Search Results - "Kızılocak, Hande"
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Late Effects of Therapy in Childhood Acute Lymphoblastic Leukemia Survivors
Published in Turkish journal of haematology (07-02-2019)“…Over the last 50 years, the survival rates in children with acute lymphoblastic leukemia (ALL) have increased remarkably. The optimal use of antileukemic…”
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Wernicke's Encephalopathy in a Child with Acute Lymphoblastic Leukemia
Published in Turkish journal of haematology (01-03-2017)Get full text
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3
Febrile Neutropenia in Children with Cancer: Approach to Diagnosis and Treatment
Published in Current pediatric reviews (01-01-2018)“…Febrile neutropenia is one of the major acute side effects of intensive treatment in pediatric cancer, necessitating prompt initiation of empirical…”
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Management of perioperative hemostasis in a severe hemophilia A patient with inhibitors on emicizumab using global hemostasis assays
Published in Therapeutic advances in hematology (01-06-2019)“…Background: Patients with severe hemophilia A and inhibitors are at risk of bleeding during invasive procedures. The standard of care for preventing…”
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5
Late Effects of Therapy in Childhood Acute Lymphoblastic Leukemia Survivors
Published in Turkish journal of haematology (06-11-2018)Get full text
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Osteosarcoma After Hematopoietic Stem Cell Transplantation in Children and Adolescents: Case Report and Review of the Literature
Published in Pediatric blood & cancer (01-09-2016)“…Osteosarcoma as a secondary malignancy after hematopoietic stem cell transplantation (HSCT) is very rare. We present a case and review of 18 other cases…”
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Successful outcome of mucormycosis in a child with acute lymphoblastic leukemia
Published in Turk Pediatri Arsivi (19-06-2020)“…Invasive fungal infections may cause morbidity and mortality in pediatric patients with hematologic and oncologic malignancies treated with intensive…”
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Treatment of plasminogen deficiency patients with fresh frozen plasma
Published in Pediatric blood & cancer (01-02-2018)“…Congenital plasminogen (Plg) deficiency leads to the development of ligneous membranes on mucosal surfaces. Here, we report our experience with local and…”
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Diagnosis and treatment of hemophilia
Published in Clinical advances in hematology & oncology (01-06-2019)“…Hemophilia A and B are inherited bleeding disorders characterized by deficiency or dysfunction of coagulation protein factors VIII and IX, respectively…”
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Emerging drugs for hemophilia A: insights into phase II and III clinical trials
Published in Expert opinion on emerging drugs (02-10-2021)“…Hemophilia is a lifelong, genetic-bleeding disorder, which inadequately treated results in permanent joint damage. It is characterized by spontaneous and…”
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Discrepancy between the Results of One-Stage and Chromogenic Factor VIII Assays: Switch in Diagnosis from Mild to Moderate Hemophilia a in Three Cases
Published in Blood (15-11-2022)Get full text
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12
Neutralizing antidrug antibody to emicizumab in a patient with severe hemophilia A with inhibitors: New case with detailed laboratory evaluation
Published in Journal of thrombosis and haemostasis (01-09-2020)“…Hemophilia A is an inherited bleeding disorder characterized by deficiency of the coagulation protein factor VIII. Development of clotting factor concentrates…”
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Neutralizing antidrug antibody to emicizumab in patients with severe hemophilia A: Case report of a first noninhibitor patient and review of the literature
Published in Research and practice in thrombosis and haemostasis (01-08-2023)“…Hemophilia A (HA) is a genetic bleeding disorder characterized by the deficiency of the coagulation protein factor (F) VIII (FVIII). The development of…”
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Safety of FEIBA and emicizumab (SAFE): Dose escalation study evaluating the safety of in vivo administration of activated prothrombin complex concentrate in haemophilia A patients on emicizumab
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-01-2023)“…Introduction Emicizumab is a humanized bispecific monoclonal antibody licensed for patients with severe haemophilia A. Breakthrough bleeding still occurs in…”
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PP-291. Comparison of histopathological placental findings in preterm and term births
Published in Early human development (01-11-2010)Get full text
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Determining the approximate factor VIII level of patients with severe haemophilia A on emicizumab using in vivo global haemostasis assays
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-09-2021)“…Introduction Emicizumab is a recombinant, humanized bispecific monoclonal antibody that mimics the function of factor VIII (FVIII) which results in a…”
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Factor VIII Level Comparison in Patients with Severe Hemophilia a on Emicizumab with Inhibitors with One Stage, Bovine and Human Chromogenic Assays and the Factor VIII Equivalency of Emicizumab Using In Vivo Global Hemostasis Assays
Published in Blood (23-11-2021)“…Introduction Emicizumab is a recombinant, humanized bispecific monoclonal antibody that mimics the function of factor VIII (FVIII) which results in a…”
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Factor VIII Level Comparison in Patients with Severe Hemophilia a on Emicizumab with Inhibitors with One Stage, Bovine and Human Chromogenic Assays and the Factor VIII Equivalency of Emicizumab Using In Vivo G lobal Hemostasis Assays
Published in Blood (05-11-2021)“…Abstract Introduction Emicizumab is a recombinant, humanized bispecific monoclonal antibody that mimics the function of factor VIII (FVIII) which results in a…”
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Comparison of bypassing agents in patients on emicizumab using global hemostasis assays
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-01-2021)“…Introduction Emicizumab is a humanized bispecific monoclonal antibody licensed for patients with severe haemophilia A with and without inhibitors. Management…”
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20
Five-year-old girl with tongue bleeding
Published in Turk Pediatri Arsivi (01-06-2016)Get full text
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