Search Results - "박영실"
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Management of Spontaneous Spinal Epidural Hematoma Developedin Children with Hemophilia
Published in Clinical pediatric hematology-oncology (01-10-2018)“…Spinal epidural hematoma (SEH) is a rare neurosurgical emergency in which pressure on the spinal cord leads to acute neurological deficits, and is a rare…”
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2
Two Cases of Infant Hemophilia A Patients with Inhibitors
Published in Clinical pediatric hematology-oncology (01-10-2015)“…Development of inhibitors is currently one of the most serious complications of hemophilia treatment. Typically, the propensity to develop an inhibitor is…”
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3
Efforts by the Republic of China Government to Convert Chinese Communist Prisoners of War during the Korean War
Published in Korea journal (01-06-2020)“…The Korean War broke out on June 25, 1950. The armistice talks, which began a year into the Korean War, lasted two years due to the issue of prisoners of war…”
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4
A Rare Case of Acquired Hemophilia A in Adolescents and Young Adults
Published in Clinical pediatric hematology-oncology (01-04-2022)“…Acquired hemophilia A (AHA) is a rare bleeding disorder, especially in adolescents and young adults (AYAs) attributable to the development of autoantibodies…”
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Septic Arthritis and Infective Endocarditis in an Adolescent Hemophilia B Patient with an Inhibitor and a Central Venous Access Device
Published in Clinical pediatric hematology-oncology (30-04-2018)“…Central venous access devices (CVAD) provide hemophilic patients, particularly children, with prolonged reliable venous access to promote routine factor…”
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6
Recombinant von Willebrand Factor for Pediatric Patient with von Willebrand Disease: First Report in Korea
Published in Clinical pediatric hematology-oncology (01-04-2021)“…von Willebrand disease (VWD) is the most common hereditary bleeding disorder. The treatment of VWD consists mainly of desmopressin and plasma-derived von…”
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7
The efficacy of bypassing agents in surgery of hemophilia patients with inhibitors
Published in Blood research (01-09-2015)“…Inhibitory antibodies to factor VIII (FVIII) or IX (FIX) are important issues when managing patients with hemophilia A or B. Advances in bypassing agents such…”
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8
단일기관에서 시행한 폰빌레브란트병 환자의 수술 경험
Published in Clinical pediatric hematology-oncology (01-04-2017)“…Background: Von Willebrand disease (VWD) is the most common inherited bleeding disorder. Surgery, even relatively minor procedures, in patients with moderate…”
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9
Various Complications after a Vascular Procedure in Patients with Hemophilia
Published in Clinical pediatric hematology-oncology (01-04-2019)“…Hemophilia, an inherited bleeding disorder, is caused by a deficiency of coagulation factor VIII or IX. Most of patients with hemophilia need vascular…”
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10
Nodular Fasciitis of External Auditory Canal
Published in Journal of pathology and translational medicine (01-09-2016)“…Nodular fasciitis is a pseudosarcomatous reactive process composed of fibroblasts and myofibroblasts, and it is most common in the upper extremities. Nodular…”
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11
Sequential therapy with activated prothrombin complex concentrates and recombinant activated factor VII to treat unresponsive bleeding in patients with hemophilia and inhibitors: a single center experience
Published in Blood research (01-12-2013)“…Currently, the greatest challenge in hemophilia treatment is managing hemophilia patients with inhibitors. The two main bypassing agents that are used to treat…”
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12
Subgroup analysis of a phase 2/3 study of rurioctocog alfa pegol in patients with severe hemophilia A: efficacy and safety in previously treated Korean patients
Published in Blood research (01-09-2019)“…The efficacy and safety of extended half-life, full-length, pegylated recombinant factor VIII rurioctocog alfa pegol [BAX 855, ADYNOVATE (USA)/ADYNOVI…”
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13
Allogeneic hematopoietic stem cell transplantation in congenital hemoglobinopathies with myeloablative conditioning and rabbit anti-thymocyte globulin
Published in Blood research (01-06-2018)“…Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative therapy for β-thalassemia major (TM) and sickle cell disease (SCD) in children…”
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14
혈우병 약물치료의 최신 지견
Published in Taehan Ŭisa Hyŏphoe chi (01-12-2009)“…Hemophilia A (factor VIII deficiency) and Hemophilia B (factor IX deficiency) are the most common and serious congenital coagulation disorders. Accurate…”
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15
The Use of Rituximab with Immune Tolerance Induction Therapy for Hemophilia A with Inhibitors
Published in Clinical pediatric hematology-oncology (30-04-2015)“…Inhibitor development is one of the major adverse events associated with increased morbidity and mortality in patients with congenital hemophilia. Recent…”
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16
Immune tolerance induction in patients with severe hemophilia A with inhibitors
Published in Blood research (01-12-2015)“…Inhibitory antibodies to factor VIII (FVIII) are an important complication when managing patients with hemophilia A. Immune tolerance induction (ITI) has been…”
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17
Recent trends in the incidence of multiple births and its consequences on perinatal problems in Korea
Published in Journal of Korean medical science (01-08-2010)“…The aim of this study was to survey multiple birth data and to analyze the recent trends of multiple births and its consequences on perinatal problems in Korea…”
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18
다기관에서의 국내 폰빌레브란트병 실태에 대한 조사
Published in Clinical pediatric hematology-oncology (01-10-2017)“…Background: von Willebrand disease (VWD) is the most common inherited bleeding disorder with a prevalence of up to 1%. However in Korea, only 126 VWD patients…”
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19
Multiple births conceived by assisted reproductive technology in Korea
Published in Korean journal of pediatrics (01-10-2010)“…The recent trends of multiple births (MBs) conceived by assisted reproductive technology (ART) in Korea were analyzed as well as the relationship with maternal…”
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20
중증 혈우병 항체 환자에서 시행한 말초삽입 중심혈관 카테터의 유용성
Published in Korean journal of pediatrics (2008)“…The most effective treatment strategy for patients with hemophilia is replacement therapy with FVIII or FIX concentrates, which usually requires long-term,…”
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