These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

390 related items for PubMed ID: 31190580

  • 1. 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]

  • 2. 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]

  • 3. 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]

  • 4. 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]

  • 5. 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]

  • 6. 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]

  • 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. 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 Feb 18; 40(2):75-84. PubMed ID: 26635043
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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]

  • 11. 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]

  • 12. Coinheritance of a Rare Nucleotide Substitution on the β-Globin Gene and Other Known Mutations in the Globin Clusters: Management in Genetic Counseling.
    Vinciguerra M, Passarello C, Leto F, Crivello A, Fustaneo M, Cassarà F, Cannata M, Maggio A, Giambona A.
    Hemoglobin; 2016 Aug 18; 40(4):231-5. PubMed ID: 27258795
    [Abstract] [Full Text] [Related]

  • 13. Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran.
    Sajadpour Z, Amini-Farsani Z, Motovali-Bashi M, Yadollahi M, Khosravi-Farsani N.
    Hemoglobin; 2020 Jan 18; 44(1):27-30. PubMed ID: 31899996
    [Abstract] [Full Text] [Related]

  • 14. Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants.
    Gupta RB, Tiwary RS, Pande PL, Kutlar F, Oner C, Oner R, Huisman TH.
    Hemoglobin; 1991 Jan 18; 15(5):441-58. PubMed ID: 1802886
    [Abstract] [Full Text] [Related]

  • 15. Hemoglobinopathies in the Çukurova Region and Neighboring Provinces.
    Yuzbasioglu Ariyurek S, Yildiz SM, Yalin AE, Guzelgul F, Aksoy K.
    Hemoglobin; 2016 Jun 18; 40(3):168-72. PubMed ID: 26984585
    [Abstract] [Full Text] [Related]

  • 16. Coinheritance of Hb City of Hope (HBB: c.208G>A) and β-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (HBB: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization.
    Zhou JY, Jiang F, Li J, Chen GL, Li DZ.
    Hemoglobin; 2019 Mar 18; 43(2):145-147. PubMed ID: 31268351
    [Abstract] [Full Text] [Related]

  • 17. 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 Mar 18; 43(4-5):223-228. PubMed ID: 31603010
    [Abstract] [Full Text] [Related]

  • 18. 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 18; 44(2):128-130. PubMed ID: 32420772
    [Abstract] [Full Text] [Related]

  • 19. 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 18; 44(1):64-66. PubMed ID: 32124638
    [Abstract] [Full Text] [Related]

  • 20. 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 18; 40(5):300-303. PubMed ID: 27690257
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 20.