These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

326 related items for PubMed ID: 28413893

  • 1. The Hb E (HBB: c.79G>A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/- -SEA α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels.
    Leckngam P, Limweeraprajak E, Kiewkarnkha T, Tatu T.
    Hemoglobin; 2017 Jan; 41(1):38-43. PubMed ID: 28413893
    [Abstract] [Full Text] [Related]

  • 2. Effective screening for double heterozygosity of Hb E/alpha0-thalassemia.
    Sanchaisuriya K, Chirakul S, Srivorakun H, Fucharoen G, Fucharoen S, Changtrakul Y, Sanchaisuriya P.
    Ann Hematol; 2008 Nov; 87(11):911-4. PubMed ID: 18575861
    [Abstract] [Full Text] [Related]

  • 3. Comprehensive screening for coexisting heterozygous α0-thalassemia in hemoglobin E trait.
    Polprasert C, Wongprachar P, Suksusut A, Settapiboon R, Amornsirivat S, Sophonphan J, Uaprasert N, Sucharitchan P, Rojnuckarin P.
    Hematology; 2020 Dec; 25(1):276-279. PubMed ID: 32633642
    [Abstract] [Full Text] [Related]

  • 4. Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn, HBB: c.[79G>A;198G>C]): A Novel β-Thalassemic Hemoglobin Variant.
    Satthakarn S, Boonmee S, Panyasai S.
    Hemoglobin; 2020 Nov; 44(6):385-390. PubMed ID: 33222574
    [Abstract] [Full Text] [Related]

  • 5. Double Heterozygosity for Hb Durham-N.C. (HBB: c.344T>C) [β114(G16)Leu→Pro] and the IVS-I-110 (HBB: c.93-21G>A) Causing a Severe β-Thalassemia Phenotype.
    Cannata M, Cassarà F, Vinciguerra M, Licari P, Passarello C, Leto F, Lo Pinto C, Pitrolo L, Ganci R, Maggio A, Giambona A.
    Hemoglobin; 2019 May; 43(3):210-213. PubMed ID: 31456457
    [Abstract] [Full Text] [Related]

  • 6. Hb A2/E levels found in co-inheritance with the α-thalassemia-1 - -(SEA)/type deletion and either Hb E or β-thalassemia.
    Pornprasert S, Treesuwan K, Punyamung M, Kongthai K.
    Hemoglobin; 2012 May; 36(4):381-7. PubMed ID: 22563848
    [Abstract] [Full Text] [Related]

  • 7. Complex interaction of Hb Hekinan [alpha27(B8) Glu-Asp] and Hb E [beta26(B8) Glu-Lys] with a deletional alpha-thalassemia 1 in a Thai family.
    Fucharoen S, Changtrakun Y, Ratanasiri T, Fucharoen G, Sanchaisuriya K.
    Eur J Haematol; 2003 May; 70(5):304-9. PubMed ID: 12694166
    [Abstract] [Full Text] [Related]

  • 8. Hb Westmead (HBA2: c.369C>G): Hematological Characteristics in Heterozygotes with and without α0-Thalassemia.
    Jiang F, Ju AP, Li J, Chen GL, Zhou JY, Tang XW, Zuo LD, Li DZ.
    Hemoglobin; 2020 May; 44(3):153-155. PubMed ID: 32436451
    [Abstract] [Full Text] [Related]

  • 9. Hematological characterization of compound heterozygous hemoglobin Hope/E patients with and without alpha-thalassemia-1 SEA type deletion.
    Pornprasert S.
    Clin Lab; 2013 May; 59(9-10):1183-5. PubMed ID: 24273946
    [Abstract] [Full Text] [Related]

  • 10. Population Screening and Prevention Strategies for Thalassemias and other Hemoglobinopathies of Eastern India: Experience of 18,166 cases.
    Chatterjee T, Chakravarty A, Chakravarty S.
    Hemoglobin; 2015 May; 39(6):384-8. PubMed ID: 26428539
    [Abstract] [Full Text] [Related]

  • 11. A Novel Mutation of the α2-Globin Gene Causing α+-Thalassemia: Hb Nanning (HBA2: c.369_370delinsGA).
    Chen B, Lin L, Yi S, Chen Q, Wei H, Li G, Zheng C, He S, Qiu X.
    Hemoglobin; 2017 Jan; 41(1):56-58. PubMed ID: 28395547
    [Abstract] [Full Text] [Related]

  • 12. Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2.
    Nuinoon M, Thipthara O, Fucharoen S.
    Hemoglobin; 2019 Jan; 43(1):52-55. PubMed ID: 31106603
    [Abstract] [Full Text] [Related]

  • 13. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene.
    Panyasai S, Jaiping K, Pornprasert S.
    Hemoglobin; 2015 Jan; 39(4):292-5. PubMed ID: 26029792
    [Abstract] [Full Text] [Related]

  • 14. Mutation spectrum and erythrocyte indices characterisation of α-thalassaemia and β-thalassaemia in Sichuan women in China: a thalassaemia screening survey of 42 155 women.
    Li B, Han X, Ma J, Yang D.
    J Clin Pathol; 2021 Mar; 74(3):182-186. PubMed ID: 32719015
    [Abstract] [Full Text] [Related]

  • 15. Hematological and Molecular Characterization of a Novel Hb A2 Variant with Homozygous α-Thalassemia-2 in a Southern Thai Individual.
    Nuinoon M, Jeenduang N, Kesornsit A, Horpet D, Plyduang T.
    Hemoglobin; 2017 May; 41(3):213-215. PubMed ID: 28795619
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. [The value of MCV, MCH and HbA(2) in laboratory screening of thalassemia].
    Li LY, Li Q, Song LL, Jin WJ, Ma ZH, Yu YH, Zhong M.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):96-100. PubMed ID: 22455739
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 17.