A Novel Marker for Screening Paroxysmal Nocturnal Hemoglobinuria Using Routine Complete Blood Count and Cell Population Data
'
A Novel Marker for Screening Paroxysmal Nocturnal Hemoglobinuria Using Routine Complete Blood Count and Cell Population Data' 의 주제별 논문영향력
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| 동일주제 총논문수 | 논문피인용 총횟수 | 주제별 논문영향력의 평균 |
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주제별 논문영향력
' A Novel Marker for Screening Paroxysmal Nocturnal Hemoglobinuria Using Routine Complete Blood Count and Cell Population Data' 의 참고문헌
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The “sugar-water” test for paroxysmal nocturnal hemoglobinuria
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The “sugar-water” test for paroxysmal nocturnal hemoglobinuria
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The molecular basis of paroxysmal nocturnal hemoglobinuria
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The molecular basis of paroxysmal nocturnal hemoglobinuria
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The complement-inhibitory activity of CD59 resides in its capacity to block incorporation of C9 into membrane C5b-9
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The complement-inhibitory activity of CD59 resides in its capacity to block incorporation of C9 into membrane C5b-9
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The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria
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The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria
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Studies on destruction of red blood cells. II. Chronic hemolytic anemia with paroxysmal nocturnal hemoglobinuria: Certain immunological aspects of the hemolytic mechanism with special reference to serum complement
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Studies on destruction of red blood cells. II. Chronic hemolytic anemia with paroxysmal nocturnal hemoglobinuria: Certain immunological aspects of the hemolytic mechanism with special reference to serum complement
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Prognostic value of paroxysmal nocturnal haemoglobinuria clone presence in aplastic anemia patients treated with combined immunosuppression: results of two-centre prospective study
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Prognostic value of paroxysmal nocturnal haemoglobinuria clone presence in aplastic anemia patients treated with combined immunosuppression: results of two-centre prospective study
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Predicting response to immunosuppressive therapy and survival in severe aplastic anaemia
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Predicting response to immunosuppressive therapy and survival in severe aplastic anaemia
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Paroxysmal nocturnal hemoglobinuria: an historical overview
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Paroxysmal nocturnal hemoglobinuria: a single Spanish center’s experience over the last 40 yr
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Paroxysmal nocturnal hemoglobinuria: a single Spanish center’s experience over the last 40 yr
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Paroxysmal nocturnal hemoglobinuria clones in children with acquired aplastic anaemia: a prospective single centre study
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Paroxysmal nocturnal hemoglobinuria clones in children with acquired aplastic anaemia: a prospective single centre study
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Paroxysmal nocturnal hemoglobinuria (PNH): higher sensitivity and validity in diagnosis and serial monitoring by flow cytometric analysis of reticulocytes
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Paroxysmal nocturnal hemoglobinuria (PNH): higher sensitivity and validity in diagnosis and serial monitoring by flow cytometric analysis of reticulocytes
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PIG-A mutations in paroxysmal nocturnal hemoglobinuria and in normal hematopoiesis
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PIG-A mutations in paroxysmal nocturnal hemoglobinuria and in normal hematopoiesis
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Origin and fate of blood cells deficient in glycosylphosphatidylinositol-anchored protein among patients with bone marrow failure
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Origin and fate of blood cells deficient in glycosylphosphatidylinositol-anchored protein among patients with bone marrow failure
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Multicenter phase 3 study of the complement inhibitor eculizumab for the treatment of patients with paroxysmal nocturnal hemoglobinuria
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Multicenter phase 3 study of the complement inhibitor eculizumab for the treatment of patients with paroxysmal nocturnal hemoglobinuria
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Minor population of CD55-CD59- blood cells predicts response to immunosuppressive therapy and prognosis in patients with aplastic anemia
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Minor population of CD55-CD59- blood cells predicts response to immunosuppressive therapy and prognosis in patients with aplastic anemia
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Long-term treatment with eculizumab in paroxysmal nocturnal hemoglobinuria: sustained efficacy and improved survival
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Long-term treatment with eculizumab in paroxysmal nocturnal hemoglobinuria: sustained efficacy and improved survival
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How I treat paroxysmal nocturnal hemoglobinuria
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How I treat paroxysmal nocturnal hemoglobinuria
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Guidelines for the diagnosis and monitoring of paroxysmal nocturnal hemoglobinuria and related disorders by flow cytometry
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Guidelines for the diagnosis and monitoring of paroxysmal nocturnal hemoglobinuria and related disorders by flow cytometry
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Evaluation of mean sphered corpuscular volume for predicting hereditary spherocytosis
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Evaluation of mean sphered corpuscular volume for predicting hereditary spherocytosis
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Diagnosis and management of paroxysmal nocturnal hemoglobinuria
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Diagnosis and management of paroxysmal nocturnal hemoglobinuria
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Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
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Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
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Clinical utility of the new Beckman-Coulter parameter red blood cell size factor in the study of erithropoiesis
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Clinical utility of the new Beckman-Coulter parameter red blood cell size factor in the study of erithropoiesis
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Clinical signs and symptoms associated with increased risk for thrombosis in patients with paroxysmal nocturnal hemoglobinuria from a Korean Registry
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Clinical signs and symptoms associated with increased risk for thrombosis in patients with paroxysmal nocturnal hemoglobinuria from a Korean Registry
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Clinical impact of HLA-DR15, a minor population of paroxysmal nocturnal hemoglobinuria-type cells, and an aplastic anaemia-associated autoantibody in children with acquired aplastic anemia
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Clinical impact of HLA-DR15, a minor population of paroxysmal nocturnal hemoglobinuria-type cells, and an aplastic anaemia-associated autoantibody in children with acquired aplastic anemia
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Automated screening for tuberculosis by multiparametric analysis of data obtained during routine complete blood count
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Automated screening for tuberculosis by multiparametric analysis of data obtained during routine complete blood count
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Aplastic anemia and paroxysmal nocturnal hemoglobinuria: search for a pathogenetic link
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Aplastic anemia and paroxysmal nocturnal hemoglobinuria: search for a pathogenetic link
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A prospective multicenter study of paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure
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A prospective multicenter study of paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure