
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    Safety and efficacy of deferasirox in patients with transfusion-dependent thalassemia: A 4-year single-center experience by Zengin Ersoy, Gizem, Ayçiçek, Ali, Odaman Al, Işık, Bayram, Cengiz, Arslantaş, Esra, Özdemir, Gül Nihal, Uysalol, Ezgi Paslı, Şalcıoğlu, Zafer, Akıcı, Ferhan, Aydoğan, Gönül

    Published in Pediatric hematology and oncology (07-09-2021)
    “…This study was organized to determine the efficacy and safety of deferasirox (DFX) in reducing the SF of patients with transfusion-dependent thalassemia (TDT)…”
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    Journal Article
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    Comparison of the efficacy of parenteral and oral treatment for nutritional vitamin B12 deficiency in children by Sezer, Rabia Gönül, Akoğlu, Handan Ayhan, Bozaykut, Abdulkadir, Özdemir, Gül Nihal

    Published in Hematology (Luxembourg) (21-10-2018)
    “…Although, oral replacement for vitamin B12 deficiency has been proved to be effective in adults, it is mainly treated with parenteral therapy. There are only…”
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    Journal Article
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    Clinical characteristics and treatment outcomes of pediatric Hodgkin lymphoma at a single center in Türkiye by Arslantaş,Esra, Ayçiçek,Ali, Bayram,Cengiz, Tekgunduz,Sibel Akpinar, Okur Acar,Sultan, Kadehci,Züleyha, Tuğcu,Deniz, Özdemir,Gül Nihal

    Published in Zeynep Kamil Medical Journal (01-03-2024)
    “…Objective: To review the 10-year experience of pediatric Hodgkin lymphoma at a single center in Türkiye. Material and Methods: This study is a retrospective…”
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    Journal Article
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    Burkitt Leukemia With Precursor B-Cell Immunophenotype and Dual Translocation of t(14;18) and t(8;14) in a Child: Case Report and Review of the Literature by Odaman Al, Işik, Bayram, Cengiz, Koç, Başak, Ersoy, Gizem, Pasli Uysalol, Ezgi, Aki, Hilal, Özdemir, Gül Nihal

    Published in Journal of pediatric hematology/oncology (01-01-2020)
    “…Burkitt leukemia (BL) with the precursor B-cell immunophenotype is a rarely reported condition. The prognosis of such patients is similar to that of classic…”
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    Journal Article
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    Glucose 6 phosphate dehydrogenase deficiency: A single-center experience by Kılıç, Mehmet Akif, Özdemir, Gül Nihal, Tahtakesen, Tuba Nur, Uysalol, Ezgi Paslı, Bayram, Cengiz, Ayçiçek, Ali, Aydoğan, Gönül

    Published in Turkish archives of pediatrics (01-05-2021)
    “…This study aims to evaluate the demographic information, clinical and laboratory findings of patients with glucose 6 phosphate dehydrogenase deficiency. We…”
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    Journal Article
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    Variant Guillain-Barré syndrome in a patient with Hodgkin lymphoma: AMSAN by Al, Işık Odaman, Koç, Başak, Bayram, Cengiz, Paslı, Ezgi Uysalol, Yıldız, Edibe Pembegül, Ayçiçek, Ali, Çalışkan, Mine, Özdemir, Gül Nihal

    Published in Turk Pediatri Arsivi (01-12-2018)
    “…Lymphomas are solid tumors characterized by the malignant proliferation of lymphoid cells. Neurologic signs encountered in patients with Hodgkin's lymphoma can…”
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    Journal Article
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    Rhabdomyosarcoma of the Tongue: Report of a Case and Review of the Literature by Kebudi, Rejin, Özdemir, Gül Nihal

    Published in Pediatric hematology and oncology (01-02-2011)
    “…Rhabdomyosarcomas are the most common soft tissue tumors in children. Head and neck is one of the most frequently affected site. Within the nonparameningeal,…”
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