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Rare Hereditary Hemolytic Anemias: Diagnostic Approach and Considerations in Management.
Risinger M, Emberesh M, Kalfa TA. Risinger M, et al. Hematol Oncol Clin North Am. 2019 Jun;33(3):373-392. doi: 10.1016/j.hoc.2019.01.002. Epub 2019 Mar 29. Hematol Oncol Clin North Am. 2019. PMID: 31030808 Review.
Congenital dyserythropoietic anemias (CDAs) are rare disorders of erythropoiesis characterized by binucleated and multinucleated erythroblasts in bone marrow. CDAs typically present with a hemolytic phenotype, as the produced RBCs have structural defects and decreas …
Congenital dyserythropoietic anemias (CDAs) are rare disorders of erythropoiesis characterized by binucleated and multinucleated e
Congenital dyserythropoietic anemia type II: molecular basis and clinical aspects.
Iolascon A, D'Agostaro G, Perrotta S, Izzo P, Tavano R, Miraglia del Giudice B. Iolascon A, et al. Haematologica. 1996 Nov-Dec;81(6):543-59. Haematologica. 1996. PMID: 9009444 Review.
It is transmitted by autosomal recessive inheritance and is characterized by the presence of a large number of multinucleate and binucleate erythroblasts in the bone marrow and typical morphological abnormalities of the membrane of circulating erythrocytes. ...
It is transmitted by autosomal recessive inheritance and is characterized by the presence of a large number of multinucleate and binu …
Congenital dyserythropoietic anemia type III.
Sandström H, Wahlin A. Sandström H, et al. Haematologica. 2000 Jul;85(7):753-7. Haematologica. 2000. PMID: 10897128 Review.
The clinical picture is characterized by hemolytic anemia and dramatic bone marrow changes dominated by active erythropoiesis with big multinucleated erythroblasts. The aim of this review is to describe the clinical manifestations, laboratory findings, and managemen …
The clinical picture is characterized by hemolytic anemia and dramatic bone marrow changes dominated by active erythropoiesis with big mu
[Hematological abnormalities in alcoholism].
Homann C, Hasselbalch HC. Homann C, et al. Ugeskr Laeger. 1992 Aug 3;154(32):2184-7. Ugeskr Laeger. 1992. PMID: 1509602 Review. Danish.
Other changes in the bone marrow are increased but ineffective erythropoiesis with defective iron metabolism, vacuolized pro-erythroblasts, multinucleated erythroblasts, megaloblasts and iron-containing plasma cells....
Other changes in the bone marrow are increased but ineffective erythropoiesis with defective iron metabolism, vacuolized pro-erythroblast
[Localized gene of the rare "Norrland disease". CDA-III blood disease with dominant heredity].
Sandström H, Wahlin A. Sandström H, et al. Lakartidningen. 1999 Jan 27;96(4):343-7. Lakartidningen. 1999. PMID: 10024825 Review. Swedish.
Bone marrow examination yields a characteristic picture of erythroid hyperplasia and multinucleate erythroblasts. A Swedish family affected with CDA-III has been reported to be characterised by a high prevalence of monoclonal gammopathy and angioid streaks, a triad …
Bone marrow examination yields a characteristic picture of erythroid hyperplasia and multinucleate erythroblasts. A Swedish fa …