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Volumn 12, Issue 3, 1998, Pages 178-200

Congenital dyserythropoietic anaemias: Clinical features, haematological morphology and new biochemical data

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA INTERFERON; OLIGOSACCHARIDE;

EID: 0031685438     PISSN: 0268960X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0268-960X(98)90016-9     Document Type: Article
Times cited : (86)

References (117)
  • 1
    • 0030879690 scopus 로고    scopus 로고
    • Dyserythropoiesis and congenital dyserythropoietic anaemias
    • Wickramasinghe SN. Dyserythropoiesis and congenital dyserythropoietic anaemias. Br J Haematol 1997; 98: 785-797.
    • (1997) Br J Haematol , vol.98 , pp. 785-797
    • Wickramasinghe, S.N.1
  • 2
    • 0030053449 scopus 로고    scopus 로고
    • Congenital dyserythropoietic anemias
    • Marks PW, Mitus AJ. Congenital dyserythropoietic anemias. Am J Hematol 1996; 51: 55-63.
    • (1996) Am J Hematol , vol.51 , pp. 55-63
    • Marks, P.W.1    Mitus, A.J.2
  • 3
    • 0029995645 scopus 로고    scopus 로고
    • Composition of the intra-erythroblastic precipitates in thalassaemia and congenital dyserythropoietic anaemia (CDA): Identification of a new type of CDA with intra-erythroblastic precipitates not reacting with monoclonal antibodies to α- and β-globin chains
    • Wickramasinghe SN, Lee MJ, Furukawa T, Eguchi M, Reid CDL. Composition of the intra-erythroblastic precipitates in thalassaemia and congenital dyserythropoietic anaemia (CDA): identification of a new type of CDA with intra-erythroblastic precipitates not reacting with monoclonal antibodies to α- and β-globin chains. Br J Haematol 1996; 93: 576-585.
    • (1996) Br J Haematol , vol.93 , pp. 576-585
    • Wickramasinghe, S.N.1    Lee, M.J.2    Furukawa, T.3    Eguchi, M.4    Reid, C.D.L.5
  • 4
    • 0021303766 scopus 로고
    • Globin chain precipitation, deranged iron metabolism and dyserythropoiesis in some thalassaemia syndromes
    • Wickramasinghe SN, Hughes M. Globin chain precipitation, deranged iron metabolism and dyserythropoiesis in some thalassaemia syndromes. Haematologia 1984; 17: 35-55.
    • (1984) Haematologia , vol.17 , pp. 35-55
    • Wickramasinghe, S.N.1    Hughes, M.2
  • 5
    • 0014264724 scopus 로고
    • Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts
    • Heimpel H, Wendt F. Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts. Helv Med Acta 1968; 34: 103-115.
    • (1968) Helv Med Acta , vol.34 , pp. 103-115
    • Heimpel, H.1    Wendt, F.2
  • 6
    • 0025292312 scopus 로고
    • Molecular basis for dominantly inherited inclusion body β-thalassaemia
    • Thein SL, Hesketh C, Taylor P et al. Molecular basis for dominantly inherited inclusion body β-thalassaemia. Proc Natl Acad Sci USA 1990; 87: 3924-3928.
    • (1990) Proc Natl Acad Sci USA , vol.87 , pp. 3924-3928
    • Thein, S.L.1    Hesketh, C.2    Taylor, P.3
  • 8
    • 0021171856 scopus 로고
    • Ultrastructure and cell cycle distribution of erythropoietic cells in heterozygotes and homozygotes for haemoglobin E
    • Wickramasinghe SN, Hughes M. Wasi P, Fucharoen S, Litwinczuk RAC. Ultrastructure and cell cycle distribution of erythropoietic cells in heterozygotes and homozygotes for haemoglobin E. Br J Haematol 1984; 57: 685-694.
    • (1984) Br J Haematol , vol.57 , pp. 685-694
    • Wickramasinghe, S.N.1    Hughes, M.2    Wasi, P.3    Fucharoen, S.4    Litwinczuk, R.A.C.5
  • 11
    • 0024328561 scopus 로고
    • Congenital dyserythropoietic anaemia variant presenting as hydrops foetalis
    • Carter C, Darbyshire PJ, Wickramasinghe SN. Congenital dyserythropoietic anaemia variant presenting as hydrops foetalis. Br J Haematol 1989; 72: 289-290.
    • (1989) Br J Haematol , vol.72 , pp. 289-290
    • Carter, C.1    Darbyshire, P.J.2    Wickramasinghe, S.N.3
  • 12
    • 0025116344 scopus 로고
    • A variant congenital dyserythropoietic anaemia presenting as a fatal hydrops foetalis
    • Williams G, Lorimer S, Merry CC, Greenberg CR, Bishop AJ. A variant congenital dyserythropoietic anaemia presenting as a fatal hydrops foetalis [comment]. Br J Haematol 1990; 76: 438-439.
    • (1990) Br J Haematol , vol.76 , pp. 438-439
    • Williams, G.1    Lorimer, S.2    Merry, C.C.3    Greenberg, C.R.4    Bishop, A.J.5
  • 13
    • 0025127735 scopus 로고
    • Congenital dyserythropoietic anaemia (CDA) with intrauterine symptoms and early lethal outcome
    • Kristiansen JD, Rasmussen LN, Vetner M. Congenital dyserythropoietic anaemia (CDA) with intrauterine symptoms and early lethal outcome. Eur J Haematol 1990; 45: 113-114.
    • (1990) Eur J Haematol , vol.45 , pp. 113-114
    • Kristiansen, J.D.1    Rasmussen, L.N.2    Vetner, M.3
  • 14
    • 0031030351 scopus 로고    scopus 로고
    • A severe transfusion-dependent congenital dyserythropoietic anaemia presenting as hydrops fetalis
    • Cantu-Rajnoldi A, Zanella A, Conter U et al. A severe transfusion-dependent congenital dyserythropoietic anaemia presenting as hydrops fetalis. Br J Haematol 1997; 96: 530-533.
    • (1997) Br J Haematol , vol.96 , pp. 530-533
    • Cantu-Rajnoldi, A.1    Zanella, A.2    Conter, U.3
  • 15
    • 0026641710 scopus 로고
    • Ultrastructure of the bone marrow in HIV infection: Evidence of dyshaemopoiesis and stromal cell damage
    • Wickramasinghe SN, Beatty C, Shiels S, Tomlinson DR, Harris JRW. Ultrastructure of the bone marrow in HIV infection: evidence of dyshaemopoiesis and stromal cell damage. Clin Lab Haematol 1992; 14: 213-229.
    • (1992) Clin Lab Haematol , vol.14 , pp. 213-229
    • Wickramasinghe, S.N.1    Beatty, C.2    Shiels, S.3    Tomlinson, D.R.4    Harris, J.R.W.5
  • 18
    • 0023147929 scopus 로고
    • Ultrastructure of bone marrow in patients with visceral leishmaniasis
    • Wickramasinghe SN, Abdalla SH, Kasili EG. Ultrastructure of bone marrow in patients with visceral leishmaniasis. J Clin Pathol 1987; 40: 267-275.
    • (1987) J Clin Pathol , vol.40 , pp. 267-275
    • Wickramasinghe, S.N.1    Abdalla, S.H.2    Kasili, E.G.3
  • 19
    • 0030670587 scopus 로고    scopus 로고
    • Neonatal manifestations of congenital dyserythropoietic anemia type I
    • Shalev H, Tamary H, Shaft D, Reznitsky P, Zaizov R. Neonatal manifestations of congenital dyserythropoietic anemia type I. J Pediatr 1997; 131: 95-97.
    • (1997) J Pediatr , vol.131 , pp. 95-97
    • Shalev, H.1    Tamary, H.2    Shaft, D.3    Reznitsky, P.4    Zaizov, R.5
  • 20
    • 0345469694 scopus 로고
    • Congenital dyserythropoietic anaemia type I
    • Lewis SM, Verwilghen RL, eds. London: Academic Press
    • Heimpel H. Congenital dyserythropoietic anaemia type I. In: Lewis SM, Verwilghen RL, eds. Dyserythropoiesis. London: Academic Press, 1977: 50-70.
    • (1977) Dyserythropoiesis , pp. 50-70
    • Heimpel, H.1
  • 21
    • 13344282062 scopus 로고    scopus 로고
    • Clinical features and studies of erythropoiesis in Israeli Bedouins with congenital dyserythropoietic anemia type I
    • Tamary H, Shalev H, Luria D et al. Clinical features and studies of erythropoiesis in Israeli Bedouins with congenital dyserythropoietic anemia type I. Blood 1996; 87: 1763-1770.
    • (1996) Blood , vol.87 , pp. 1763-1770
    • Tamary, H.1    Shalev, H.2    Luria, D.3
  • 22
    • 0020324773 scopus 로고
    • Use of subcutaneous deferoxamine in a child with hemochromatosis associated with congenital dyserythropoietic anemia, type I
    • Smithson WA, Perrault J. Use of subcutaneous deferoxamine in a child with hemochromatosis associated with congenital dyserythropoietic anemia, type I. Mayo Clin Proc 1982; 57: 322-325.
    • (1982) Mayo Clin Proc , vol.57 , pp. 322-325
    • Smithson, W.A.1    Perrault, J.2
  • 23
    • 0022442656 scopus 로고
    • Studies of erythroblast function in congenital dyserythropoietic anaemia, type I: Evidence of impaired DNA, RNA, and protein synthesis and unbalanced globin chain synthesis in ultrastructurally abnormal cells
    • Wickramasinghe SN, Pippard MJ. Studies of erythroblast function in congenital dyserythropoietic anaemia, type I: evidence of impaired DNA, RNA, and protein synthesis and unbalanced globin chain synthesis in ultrastructurally abnormal cells. J Clin Pathol 1986; 39: 881-890.
    • (1986) J Clin Pathol , vol.39 , pp. 881-890
    • Wickramasinghe, S.N.1    Pippard, M.J.2
  • 25
    • 0021215339 scopus 로고
    • CDA type I with persistent haemosiderinuria: Absence of iron loading
    • Hewitt PE, Win AA, Davies SC. CDA type I with persistent haemosiderinuria: absence of iron loading [letter]. Br J Haematol 1984; 56: 682-684.
    • (1984) Br J Haematol , vol.56 , pp. 682-684
    • Hewitt, P.E.1    Win, A.A.2    Davies, S.C.3
  • 29
    • 0018149616 scopus 로고
    • Type I congenital dyserythropoietic anaemia with myelopoietic abnormalities and hand malformations
    • Holmberg L, Jansson L, Rausing A, Henriksson P. Type I congenital dyserythropoietic anaemia with myelopoietic abnormalities and hand malformations. Scand J Haematol 1978; 21: 72-79.
    • (1978) Scand J Haematol , vol.21 , pp. 72-79
    • Holmberg, L.1    Jansson, L.2    Rausing, A.3    Henriksson, P.4
  • 30
    • 0020521898 scopus 로고
    • Congenital dyserythropoietic anemia type I: A freeze-fracture and thin section electron microscopic study
    • Hiraoka A, Kanayama Y, Yonezawa T, Kitani T, Tarui S, Hashimoto PH. Congenital dyserythropoietic anemia type I: a freeze-fracture and thin section electron microscopic study. Blut 1983; 46: 329-338.
    • (1983) Blut , vol.46 , pp. 329-338
    • Hiraoka, A.1    Kanayama, Y.2    Yonezawa, T.3    Kitani, T.4    Tarui, S.5    Hashimoto, P.H.6
  • 31
    • 0028236547 scopus 로고
    • Two cases of congenital dyserythropoietic anaemia type I associated with unusual skeletal abnormalities of the limbs
    • Brichard B, Vermylen C, Scheiff JM, Michaux JL, Ninane J, Cornu G. Two cases of congenital dyserythropoietic anaemia type I associated with unusual skeletal abnormalities of the limbs. Br J Haematol 1994; 86: 201-202.
    • (1994) Br J Haematol , vol.86 , pp. 201-202
    • Brichard, B.1    Vermylen, C.2    Scheiff, J.M.3    Michaux, J.L.4    Ninane, J.5    Cornu, G.6
  • 33
    • 0020421533 scopus 로고
    • Alterations of globin chain synthesis and of red cell membrane proteins in congenital dyserythropoietic anemia I and II
    • Alloisio N, Jaccoud P, Dorleac E et al. Alterations of globin chain synthesis and of red cell membrane proteins in congenital dyserythropoietic anemia I and II. Pediatr Res 1982; 16: 1016-1021.
    • (1982) Pediatr Res , vol.16 , pp. 1016-1021
    • Alloisio, N.1    Jaccoud, P.2    Dorleac, E.3
  • 34
    • 0030831828 scopus 로고    scopus 로고
    • Serum thymidine kinase in congenital dyserythropoietic anaemia, type I and homozygous β-thalassaemia
    • Wickramasinghe SN, Hasan R, Menike D, Sandström H, Wahlin A. Serum thymidine kinase in congenital dyserythropoietic anaemia, type I and homozygous β-thalassaemia. Eur J Haematol 1997; 59: 333-334.
    • (1997) Eur J Haematol , vol.59 , pp. 333-334
    • Wickramasinghe, S.N.1    Hasan, R.2    Menike, D.3    Sandström, H.4    Wahlin, A.5
  • 35
    • 0015027830 scopus 로고
    • Electron and light microscopic study of the erythroblasts of patients with congenital dyserythropoietic anemia
    • Heimpel H, Forteza-Vila J, Queisser W, Spiertz E. Electron and light microscopic study of the erythroblasts of patients with congenital dyserythropoietic anemia. Blood 1971; 37: 299-310.
    • (1971) Blood , vol.37 , pp. 299-310
    • Heimpel, H.1    Forteza-Vila, J.2    Queisser, W.3    Spiertz, E.4
  • 36
    • 0022652490 scopus 로고
    • Nuclear bridging of erythroblasts in acquired dyserythropoiesis: An early and transient preleukemic marker
    • Bethlenfalvay NC, Phaure TA, Phyliky RL, Bowman RP. Nuclear bridging of erythroblasts in acquired dyserythropoiesis: an early and transient preleukemic marker. Am J Hematol 1986; 21: 315-322.
    • (1986) Am J Hematol , vol.21 , pp. 315-322
    • Bethlenfalvay, N.C.1    Phaure, T.A.2    Phyliky, R.L.3    Bowman, R.P.4
  • 37
    • 0024422466 scopus 로고
    • Pathogenetic implications of internuclear bridging in myelodysplastic syndrome. An Eastern Cooperative Oncology Group/Southwest Oncology Group Cooperative Study
    • Head DR, Kopecky K, Bennett JM et al. Pathogenetic implications of internuclear bridging in myelodysplastic syndrome. An Eastern Cooperative Oncology Group/Southwest Oncology Group Cooperative Study. Cancer 1989; 64: 2199-2202.
    • (1989) Cancer , vol.64 , pp. 2199-2202
    • Head, D.R.1    Kopecky, K.2    Bennett, J.M.3
  • 38
    • 0015372396 scopus 로고
    • Clinical and ultrastructural aspects of congenital dyserythropoietic anaemia type I
    • Lewis SM, Nelson DA, Pitcher CS. Clinical and ultrastructural aspects of congenital dyserythropoietic anaemia type I. Br J Haematol 1972; 23: 113-119.
    • (1972) Br J Haematol , vol.23 , pp. 113-119
    • Lewis, S.M.1    Nelson, D.A.2    Pitcher, C.S.3
  • 39
    • 0015538559 scopus 로고
    • Anomalies ultrastructurales des érythroblastes et des érythrocytes dans six cas de dysérythropoièse congénitale
    • Breton-Gorius J, Daniel MT, Clauvel JP, Dreyfus B. Anomalies ultrastructurales des érythroblastes et des érythrocytes dans six cas de dysérythropoièse congénitale. Nouv Rev Fr Hematol 1973; 13: 23-49.
    • (1973) Nouv Rev Fr Hematol , vol.13 , pp. 23-49
    • Breton-Gorius, J.1    Daniel, M.T.2    Clauvel, J.P.3    Dreyfus, B.4
  • 40
    • 0014991513 scopus 로고
    • Proliferation disturbances of erythroblasts in congenital dyserythropoietic anemia type I and II
    • Queisser W, Spiertz E, Jost E, Heimpel H. Proliferation disturbances of erythroblasts in congenital dyserythropoietic anemia type I and II, Acta Haematol 1971; 45: 65-76.
    • (1971) Acta Haematol , vol.45 , pp. 65-76
    • Queisser, W.1    Spiertz, E.2    Jost, E.3    Heimpel, H.4
  • 41
    • 0028934962 scopus 로고
    • Alpha-interferon therapy for congenital dyserythropoiesis type I
    • Lavabre-Bertrand T, Blanc P, Navarro R et al. Alpha-interferon therapy for congenital dyserythropoiesis type I. Br J Haematol 1995; 89: 929-932.
    • (1995) Br J Haematol , vol.89 , pp. 929-932
    • Lavabre-Bertrand, T.1    Blanc, P.2    Navarro, R.3
  • 42
    • 0029816327 scopus 로고    scopus 로고
    • Congenital dyserythropoiesis type I and alpha-interferon therapy
    • Virjee S, Hatton C. Congenital dyserythropoiesis type I and alpha-interferon therapy. Br J Haematol 1996; 94: 581-582.
    • (1996) Br J Haematol , vol.94 , pp. 581-582
    • Virjee, S.1    Hatton, C.2
  • 43
    • 0008908913 scopus 로고    scopus 로고
    • Congenital dyserythropoietic anaemia (CDA) type I; survey of cases in the UK and response to alpha interferon
    • Wickramasinghe SN. Congenital dyserythropoietic anaemia (CDA) type I; survey of cases in the UK and response to alpha interferon. Internat J Hematol 1996; 64: Suppl 1, S22.
    • (1996) Internat J Hematol , vol.64 , Issue.1 SUPPL.
    • Wickramasinghe, S.N.1
  • 44
    • 0030890512 scopus 로고    scopus 로고
    • Response of CDA type I to alpha-interferon
    • Wickramasinghe SN. Response of CDA type I to alpha-interferon. Eur J Haematol 1997; 58: 121-123.
    • (1997) Eur J Haematol , vol.58 , pp. 121-123
    • Wickramasinghe, S.N.1
  • 45
    • 0030810448 scopus 로고    scopus 로고
    • Reduced interferon-alpha production by Epstein-Barr virus-transformed B-lymphoblastoid cell lines and lectin-stimulated lymphocytes in congenital dyserythropoietic anaemia, type I
    • Wickramasinghe SN, Hasan R, Smythe J. Reduced interferon-alpha production by Epstein-Barr virus-transformed B-lymphoblastoid cell lines and lectin-stimulated lymphocytes in congenital dyserythropoietic anaemia, type I. Br J Haematol 1997; 98: 295-298.
    • (1997) Br J Haematol , vol.98 , pp. 295-298
    • Wickramasinghe, S.N.1    Hasan, R.2    Smythe, J.3
  • 46
    • 4243227931 scopus 로고    scopus 로고
    • Localization of the gene for congenital dyserythropoietic anemia type I to chromosome 15q15.1-15.3
    • Tamary H, Shalmon L, Shaley H et al. Localization of the gene for congenital dyserythropoietic anemia type I to chromosome 15q15.1-15.3. Blood 1996; 88: Suppl 1, 144a.
    • (1996) Blood , vol.88 , Issue.1 SUPPL.
    • Tamary, H.1    Shalmon, L.2    Shaley, H.3
  • 48
    • 0014545231 scopus 로고
    • Hereditary erythroblastic multinuclearity associated with a positive acidified-serum test: A type of congenital dyserythropoietic anaemia
    • Crookston JH, Crookston MC, Brunie KL et al. Hereditary erythroblastic multinuclearity associated with a positive acidified-serum test: a type of congenital dyserythropoietic anaemia. Br J Haematol 1969; 17: 11-26.
    • (1969) Br J Haematol , vol.17 , pp. 11-26
    • Crookston, J.H.1    Crookston, M.C.2    Brunie, K.L.3
  • 50
    • 0023525966 scopus 로고
    • Congenital dyserythropoietic anaemia (type II) presenting with haemosiderosis
    • Bird AR, Jacobs P, Moores P. Congenital dyserythropoietic anaemia (type II) presenting with haemosiderosis. Acta Haematol 1987; 78: 33-36.
    • (1987) Acta Haematol , vol.78 , pp. 33-36
    • Bird, A.R.1    Jacobs, P.2    Moores, P.3
  • 51
    • 0022368257 scopus 로고
    • Severe hemochromatosis: The predominant clinical manifestation of congenital dyserythropoietic anemia type 2
    • Halpern Z, Rahmani R, Levo Y. Severe hemochromatosis: the predominant clinical manifestation of congenital dyserythropoietic anemia type 2. Acta Haematol 1985; 74: 178-180.
    • (1985) Acta Haematol , vol.74 , pp. 178-180
    • Halpern, Z.1    Rahmani, R.2    Levo, Y.3
  • 52
    • 0026822930 scopus 로고
    • A case of congenital dyserythropoietic anemia type II associated with hemochromatosis
    • Tamura H, Matsumoto G, Itakura Y et al. A case of congenital dyserythropoietic anemia type II associated with hemochromatosis. Intern Med 1992; 31: 380-384.
    • (1992) Intern Med , vol.31 , pp. 380-384
    • Tamura, H.1    Matsumoto, G.2    Itakura, Y.3
  • 53
    • 0022470943 scopus 로고
    • Paravertebral extramedullary hematopoiesis associated with improvement of anemia in congenital dyserythropoietic anemia type II
    • Lugassy G, Michaeli J, Harats N, Libson E, Rachmilewitz EA. Paravertebral extramedullary hematopoiesis associated with improvement of anemia in congenital dyserythropoietic anemia type II. Am J Hematol 1986; 22: 295-300.
    • (1986) Am J Hematol , vol.22 , pp. 295-300
    • Lugassy, G.1    Michaeli, J.2    Harats, N.3    Libson, E.4    Rachmilewitz, E.A.5
  • 54
    • 0022523240 scopus 로고
    • Parvovirus infection associated with aplastic crisis in a patient with HEMPAS
    • West NC, Meigh RE, Mackie M, Anderson MJ. Parvovirus infection associated with aplastic crisis in a patient with HEMPAS. J Clin Pathol 1986; 39: 1019-1020.
    • (1986) J Clin Pathol , vol.39 , pp. 1019-1020
    • West, N.C.1    Meigh, R.E.2    Mackie, M.3    Anderson, M.J.4
  • 55
    • 0018663467 scopus 로고
    • Studies of ineffective erythropoiesis and peripheral haemolysis in congenital dyserythropoietic anaemia type II
    • Barosi G, Cazzola M, Stefanelli M, Ascari E. Studies of ineffective erythropoiesis and peripheral haemolysis in congenital dyserythropoietic anaemia type II. Br J Haematol 1979; 43: 243-250.
    • (1979) Br J Haematol , vol.43 , pp. 243-250
    • Barosi, G.1    Cazzola, M.2    Stefanelli, M.3    Ascari, E.4
  • 57
    • 0015253170 scopus 로고
    • Congenital dyserythropoietic anemia type II: Ultrastructural and radioautographic studies of blood and bone marrow
    • Wong KY, Hug G, Lampkin BC. Congenital dyserythropoietic anemia type II: ultrastructural and radioautographic studies of blood and bone marrow. Blood 1972; 39: 23-30.
    • (1972) Blood , vol.39 , pp. 23-30
    • Wong, K.Y.1    Hug, G.2    Lampkin, B.C.3
  • 58
    • 9344251085 scopus 로고    scopus 로고
    • The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum
    • Alloisio N, Texier P, Denoroy L et al. The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum. Blood 1996; 87: 4433-4439.
    • (1996) Blood , vol.87 , pp. 4433-4439
    • Alloisio, N.1    Texier, P.2    Denoroy, L.3
  • 59
    • 0018151527 scopus 로고
    • Electron microscope autoradiographic studies of the erythroblasts of a case of congenital dyserythropoietic anaemia, type II
    • Wickramasinghe SN, Parry TE, Hughes M. Electron microscope autoradiographic studies of the erythroblasts of a case of congenital dyserythropoietic anaemia, type II. Scand J Haematol 1978; 20: 429-439.
    • (1978) Scand J Haematol , vol.20 , pp. 429-439
    • Wickramasinghe, S.N.1    Parry, T.E.2    Hughes, M.3
  • 61
    • 0003522262 scopus 로고
    • Oxford: Blackwell Scientific Publications
    • Wickramasinghe SN. Human bone marrow. Oxford: Blackwell Scientific Publications, 1975: 349.
    • (1975) Human Bone Marrow , pp. 349
    • Wickramasinghe, S.N.1
  • 62
    • 0020454782 scopus 로고
    • Evidence for the existence of two populations of erythroid cells in a case of congenital dyserythropoietic anaemia type II
    • Cazzola M, Barosi G, Lambertenghi-Deliliers G, Paolini F, Riccardi A. Evidence for the existence of two populations of erythroid cells in a case of congenital dyserythropoietic anaemia type II. Haematologica 1982; 67: 508-516.
    • (1982) Haematologica , vol.67 , pp. 508-516
    • Cazzola, M.1    Barosi, G.2    Lambertenghi-Deliliers, G.3    Paolini, F.4    Riccardi, A.5
  • 63
    • 0006977692 scopus 로고
    • Congenital dyserythropoietic anemia type IV
    • McBride JA, Wilson WEC, Baillie B. Congenital dyserythropoietic anemia type IV. Blood 1971; 38: 837.
    • (1971) Blood , vol.38 , pp. 837
    • McBride, J.A.1    Wilson, W.E.C.2    Baillie, B.3
  • 64
    • 0022512321 scopus 로고
    • A variant of the congenital dyserythropoietic anaemia type II with structural abnormalities in the granulocytic series
    • Vermylen C, Scheiff JM, Rodhain J, Ninane J, Cornu G. A variant of the congenital dyserythropoietic anaemia type II with structural abnormalities in the granulocytic series. Eur J Pediatr 1986; 145: 232-235.
    • (1986) Eur J Pediatr , vol.145 , pp. 232-235
    • Vermylen, C.1    Scheiff, J.M.2    Rodhain, J.3    Ninane, J.4    Cornu, G.5
  • 66
    • 0020407280 scopus 로고
    • Variants of congenital dyserythropoietic anaemia: An update
    • Boogaerts MA, Verwilghen RL. Variants of congenital dyserythropoietic anaemia: an update. Haematologia 1982; 15: 211-219.
    • (1982) Haematologia , vol.15 , pp. 211-219
    • Boogaerts, M.A.1    Verwilghen, R.L.2
  • 67
    • 0018922436 scopus 로고
    • Congenital dyserythropoietic anaemia (CDA) with severe gout, rare Kell phenotype and erythrocyte, granulocyte and platelet membrane reduplication: A new variant of CDA type II
    • Lowenthal RM, Marsden KA, Dewar CL, Thompson GR. Congenital dyserythropoietic anaemia (CDA) with severe gout, rare Kell phenotype and erythrocyte, granulocyte and platelet membrane reduplication: a new variant of CDA type II. Br J Haematol 1980; 44: 211-220.
    • (1980) Br J Haematol , vol.44 , pp. 211-220
    • Lowenthal, R.M.1    Marsden, K.A.2    Dewar, C.L.3    Thompson, G.R.4
  • 68
    • 0020045220 scopus 로고
    • Red cell membrane protein anomalies in congenital dyserythropoietic anaemia, type II (HEMPAS)
    • Baines AJ, Banga JP, Gratzer WB, Linch DC, Huehns ER. Red cell membrane protein anomalies in congenital dyserythropoietic anaemia, type II (HEMPAS). Br J Haematol 1982; 50: 563-574.
    • (1982) Br J Haematol , vol.50 , pp. 563-574
    • Baines, A.J.1    Banga, J.P.2    Gratzer, W.B.3    Linch, D.C.4    Huehns, E.R.5
  • 69
    • 0019977542 scopus 로고
    • Decreased glycosylation of band 3 and band 4.5 glycoproteins of erythrocyte membrane in congenital dyserythropoietic anaemia type II
    • Scartezzini P, Forni GL, Baldi M, Izzo C, Sansone G. Decreased glycosylation of band 3 and band 4.5 glycoproteins of erythrocyte membrane in congenital dyserythropoietic anaemia type II. Br J Haematol 1982; 51: 569-576.
    • (1982) Br J Haematol , vol.51 , pp. 569-576
    • Scartezzini, P.1    Forni, G.L.2    Baldi, M.3    Izzo, C.4    Sansone, G.5
  • 70
    • 0020571298 scopus 로고
    • Incomplete glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (CDA II)
    • Mawby WJ, Tanner MJ, Anstee DJ, Clamp JR. Incomplete glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (CDA II). Br J Haematol 1983; 55: 357-368.
    • (1983) Br J Haematol , vol.55 , pp. 357-368
    • Mawby, W.J.1    Tanner, M.J.2    Anstee, D.J.3    Clamp, J.R.4
  • 71
    • 0021986428 scopus 로고
    • Abnormal fatty acid composition of erythrocyte glycosphingolipids in congenital dyserythropoietic anemia type II
    • Bouhours JF, Bouhours D, Delaunay J. Abnormal fatty acid composition of erythrocyte glycosphingolipids in congenital dyserythropoietic anemia type II. J Lipid Res 1985; 26: 435-441.
    • (1985) J Lipid Res , vol.26 , pp. 435-441
    • Bouhours, J.F.1    Bouhours, D.2    Delaunay, J.3
  • 72
    • 0023225205 scopus 로고
    • Glycolipids and glycopeptides of red cell membranes in congenital dyserythropoietic anaemia type II (CDA II)
    • Zdebska E, Anselstetter V, Pacuszka T et al. Glycolipids and glycopeptides of red cell membranes in congenital dyserythropoietic anaemia type II (CDA II). Br J Haematol 1987; 66: 385-391.
    • (1987) Br J Haematol , vol.66 , pp. 385-391
    • Zdebska, E.1    Anselstetter, V.2    Pacuszka, T.3
  • 73
    • 0022520245 scopus 로고
    • Anomalous clustering of underglycosylated band 3 in erythrocytes and their precursor cells in congenital dyserythropoietic anemia type II
    • Fukuda MN, Klier G, Yu J, Scartezzini P. Anomalous clustering of underglycosylated band 3 in erythrocytes and their precursor cells in congenital dyserythropoietic anemia type II. Blood 1986; 68: 521-529.
    • (1986) Blood , vol.68 , pp. 521-529
    • Fukuda, M.N.1    Klier, G.2    Yu, J.3    Scartezzini, P.4
  • 74
    • 0027081573 scopus 로고
    • Incompletely processed N-glycans of serum glycoproteins in congenital dyserythropoietic anaemia, type II (HEMPAS)
    • Fukuda MN, Gaetani GF, Izzo P, Scartezzini P, Dell A. Incompletely processed N-glycans of serum glycoproteins in congenital dyserythropoietic anaemia, type II (HEMPAS). Br J Haematol 1992; 82: 745-752.
    • (1992) Br J Haematol , vol.82 , pp. 745-752
    • Fukuda, M.N.1    Gaetani, G.F.2    Izzo, P.3    Scartezzini, P.4    Dell, A.5
  • 75
    • 0023227217 scopus 로고
    • Primary defect of congenital dyserythropoietic anemia type II. Failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N-acetylglucosaminyltransferase II
    • Fukuda MN, Dell A, Scartezzini P. Primary defect of congenital dyserythropoietic anemia type II. Failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N-acetylglucosaminyltransferase II. J Biol Chem 1987; 262: 7195-7206.
    • (1987) J Biol Chem , vol.262 , pp. 7195-7206
    • Fukuda, M.N.1    Dell, A.2    Scartezzini, P.3
  • 76
    • 0024506085 scopus 로고
    • Defective glycosylation of erythrocyte membrane glycoconjugates in a variant of congenital dyserythropoietic anemia type II: Association of low level of membrane-bound form of galactosyltransferase
    • Fukuda MN, Masri KA, Dell A, Thonar EJ, Klier G, Lowenthal RM. Defective glycosylation of erythrocyte membrane glycoconjugates in a variant of congenital dyserythropoietic anemia type II: association of low level of membrane-bound form of galactosyltransferase. Blood 1989; 73: 1331-1339.
    • (1989) Blood , vol.73 , pp. 1331-1339
    • Fukuda, M.N.1    Masri, K.A.2    Dell, A.3    Thonar, E.J.4    Klier, G.5    Lowenthal, R.M.6
  • 77
    • 0025607312 scopus 로고
    • HEMPAS disease: Genetic defect of glycosylation
    • Fukuda MN. HEMPAS disease: genetic defect of glycosylation. Glycobiology 1990; 1: 9-15.
    • (1990) Glycobiology , vol.1 , pp. 9-15
    • Fukuda, M.N.1
  • 78
    • 11944260919 scopus 로고
    • Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II
    • Fukuda MN, Masri KA, Dell A, Luzzatto L, Moremen KW. Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II. Proc Natl Acad Sci USA 1990; 87: 7443-7447.
    • (1990) Proc Natl Acad Sci USA , vol.87 , pp. 7443-7447
    • Fukuda, M.N.1    Masri, K.A.2    Dell, A.3    Luzzatto, L.4    Moremen, K.W.5
  • 80
    • 0030775892 scopus 로고    scopus 로고
    • Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II)
    • Iolascon A, de Giudice EM, Perrotta S, Granatiero M, Zelante L, Gasparini P. Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II). Blood 1997; 90: 4197-4200.
    • (1997) Blood , vol.90 , pp. 4197-4200
    • Iolascon, A.1    De Giudice, E.M.2    Perrotta, S.3    Granatiero, M.4    Zelante, L.5    Gasparini, P.6
  • 81
    • 16944367512 scopus 로고    scopus 로고
    • Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search
    • Gasparini P, del Giudice EM, Delaunay J et al. Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search. Am J Hum Genet 1997; 61: 1112-1116.
    • (1997) Am J Hum Genet , vol.61 , pp. 1112-1116
    • Gasparini, P.1    Del Giudice, E.M.2    Delaunay, J.3
  • 82
    • 0000738334 scopus 로고
    • Hereditary benign erythroreticulosis
    • Bergström I, Jacobsson L. Hereditary benign erythroreticulosis. Blood 1962; 19: 296-303.
    • (1962) Blood , vol.19 , pp. 296-303
    • Bergström, I.1    Jacobsson, L.2
  • 83
    • 0028869553 scopus 로고
    • Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25
    • Lind L, Sandström H, Wahlin A et al. Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25. Hum Mol Genet 1995; 4: 109-112.
    • (1995) Hum Mol Genet , vol.4 , pp. 109-112
    • Lind, L.1    Sandström, H.2    Wahlin, A.3
  • 84
  • 85
    • 0000289308 scopus 로고
    • Familial erythroid multinuclearity
    • Wolff JA, von Hofe FH. Familial erythroid multinuclearity. Blood 1951; 6: 1274-1283.
    • (1951) Blood , vol.6 , pp. 1274-1283
    • Wolff, J.A.1    Von Hofe, F.H.2
  • 86
    • 0019755203 scopus 로고
    • Diseritropoyesis congénita con polyploidía eritoblástica. A propósito de una variedad hallada en la Mesopotamia argentina
    • Accame EA, de Tezanos Pinto M. Diseritropoyesis congénita con polyploidía eritoblástica. A propósito de una variedad hallada en la Mesopotamia argentina. Sangre 1981; 26: 545-555.
    • (1981) Sangre , vol.26 , pp. 545-555
    • Accame, E.A.1    De Tezanos Pinto, M.2
  • 87
    • 0028155927 scopus 로고
    • Intravascular haemolysis and increased prevalence of myeloma and monoclonal gammopathy in congenital dyserythropoietic anaemia, type III
    • Sandström H, Wahlin A, Eriksson M, Bergström I, Wickramasinghe, SN. Intravascular haemolysis and increased prevalence of myeloma and monoclonal gammopathy in congenital dyserythropoietic anaemia, type III. Eur J Haematol 1994; 52: 42-46.
    • (1994) Eur J Haematol , vol.52 , pp. 42-46
    • Sandström, H.1    Wahlin, A.2    Eriksson, M.3    Bergström, I.4    Wickramasinghe, S.N.5
  • 88
    • 0015370064 scopus 로고
    • Congenital dyserythropoietic anaemia, type III
    • Goudsmit R, Beckers D, de Bruijne JI et al. Congenital dyserythropoietic anaemia, type III. Br J Haematol 1972; 23: 97-105.
    • (1972) Br J Haematol , vol.23 , pp. 97-105
    • Goudsmit, R.1    Beckers, D.2    De Bruijne, J.I.3
  • 89
    • 0020382258 scopus 로고
    • A new case of congenital dyserythropoietic anaemia, type III: Studies of the cell cycle distribution and ultrastructure of erythroblasts and of nucleic acid synthesis in marrow cells
    • Wickramasinghe SN, Parry TE, Williams C, Bond AN, Hughes M, Crook S. A new case of congenital dyserythropoietic anaemia, type III: studies of the cell cycle distribution and ultrastructure of erythroblasts and of nucleic acid synthesis in marrow cells. J Clin Pathol 1982; 35: 1103-1109.
    • (1982) J Clin Pathol , vol.35 , pp. 1103-1109
    • Wickramasinghe, S.N.1    Parry, T.E.2    Williams, C.3    Bond, A.N.4    Hughes, M.5    Crook, S.6
  • 91
    • 0019061479 scopus 로고
    • Congenital dyserythropoietic anemia in treated Hodgkin's disease
    • Byrnes RK, Dhru R, Brady AM, Galen WP, Hopper B. Congenital dyserythropoietic anemia in treated Hodgkin's disease. Hum Pathol 1980; 11: 485-486.
    • (1980) Hum Pathol , vol.11 , pp. 485-486
    • Byrnes, R.K.1    Dhru, R.2    Brady, A.M.3    Galen, W.P.4    Hopper, B.5
  • 92
    • 0028322296 scopus 로고
    • Serum thymidine kinase in congenital dyserythropoietic anaemia type III
    • Sandström H, Wahlin A, Eriksson M, Bergström I. Serum thymidine kinase in congenital dyserythropoietic anaemia type III. Br J Haematol 1994; 87: 653-654.
    • (1994) Br J Haematol , vol.87 , pp. 653-654
    • Sandström, H.1    Wahlin, A.2    Eriksson, M.3    Bergström, I.4
  • 93
    • 0028337771 scopus 로고
    • Congenital dyserythropoietic anemia type III with unbalanced globin chain synthesis
    • Villegas A, Gonzalez L, Furio V et al. Congenital dyserythropoietic anemia type III with unbalanced globin chain synthesis. Eur J Haematol 1994; 52: 251-253.
    • (1994) Eur J Haematol , vol.52 , pp. 251-253
    • Villegas, A.1    Gonzalez, L.2    Furio, V.3
  • 94
    • 9044251877 scopus 로고
    • Congenital dyserythropoietic anaemia, type III
    • Lewis SM, Verwilghen RL, eds. London: Academic Press
    • Goudsmit R. Congenital dyserythropoietic anaemia, type III. In: Lewis SM, Verwilghen RL, eds. Dyserythropoiesis. London: Academic Press, 1977: 83-92.
    • (1977) Dyserythropoiesis , pp. 83-92
    • Goudsmit, R.1
  • 95
    • 0017893847 scopus 로고
    • Congenital dyserythropoietic anaemia type III: An electron microscopic study
    • Björksten B, Holmgren G, Roos G, Stenling R. Congenital dyserythropoietic anaemia type III: an electron microscopic study. Br J Haematol 1978; 38: 37-42.
    • (1978) Br J Haematol , vol.38 , pp. 37-42
    • Björksten, B.1    Holmgren, G.2    Roos, G.3    Stenling, R.4
  • 96
    • 0018373473 scopus 로고
    • Some aspects of the biology of multinucleate and giant mononucleate erythroblasts in a patient with CDA, type III
    • Wickramasinghe SN, Goudsmit R. Some aspects of the biology of multinucleate and giant mononucleate erythroblasts in a patient with CDA, type III. Br J Haematol 1979; 41: 485-495.
    • (1979) Br J Haematol , vol.41 , pp. 485-495
    • Wickramasinghe, S.N.1    Goudsmit, R.2
  • 97
    • 0027252961 scopus 로고
    • Observations on two members of the Swedish family with congenital dyserythropoietic anaemia, type III
    • Wickramasinghe SN, Wahlin A, Anstee D et al. Observations on two members of the Swedish family with congenital dyserythropoietic anaemia, type III. Eur J Haematol 1993 ; 50: 213-221.
    • (1993) Eur J Haematol , vol.50 , pp. 213-221
    • Wickramasinghe, S.N.1    Wahlin, A.2    Anstee, D.3
  • 98
    • 0023282950 scopus 로고
    • Precipitation of beta-globin chains within the erythropoietic cells of a patient with congenital dyserythropoietic anemia, type III
    • Wickramasinghe SN, Goudsmit R. Precipitation of beta-globin chains within the erythropoietic cells of a patient with congenital dyserythropoietic anemia, type III [letter]. Br J Haematol 1987; 65: 250-251.
    • (1987) Br J Haematol , vol.65 , pp. 250-251
    • Wickramasinghe, S.N.1    Goudsmit, R.2
  • 99
    • 0031895307 scopus 로고    scopus 로고
    • Transfusion-dependent congenital dyserythropoietic anaemia with non-specific dysplastic changes in erythroblasts
    • Wickramasinghe SN, Vora AJ, Will A et al. Transfusion-dependent congenital dyserythropoietic anaemia with non-specific dysplastic changes in erythroblasts. Eur J Haematol 1998; 60: 140-142.
    • (1998) Eur J Haematol , vol.60 , pp. 140-142
    • Wickramasinghe, S.N.1    Vora, A.J.2    Will, A.3
  • 100
    • 0014704483 scopus 로고
    • The bilirubin shunt and shunt hyperbilirubinemia
    • Popper H, Schaffner F, eds. New York and London: Grune and Stratton Inc
    • Israels LG. The bilirubin shunt and shunt hyperbilirubinemia. In: Popper H, Schaffner F, eds. Progess in liver disease III. New York and London: Grune and Stratton Inc, 1970: 1-12.
    • (1970) Progess in Liver Disease III , pp. 1-12
    • Israels, L.G.1
  • 101
    • 0015610052 scopus 로고
    • Disturbed bone marrow cell proliferation in primary shunt hyperbilirubinaemia
    • Hamer JW, Fitzgerald PH. Disturbed bone marrow cell proliferation in primary shunt hyperbilirubinaemia. Blood 1973; 41: 539-547.
    • (1973) Blood , vol.41 , pp. 539-547
    • Hamer, J.W.1    Fitzgerald, P.H.2
  • 102
    • 0018321522 scopus 로고
    • Primary shunt hyperbilirubinemia with secondary iron overload: A case report
    • Frank DJ, Dusol M Jr, Schiff ER. Primary shunt hyperbilirubinemia with secondary iron overload: a case report. Gastroenterology 1979; 77: 754-757.
    • (1979) Gastroenterology , vol.77 , pp. 754-757
    • Frank, D.J.1    Dusol Jr., M.2    Schiff, E.R.3
  • 104
    • 0025857206 scopus 로고
    • Primary shunt hyperbilirubinaemia: A variant of the congenital dyserythropoietic anaemias
    • Bird AR, Knottenbelt E, Jacobs P, Maigrot J. Primary shunt hyperbilirubinaemia: a variant of the congenital dyserythropoietic anaemias. Postgrad Med J 1991; 67: 396-398.
    • (1991) Postgrad Med J , vol.67 , pp. 396-398
    • Bird, A.R.1    Knottenbelt, E.2    Jacobs, P.3    Maigrot, J.4
  • 105
    • 0029798353 scopus 로고    scopus 로고
    • 12- and folate-independent megaloblastic change and absence of the defining features of congenital dyserythropoietic anaemia types I or III
    • 12- and folate-independent megaloblastic change and absence of the defining features of congenital dyserythropoietic anaemia types I or III. Br J Haematol 1996; 95: 73-76.
    • (1996) Br J Haematol , vol.95 , pp. 73-76
    • Wickramasinghe, S.N.1    Andrews, V.E.2    O'Hea, A.M.3
  • 108
    • 0025992718 scopus 로고
    • Congenital dyserythropoietic anaemia with novel intra-erythroblastic and intra-erythrocytic inclusions
    • Wickramasinghe SN, Ilium N, Wimberley PD. Congenital dyserythropoietic anaemia with novel intra-erythroblastic and intra-erythrocytic inclusions. Br J Haematol 1991; 79: 322-330.
    • (1991) Br J Haematol , vol.79 , pp. 322-330
    • Wickramasinghe, S.N.1    Ilium, N.2    Wimberley, P.D.3
  • 109
    • 0027980006 scopus 로고
    • A novel form of congenital dyserythropoietic anaemia (CDA) associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]
    • Parsons SF, Jones J, Anstee DJ et al. A novel form of congenital dyserythropoietic anaemia (CDA) associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]. Blood 1994; 83: 860-868.
    • (1994) Blood , vol.83 , pp. 860-868
    • Parsons, S.F.1    Jones, J.2    Anstee, D.J.3
  • 110
    • 0027968603 scopus 로고
    • Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia
    • Agre P, Smith BL, Baumgarten R et al. Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia. J Clin Invest 1994; 94: 1050-1058.
    • (1994) J Clin Invest , vol.94 , pp. 1050-1058
    • Agre, P.1    Smith, B.L.2    Baumgarten, R.3
  • 111
    • 0018200696 scopus 로고
    • Congenital dyserythropoietic anaemia with unusual cytoplasmic inclusions
    • Kenny MW, Ibbotson RM, Hand MJ, Tector MJ. Congenital dyserythropoietic anaemia with unusual cytoplasmic inclusions. J Clin Pathol 1978; 31: 1228-1233.
    • (1978) J Clin Pathol , vol.31 , pp. 1228-1233
    • Kenny, M.W.1    Ibbotson, R.M.2    Hand, M.J.3    Tector, M.J.4
  • 112
    • 0023267797 scopus 로고
    • Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemia
    • Pothier B, Morlé L, Alloisio N et al. Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemia. Br J Haematol 1987; 66: 393-400.
    • (1987) Br J Haematol , vol.66 , pp. 393-400
    • Pothier, B.1    Morlé, L.2    Alloisio, N.3
  • 114
    • 0017346214 scopus 로고
    • Congenital dyserythropoietic anaemia: Response to splenectomy and quantitation of ineffective erythropoiesis
    • Samson D, Halliday D, Chanarin I. Congenital dyserythropoietic anaemia: response to splenectomy and quantitation of ineffective erythropoiesis. J Clin Pathol 1977; 30: 184-190.
    • (1977) J Clin Pathol , vol.30 , pp. 184-190
    • Samson, D.1    Halliday, D.2    Chanarin, I.3
  • 115
    • 0019414454 scopus 로고
    • Congenital dyserythropoietic anaemias: Splenectomy as a mode of therapy
    • Choudhry VP, Saraya AK, Kasturi J, Rath PK. Congenital dyserythropoietic anaemias: splenectomy as a mode of therapy. Acta Haematol 1981; 66: 195-201.
    • (1981) Acta Haematol , vol.66 , pp. 195-201
    • Choudhry, V.P.1    Saraya, A.K.2    Kasturi, J.3    Rath, P.K.4
  • 116
  • 117
    • 0022079241 scopus 로고
    • Type IV congenital dyserythropoietic anemia with an unusual response to splenectomy
    • Bird AR, Karabus CD, Hartley PS. Type IV congenital dyserythropoietic anemia with an unusual response to splenectomy. Am J Ped Hematol/Oncol 1985; 7: 196-199.
    • (1985) Am J Ped Hematol/Oncol , vol.7 , pp. 196-199
    • Bird, A.R.1    Karabus, C.D.2    Hartley, P.S.3


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