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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Transplant-associated thrombotic microangiopathy: opening Pandora's box.Paroxysmal nocturnal haemoglobinuria. Experience over a 10 years period.Modified Ham test for atypical hemolytic uremic syndromeDirect evidence of complement activation in HELLP syndrome: A link to atypical hemolytic uremic syndrome.Leukemia arising out of paroxysmal nocturnal hemoglobinuria.Implications of recent insights into the pathophysiology of paroxysmal nocturnal haemoglobinuria.Paroxysmal nocturnal haemoglobinuria: nature's gene therapy?THE INITIATION AND ENHANCEMENT OF HUMAN RED CELL LYSIS BY ACTIVATORS OF THE FIRST COMPONENT OF COMPLEMENT AND BY FIRST COMPONENT ESTERASE; STUDIES USING NORMAL RED CELLS AND RED CELLS FROM PATIENTS WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA.Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. I. The sensitivity of PNH red cells to lysis by complement and specific antibodyDetection of complement components on unlysed erythrocytes from acid hemolysis and thrombin test reactions in paroxysmal nocturnal hemoglobinuria.Paroxysmal nocturnal hemoglobinuria--present status and future prospects.Multiparameter flow cytometry for the diagnosis and monitoring of small GPI-deficient cellular populationsHistorical aspects of paroxysmal nocturnal haemoglobinuria: 'defining the disease'.Long-term outcome of fludarabine-based reduced-intensity allogeneic hematopoietic cell transplantation for debilitating paroxysmal nocturnal hemoglobinuria.Mechanisms of immune lysis of red blood cells in vitro. I. Paroxysmal nocturnal hemoglobinuria cells.Interactions of the platelets in paroxysmal nocturnal hemoglobinuria with complement. Relationship to defects in the regulation of complement and to platelet survival in vivo.The properdin system and immunity. IV. The hemolysis of erythrocytes from patients with paroxysmal nocturnal hemoglobinuria.A novel marker for screening paroxysmal nocturnal hemoglobinuria using routine complete blood count and cell population data.Retrovirus-induced feline pure red cell aplasia. Hematopoietic progenitors are infected with feline leukemia virus and erythroid burst-forming cells are uniquely sensitive to heterologous complementDevelopment of complement therapeutics for inhibition of immune-mediated red cell destructionStudies on immune human hemolysis. I. The kinetics of the Donath-Land-steiner reaction and the requirement for complement in the reaction.Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. 3. The membrane defects caused by complement lysis.Paroxysmal nocturnal hemoglobinuria: a complement-mediated hemolytic anemiaAdvances in the diagnosis and therapy of paroxysmal nocturnal hemoglobinuriaParoxysmal nocturnal hemoglobinuria and glycosyl phosphatidylinositol anchored proteins that regulate complement.Hepatic manifestations in hematological disorders.Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor.Enhanced complement-mediated lysis of type III paroxysmal nocturnal hemoglobinuria erythrocytes involves increased C9 binding and polymerization.Anti-Complement Treatment in Paroxysmal Nocturnal Hemoglobinuria: Where we Stand and Where we are Going.Laboratory tests for paroxysmal nocturnal hemoglobinuria.Paroxysmal nocturnal hemoglobinuria and the glycosylphosphatidylinositol anchor.Paroxysmal nocturnal hemoglobinuria and eculizumab.Functional and structural characterization of four mouse monoclonal antibodies to complement C3 with potential therapeutic and diagnostic applications.Paroxysmal nocturnal haemoglobinuria clones in patients with myelodysplastic syndromes.Paroxysmal nocturnal haemoglobinuria testing in blood transfusion laboratories: do they go with the flow?Flow cytometric testing for paroxysmal nocturnal hemoglobinuria: CD64 is better for gating monocytes than CD33.Blood Transfusion in Nocturnal Haemoglobinuria.
P2860
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P2860
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.
description
1939 nî lūn-bûn
@nan
1939年の論文
@ja
1939年論文
@yue
1939年論文
@zh-hant
1939年論文
@zh-hk
1939年論文
@zh-mo
1939年論文
@zh-tw
1939年论文
@wuu
1939年论文
@zh
1939年论文
@zh-cn
name
STUDIES ON DESTRUCTION OF RED ...... REFERENCE TO SERUM COMPLEMENT.
@en
type
label
STUDIES ON DESTRUCTION OF RED ...... REFERENCE TO SERUM COMPLEMENT.
@en
prefLabel
STUDIES ON DESTRUCTION OF RED ...... REFERENCE TO SERUM COMPLEMENT.
@en
P356
P1476
STUDIES ON DESTRUCTION OF RED ...... REFERENCE TO SERUM COMPLEMENT.
@en
P2093
P2860
P304
P356
10.1172/JCI101081
P407
P577
1939-11-01T00:00:00Z