Copyright © 2015 Shin-ichiro Suemori et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Flow cytometric test for analyzing the eosin-5-maleimide (EMA) binding to red blood cells has been believed to be a specific method for diagnosing hereditary spherocytosis (HS). However, it has been reported that diseases other thanHS, such as hereditary pyropoikilocytosis (HPP) and Southeast Asian ovalocytosis (SAO), which are forms in the category of hereditary elliptocytosis (HE), show decreased EMA binding to red blood cells. We analyzed EMA binding to red blood cells in 101 healthy...
Purpose Sodium dodecyl sulphate-polyacrylamide gel electrophoresis (1DE) may reveal qualitative or q...
H EREDITA1Y ELLIPTOCYTOSIS is oftets a l)enigts hereditary condi-tion matoifested by the presetsce o...
Hereditary erythrocyte membrane disorders are caused by mutations in genes encoding various transmem...
Flow cytometric test for analyzing the eosin-5-maleimide (EMA) binding to red blood cells has been b...
Objective: The diagnosis of hereditary red blood cell (RBC) membrane disorders, and in particular he...
Red blood cell (RBC) morphology is, in general, the key diagnostic feature for hereditary spherocyto...
OBJECTIVE: The diagnosis of hereditary red blood cell (RBC) membrane disorders, and in particular he...
Hereditary elliptocytosis an abnormality of red blood cell may provide a selective advantage to prot...
The clinical severity of common hereditary elliptocytosis (HE) is highly variable. ranging from an a...
Hereditary elliptocytosis (HE) is a group of disorders character-ized by abnormal erythrocyte shapes...
A 17-day-old boy was admitted because of jaundice and anemia. He was born weighing 2900 g subsequen...
Copyright © 2013 Carla Luana Dinardo et al. This is an open access article distributed under the Cre...
Hereditary spherocytosis is a common hemolytic disorder characterized by a defect or deficiency in o...
Abstract. Conventional diagnosis of hereditary red blood cell (RBC) membrane disor-ders, in particul...
The 4.1(-) hereditary elliptocytosis is a variety of hereditary elliptocytosis that results from the...
Purpose Sodium dodecyl sulphate-polyacrylamide gel electrophoresis (1DE) may reveal qualitative or q...
H EREDITA1Y ELLIPTOCYTOSIS is oftets a l)enigts hereditary condi-tion matoifested by the presetsce o...
Hereditary erythrocyte membrane disorders are caused by mutations in genes encoding various transmem...
Flow cytometric test for analyzing the eosin-5-maleimide (EMA) binding to red blood cells has been b...
Objective: The diagnosis of hereditary red blood cell (RBC) membrane disorders, and in particular he...
Red blood cell (RBC) morphology is, in general, the key diagnostic feature for hereditary spherocyto...
OBJECTIVE: The diagnosis of hereditary red blood cell (RBC) membrane disorders, and in particular he...
Hereditary elliptocytosis an abnormality of red blood cell may provide a selective advantage to prot...
The clinical severity of common hereditary elliptocytosis (HE) is highly variable. ranging from an a...
Hereditary elliptocytosis (HE) is a group of disorders character-ized by abnormal erythrocyte shapes...
A 17-day-old boy was admitted because of jaundice and anemia. He was born weighing 2900 g subsequen...
Copyright © 2013 Carla Luana Dinardo et al. This is an open access article distributed under the Cre...
Hereditary spherocytosis is a common hemolytic disorder characterized by a defect or deficiency in o...
Abstract. Conventional diagnosis of hereditary red blood cell (RBC) membrane disor-ders, in particul...
The 4.1(-) hereditary elliptocytosis is a variety of hereditary elliptocytosis that results from the...
Purpose Sodium dodecyl sulphate-polyacrylamide gel electrophoresis (1DE) may reveal qualitative or q...
H EREDITA1Y ELLIPTOCYTOSIS is oftets a l)enigts hereditary condi-tion matoifested by the presetsce o...
Hereditary erythrocyte membrane disorders are caused by mutations in genes encoding various transmem...