Hereditary spherocytosis and elliptocytosis are the two most common inherited red cell
membrane disorders resulting from mutations in genes encoding various red cell membrane …

Inherited red blood cell (RBC) membrane disorders, such as hereditary spherocytosis,
elliptocytosis and hereditary ovalocytosis, result from mutations in genes encoding various …

3.1 Лечение CIN III 3.2 Лечение микроинвазивного рака шейки матки 3.3 Лечение рака
шейки матки IB1 и IIА1 стадий 3.4. Лечение рака шейки матки IB2 и IIА2 стадий 3.5 …

It is estimated that there are 100,000 people living with sickle cell disease (SCD) in the
United States. 1 The most common manifestation of sickle cell disease is vaso-occlusive …

Background The laboratory diagnosis of hereditary spherocytosis commonly relies on NaCl-
based or glycerol-based red cell osmotic fragility tests; more recently, an assay directly …

Hemolytic anemias are a group of disorders with varied clinical and molecular
heterogeneity. They are characterized by decreased levels of circulating erythrocytes in …

The plasma membrane of the erythrocyte accounts for all of this cell's antigenic, transport,
and mechanical characteristics, particularly its ability to undergo large passive deformations …

Short circulation time and off‐target toxicity are the main challenges faced by small‐
molecule chemotherapeutics. To overcome these shortcomings, an albumin‐binding …

Among the red cell membrane disorders, hereditary spherocytosis (HS) is one of the most
common causes of inherited hemolytic anemia. HS results from the deficiency or dysfunction …

Thalassemia is an inherited blood disorder that requires lifelong adherence to a complicated
and burdensome medical regimen which could potentially impact emotional functioning of …