共 92 条
- [1] Marks PW(1996)Congenital dyserythropoietic anemias Am J Hematol 51 55-63
- [2] Mitus AJ(2010)Frequency of congenital dyserythropoietic anemias in Europe Eur J Haematol 85 20-25
- [3] Heimpel H(1969)Hereditary erythroblastic multinuclearity associated with a positive acidified-serum test: a type of congenital dyserythropoietic anaemia Br J Haematol 17 11-26
- [4] Matuschek A(2003)Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation Blood 102 4576-4581
- [5] Ahmed M(1996)Congenital dyserythropoietic anemia type II: molecular basis and clinical aspects Haematologica 81 543-559
- [6] Bader-Meunier B(2010)The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells Haematologica 95 1034-1036
- [7] Colita A(2009)The congenital dyserythropoietic anemias Hematol Oncol Clin North Am 23 283-306
- [8] Crookston JH(1996)The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum Blood 87 4433-4439
- [9] Crookston MC(1977)Congenital dyserythropoietic anaemia, types I and II: aberrant pattern of erythrocyte membrane proteins in CDA II, as revealed by two-dimensional polyacrylamide gel electrophoresis Br J Haematol 35 209-215
- [10] Burnie KL(2009)Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene Hum Mutat 30 1292-1298