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Anemia

Free Subscription Articles published in Hemoglobin Retrieve available abstracts of 107 articles: HTML format Text format

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January 2011
1. LIAO C , Zhou JY, Xie XM, Li DZ, et al
   Screening for Hb Constant Spring in the Guangdong Province, South China, using the Sebia capillary electrophoresis system.
   Hemoglobin. 2011;35:87-90.
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2. WAYE JS , Nakamura-Garrett LM, Eng B, Kanavakis E, et al
   beta+-Thalassemia trait due to a novel mutation in the beta-globin gene promoter: -26 (A>C) [HBB c.-76A>C].
   Hemoglobin. 2011;35:84-6.
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3. GUZMAN LF , Perea FJ, Morales-Gonzalez KR, Sanchez-Lopez JY, et al
   Characterization of the 5' and 3' breakpoints of the Spanish (deltabeta)0-thalassemia deletion in Mexican patients.
   Hemoglobin. 2011;35:80-3.
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4. ABDALLA MY , Fawzi M, Al-Maloul SR, El-Banna N, et al
   Increased oxidative stress and iron overload in Jordanian beta-thalassemic children.
   Hemoglobin. 2011;35:67-79.
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5. ZACHAKI S , Vrettou C, Destouni A, Kokkali G, et al
   Novel and known microsatellite markers within the beta-globin cluster to support robust preimplantation genetic diagnosis of beta-thalassemia and sickle cell syndromes.
   Hemoglobin. 2011;35:56-66.
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6. MENDILCIOGLU I , Yakut S, Keser I, Simsek M, et al
   Prenatal diagnosis of beta-thalassemia and other hemoglobinopathies in southwestern Turkey.
   Hemoglobin. 2011;35:47-55.
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7. EBRAHIMKHANI S , Azarkeivan A, Bayat N, Houry-Parvin M, et al
   Genotype-phenotype correlation in Iranian patients with Hb H disease.
   Hemoglobin. 2011;35:40-6.
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8. ZHENG CG , Liu M, Du J, Chen K, et al
   Molecular spectrum of alpha- and beta-globin gene mutations detected in the population of Guangxi Zhuang Autonomous Region, People's Republic of China.
   Hemoglobin. 2011;35:28-39.
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9. AL-NOOD HA , Al-Khawlani MM, Al-Akwa A
   Fetal hemoglobin response to hydroxyurea in Yemeni sickle cell disease patients.
   Hemoglobin. 2011;35:13-21.
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10. SERJEANT GR , Serjeant BE, Fraser RA, Hambleton IR, et al
    Hb S-beta-thalassemia: molecular, hematological and clinical comparisons.
    Hemoglobin. 2011;35:1-12.
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11. QARI MH , Zaki WA
    Flow cytometric assessment of leukocyte function in sickle cell anemia.
    Hemoglobin. 2011;35:367-81.
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12. NICK HP
    Iron chelation therapy in hereditary hemochromatosis and thalassemia intermedia: regulatory and non regulatory mechanisms of increased iron absorption [Kontoghiorghes GJ, Spyrou A, Kolganou A. Hemoglobin. 2010;34(3); 251-264].
    Hemoglobin. 2011;35:175-9.
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13. KAR R , Sharma CB
    Bilirubin peak can be mistaken as Hb Bart's or Hb H on High-performance liquid chromatography.
    Hemoglobin. 2011;35:171-4.
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14. LIAO C , Zhou JY, Xie XM, Liu YN, et al
    Identification of a new alpha chain variant at codons 22-25 (-9 nts) using the Sebia capillarys 2 electrophoresis system.
    Hemoglobin. 2011;35:166-70.
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15. SO CC , Chan AY, Luo HY, Verhovsek M, et al
    Hb A2 Hong Kong - A novel delta-globin variant in a Chinese family masks the diagnosis of beta-thalassemia trait.
    Hemoglobin. 2011;35:162-5.
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16. GHEDIRA ES , Dupin-Deguine D, Duffilot D, Lemetayer N, et al
    A second observation of the rare frameshift mutation in the beta-globin gene: codon 46 (+A) (Hbb:c.138_139insA).
    Hemoglobin. 2011;35:157-61.
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17. JOLY P , Garcia C, Lacan P, Couprie N, et al
    Two new hemoglobin variants: Hb Aix-Les-Bains [beta5(A2)Pro-->Leu; HBB:c.17 C>T] and Hb Dubai [alpha122(H5)His-->Leu (alpha2); HBA2:c.368 A>T].
    Hemoglobin. 2011;35:147-51.
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18. FINLAYSON J , Ghassemifar R, Holmes P, Grey D, et al
    Hb Lynwood [alpha107(G14) (-T) (alpha2) HBA2:c.323delT)] in conjunction with the alpha(3.7) deletion produces a moderately severe alpha-thalassemia phenotype.
    Hemoglobin. 2011;35:142-6.
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19. AL-SULTAN A , Phanasgaonkar S, Suliman A, Al-Baqushi M, et al
    Spectrum of beta-thalassemia mutations in the eastern province of Saudi Arabia.
    Hemoglobin. 2011;35:125-34.
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20. DAAR S , Al Zadjali S, Gravell D, Al Haddabi H, et al
    Hb A2' (Hb B2) in the Omani population and diagnostic significance.
    Hemoglobin. 2011;35:117-24.
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21. VERSTEEGH FG , Arkesteijn SG, Bakker-Verweij M, Haanappel K, et al
    Hb Boskoop [HBA2c.112C>T p.Pro38Ser]: a new alpha2 chain variant observed in a Morrocan family.
    Hemoglobin. 2011;35:97-102.
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22. LIU SC , Peng CT, Lin TH, Wang SJ, et al
    Molecular lesion frequency of hemoglobin gene disorders in Taiwan.
    Hemoglobin. 2011;35:228-36.
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23. PANTALONE GR , Maggio A, Vitrano A, Capra M, et al
    Sequential alternating deferiprone and deferoxamine treatment compared to deferiprone monotherapy: main findings and clinical follow-up of a large multicenter randomized clinical trial in -thalassemia major patients.
    Hemoglobin. 2011;35:206-16.
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24. HA SY , Mok AS, Chu WC, Rasalkar DD, et al
    Intermediate-term evaluation of a pratical chelation protocol based on stratification of thalassemic patients by serum ferritin and magnetic resonance imaging cardiac t2*.
    Hemoglobin. 2011;35:199-205.
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25. KOLNAGOU A , Kleanthous M, Kontoghiorghes GJ
    Efficacy, compliance and toxicity factors are affecting the rate of normalization of body iron stores in thalassemia patients using the deferiprone and deferoxamine combination therapy.
    Hemoglobin. 2011;35:186-98.
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26. POGGI M , Sorrentino F, Pascucci C, Monti S, et al
    Malignancies in beta-thalassemia patients: first description of two cases of thyroid cancer and review of the literature.
    Hemoglobin. 2011;35:439-46.
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27. LIAO C , Pan M, Han J, Yang X, et al
    Early prenatal diagnosis of thalassemia: the first report of experience in mainland China.
    Hemoglobin. 2011;35:434-8.
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28. GUEST EM , Neville KA, Hoyer JD, Safo MK, et al
    Hb Lake Tapawingo [alpha46(CE4)Phe-->Ser; HBA2:c.140T>C]: a new unstable alpha chain hemoglobin variant associated with low systemic arterial saturation.
    Hemoglobin. 2011;35:411-6.
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29. DANIEL Y , Hill K, Inusa B, Thein SL, et al
    Sickle cell/beta0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotype.
    Hemoglobin. 2011;35:406-10.
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30. MOKHTAR GM , Tantawy AA, Adly AA, Ismail EA, et al
    Clinicopathological and radiological study of Egyptian beta-thalassemia intermedia and beta-thalassemia major patients: relation to complications and response to therapy.
    Hemoglobin. 2011;35:382-405.
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31. FERNANDES AC , Shimmoto MM, Furuzawa GK, Vicari P, et al
    Molecular analysis of beta-thalassemia patients: first identification of mutations HBB:c.93-2A>G and HBB:c.114G>A in Brazil.
    Hemoglobin. 2011;35:358-66.
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32. ABUZENADAH AM , Hussein IM, Damanhouri GA, A-Sayes FM, et al
    Molecular basis of beta-thalassemia in the western province of Saudi Arabia: identification of rare beta-thalassemia mutations.
    Hemoglobin. 2011;35:346-57.
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33. WANEESORN J , Panyasai S, Kongthai K, Singboottra P, et al
    Comparison between capillary electrophoresis and high performance liquid chromatography for detection and quantification of Hb constant spring [Hb CS; alpha142, Term-->Gln (TAA>CAA IN alpha2)].
    Hemoglobin. 2011;35:338-45.
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34. RAHIMINEJAD MS , Zeinali S, Afrasiabi A, Valeshabad AK, et al
    beta-Thalassemia mutations found during 1 year of prenatal diagnoses in Fars Province, Iran.
    Hemoglobin. 2011;35:331-7.
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35. MOOSAVI SF , Amirian A, Zarbakhsh B, Kordafshari A, et al
    The carrier frequency of alpha-globin gene triplication in an Iranian population with normal or borderline hematological parameters.
    Hemoglobin. 2011;35:323-30.
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36. JOLY P , Lacan P, Garcia C, Meley R, et al
    A novel deletion/insertion caused by a replication error in the beta-globin gene locus control region.
    Hemoglobin. 2011;35:316-22.
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    June 2010
37. 
    Proceedings of the 18th International Conference on Chelation (ICOC). December 13-16, 2008, Athens, Greece.
    Hemoglobin. 2010;34:199-331.
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38. HERGERSBERG M , Brunner-Agten S, Kuhne T, Paulussen M, et al
    A new stable alpha chain variant: Hb Basel [alpha14(A12)Trp-->Leu (alpha1)].
    Hemoglobin. 2010;34:327-31.
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39. BROQUERE C , Brudey K, Harteveld CL, Saint-Martin C, et al
    Phenotypic expression and origin of the rare beta-thalassemia splice site mutation HBB:c.315 + 1G>T.
    Hemoglobin. 2010;34:322-6.
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40. EVANGELI M , Mughal K, Porter JB
    Which psychosocial factors are related to chelation adherence in thalassemia? A systematic review.
    Hemoglobin. 2010;34:305-21.
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41. KONTOGHIORGHES GJ , Spyrou A, Kolnagou A
    Iron chelation therapy in hereditary hemochromatosis and thalassemia intermedia: regulatory and non regulatory mechanisms of increased iron absorption.
    Hemoglobin. 2010;34:251-64.
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42. TSIRONI M , Karagiorga M, Aessopos A
    Iron overload, cardiac and other factors affecting pregnancy in thalassemia major.
    Hemoglobin. 2010;34:240-50.
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43. FRAGATOU S , Tsourveloudis I, Manesis G
    Incidence of hepatocellular carcinoma in a thalassemia unit.
    Hemoglobin. 2010;34:221-6.
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44. TSIAPRAS D , Fragatou S, Farmaki K, Kyrzopoulos S, et al
    Effect of combined chelation therapy with deferiprone and deferoxamine on left ventricular diastolic function in adult beta-thalassemia major patients.
    Hemoglobin. 2010;34:210-20.
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45. KOLNAGOU A , Kontoghiorghes GJ
    Maintenance of normal range body iron store levels for up to 4.5 years in thalassemia major patients using deferiprone monotherapy.
    Hemoglobin. 2010;34:204-9.
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46. KONTOGHIORGHES GJ
    The 18th ICOC Proceedings in Athens, Greece: New breakthrough in thalassemia leading to the complete treatment of iron overload and to hundreds of patients achieving and maintaining normal body iron stores. Ethical questions on chelation therapy.
    Hemoglobin. 2010;34:199-203.
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    January 2010
47. SALEHI R , Fisher CA, Bignell PA, Eslami G, et al
    Identification of three novel mutations [-41 (A>C), codon 24 (-G), and IVS-I-109 (-T)], in a study of beta-thalassemia alleles in the Isfahan region of Iran.
    Hemoglobin. 2010;34:115-20.
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48. GALLIENNE AE , Iberson NM, Dreau HM, Jackson H, et al
    Characterization of a novel deletion causing beta-thalassemia major in an Afghan family.
    Hemoglobin. 2010;34:110-4.
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49. DRAKONAKI EE , Maris TG, Maragaki S, Klironomos V, et al
    Deferoxamine versus combined therapy for chelating liver, spleen and bone marrow iron in beta-thalassemic patients: a quantitative magnetic resonance imaging study.
    Hemoglobin. 2010;34:95-106.
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50. MOKHTAR GM , Adly AA, Alfy MS, Tawfik LM, et al
    N-terminal natriuretic Peptide and ventilation-perfusion lung scan in sickle cell disease and thalassemia patients with pulmonary hypertension.
    Hemoglobin. 2010;34:78-94.
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51. AL-SAQLADI AW , Harper G, Delpisheh A, Fijnvandraat K, et al
    Frequency of the MTHFR C677T polymorphism in Yemeni children with sickle cell disease.
    Hemoglobin. 2010;34:67-77.
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52. DERCHI G , Lai ME, Marcaccini P, Carta MP, et al
    Human immunodeficiency virus and beta-thalassemia major: A "competition of guilt" for pulmonary arterial hypertension. Report of a case and a review of the literature.
    Hemoglobin. 2010;34:61-6.
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53. ZHANG CM , Wang Y, Gao LS, Gao JH, et al
    Molecular epidemiology investigation of beta-thalassemia in Zhongshan City, Guangdong Province, People's Republic of China.
    Hemoglobin. 2010;34:55-60.
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54. KARIMI M , Johari S, Cohan N
    Attitude toward prenatal diagnosis for beta-thalassemia major and medical abortion in Southern Iran.
    Hemoglobin. 2010;34:49-54.
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55. WARANG P , Nair S, Nadkarni A, Ghosh K, et al
    Hb H disease due to homozygosity for a rare alpha2-globin variant, Hb Sallanches.
    Hemoglobin. 2010;34:45-8.
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56. PRESLEY TD , Perlegas AS, Bain LE, Ballas SK, et al
    Effects of a single sickling event on the mechanical fragility of sickle cell trait erythrocytes.
    Hemoglobin. 2010;34:24-36.
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57. HAJ KHELIL A , Denden S, Leban N, Daimi H, et al
    Hemoglobinopathies in North Africa: a review.
    Hemoglobin. 2010;34:1-23.
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58. YI P , Guo J, Chen Z, Liu Q, et al
    Misdiagnosis of a beta-thalassemia heterozygote using a reverse dot-blot method may be caused by a polymorphic locus in the wild type sequence of the beta-globin gene.
    Hemoglobin. 2010;34:191-5.
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59. DE MARE A , Groeneger AH, Schuurman S, van den Bergh FA, et al
    A rapid single-tube multiplex polymerase chain reaction assay for the seven most prevalent alpha-thalassemia deletions and alphaalphaalpha(anti 3.7) alpha-globin gene triplication.
    Hemoglobin. 2010;34:184-90.
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60. HUANG G , Jiang WL, Rong KB, Li YX, et al
    Molecular characterization of a Chinese pedigree with beta-thalassemia intermedia.
    Hemoglobin. 2010;34:179-83.
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61. LIAO C , Zhou JY, Xie XM, Li J, et al
    Detection of Hb Constant Spring by a capillary electrophoresis method.
    Hemoglobin. 2010;34:175-8.
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62. HONIG GR , Lu SJ, Feng Q, Vida LN, et al
    alpha-Thalassemia-like globin gene expression by primitive erythrocytes derived from human embryonic stem cells.
    Hemoglobin. 2010;34:145-50.
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63. ALKINDI S , Al Zadjali S, Al Madhani A, Daar S, et al
    Forecasting hemoglobinopathy burden through neonatal screening in Omani neonates.
    Hemoglobin. 2010;34:135-44.
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64. HASSAN SM , Hamza N, Jaffer Al-Lawatiya F, Jaffer Mohammed A, et al
    Extended molecular spectrum of beta- and alpha-thalassemia in Oman.
    Hemoglobin. 2010;34:127-34.
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65. PHYLIPSEN M , Prior JF, Lim E, Lingam N, et al
    Two new alpha1-globin gene point mutations: Hb Nedlands (HBA1:c.86C>T) [alpha28(B9)Ala-->Val] and Hb Queens Park (HBA1:c.98T>A) [alpha32(B13)Met-->Lys].
    Hemoglobin. 2010;34:123-6.
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66. BALLAS SK , McCarthy WF, Guo N, Brugnara C, et al
    Early detection of response to hydroxyurea therapy in patients with sickle cell anemia.
    Hemoglobin. 2010;34:424-9.
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67. BRENNAN SO , Ryken S, Chan T
    Hb Koya Dora [alpha142, Term-->Ser (TAA>TCA in alpha2)]: a rare mutation of the alpha2 gene stop codon associated with alpha-thalassemia.
    Hemoglobin. 2010;34:402-5.
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68. GEORGEL AF , Mereau C, Willekens C, Bourgeois E, et al
    Identification of a new mutation on the beta-globin gene: codons 8/9 (+AGAA); GAG.AAG.TCT(Glu-Lys-Ser)>GAG. AAAGAAG, in a patient from the north of France with a phenotype of beta-thalassemia minor.
    Hemoglobin. 2010;34:389-93.
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69. KALOTYCHOU V , Tzanetea R, Konstantopoulos K, Papassotiriou I, et al
    Erythrocytosis due to a combination of the high oxygen affinity hemoglobin variant, Hb Olympia [beta20(B2)Val-->Met] with beta- and alpha-thalassemia mutations: first case in the literature.
    Hemoglobin. 2010;34:383-8.
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70. FRISCHKNECHT H , Troxler H, Dutly F, Walker L, et al
    Characterization of three novel delta chain hemoglobin variants and two delta-thalassemia alleles.
    Hemoglobin. 2010;34:374-82.
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71. JOLY P , Szymanowicz A, Neyron MJ, Zine A, et al
    Hb Charlieu [alpha106(G13)Leu-->Pro (alpha1)]: a new phenotypically silent hemoglobin variant associated with a mild alpha-thalassemia phenotype.
    Hemoglobin. 2010;34:366-73.
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72. GIORDANO PC , Cnossen MH, Joosten AM, Jansen CA, et al
    Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb Rotterdam): two novel alpha2 gene mutations associated with mild alpha-thalassemia found in the same family after newborn screening.
    Hemoglobin. 2010;34:354-65.
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73. LOU JW , Li Q, Wei XF, Huang JW, et al
    Identification of the linkage of a 1.357 KB beta-globin gene deletion and A gamma-globin gene triplication in a Chinese family.
    Hemoglobin. 2010;34:343-53.
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74. PAPACHATZOPOULOU A , Kourakli A, Stavrou EF, Fragou E, et al
    Region-specific genetic heterogeneity of HBB mutation distribution in South-Western Greece.
    Hemoglobin. 2010;34:333-42.
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75. GARCON L , Iolascon A, Pissard S, Esposito MR, et al
    A Dyserythropoietic Anemia Associated with Homozygous Hb Plasencia [alpha125(H8)Leu-->Arg (alpha2)] (HBA2:c.377T>G), A Variant with an Unstable alpha Chain.
    Hemoglobin. 2010;34:576-81.
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76. BELISARIO AR , Rodrigues CV, Martins ML, Silva CM, et al
    Coinheritance of alpha-Thalassemia Decreases the Risk of Cerebrovascular Disease in a Cohort of Children with Sickle Cell Anemia.
    Hemoglobin. 2010;34:516-29.
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77. GRIFFON C , Joly P, Senechal A, Philit F, et al
    Severe beta-thalassemia intermedia in a compound heterozygous patient for the -30 (T>A) beta(+)-thalassemia mutation and the delta(0)beta(+)-Senegalese deletion.
    Hemoglobin. 2010;34:505-8.
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78. PORNPRASERT S , Kasemrad C, Sukunthamala K
    Diagnosis of thalassemia on dried blood spot samples by high performance liquid chromatography.
    Hemoglobin. 2010;34:486-94.
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79. RADMILOVIC M , Zukic B, Stankovic B, Karan-Djurasevic T, et al
    Thalassemia syndromes in Serbia: an update.
    Hemoglobin. 2010;34:477-85.
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80. JALAL SD , Al-Allawi NA, Bayat N, Imanian H, et al
    beta-Thalassemia mutations in the Kurdish population of northeastern Iraq.
    Hemoglobin. 2010;34:469-76.
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81. GALEHDARI H , Salehi B, Azmoun S, Keikhaei B, et al
    Comprehensive spectrum of the beta-Thalassemia mutations in Khuzestan, southwest Iran.
    Hemoglobin. 2010;34:461-8.
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82. SALEH-GOHARI N , Khosravi-Mashizi A
    Spectrum of alpha-globin gene mutations in the Kerman Province of Iran.
    Hemoglobin. 2010;34:451-60.
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83. PHYLIPSEN M , Harteveld CL, de Metz M, Gallivan MV, et al
    New and known beta-thalassemia determinants masked by known and new delta gene defects [Hb A(2)-Ramallah or delta6(A3)Glu-->Gln, GAG>>CAG].
    Hemoglobin. 2010;34:445-50.
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84. TRAEGER-SYNODINOS J , Douna V, Papassotiriou I, Stamoulakatou A, et al
    Variable and often severe phenotypic expression in patients with the alpha-thalassemic variant Hb Agrinio [alpha29(B10)Leu-->Pro (alpha2)].
    Hemoglobin. 2010;34:430-8.
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85. LACERRA G , Scarano C, Lagona LF, Testa R, et al
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