DEFINITION OF THE MOLECULAR BASIS OF THE CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE II (CDA-II OR HEMPAS)

Pubblicazioni Scientifiche

• ACTA HAEMATOLOGICA

  Homozygous prothrombin gene mutation and ischemic cerebrovascular disease

• BLOOD

  Genetic heterogeneity of congenital dyserythropoietic anemia type II

• BONE MARROW TRANSPLANTATION

  Bone marrow transplantation in a case of severe, type II congenital dyserythropoietic anaemia (CDA II)

• BRITISH JOURNAL OF HAEMATOLOGY

  Suppression of CDA II expression in a homozygote

• CLINICAL AND LABORATORY HAEMATOLOGY

  Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis

• EUROPEAN JOURNAL OF HAEMATOLOGY

  Transfusion-dependent congenital dyserythropoietic anaemia with intraerythroblastic inclusions of a non-globin protein

• EXPERIMENTAL HEMATOLOGY

  Decreased band 3 anion transport activity and band 3 clusterization in congenital dyserythropoietic anemia type II

• HAEMATOLOGICA

  Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?

• JOURNAL OF PEDIATRICS

  Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II)