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21 results

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Page 1
Morbidity and mortality of adult patients with congenital dyserythropoietic anemia type I.
Shalev H, Al-Athamen K, Levi I, Levitas A, Tamary H. Shalev H, et al. Eur J Haematol. 2017 Jan;98(1):13-18. doi: 10.1111/ejh.12778. Epub 2016 Jun 15. Eur J Haematol. 2017. PMID: 27206021
Congenital dyserythropoietic anemia type I (CDAI) is a rare autosomal recessive disease characterized by macrocytic anemia, ineffective erythropoiesis, and secondary hemochromatosis. ...
Congenital dyserythropoietic anemia type I (CDAI) is a rare autosomal recessive disease characterized by …
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
OBJECTIVES: To analyze the relative frequency of both light microscopic (LM) and electron microscopic (EM) morphological features of erythroblasts in a large group of patients with molecular proven congenital dyserythropoietic anemia type I (CDA …
OBJECTIVES: To analyze the relative frequency of both light microscopic (LM) and electron microscopic (EM) morphological features of erythro …
Glycophorin A in two patients with congenital dyserythropoietic anemia type I and type II is partly unglycosylated.
Zdebska E, Adamczyk-Popławska M, Kościelak J. Zdebska E, et al. Acta Biochim Pol. 2000;47(3):773-9. Acta Biochim Pol. 2000. PMID: 11310976
Glycophorins A from erythrocyte membranes of two patients with congenital dyserythropoietic anemia type I and type II (CDA type I and II) were analyzed for carbohydrate molar composition employing a modification of the recently published method …
Glycophorins A from erythrocyte membranes of two patients with congenital dyserythropoietic anemia type I …
Hepatic and cardiac iron load as determined by MRI T2* in patients with congenital dyserythropoietic anemia type I.
Asleh M, Levitas A, Daniel S, Abu-Quider A, Ben-Harosh M, Kapelushnik J. Asleh M, et al. Ann Hematol. 2020 Nov;99(11):2507-2512. doi: 10.1007/s00277-020-04263-4. Epub 2020 Sep 12. Ann Hematol. 2020. PMID: 32918595
Iron overload comprises one of the main complications of congenital dyserythropoietic anemia type I (CDA-I). When analyzing magnetic resonance imaging T2* (MRI T2*) results in CDA patients, two previous studies reported discordant results regard …
Iron overload comprises one of the main complications of congenital dyserythropoietic anemia type I (CDA- …
Pregnancy outcome in congenital dyserythropoietic anemia type I.
Shalev H, Avraham GP, Hershkovitz R, Levy A, Sheiner E, Levi I, Tamary H. Shalev H, et al. Eur J Haematol. 2008 Oct;81(4):317-21. doi: 10.1111/j.1600-0609.2008.01109.x. Epub 2008 Jun 28. Eur J Haematol. 2008. PMID: 18573172
OBJECTIVES: Congenital dyserythropoietic anemia type I (CDA I) is a rare inherited disease characterized by moderate to severe macrocytic anemia and abnormal erythroid precursors with nuclear chromatin bridges and spongy heterochromatin. ...
OBJECTIVES: Congenital dyserythropoietic anemia type I (CDA I) is a rare inherited disease characterized …
Fetal presentation of congenital dyserythropoietic anemia type 1 with novel compound heterozygous CDAN1 mutations.
Meznarich JA, Draper L, Christensen RD, Yaish HM, Luem ND, Pysher TJ, Jung G, Nemeth E, Ganz T, Ward DM. Meznarich JA, et al. Blood Cells Mol Dis. 2018 Jul;71:63-66. doi: 10.1016/j.bcmd.2018.03.002. Epub 2018 Mar 20. Blood Cells Mol Dis. 2018. PMID: 29599085 Free PMC article.
The congenital dyserythropoietic anemias are a heterogeneous group of disorders characterized by anemia and ineffective erythropoiesis. Congenital dyserythropoietic anemia type I (CDA1) can present in utero with hydrops fetalis, but more often i …
The congenital dyserythropoietic anemias are a heterogeneous group of disorders characterized by anemia and ineffective erythropoiesis. C …
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. ...
Congenital dyserythropoietic anemia type I (CDA I) is a rare autosomal recessive disorder with ineffectiv …
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. ...
Congenital dyserythropoietic anemia type I (CDA I) is a rare disorder of erythropoiesis. ...
Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.
Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Crétien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rössler J, Le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H. Dgany O, et al. Am J Hum Genet. 2002 Dec;71(6):1467-74. doi: 10.1086/344781. Epub 2002 Nov 14. Am J Hum Genet. 2002. PMID: 12434312 Free PMC article.
21 results