Historical aspects of paroxysmal nocturnal haemoglobinuria: 'defining the disease'. (Q34120817)

31 July 2017

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title

Historical aspects of paroxysmal nocturnal haemoglobinuria: 'defining the disease'. (English)

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31 July 2017

Charles J Parker

1

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31 July 2017

language of work or name

English

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publication date

1 April 2002

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British Journal of Haematology

31 July 2017

published in

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31 July 2017

volume

117

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31 July 2017

issue

1

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31 July 2017

page(s)

3-22

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A platelet and granulocyte membrane defect in paroxysmal nocturnal hemoglobinuria: usefulness for the detection of platelet antibodies

31 July 2017

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1 reference

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Paroxysmal nocturnal hemoglobinuria. II. Erythrocyte acetylcholinesterase defect.

21 January 2018

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Refractory anaemia (Fanconi type): Its Incidence in Three Members of One Family, with in One Case a Relationship to Chronic Haemolytic Anaemia with Nocturnal Haemo-Globinuria (Marchiafava-Micheli Disease or `Nocturnal Haemoglobinuria')

21 January 2018

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Release of decay-accelerating factor (DAF) from the cell membrane by phosphatidylinositol-specific phospholipase C (PIPLC). Selective modification of a complement regulatory protein

21 January 2018

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Regulation of the amplification C3 convertase of human complement by an inhibitory protein isolated from human erythrocyte membrane

21 January 2018

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Identification of the membrane glycoprotein that is the C3b receptor of the human erythrocyte, polymorphonuclear leukocyte, B lymphocyte, and monocyte

21 January 2018

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Chronic Hemolytic Anemia with Paroxysmal Nocturnal Hemoglobinuria

21 January 2018

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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.

21 January 2018

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Paroxysmal nocturnal hemoglobinuria type III. Lack of an erythrocyte membrane protein restricting the lysis by C5b-9.

21 January 2018

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The properdin system and immunity. IV. The hemolysis of erythrocytes from patients with paroxysmal nocturnal hemoglobinuria

21 January 2018

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Isolation and characterization of a membrane protein from normal human erythrocytes that inhibits reactive lysis of the erythrocytes of paroxysmal nocturnal hemoglobinuria

21 January 2018

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Relationship between the membrane inhibitor of reactive lysis and the erythrocyte phenotypes of paroxysmal nocturnal hemoglobinuria

21 January 2018

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Cell-surface-antigen mutants of haematopoietic cells. Tools to study differentiation, biosynthesis and function

21 January 2018

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Somatic genetic analysis of the expression of cell surface molecules

21 January 2018

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Novel protein/membrane attachment

21 January 2018

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Mechanisms of immune lysis of red blood cells in vitro. I. Paroxysmal nocturnal hemoglobinuria cells

21 January 2018

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Relationship between decay accelerating factor deficiency, diminished acetylcholinesterase activity, and defective terminal complement pathway restriction in paroxysmal nocturnal hemoglobinuria erythrocytes

21 January 2018

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The Cloning of PIG-A, a Component in the Early Step of GPI-Anchor Biosynthesis

21 January 2018

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Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor

21 January 2018

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Complement lysis of human erythrocytes. Differeing susceptibility of two types of paroxysmal nocturnal hemoglobinuria cells to C5b-9

21 January 2018

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Deficiency of an erythrocyte membrane protein with complement regulatory activity in paroxysmal nocturnal hemoglobinuria

21 January 2018

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Molecular basis of paroxysmal nocturnal hemoglobinuria

21 January 2018

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Increased enzymatic activity of the alternative pathway convertase when bound to the erythrocytes of paroxysmal nocturnal hemoglobinuria

21 January 2018

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Abnormality of glycophorin-alpha on paroxysmal nocturnal hemoglobinuria erythrocytes

21 January 2018

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Increased efficiency of binding of nascent C3b to the erythrocytes of chronic cold agglutinin disease.

21 January 2018

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Characterization of the complement sensitivity of paroxysmal nocturnal hemoglobinuria erythrocytes

21 January 2018

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The properdin system and immunity. I. Demonstration and isolation of a new serum protein, properdin, and its role in immune phenomena

21 January 2018

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Variations in the Red Cells in Paroxysmal Nocturnal Haemoglobinuria

21 January 2018

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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 antibody

21 January 2018

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The Population of Cells in Paroxysmal Nocturnal Haemoglobinuria of Intermediate Sensitivity to Complement Lysis: Significance and Mechanism of Increased Immune Lysis

21 January 2018

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Deficient biosynthesis of N-acetylglucosaminyl-phosphatidylinositol, the first intermediate of glycosyl phosphatidylinositol anchor biosynthesis, in cell lines established from patients with paroxysmal nocturnal hemoglobinuria

21 January 2018

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Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria

21 January 2018

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Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria

21 January 2018

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Isolation of a human erythrocyte membrane protein capable of inhibiting expression of homologous complement transmembrane channels

21 January 2018

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Deficiency of the homologous restriction factor in paroxysmal nocturnal hemoglobinuria

21 January 2018

1 reference

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10.1046/J.1365-2141.2002.03374.X

21 January 2018

Identifiers

DOI

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31 July 2017

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