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226 related items for PubMed ID: 34396882

  • 1. IVS-II-16 (G>C) (HBB: c.315+16G>C) or IVS-II-666 (C>T) (HBB: c.316-185C>T) Mutations Trigger an Hb S (HBB: c.20A>T)/β+-Thalassemia Phenotype in an Hb S Trait Patient.
    Uçucu S, Karabıyık T, Azik FM.
    Hemoglobin; 2021 Jul; 45(4):225-227. PubMed ID: 34396882
    [Abstract] [Full Text] [Related]

  • 2. Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics.
    Belisário AR, Carneiro-Proietti AB, Sabino EC, Araújo A, Loureiro P, Máximo C, Flor-Park MV, Rodrigues DDOW, Ozahata MC, McClure C, Mota RA, Gomes Moura IC, Custer B, Kelly S, Recipient Epidemiology and Donor Evaluation Study (REDS-III) International Component Brazil.
    Hemoglobin; 2020 Jan; 44(1):1-9. PubMed ID: 32172616
    [Abstract] [Full Text] [Related]

  • 3. A Triple-Heterozygous β-Thalassemia Patient Demonstrated an Unusual Electrophoresis Pattern Due to a Novel β0 Mutation [an IVS-II-654 (C>T) mutation with a Hb Zürich-Langstrasse (HBB: c.151A>T) mutation in cis].
    Liao J, Li Q, Ling LQ, Liu CN, Huang XB, Zhou J.
    Hemoglobin; 2022 Jul; 46(4):249-252. PubMed ID: 35575165
    [Abstract] [Full Text] [Related]

  • 4. Profiling of 35 Cases of Hb S/Hb E (HBB: c.20A>T/HBB: c.79G>a), Disease and Association with α-Thalassemia and β-Globin Gene Cluster Haplotypes from Odisha, India.
    Dehury S, Mohanty PK, Patel S, Meher S, Das K, Purohit P, Sahoo S, Ratha J.
    Hemoglobin; 2021 Nov; 45(6):380-386. PubMed ID: 35243949
    [Abstract] [Full Text] [Related]

  • 5. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM.
    Hemoglobin; 2016 Nov; 40(2):75-84. PubMed ID: 26635043
    [Abstract] [Full Text] [Related]

  • 6. The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern Turkey.
    Yılmaz S.
    Hemoglobin; 2019 May; 43(3):174-181. PubMed ID: 31411089
    [Abstract] [Full Text] [Related]

  • 7. First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family.
    Murad H, Moassas F.
    Hemoglobin; 2019 Jan; 43(1):66-68. PubMed ID: 30843739
    [Abstract] [Full Text] [Related]

  • 8. β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey.
    Guzelgul F, Seydel GS, Aksoy K.
    Hemoglobin; 2020 Jul; 44(4):249-253. PubMed ID: 32664780
    [Abstract] [Full Text] [Related]

  • 9. The Spectrum of β-Thalassemia Mutations in a Population from the Brazilian Amazon.
    Silva AN, Cardoso GL, Cunha DA, Diniz IG, Santos SE, Andrade GB, Trindade SM, Cardoso Mdo S, Francês LT, Guerreiro JF.
    Hemoglobin; 2016 Jul; 40(1):20-4. PubMed ID: 26372288
    [Abstract] [Full Text] [Related]

  • 10. The Prevalence of HBB Mutations among the Transfusion-Dependent and Non Transfusion-Dependent Hb E/β-Thalassemia Children in a Tertiary Center of West Bengal, India.
    Saha J, Panja A, Nayek K.
    Hemoglobin; 2021 May; 45(3):157-162. PubMed ID: 34060430
    [Abstract] [Full Text] [Related]

  • 11. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
    Moassas F, Nweder MS, Murad H.
    BMC Pediatr; 2019 Feb 18; 19(1):61. PubMed ID: 30777047
    [Abstract] [Full Text] [Related]

  • 12. 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 18; 43(3):210-213. PubMed ID: 31456457
    [Abstract] [Full Text] [Related]

  • 13. The Frequency of HBB Mutations Among β-Thalassemia Patients in Hamadan Province, Iran.
    Jalilian M, Azizi Jalilian F, Ahmadi L, Amini R, Esfehani H, Sosanian M, Rabbani B, Maleki M, Mahdieh N.
    Hemoglobin; 2017 Jan 18; 41(1):61-64. PubMed ID: 28391758
    [Abstract] [Full Text] [Related]

  • 14. Characterization of the IVS-II-821 (A>C) (HBB: c.316-30A>C) Mutation in a β-Thalassemia Phenotype in Iran.
    Azimi A, Nejati P, Tahmasebi S, Alimoradi S, Alibakhshi R.
    Hemoglobin; 2019 Jan 18; 43(1):23-26. PubMed ID: 31146650
    [Abstract] [Full Text] [Related]

  • 15. β-Thalassemia major resulting from compound heterozygosity for HBB: c.92+2T>C [formerly known as IVS-I-2 (T>C)] and a novel β(0)-thalassemia frameshift mutation: HBB: c.209delG; p.Gly70Valfs*20.
    Kluge ML, Hoyer JD, Swanson KC, Oliveira JL.
    Hemoglobin; 2014 Jan 18; 38(4):292-4. PubMed ID: 24986053
    [Abstract] [Full Text] [Related]

  • 16. Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients.
    Azarkeivan A, Cohan N, Niazkar HR, Azizi A, Rad F.
    Hemoglobin; 2020 Mar 18; 44(2):109-112. PubMed ID: 32370567
    [Abstract] [Full Text] [Related]

  • 17. The Spectrum of β-Thalassemia Mutations in Hamadan Province, West Iran.
    Alibakhshi R, Moradi K, Aznab M, Azimi A, Shafieenia S, Biglari M.
    Hemoglobin; 2019 Jan 18; 43(1):18-22. PubMed ID: 31096791
    [Abstract] [Full Text] [Related]

  • 18. Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran.
    Miri-Moghaddam E, Bahrami S, Naderi M, Bazi A, Karimipoor M.
    Hemoglobin; 2016 Jun 18; 40(3):173-8. PubMed ID: 27117567
    [Abstract] [Full Text] [Related]

  • 19. Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India.
    Dehury S, Meher S, Patel S, Das K, Jana A, Bhattacharya S, Sahoo S, Sarkar B, Mohanty PK.
    Hemoglobin; 2019 Mar 18; 43(2):132-136. PubMed ID: 31190580
    [Abstract] [Full Text] [Related]

  • 20. The Spectrum of β-Thalassemia Mutations in the Population Migration in Lebanon: A 6-Year Retrospective Study.
    Farra C, Abdouni L, Souaid M, Awwad J, Yazbeck N, Abboud M.
    Hemoglobin; 2021 Nov 18; 45(6):365-370. PubMed ID: 33947296
    [Abstract] [Full Text] [Related]

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