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251 related items for PubMed ID: 35243949

  • 1. 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]

  • 2. 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; 44(2):109-112. PubMed ID: 32370567
    [Abstract] [Full Text] [Related]

  • 3. 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; 43(2):132-136. PubMed ID: 31190580
    [Abstract] [Full Text] [Related]

  • 4. Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-Thalassemia.
    Dash PM, Sahu PK, Patel S, Mashon RS, Kharat KR, Mukherjee MB.
    Hemoglobin; 2018 Jul; 42(4):236-242. PubMed ID: 30486691
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. 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 May; 40(2):75-84. PubMed ID: 26635043
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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 18; 45(4):225-227. PubMed ID: 34396882
    [Abstract] [Full Text] [Related]

  • 9. 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 18; 44(1):1-9. PubMed ID: 32172616
    [Abstract] [Full Text] [Related]

  • 10. 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 18; 44(6):385-390. PubMed ID: 33222574
    [Abstract] [Full Text] [Related]

  • 11. Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients.
    Mahmoud T, Sahli C, Hadj Fredj S, Amri Y, Othmani R, Mohamed GS, Zein E, Messaoud T.
    Mol Genet Genomic Med; 2022 Oct 18; 10(10):e2048. PubMed ID: 36106931
    [Abstract] [Full Text] [Related]

  • 12. Unusual β-Globin Haplotype Distribution in Newborns from Bengo, Angola.
    Borges E, Tchonhi C, Couto CSB, Gomes V, Amorim A, Prata MJ, Brito M.
    Hemoglobin; 2019 May 18; 43(3):149-154. PubMed ID: 31394941
    [Abstract] [Full Text] [Related]

  • 13. Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift β-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2].
    Gueye Tall F, Martin C, Malick Ndour EH, Déme Ly I, Renoux C, Chillotti L, Veyrenche N, Connes P, Madieye Gueye P, Ndiaye Diallo R, Lacan P, Diagne I, Amadou Diop P, Cissé A, Lopez Sall P, Joly P.
    Hemoglobin; 2017 Mar 18; 41(2):89-95. PubMed ID: 28670947
    [Abstract] [Full Text] [Related]

  • 14. Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations.
    Qiu Y, Wei S, Hou W, Lai K, Zhu H, Li W, Li Q, Yang Z, Shu Q, Chen P, Mo W.
    Hemoglobin; 2023 Nov 18; 47(2):52-55. PubMed ID: 37309066
    [Abstract] [Full Text] [Related]

  • 15. First Report of Compound Heterozygosity for Hb S (HBB: c.20A>T) and Hb Haringey (HBB: c.131A>G).
    Ogu UO, Reyes Gil M, Tolu SS, Acharya SA, Minniti CP.
    Hemoglobin; 2021 Mar 18; 45(2):136-139. PubMed ID: 34134586
    [Abstract] [Full Text] [Related]

  • 16. 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 18; 43(1):52-55. PubMed ID: 31106603
    [Abstract] [Full Text] [Related]

  • 17. Sickle cell disease in the Kurdish population of northern Iraq.
    Al-Allawi NA, Jalal SD, Nerwey FF, Al-Sayan GO, Al-Zebari SS, Alshingaly AA, Markous RD, Jubrael JM, Hamamy H.
    Hemoglobin; 2012 Jan 18; 36(4):333-42. PubMed ID: 22686351
    [Abstract] [Full Text] [Related]

  • 18. Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A2 Levels.
    Satthakarn S, Panyasai S, Pornprasert S.
    Hemoglobin; 2020 Sep 18; 44(5):349-353. PubMed ID: 33023363
    [Abstract] [Full Text] [Related]

  • 19. Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.
    Jha AN, Mishra H, Verma HK, Pandey I, Lakkakula BVKS.
    Hemoglobin; 2018 Mar 18; 42(2):84-90. PubMed ID: 30200838
    [Abstract] [Full Text] [Related]

  • 20. 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 18; 43(1):66-68. PubMed ID: 30843739
    [Abstract] [Full Text] [Related]

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