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Journal Abstract Search

365 related items for PubMed ID: 15224363

  • 1. Hydrops fetalis associated with homozygosity for hemoglobin Taybe (alpha 38/39 THR deletion) in newborn triplets.
    Arnon S, Tamary H, Dgany O, Litmanovitz I, Regev R, Bauer S, Dolfin T, Yacobovich J, Wolach B, Jaber L.
    Am J Hematol; 2004 Jul; 76(3):263-6. PubMed ID: 15224363
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  • 2. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
    Karnpean R, Fucharoen G, Fucharoen S, Sae-ung N, Sanchaisuriya K, Ratanasiri T.
    Acta Haematol; 2009 Jul; 121(4):227-33. PubMed ID: 19546525
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  • 3. Anemia and hydrops in a fetus with homozygous hemoglobin constant spring.
    Charoenkwan P, Sirichotiyakul S, Chanprapaph P, Tongprasert F, Taweephol R, Sae-Tung R, Sanguansermsri T.
    J Pediatr Hematol Oncol; 2006 Dec; 28(12):827-30. PubMed ID: 17164653
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  • 4. Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygous.
    Galacteros F, Girodon E, M'Rad A, Martin J, Goossens M, Jaber L, Cohen IJ, Tamary H, Goshen Y, Zaizov R.
    C R Acad Sci III; 1994 May; 317(5):437-44. PubMed ID: 7994622
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  • 5. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N, Pinmuang-Ngam C, Fucharoen G, Fucharoen S.
    Fetal Diagn Ther; 2007 May; 22(4):264-8. PubMed ID: 17369692
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  • 7. Hydrops fetalis due to homozygosity for alpha-thalassemia-1, -(alpha)-20.5 kb: the first observation in a Turkish family.
    Gurgey A, Altay C, Beksaç MS, Bhattacharya R, Kutlar F, Huisman TH.
    Acta Haematol; 1989 May; 81(3):169-71. PubMed ID: 2496567
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  • 8. Hemoglobin barts hydrops fetalis syndrome.
    Bowman E, Watts J, Burrows R, Chui DH.
    Haematologia (Budap); 1987 May; 20(3):125-30. PubMed ID: 3692334
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  • 10. First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child.
    Paglietti ME, Sollaino MC, Loi D, Barella S, Desogus MF, Galanello R.
    Hemoglobin; 2012 May; 36(3):299-304. PubMed ID: 22428534
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  • 11. Homozygosity for the Mediterranean a-thalassemic deletion (hemoglobin Barts hydrops fetalis).
    Al-Allawi NA, Shamdeen MY, Rasheed NS.
    Ann Saudi Med; 2010 May; 30(2):153-5. PubMed ID: 20220267
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  • 12. Prenatal diagnosis of Hb Bart's hydrops fetalis by PCR technique: Pramongkutklao experience.
    Torcharus K, Sriphaisal T, Krutvecho T, Ketupanya A, Vuthiwong C, Suwanasophon C, Noonai A.
    Southeast Asian J Trop Med Public Health; 1995 May; 26 Suppl 1():287-90. PubMed ID: 8629126
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  • 13. Rapid prenatal diagnosis of Hb Bart's hydrops fetalis in southeast Asia area by polymerase chain reaction.
    Chang JG, Chen CP, Ho HJ, Lin CP, Lee LS, Chen PH.
    Int J Hematol; 1992 Oct; 56(2):155-9. PubMed ID: 1421177
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  • 17. Screening for (--SEA) alpha-globin gene deletion in beta-thalassemia carriers and prevention of hydrops fetalis.
    Kwan Ma ES, Yin Chan AY, Yin Ha S, Fung Chan GC, Lung Lau Y, Chan LC.
    Haematologica; 2000 Sep; 85(9):991-3. PubMed ID: 10980643
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