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Journal Abstract Search

233 related items for PubMed ID: 32124638

  • 1. Hb Rush (HBB: c.304G>C): A Rare Variant Hemoglobin Mimicking the Hb S (HBB: c.20A>T) Variant on High Performance Liquid Chromatography.
    Mashon RS, Das R, Dhawan R, Kakkar N, Dhar T.
    Hemoglobin; 2020 Jan; 44(1):64-66. PubMed ID: 32124638
    [Abstract] [Full Text] [Related]

  • 2. A novel β-globin gene mutation HBB.c.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC.
    Edison ES, Sathya M, Rajkumar SV, Nair SC, Srivastava A, Shaji RV.
    Int J Lab Hematol; 2012 Oct; 34(5):556-8. PubMed ID: 22471768
    [Abstract] [Full Text] [Related]

  • 3. Hb Matera (HBB: c.167 T > A): A Second Case Detected in a Pregnant Chinese Woman by the Capillary Electrophoresis Method.
    Li YQ, Ye LH, Mo Y.
    Hemoglobin; 2016 Oct; 40(2):125-6. PubMed ID: 26911301
    [Abstract] [Full Text] [Related]

  • 4. An Unusual Compound Heterozygosity for Hb O-Arab (HBB: c.364G>A) and Hb D-Los Angeles (HBB: c.364G>C).
    van Gammeren AJ, Pelkmans L, Endschot CCWV, Roelofsen-de Beer RJAC, Harteveld CL.
    Hemoglobin; 2020 Jan; 44(1):61-63. PubMed ID: 31973650
    [Abstract] [Full Text] [Related]

  • 5. Hb Tianshui (HBB: C.119A > G) in Compound Heterozygosity with Hb S (HBB: C.20A > T) from Odisha, India.
    Meher S, Dehury S, Mohanty PK, Patel S, Pattanayak C, Bhattacharya S, Das K, Sarkar B.
    Hemoglobin; 2016 Aug; 40(4):270-2. PubMed ID: 27254408
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. First Report of a Coincidental Discovery of Hb Antibes-Juan-Les-Pins (HBB: c.349_350insGTGTGCTGGCCC) in a Greek Woman.
    Theodoridou S, Boutou E, Vyzantiadis TA, Balassopoulou A, Vlachaki E.
    Hemoglobin; 2020 Sep; 44(5):361-363. PubMed ID: 33267629
    [Abstract] [Full Text] [Related]

  • 9. Hb Midnapore [β53(D4)Ala→Val; HBB: c.161C>T]: A Novel Hemoglobin Variant with a Structural Abnormality Associated with IVS-I-5 (G>C) (HBB: c.92+5G>C) Found in a Bengali Indian Family.
    Panja A, Chowdhury P, Basu A.
    Hemoglobin; 2016 Sep; 40(5):300-303. PubMed ID: 27690257
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Coinheritance of Hb D-Punjab and β-thalassemia: diagnosis and implications in prenatal diagnosis.
    Das S, Mashon RS.
    Hemoglobin; 2015 Mar; 39(2):138-40. PubMed ID: 25666204
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. 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]

  • 14. 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]

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

  • 16. Interactions of unstable hemoglobin Rush with thalassemia and hemoglobin E result in thalassemia intermedia.
    Huang K, Ge S, Yi W, Bi H, Lin K, Sun H, Huang X, Chu J, Ma S, Yang Z.
    Hematology; 2019 Dec; 24(1):459-466. PubMed ID: 31124399
    [Abstract] [Full Text] [Related]

  • 17. Novel Insights into Hb Shaare Zedek Associated with β0-Thalassemia: Molecular Characteristics, Genetic Origin and Diagnostic Approaches.
    Satthakarn S, Srisuwan W, Kunyanone N, Panyasai S.
    Int J Mol Sci; 2024 Aug 06; 25(16):. PubMed ID: 39201263
    [Abstract] [Full Text] [Related]

  • 18. Splice Acceptor Mutation [HBB:c.93-2A > T] in a Patient with Hb S/β0-Thalassemia.
    Waye JS, Hanna M, Nakamura L, Walker L, Eng B, Nfonsam LE.
    Hemoglobin; 2024 Mar 06; 48(2):116-117. PubMed ID: 38360540
    [Abstract] [Full Text] [Related]

  • 19. 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 06; 45(2):136-139. PubMed ID: 34134586
    [Abstract] [Full Text] [Related]

  • 20. Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a β-Thalassemia Major Phenotype.
    Martin G, Grimholt RM, Le D, Bechensteen AG, Klingenberg O, Fjeld B, Fourie T, Perrier R, Proven M, Henderson SJ, Roy NBA.
    Hemoglobin; 2021 Jul 06; 45(4):215-219. PubMed ID: 34311670
    [Abstract] [Full Text] [Related]

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