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Journal Abstract Search

125 related items for PubMed ID: 38360540

  • 21. 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; 45(2):136-139. PubMed ID: 34134586
    [Abstract] [Full Text] [Related]

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

  • 23. 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]

  • 24. First Detection of a Splice Site β-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family.
    Chen B, Huang P, Yi S, Chen Q, Tang Y, Zhang Q, He S.
    Hemoglobin; 2015 Jul; 39(3):207-8. PubMed ID: 25856402
    [Abstract] [Full Text] [Related]

  • 25. 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; 43(3):149-154. PubMed ID: 31394941
    [Abstract] [Full Text] [Related]

  • 26. A Case Report of Compound Heterozygosity for β0/β+-Thalassemia Resulting from under Diagnosed β-Thalassemia Found in a Hb A'2 Sample.
    Intasai N, Phasit A, Panyasai S, Pornprasert S.
    Hemoglobin; 2019 Jan; 43(1):63-65. PubMed ID: 31037981
    [Abstract] [Full Text] [Related]

  • 27. 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; 43(1):23-26. PubMed ID: 31146650
    [Abstract] [Full Text] [Related]

  • 28. Non-thalassemic phenotype associated with the -83 (G > A) mutation of the β-globin gene promoter (HBB: c.-133G > A).
    Waye JS, Eng B, Hanna M, Hohenadel BA, Nakamura LN, Walker L.
    Hemoglobin; 2014 Jan; 38(6):447-8. PubMed ID: 25405919
    [Abstract] [Full Text] [Related]

  • 29. β0-Thalassemia Caused by a Novel Nonsense Mutation [HBB:c.199A > T].
    Waye JS, Hanna M, Hohenadel BA, Nakamura L, Walker L, Eng B, Nfonsam LE.
    Hemoglobin; 2024 Jan; 48(1):69-70. PubMed ID: 38425097
    [Abstract] [Full Text] [Related]

  • 30. Mutational Profile of Homozygous β-Thalassemia in Rio de Janeiro, Brazil.
    Carrocini GCS, Venancio LPR, Pessoa VLR, Lobo CLC, Bonini-Domingos CR.
    Hemoglobin; 2017 Jan; 41(1):12-15. PubMed ID: 28366028
    [Abstract] [Full Text] [Related]

  • 31. Compound Heterozygosity for Hb Alperton (HBB: c.407C>T) and IVS-I-5 (G>C) (HBB: c.92+5G>C) Mutations Presenting as a Moderate Anemia in an Indian Family.
    Godbole KG, Ramachandran A, Karkamkar AS, Dalal AB.
    Hemoglobin; 2018 Mar; 42(2):141-142. PubMed ID: 29651865
    [Abstract] [Full Text] [Related]

  • 32. A Clinical Update of the Hb Siirt [β27(B9)Ala→Gly; HBB: c.83C>G] Hemoglobin Variant.
    Cappabianca MP, Colosimo A, Sabatucci A, Dainese E, Di Biagio P, Piscitelli R, Sarra O, Zei D, Amato A.
    Hemoglobin; 2017 Jan; 41(1):53-55. PubMed ID: 28391745
    [Abstract] [Full Text] [Related]

  • 33. Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β0-Thalassemia in a Chinese Patient with β-Thalassemia Intermedia.
    Li Y, Yan JM, Zhou JY, Lu YC, Li DZ.
    Hemoglobin; 2017 Jan; 41(1):47-49. PubMed ID: 28366026
    [Abstract] [Full Text] [Related]

  • 34. 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]

  • 35. Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia.
    Vinciguerra M, Passarello C, Cassarà F, Leto F, Cannata M, Calvaruso G, Di Maggio R, Renda D, Maggio A, Giambona A.
    Int J Lab Hematol; 2016 Feb; 38(1):17-26. PubMed ID: 26418075
    [Abstract] [Full Text] [Related]

  • 36. Compound Heterozygosity for a Novel Mutation Codon 104 (-A) (HBB: c.313delA) and Codons 41/42 (-CTTT) (HBB: c.126_129delCTTT) Leading to β-Thalassemia Major in a Chinese Family.
    Qiu Y, Huang Y, Chen P, Wei S, Su Q, Zhang Z, Yang Z, Ye L, Huang J, Shen X, Mo W.
    Hemoglobin; 2020 Nov; 44(6):402-405. PubMed ID: 33198537
    [Abstract] [Full Text] [Related]

  • 37. A novel promoter mutation (HBB: c.-75G>T) was identified as a cause of β(+)-thalassemia.
    Li Z, Li L, Yao Y, Li N, Li Y, Zhang Z, Yan F, Qiu H, Wu C, Zhang Z.
    Hemoglobin; 2015 Nov; 39(2):115-20. PubMed ID: 25657036
    [Abstract] [Full Text] [Related]

  • 38. Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study.
    Kolliopoulou A, Siamoglou S, John A, Sgourou A, Kourakli A, Symeonidis A, Vlachaki E, Chalkia P, Theodoridou S, Ali BR, Katsila T, Patrinos GP, Papachatzopoulou A.
    Hemoglobin; 2019 Jan; 43(1):27-33. PubMed ID: 31039620
    [Abstract] [Full Text] [Related]

  • 39. A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (HBB: c.27delG) in a Bangladeshi Family Acquired De Novo.
    Hasan KN, Sufian A, Mazumder AK, Khaleque MA, Rahman M, Akhteruzzaman S.
    Hemoglobin; 2019 May; 43(3):162-165. PubMed ID: 31339392
    [Abstract] [Full Text] [Related]

  • 40. Dominant β-Thalassemia Phenotype Caused by Hb Dieppe (HBB: c.383A>G): Another Case Report.
    Chen HQ, Wu LS, Jiang F, Li DZ.
    Hemoglobin; 2021 Sep; 45(5):329-331. PubMed ID: 34957901
    [Abstract] [Full Text] [Related]

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