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Journal Abstract Search

362 related items for PubMed ID: 16840226

  • 21. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN.
    Hemoglobin; 2007; 31(2):233-41. PubMed ID: 17486506
    [Abstract] [Full Text] [Related]

  • 22. THE Hb S/beta+ -thalassemia phenotype demonstrates that the IVS-I (-2) (A>C) mutation is a mild beta-thalassemia allele.
    Schmugge M, Waye JS, Basran RK, Zurbriggen K, Frischknecht H.
    Hemoglobin; 2008; 32(3):303-7. PubMed ID: 18473247
    [Abstract] [Full Text] [Related]

  • 23. Prenatal diagnosis of beta-thalassemia/Hb E by hemoglobin typing compared to DNA analysis.
    Sirichotiyakul S, Saetung R, Sanguansermsri T.
    Hemoglobin; 2009; 33(1):17-23. PubMed ID: 19205969
    [Abstract] [Full Text] [Related]

  • 24. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
    Esteghamat F, Imanian H, Azarkeivan A, Pourfarzad F, Almadani N, Najmabadi H.
    Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
    [Abstract] [Full Text] [Related]

  • 25. Spectrum of beta thalassemia mutations and HbF levels in the heterozygous Moroccan population.
    Lemsaddek W, Picanço I, Seuanes F, Mahmal L, Benchekroun S, Khattab M, Nogueira P, Osório-Almeida L.
    Am J Hematol; 2003 Jul; 73(3):161-8. PubMed ID: 12827652
    [Abstract] [Full Text] [Related]

  • 26. Surface plasmon resonance-based molecular detection of Hb S [beta6(A3)Glu-->Val, GAG-->GTG] at the gene level.
    Atalay EO, Ustel E, Yildiz S, Atalay A.
    Hemoglobin; 2006 Jul; 30(3):385-91. PubMed ID: 16840230
    [Abstract] [Full Text] [Related]

  • 27. 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]

  • 28. Observation of a rare hemoglobin variant [Hb Lulu island, beta107(G9)Gly-->Asp, GGC-->GAC] co-inherited with a beta+-thalassemia mutation [IVS-I-110 (G-->A)] or in the heterozygous state in a Greek-Albanian family.
    Papassotiriou I, Stamoulakatou A, Wajcman H, Kister J, Dimisianos G, Lazaropoulou C, Kanavaki I, Vavourakis E, Kattamis A, Kanavakis E, Traeger-Synodinos J.
    Hemoglobin; 2006 Jun; 30(4):409-18. PubMed ID: 16987796
    [Abstract] [Full Text] [Related]

  • 29. Chromatographic measurements of hemoglobin A2 in blood samples that contain sickle hemoglobin.
    Shokrani M, Terrell F, Turner EA, Aguinaga MD.
    Ann Clin Lab Sci; 2000 Apr; 30(2):191-4. PubMed ID: 10807164
    [Abstract] [Full Text] [Related]

  • 30. 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 Apr; 38(6):390-3. PubMed ID: 25405916
    [Abstract] [Full Text] [Related]

  • 31. Delta-thalassemia in Cyprus.
    Pavlou E, Phylactides M, Kyrri A, Kalogerou E, Makariou C, Georgiou I, Kleanthous M.
    Hemoglobin; 2006 Apr; 30(4):455-62. PubMed ID: 16987800
    [Abstract] [Full Text] [Related]

  • 32. Phenotype and genotype frequency of β-thalassemia and sickle cell disease carriers in Halkidiki, Northern Greece.
    Kalleas C, Anagnostopoulos K, Sinopoulou K, Delaki E, Margaritis D, Bourikas G, Tsatalas C, Kortsaris A, Tentes I.
    Hemoglobin; 2012 Apr; 36(1):64-72. PubMed ID: 22188117
    [Abstract] [Full Text] [Related]

  • 33. First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders.
    Upadhye DS, Jain D, Nair SB, Nadkarni AH, Ghosh K, Colah RB.
    J Clin Pathol; 2012 Jul; 65(7):654-9. PubMed ID: 22461654
    [Abstract] [Full Text] [Related]

  • 34. Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion.
    Harteveld CL, Versteegh FG, van Leer EH, Starreveld JS, Kok PJ, van Rooijen-Nijdam I, van Delft P, Zanella-Cleon I, Becchi M, Wajcman H, Giordano PC.
    Hemoglobin; 2007 Jul; 31(3):313-23. PubMed ID: 17654068
    [Abstract] [Full Text] [Related]

  • 35. Spectrum of β-thalassemia mutations in the eastern province of Saudi Arabia.
    Al-Sultan A, Phanasgaonkar S, Suliman A, Al-Baqushi M, Nasrullah Z, Al-Ali A.
    Hemoglobin; 2011 Jul; 35(2):125-34. PubMed ID: 21417569
    [Abstract] [Full Text] [Related]

  • 36. Heterozygous Hb Hope [beta136(H14)Gly --> Asp] in association with heterozygous beta0-thalassemia with apparent homozygous expression, in a Spanish patient.
    Beneitez D, Carrera A, Duran-Suárez JR, Paz V, León A, García Talavera J.
    Hemoglobin; 2006 Jul; 30(1):45-9. PubMed ID: 16540415
    [Abstract] [Full Text] [Related]

  • 37. Hemoglobinopathy carrier prevalence in the United Arab Emirates: first analysis of the Dubai Health Authority premarital screening program results.
    Belhoul KM, Abdulrahman M, Alraei RF.
    Hemoglobin; 2013 Jul; 37(4):359-68. PubMed ID: 23647352
    [Abstract] [Full Text] [Related]

  • 38. Hb A2' (Hb B2) in the Omani population and diagnostic significance.
    Daar S, Al Zadjali S, Gravell D, Al Haddabi H, Al Riyami M, Al Belushi A, Berbar T, Krishnamoorthy R.
    Hemoglobin; 2011 Jul; 35(2):117-24. PubMed ID: 21417568
    [Abstract] [Full Text] [Related]

  • 39. Detection of two rare beta-thalassemia alleles found in the Tunisian population: codon 47 (+A) and codons 106/107 (+G).
    Bibi A, Messaoud T, Beldjord C, Fattoum S.
    Hemoglobin; 2006 Jul; 30(4):437-47. PubMed ID: 16987798
    [Abstract] [Full Text] [Related]

  • 40. DNA haplotypes in Africans and West Indians with sickle cell anaemia or SC disease.
    Konstantopoulos K, Vulliamy T, Swirsky D, Reeves JD, Kaeda J, Luzzatto L.
    Gene Geogr; 1996 Apr; 10(1):19-24. PubMed ID: 8913718
    [Abstract] [Full Text] [Related]

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