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Journal Abstract Search

232 related items for PubMed ID: 31030808

  • 1. Rare Hereditary Hemolytic Anemias: Diagnostic Approach and Considerations in Management.
    Risinger M, Emberesh M, Kalfa TA.
    Hematol Oncol Clin North Am; 2019 Jun; 33(3):373-392. PubMed ID: 31030808
    [Abstract] [Full Text] [Related]

  • 2. Congenital dyserythropoietic anemia type 1 with a novel mutation in the CDAN1 gene previously diagnosed as congenital hemolytic anemia.
    Fujino H, Doisaki S, Park YD, Hama A, Muramatsu H, Kojima S, Sumimoto S.
    Int J Hematol; 2013 May; 97(5):650-3. PubMed ID: 23605369
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  • 3. Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias.
    Shefer Averbuch N, Steinberg-Shemer O, Dgany O, Krasnov T, Noy-Lotan S, Yacobovich J, Kuperman AA, Kattamis A, Ben Barak A, Roth-Jelinek B, Chubar E, Shabad E, Dufort G, Ellis M, Wolach O, Pazgal I, Abu Quider A, Miskin H, Tamary H.
    Eur J Haematol; 2018 Sep; 101(3):297-304. PubMed ID: 29786897
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  • 4. The congenital dyserythropoietic anemias.
    Renella R, Wood WG.
    Hematol Oncol Clin North Am; 2009 Apr; 23(2):283-306. PubMed ID: 19327584
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  • 7. Confounding factors in the diagnosis and clinical course of rare congenital hemolytic anemias.
    Fattizzo B, Giannotta JA, Cecchi N, Barcellini W.
    Orphanet J Rare Dis; 2021 Oct 09; 16(1):415. PubMed ID: 34627331
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  • 8. Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia.
    Hamada M, Doisaki S, Okuno Y, Muramatsu H, Hama A, Kawashima N, Narita A, Nishio N, Yoshida K, Kanno H, Manabe A, Taga T, Takahashi Y, Miyano S, Ogawa S, Kojima S.
    Int J Hematol; 2018 Sep 09; 108(3):306-311. PubMed ID: 29936674
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  • 10. Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients.
    Zaninoni A, Fermo E, Vercellati C, Consonni D, Marcello AP, Zanella A, Cortelezzi A, Barcellini W, Bianchi P.
    Front Physiol; 2018 Sep 09; 9():451. PubMed ID: 29755372
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  • 11. Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias.
    Russo R, Iolascon A, Andolfo I, Marra R, Rosato BE.
    Int J Lab Hematol; 2024 Aug 09; 46(4):595-605. PubMed ID: 38747503
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  • 13. Congenital dyserythropoietic anemias.
    Marks PW, Mitus AJ.
    Am J Hematol; 1996 Jan 09; 51(1):55-63. PubMed ID: 8571938
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  • 14. [Genetic diagnosis for congenital hemolytic anemia].
    Ohga S.
    Rinsho Ketsueki; 2016 Jan 09; 57(10):1908-1912. PubMed ID: 27725587
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  • 15. Congenital dyserythropoietic anemias: molecular insights and diagnostic approach.
    Iolascon A, Heimpel H, Wahlin A, Tamary H.
    Blood; 2013 Sep 26; 122(13):2162-6. PubMed ID: 23940284
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  • 16. [Dyserythropoietic anemia].
    Fereberger W.
    Acta Med Austriaca Suppl; 1979 Sep 26; 6():281-6. PubMed ID: 299214
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  • 17. Congenital dyserythropoietic anemias: epidemiology, clinical significance, and progress in understanding their pathogenesis.
    Heimpel H.
    Ann Hematol; 2004 Oct 26; 83(10):613-21. PubMed ID: 15278299
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  • 18. Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR).
    Niss O, Lorsbach RB, Berger M, Chonat S, McLemore M, Buchbinder D, McCavit T, Shaffer LG, Simpson J, Schwartz JH, Meznarich J, Emberesh M, Seu KG, Zhang W, Kalfa TA, CDAR consortium.
    Blood Cells Mol Dis; 2021 Mar 26; 87():102534. PubMed ID: 33401150
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