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Journal Abstract Search

312 related items for PubMed ID: 31603010

  • 1. Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15).
    Abdaoui W, Benouareth DE, Djenouni A, Renoux C, Grifi F, Gouri A, Athamnia F, Benalioua M, Joly P.
    Hemoglobin; 2019; 43(4-5):223-228. PubMed ID: 31603010
    [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. 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; 41(2):89-95. PubMed ID: 28670947
    [Abstract] [Full Text] [Related]

  • 4. 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]

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

  • 6. Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
    Muszlak M, Pissard S, Badens C, Chamouine A, Maillard O, Thuret I.
    Hemoglobin; 2015 Mar; 39(3):156-61. PubMed ID: 25806420
    [Abstract] [Full Text] [Related]

  • 7. Hb A1c Determination by Capillary Electrophoresis is an Efficient Method for Detecting β-Thalassemias and Hemoglobin Variants.
    Orts JA, Zúñiga Á, Bello Y, Fabregat AB, Vicente AI.
    Hemoglobin; 2016 Sep; 40(5):335-340. PubMed ID: 27535164
    [Abstract] [Full Text] [Related]

  • 8. 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; 42(2):84-90. PubMed ID: 30200838
    [Abstract] [Full Text] [Related]

  • 9. Molecular Understanding of Severe Cases of β-Thalassemia in the Nablus Region, West Bank, Palestine.
    Samha L, Sirdah MM, Reading NS, Karmi B, Agarwal AM.
    Hemoglobin; 2020 Mar; 44(2):128-130. PubMed ID: 32420772
    [Abstract] [Full Text] [Related]

  • 10. 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 Mar; 40(1):20-4. PubMed ID: 26372288
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. 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]

  • 13. 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]

  • 14. Hemoglobinopathies in the Çukurova Region and Neighboring Provinces.
    Yuzbasioglu Ariyurek S, Yildiz SM, Yalin AE, Guzelgul F, Aksoy K.
    Hemoglobin; 2016 Jun; 40(3):168-72. PubMed ID: 26984585
    [Abstract] [Full Text] [Related]

  • 15. Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population.
    Ben Charfeddine I, Ben Lazreg T, M'sakni A, Amara A, Mlika A, Chaïeb A, Hlel K, Zouari N, Zbidi F, Bouguila J, Soyah N, Ayedi A, Ben Hamouda H, Abroug S, Boughamoura L, Saad A, Gribaa M.
    Hemoglobin; 2015 Jun; 39(4):251-5. PubMed ID: 26016902
    [Abstract] [Full Text] [Related]

  • 16. 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; 43(1):18-22. PubMed ID: 31096791
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.
    Murad H, Moassas F, Jarjour R, Mukhalalaty Y, Al-Achkar W.
    Hemoglobin; 2014 Jul; 38(6):390-3. PubMed ID: 25405916
    [Abstract] [Full Text] [Related]

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

  • 20. The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.
    Charoenkwan P, Teerachaimahit P, Sanguansermsri T.
    Hemoglobin; 2014 Jun; 38(5):335-8. PubMed ID: 25238043
    [Abstract] [Full Text] [Related]

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