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Quoted phrase not found in phrase index: "Congenital dyserythropoietic anemia type 4"
Page 1
A stepwise diagnostic approach for undiagnosed Anemia in children: A model for low-middle income country.
Aly NH, Elalfy MS, Elhabashy SA, Mowafy NM, Russo R, Andolfo I, Iolascon A, Ragab IA. Aly NH, et al. Blood Cells Mol Dis. 2023 Nov;103:102779. doi: 10.1016/j.bcmd.2023.102779. Epub 2023 Jul 16. Blood Cells Mol Dis. 2023. PMID: 37558589
BACKGROUND: Reaching a precise diagnosis in rare inherited anemia is extremely difficult and challenging, especially in areas with limited use of genetic studies, which makes undiagnosed anemia a unique clinical entity in tertiary hematology centers. ...In the normo …
BACKGROUND: Reaching a precise diagnosis in rare inherited anemia is extremely difficult and challenging, especially in areas with li …
Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosis.
Resnitzky P, Shaft D, Shalev H, Kapelushnik J, Dgany O, Krasnov T, Tamary H. Resnitzky P, et al. Eur J Haematol. 2017 Oct;99(4):366-371. doi: 10.1111/ejh.12931. Epub 2017 Aug 29. Eur J Haematol. 2017. PMID: 28755517
INTRODUCTION: Congenital dyserythropoietic anemias are rare blood disorders characterized by congenital anemia and a wide range of morphological and functional abnormalities of erythroid precursors. OBJECTIVES: To analyze the relative frequency of both …
INTRODUCTION: Congenital dyserythropoietic anemias are rare blood disorders characterized by congenital anemia a …
Managing the Unusual Causes of Fetal Anemia.
Maisonneuve E, Ben M'Barek I, Leblanc T, Da Costa L, Friszer S, Pernot F, Thomas P, Castaigne V, Toly N'Dour C, Mailloux A, Cortey A, Jouannic JM. Maisonneuve E, et al. Fetal Diagn Ther. 2020;47(2):156-164. doi: 10.1159/000501554. Epub 2019 Sep 10. Fetal Diagn Ther. 2020. PMID: 31505487
The fetuses received between 1 and 6 IUT (39% received at least 2 IUT). The definitive etiologies for central anemia were: congenital syphilis, neonatal poikilocytosis, type II congenital dyserythropoietic anemia (CDA), and neonatal hemoc …
The fetuses received between 1 and 6 IUT (39% received at least 2 IUT). The definitive etiologies for central anemia were: congeni …
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II).
Perrotta S, del Giudice EM, Carbone R, Servedio V, Schettini F Jr, Nobili B, Iolascon A. Perrotta S, et al. J Pediatr. 2000 Apr;136(4):556-9. doi: 10.1016/s0022-3476(00)90026-x. J Pediatr. 2000. PMID: 10753261 Review.
The molecular basis for the considerable variation of serum bilirubin levels and the incidence of gallstone formation in patients with congenital dyserythropoietic anemia (CDA) type II are unknown. We show that the combined effect of an increased bilir …
The molecular basis for the considerable variation of serum bilirubin levels and the incidence of gallstone formation in patients with co …
Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in a cohort of French children.
Bader-Meunier B, Leverger G, Tchernia G, Schischmanoff O, Cynober T, Bernaudin F, Leblanc T, Munzer M, Roda L, Soler C, Thuret I, Delaunay J. Bader-Meunier B, et al. J Pediatr Hematol Oncol. 2005 Aug;27(8):416-9. doi: 10.1097/01.mph.0000175406.42427.c9. J Pediatr Hematol Oncol. 2005. PMID: 16096522
Congenital dyserythropoietic anemia type I (CDA I) is a rare disorder of erythropoiesis. ...It should be sought in patients with unexplained chronic anemia, especially when associated with neonatal manifestations, jaundice, splenomegaly, subnorm …
Congenital dyserythropoietic anemia type I (CDA I) is a rare disorder of erythropoiesis. ...It should be sought …
Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation.
Heimpel H, Schwarz K, Ebnöther M, Goede JS, Heydrich D, Kamp T, Plaumann L, Rath B, Roessler J, Schildknecht O, Schmid M, Wuillemin W, Einsiedler B, Leichtle R, Tamary H, Kohne E. Heimpel H, et al. Blood. 2006 Jan 1;107(1):334-40. doi: 10.1182/blood-2005-01-0421. Epub 2005 Sep 1. Blood. 2006. PMID: 16141353 Free article.
Congenital dyserythropoietic anemia type I (CDA I) is a rare autosomal recessive disorder with ineffective erythropoiesis and iron overloading. ...Twenty-one patients with a confirmed diagnosis of CDA I exhibited chronic macrocytic anemia of var …
Congenital dyserythropoietic anemia type I (CDA I) is a rare autosomal recessive disorder with ineffective eryth …
Advances in the understanding of the congenital dyserythropoietic anaemias.
Wickramasinghe SN, Wood WG. Wickramasinghe SN, et al. Br J Haematol. 2005 Nov;131(4):431-46. doi: 10.1111/j.1365-2141.2005.05757.x. Br J Haematol. 2005. PMID: 16281933 Free article. Review.
The congenital dyserythropoietic anaemias (CDAs) are a heterogeneous group of diseases in which the anaemia is predominantly caused by dyserythropoiesis and marked ineffective erythropoiesis; three major (types I, II and III) and several minor subgroups have been id …
The congenital dyserythropoietic anaemias (CDAs) are a heterogeneous group of diseases in which the anaemia is predominantly c …
Natural history of congenital dyserythropoietic anemia type II.
Iolascon A, Delaunay J, Wickramasinghe SN, Perrotta S, Gigante M, Camaschella C. Iolascon A, et al. Blood. 2001 Aug 15;98(4):1258-60. doi: 10.1182/blood.v98.4.1258. Blood. 2001. PMID: 11493480 Free article.
Congenital dyserythropoietic anemia type II (CDA-II) is an autosomal recessive disease characterized by anemia, jaundice, splenomegaly, and erythroblast multinuclearity. ...Retrospective data were obtained using an appropriate questionnaire. The …
Congenital dyserythropoietic anemia type II (CDA-II) is an autosomal recessive disease characterized by anemi …
Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.
Scott C, Downes DJ, Brown JM, Beagrie R, Olijnik AA, Gosden M, Schwessinger R, Fisher CA, Rose A, Ferguson DJP, Johnson E, Hill QA, Okoli S, Renella R, Ryan K, Brand M, Hughes J, Roy NBA, Higgs DR, Babbs C, Buckle VJ. Scott C, et al. Haematologica. 2021 Nov 1;106(11):2960-2970. doi: 10.3324/haematol.2020.260158. Haematologica. 2021. PMID: 33121234 Free PMC article.
The investigation of inherited disorders of erythropoiesis has elucidated many of the principles underlying the production of normal red blood cells and how this is perturbed in human disease. Congenital Dyserythropoietic Anaemia type 1 (CDA-I) is a ra …
The investigation of inherited disorders of erythropoiesis has elucidated many of the principles underlying the production of normal red blo …
28 results