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

Pubblicazioni Scientifiche

• 1999-01-01 ACTA HAEMATOLOGICA

  Homozygous prothrombin gene mutation and ischemic cerebrovascular disease

• 1998-10-01 BLOOD

  Genetic heterogeneity of congenital dyserythropoietic anemia type II

• 2001-01-01 BONE MARROW TRANSPLANTATION

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

• 1999-09-01 BRITISH JOURNAL OF HAEMATOLOGY

  Suppression of CDA II expression in a homozygote

• 2001-02-01 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

• 2000-08-01 EUROPEAN JOURNAL OF HAEMATOLOGY

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

• 1998-08-01 EXPERIMENTAL HEMATOLOGY

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

• 2000-05-01 HAEMATOLOGICA

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

• 2000-04-01 JOURNAL OF PEDIATRICS

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