Search Results - "Kızılocak, Hande"

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    Late Effects of Therapy in Childhood Acute Lymphoblastic Leukemia Survivors by Kızılocak, Hande, Okcu, Fatih

    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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    Journal Article
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    Febrile Neutropenia in Children with Cancer: Approach to Diagnosis and Treatment by Kebudi, Rejin, Kizilocak, Hande

    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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    Journal Article
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    Management of perioperative hemostasis in a severe hemophilia A patient with inhibitors on emicizumab using global hemostasis assays by Kizilocak, Hande, Yukhtman, Clara Lana, Marquez-Casas, Elizabeth, Lee, Jeanie, Donkin, Jennifer, Young, Guy

    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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    Osteosarcoma After Hematopoietic Stem Cell Transplantation in Children and Adolescents: Case Report and Review of the Literature by Kebudi, Rejin, Ozger, Harzem, Kızılocak, Hande, Bay, Sema Buyukkapu, Bilgiç, Bilge

    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 by kebudi, rejin

    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 by Kızılocak, Hande, Ozdemir, Nihal, Dikme, Gürcan, Koç, Begüm, Atabek, Ayşe Ayzıt, Çokuğraş, Haluk, İskeleli, Güzin, Dönmez‐Demir, Buket, Christiansen, Nina Merete, Ziegler, Maike, Ozdağ, Hilal, Schuster, Volker, Celkan, Tiraje

    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 by Kizilocak, Hande, Young, Guy

    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 by Kizilocak, Hande, Young, Guy

    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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    Neutralizing antidrug antibody to emicizumab in a patient with severe hemophilia A with inhibitors: New case with detailed laboratory evaluation by Harkins Druzgal, Colleen, Kizilocak, Hande, Brown, Joshua, Sennett, Margaret, Young, Guy

    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 by Kizilocak, Hande, Guerrera, Michael F., Young, Guy

    “…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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    Determining the approximate factor VIII level of patients with severe haemophilia A on emicizumab using in vivo global haemostasis assays by Kizilocak, Hande, Marquez‐Casas, Elizabeth, Malvar, Jemily, Carmona, Roxana, Young, Guy

    “…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 by Kizilocak, Hande, Marquez-Casas, Elizabeth, Brown, Joshua, Malvar, Jemily, Young, Guy

    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 by Kizilocak, Hande, Marquez‐Casas, Elizabeth, Phei Wee, Choo, Malvar, Jemily, Carmona, Roxana, Young, Guy

    “…Introduction Emicizumab is a humanized bispecific monoclonal antibody licensed for patients with severe haemophilia A with and without inhibitors. Management…”
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