Red-cell abnormalities in HEMPAS (hereditary erythroblastic multinuclearity with a positive acidified-serum test)

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Red-cell abnormalities in HEMPAS (hereditary erythroblastic multinuclearity with a positive acidified-serum test)

Abstract

References

Granulopoiesis in chronic granulocytic leukaemia

Erythrocyte enzymatic abnormalities in HEMPAS (hereditary erythroblastic multinuclearity with a positive acidified-serum test)

Cell membrane anomaly impeding cell division

Lysis by anti-I in dyserythropoietic anaemias: role of increased uptake of antibody

Increased agglutinability by anti-i of red cells in sideroblastic and megaloblastic anaemia

Hereditary erythroblastic multinuclearity associated with a positive acidified-serum test: a type of congenital dyserythropoietic anaemia

Ineffective erythropoiesis with morphologically abnormal erythroblasts and unconjugated hyperbilirubinaemia

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

The "sugar-water" test for paroxysmal nocturnal hemoglobinuria

Comparative sensitivity of the erythrocytes in paroxysmal nocturnal haemoglobinuria to haemolysis by acidified normal serum and by high-titre cold antibody

Comparison of the sensitivity to agglutination and haemolysis by a high-titre cold antibody of the erythrocytes of normal subjects and of patients with a variety of blood diseases including paroxysmal nocturnal haemoglobinuria

Chromosomal study in erythroblastic endopolyploidy

AGGLUTINABILITY OF RED CELLS BY ANTI-I IN PATIENTS WITH THALASSEMIA MAJOR AND OTHER HAEMATOLOGICAL DISORDERS

Citations

Isolation and characterization of poly-N-acetyllactosaminylceramides accumulated in the erythrocytes of congenital dyserythropoietic anemia type II patients

The classification, recognition and significance of polyagglutination in transfusion medicine

Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

Congenital dyserythropoietic anaemia, types I and II: aberrant pattern of erythrocyte membrane proteins in CDA II, as revealed by two-dimensional polyacrylamide gel electrophoresis

Morphological Abnormalities in cultured erythroid colonies (BFU-E) from the blood of two patients with HEMPAS

Congenital dyserythropoietic anaemia type II (HEMPAS): a family study

Cell membrane receptors for serological reagents

Mechanisms of immune lysis of the red cells in hereditary erythroblastic multinuclearity with a positive acidified serum test and paroxysmal nocturnal hemoglobinuria

Congenital dyserythropoietic anemia, type II (Hempas). First five reported cases in Italy

Red cell membrane protein anomalies in congenital dyserythropoietic anaemia, type II (HEMP AS)

Congenital dyserythropoietic anaemia (CDA) with severe gout, rare Kell phenotype and erythrocyte, granulocyte and platelet membrane reduplication: a new variant of CDA type II

The carcinogenicity of lead

The role of lectins in blood group serology

Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation.

The Di Guglielmo syndrome: a study of 17 cases. I. Clinical and haematological manifestations

Congenital dyserythropoietic anemias

'VA', a new type of erythrocyte polyagglutination characterized by depressed H receptors and associated with hemolytic anemia. II. Observations by immunofluorescence, electron microscopy, cell electrophoresis and Biochemistry.

Ultrastructure of erythroid cells in a case of congenital dyserythropoietic anaemia type II (author's transl)

Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)

Congenital dyserythropoietic anaemia type II (HEMPAS) and haemochromatosis: a report of two cases

Red blood cell polyagglutination: clinical aspects

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