Browsing by Author "Fisgin, Tunc"
Now showing items 1-16 of 16
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Cerebral thrombosis associated with heterozygous factor V Leiden mutation and high lipoprotein(a) level in a girl with factor XIII deficiency
Akbalik, Mehtap; Duru, Feride; Fisgin, Tunc; Tasdemir, Haydar Ali; Incesu, Lutfi; Albayrak, Davut; Ozyurek, Emel (Lippincott Williams & Wilkins, 2007)A 5-year-old girl in whom the diagnosis of inherited factor XIII deficiency was established at the age of 1 day presented with cryptic tonsillitis along with drowsiness and an abrupt occurrence of getting left interior ... -
Clinical and laboratory data of primary hemophagocytic lymphohistiocytosis: A retrospective review of the Turkish Histiocyte Study Group
Fisgin, Tunc; Patiroglu, Turkan; Ozdemir, Akif; Celkan, Tiraje; Caliskan, Umran; Ertem, Mehmet; Karapinar, Deniz Yilmaz (Galenos Yayincilik, 2010)Objective: This study analyzes the clinical and laboratory findings of children with primary hemophagocytic lymphohistiocytosis (HLH) followed in various referral centers of Turkey. Materials and Methods: A simple three-page ... -
Comparison of the approaches to non-febrile neutropenia developing in children with acute lymphoblastic leukemia
Paksu, Muhammet Sukru; Paksu, Sule; Akbalik, Mehtap; Ozyurek, Emel; Duru, Feride; Albayrak, Davut; Fisgin, Tunc (Wiley, 2012)The objectives of this study was to investigate of the influences of high-dose (20 mg/kg/day) methyl prednisolone (HDMP) and granulocyte colony stimulating factor (G-CSF) in shortening the duration of chemotherapy-induced ... -
Crimean-Congo hemorrhagic fever: Five patients with hemophagocytic syndrome
Fisgin, Nuriye Tasdelen; Fisgin, Tunc; Tanyel, Esra; Doganci, Levent; Tulek, Necla; Guler, Nil; Duru, Feride (Wiley, 2008)Three pediatric and two adult Turkish patients with Crimean Congo Hemorrhagic Fever (CCHF) induced hemophagocytic syndrome (HPS) were admitted to Ondokuz Mayis University Hospital, which is in the Middle Black Sea Region ... -
Hair selenium status in children with leukemia and lymphoma
Ozgen, Ilker Tolga; Dagdemir, Ayhan; Elli, Murat; Saraymen, Recep; Pinarli, Faruk Guclu; Fisgin, Tunc; Acar, Sabri (Lippincott Williams & Wilkins, 2007)Selenium (Se) is a trace element contributing to the structure of antioxidant system that saves cells from reactive oxygen species. Low serum Se levels have been reported in pediatric and adult patients with cancers. On ... -
Hematological aspects of Crimean-Congo hemorrhagic fever
Duru, Feride; Fisgin, Tunc (Galenos Yayincilik, 2009)Crimean-Congo hemorrhagic fever (CCHF) is an acute tick-borne viral disease transmitted to humans by Hyalomma ticks or by direct contact with the blood of infected humans or domestic animals. In certain areas of the world, ... -
Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Patients in the Black Sea Region of Turkey
Yildiran, Alisan; Celiksoy, Mehmet Halil; Borte, Stephan; Guner, Sukru Nail; Elli, Murat; Fisgin, Tunc; Ogur, Gonul (Galenos Yayincilik, 2017)Hematopoietic stem cell transplantation is a promising curative therapy for many combined primary immunodeficiencies and phagocytic disorders. We retrospectively reviewed pediatric cases of patients diagnosed with primary ... -
Hemophagocytic Bone Marrow Aplasia With Plasma Cells in a RAG2-deficient SCID Case After a Nonconditioned Transplantation From a Fully Matched Sibling
Yildiran, Alisan; Fisgin, Tunc; Guner, Sukru N.; Kilic, Mehtap; Sancak, Recep; Ozyurek, Emel; Duru, Feride (Lippincott Williams & Wilkins, 2013)We report a RAG2-deficient patient with severe combined immunodeficiency and hemophagocytic bone marrow aplasia with plasma cells after a nonconditioned transplantation from a fully matched sibling. After engraftment, ... -
Immune thrombocytopenic purpura-related hemotympanum presenting with hearing loss
Fisgin, Tunc; Atmaca, Sinan; Duru, Feride; Ozyurek, Emel; Cetin, Recep; Albayrak, Davut (Lippincott Williams & Wilkins, 2009)A 5-year-old boy was admitted to our center with a major complaint of bilateral hearing loss for 2 days. He was diagnosed with acute immune thrombocytopenic purpura 3 months before the admission and treated with high-dose ... -
Immunoreconstitution in the First Thre Year After Hsct in A Newly Established Transplantation Unit
Yildiran, Alisan; Borte, Stephan; Elli, Murat; Fisgin, Tunc (Springer/Plenum Publishers, 2014)… -
Keratinocyte growth factor-2 and autologous serum potentiate the regenerative effect of mesenchymal stem cells in cornea damage in rats
Pinarli, Ferda Alpaslan; Okten, Gulsen; Beden, Umit; Fisgin, Tunc; Kefeli, Mehmet; Kara, Narten; Tomak, Leman (Ijo Press, 2014)AIM: To investigate the healing process after severe corneal epithelial damage in rats treated with mesenchymal stem cells (MSCs) cultured with or without keratinocyte growth factor (KGF -2) and autologous serum (AS) on ... -
Low protein Z levels in children with nephrotic syndrome
Ozkaya, Ozan; Bek, Kenan; Fisgin, Tunc; Aliyazicioglu, Yuksel; Sultansuyu, Sevinc; Acikgoz, Yonca; Baysal, Kemal (Springer, 2006)Acquired deficiency of anticoagulant proteins, due to loss in the urine, has been proposed as one of the major thrombogenic alterations in nephrotic syndrome (NS). Protein Z (PZ) is a single-chain vitamin K-dependent ... -
Protein Z and natural anticoagulants in children on peritoneal dialysis and hemodialysis
Bek, Kenan; Ozkaya, Ozan; Fisgin, Tunc; Aliyazicioglu, Yuksel; Paksu, M. Sukru; Ozgen, Tolga; Baysal, Kemal (Springer, 2007)Hemostatic alterations due to abnormalities in the coagulation and fibrinolytic system may occur in dialysis patients. Protein Z (PZ) is a vitamin K-dependent coagulation protein promoting assembly of thrombin with ... -
Rare Coagulation Disorders: A Retrospective Analysis of 156 Patients in Turkey
Fisgin, Tunc; Balkan, Can; Celkan, Tiraje; Kilinc, Yurdanur; Turker, Meral; Timur, Cetin; Kavakli, Kaan (Galenos Yayincilik, 2012)Objective: To retrospectively evaluate the clinical findings, laboratory data, management, and outcome in a group of Turkish children diagnosed with rare coagulation deficiencies (RCDs) between January 1999 and June 2009. ... -
t(6;9)(p23;q34) Presenting Acute Myeloid Leukemia in a Child With an Unsuspected 45,X/46,X,derY [?t(Yp;Yq)] Chromosomal Constitution: Yet Another Y Chromosome Overdosage and Malignancy Association
Ogur, Gonul; Duru, Feride; Ozyurek, Emel; Fisgin, Tunc (Lippincott Williams & Wilkins, 2012)Development of leukemia in patients with sexual chromosome abnormalities is relatively rare and mostly involves cases of monosomy X, Turner syndrome. Here, we report on a child having a 45,X/46,X,derY [?t(Yp;Yq)] chromosomal ...
