Introduction: Flow cytometry with eosin-5´-maleimide (EMA), anti-CD55 and anti-CD59 is commonly used when investigating non-autoimmune hemolytic anemias. Reduced fluorescence of EMA, typically detected in hereditary spherocytosis is also seen in congenital dyserythropoietic anemia type II (CDA II). Reduction of CD55 and CD59 characterizes paroxysmal nocturnal hemoglobinuria (PNH). We studied the flow cytometric profile of EMA, CD55 and CD59 on erythrocytes in congenital dyserythropoietic anemia type III (CDA III). Methods: Erythrocytes from 16 CDA III positive individuals, 14 CDA III negative relatives and three normal controls per assay were studied with flow cytometry after EMA staining. Flow cytometry after anti-CD55 and anti- CD59 was ...
Introduction:The laboratory diagnosis of paroxysmal nocturnal hemoglobinuria (PNH), disease that is ...
The congenital dyserythropoietic anemias (CDAs) are a heterogeneous group of hereditary disorders th...
Erythroid dysplasia is the pathologic hallmark of myelodysplastic syndromes (MDS). To develop a quan...
Introduction: Flow cytometry with eosin-5´-maleimide (EMA), anti-CD55 and anti-CD59 is commonly used...
Context: Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal stem cell disorder characte...
Congenital dyserythropoietic anaemia type II (CDA II) is the most common congenital dyserythropoieti...
OBJECTIVE: The diagnosis of hereditary red blood cell (RBC) membrane disorders, and in particular he...
Congenital dyserythropoietic anemias (CDAs) are a heterogeneous group of inherited anemias that affe...
PNH is a rare clonal disorder of hematopoietic stem cells, therefore all blood cells lineages are in...
A term male newborn born to a mother who had hereditary spherocytosis presented with neonatal jaundi...
Congenital Dyserythropoietic Anemias (CDAs) are subtypes of bone marrow failure syndromes, hallmarke...
Abstract. Conventional diagnosis of hereditary red blood cell (RBC) membrane disor-ders, in particul...
Congenital dyserythropoietic anemia type II (CDA-II) is the most common form of inherited dyserythro...
Flow cytometric test for analyzing the eosin-5-maleimide (EMA) binding to red blood cells has been b...
Current recommendations for diagnosing myelodysplastic syndromes endorse flow cytometry as an inform...
Introduction:The laboratory diagnosis of paroxysmal nocturnal hemoglobinuria (PNH), disease that is ...
The congenital dyserythropoietic anemias (CDAs) are a heterogeneous group of hereditary disorders th...
Erythroid dysplasia is the pathologic hallmark of myelodysplastic syndromes (MDS). To develop a quan...
Introduction: Flow cytometry with eosin-5´-maleimide (EMA), anti-CD55 and anti-CD59 is commonly used...
Context: Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal stem cell disorder characte...
Congenital dyserythropoietic anaemia type II (CDA II) is the most common congenital dyserythropoieti...
OBJECTIVE: The diagnosis of hereditary red blood cell (RBC) membrane disorders, and in particular he...
Congenital dyserythropoietic anemias (CDAs) are a heterogeneous group of inherited anemias that affe...
PNH is a rare clonal disorder of hematopoietic stem cells, therefore all blood cells lineages are in...
A term male newborn born to a mother who had hereditary spherocytosis presented with neonatal jaundi...
Congenital Dyserythropoietic Anemias (CDAs) are subtypes of bone marrow failure syndromes, hallmarke...
Abstract. Conventional diagnosis of hereditary red blood cell (RBC) membrane disor-ders, in particul...
Congenital dyserythropoietic anemia type II (CDA-II) is the most common form of inherited dyserythro...
Flow cytometric test for analyzing the eosin-5-maleimide (EMA) binding to red blood cells has been b...
Current recommendations for diagnosing myelodysplastic syndromes endorse flow cytometry as an inform...
Introduction:The laboratory diagnosis of paroxysmal nocturnal hemoglobinuria (PNH), disease that is ...
The congenital dyserythropoietic anemias (CDAs) are a heterogeneous group of hereditary disorders th...
Erythroid dysplasia is the pathologic hallmark of myelodysplastic syndromes (MDS). To develop a quan...