Hasil Pencarian - Mualla Çetin

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  1. 1
    Vacuolization in Myeloid and Erythroid Precursors in a Child with Menkes Disease

    Vacuolization in Myeloid and Erythroid Precursors in a Child with Menkes Disease oleh Seçil Sayın, Şule Ünal, Mualla Çetin, Fatma Gümrük

    Diterbitkan 2019-08-01
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  2. 2
    The Relationship Between Hematological Findings and Coronary Artery Aneurysm in Kawasaki Disease

    The Relationship Between Hematological Findings and Coronary Artery Aneurysm in Kawasaki Disease oleh Burçin Beken, Şule Ünal, Mualla Çetin, Fatma Gümrük

    Diterbitkan 2014-05-01
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  3. 3
    Immune Thrombocytopenic Purpura During Maintenance Phase of Acute Lymphoblastic Leukemia: A Rare Coexistence Requiring a High Degree of Suspicion, a Case Report and Review of the Literature

    Immune Thrombocytopenic Purpura During Maintenance Phase of Acute Lymphoblastic Leukemia: A Rare Coexistence Requiring a High Degree of Suspicion, a Case Report and Review of the... oleh Turan Bayhan, Şule Ünal, Fatma Gümrük, Mualla Çetin

    Diterbitkan 2015-11-01
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  4. 4
    Reliability and Validity of the Turkish Version of the PedsQL 3.0 Cancer Module for 2- to 7-Year-Old and the PedsQL 4.0 Generic Core Scales for 5- to 7-Year-Old: The Hacettepe University Experience

    Reliability and Validity of the Turkish Version of the PedsQL 3.0 Cancer Module for 2- to 7-Year-Old and the PedsQL 4.0 Generic Core Scales for 5- to 7-Year-Old: The Hacettepe Uni... oleh Vesile Yıldız Kabak, Yavuz Yakut, Mualla Çetin, Tülin Düger

    Diterbitkan 2016-08-01
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  5. 5
    Serum Erythropoietin Levels in Pediatric Hematologic Disorders and Impact of Recombinant Human Erythropoietin Use

    Serum Erythropoietin Levels in Pediatric Hematologic Disorders and Impact of Recombinant Human Erythropoietin Use oleh Mualla Çetin, Şule Ünal, Fatma Gümrük, Aytemiz Gürgey, Çiğdem Altay

    Diterbitkan 2009-06-01
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  6. 6
    Rare Cytogenetic Anomalies in Two Pediatric Patients with Acute Leukemia

    Rare Cytogenetic Anomalies in Two Pediatric Patients with Acute Leukemia oleh Süreyya Bozkurt, Şule Ünal, Turan Bayhan, Fatma Gümrük, Mualla Çetin

    Diterbitkan 2020-05-01
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  7. 7
    Acute Megakaryoblastic Leukemia with t(1;22) Mimicking Neuroblastoma in an Infant

    Acute Megakaryoblastic Leukemia with t(1;22) Mimicking Neuroblastoma in an Infant oleh Müge Gökçe, Selin Aytaç, Şule Ünal, İlhan Altan, Fatma Gümrük, Mualla Çetin

    Diterbitkan 2015-02-01
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  8. 8
    Long term biweekly 1 mg oral vitamin B12 ensures normal hematological parameters, but does not correct all other markers of vitamin B12 deficiency. A study in patients with inherited vitamin B12 deficiency

    Long term biweekly 1 mg oral vitamin B12 ensures normal hematological parameters, but does not correct all other markers of vitamin B12 deficiency. A study in patients with inherit... oleh Mustafa Vakur Bor, Mualla Çetin, Selin Aytaç, Çigdem Altay, Per Magne Ueland, Ebba Nexo

    Diterbitkan 2008-11-01
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  9. 9
    Transcobalamin II Deficiency in Four Cases with Novel Mutations

    Transcobalamin II Deficiency in Four Cases with Novel Mutations oleh Sule Unal, Tony Rupar, Sevgi Yetgin, Nese Yarali, Ali Dursun, Türkiz Gürsel, Mualla Cetin

    Diterbitkan 2015-11-01
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  10. 10
    The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experience

    The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experience oleh Burcin Beken, Selin Aytac, Gunay Balta, Baris Kuskonmaz, Duygu Uckan, Sule Unal, Mualla Cetin, Fatma Gumruk

    Diterbitkan 2018-02-01
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  11. 11
    The frequency of A91V in the perforin gene and the effect of tumor necrosis factor-α promoter polymorphism on acquired hemophagocytic lymphohistiocytosis

    The frequency of A91V in the perforin gene and the effect of tumor necrosis factor-α promoter polymorphism on acquired hemophagocytic lymphohistiocytosis oleh Hamza Okur, Şule Ünal, Günay Balta, Didem Efendioğlu, Eren Çimen, Mualla Çetin, Aytemiz Gürgey, Çiğdem Altay, Fatma Gümrük

    Diterbitkan 2011-06-01
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  12. 12
    Early detection of pulmonary fungal infection by CT scan in pediatric ALL patients under chemotherapy or in post-transplantation period with primary complaint of chest pain

    Early detection of pulmonary fungal infection by CT scan in pediatric ALL patients under chemotherapy or in post-transplantation period with primary complaint of chest pain oleh Şule Ünal, Barış Kuşkonmaz, Betul Tavil, Selin Aytaç Elmas, Duygu Uçkan Çetinkaya, Mualla Çetin, Mithat Haliloğlu, Fatma Gümrük

    Diterbitkan 2010-03-01
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  13. 13
    The frequency of A91V in the perforin gene and the effect of tumor necrosis factor-α promoter polymorphism on acquired hemophagocytic lymphohistiocytosis

    The frequency of A91V in the perforin gene and the effect of tumor necrosis factor-α promoter polymorphism on acquired hemophagocytic lymphohistiocytosis oleh Hamza Okur, Şule Ünal, Günay Balta, Didem Efendioğlu, Eren Çimen, Mualla Çetin, Aytemiz Gürgey, Çiğdem Altay, Fatma Gümrük

    Diterbitkan 2011-05-01
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  14. 14
    Autoimmune hemolytic anemia and giant cell hepatitis: Report of three infants

    Autoimmune hemolytic anemia and giant cell hepatitis: Report of three infants oleh Şule Ünal, Barış Kuşkonmaz, Necati Balamtekin, Gökhan Baysoy, Selin Aytaç Elmas, Diclehan Orhan, Gülsev Kale, Aysel Yüce, Figen Gürakan, Fatma Gümrük, Mualla Çetin

    Diterbitkan 2010-12-01
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  15. 15
    Autoimmune hemolytic anemia and giant cell hepatitis: Report of three infants

    Autoimmune hemolytic anemia and giant cell hepatitis: Report of three infants oleh Şule Ünal, Barış Kuşkonmaz, Necati Balamtekin, Gökhan Baysoy, Selin Aytaç Elmas, Diclehan Orhan, Gülsev Kale, Aysel Yüce, Figen Gürakan, Fatma Gümrük, Mualla Çetin

    Diterbitkan 2010-12-01
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  16. 16
    Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases

    Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases oleh Elisa Fermo, Cristina Vercellati, Anna Paola Marcello, Anna Zaninoni, Selin Aytac, Mualla Cetin, Ilaria Capolsini, Maddalena Casale, Sabrina Paci, Alberto Zanella, Wilma Barcellini, Paola Bianchi

    Diterbitkan 2019-05-01
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