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Anemia

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Single Articles

January 2007
1. LI D , Liao C, Xie X, Zhong H, et al
   Four cases of Hb Q-H disease found in Southern China.
   Hemoglobin. 2007;31:109-11.
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2. LI D , Liao C, Li J
   Misdiagnosis of Hb constant spring (alpha142, Term-->Gln, TAA-->CAA in alpha2) in a Hb H (beta4) disease child.
   Hemoglobin. 2007;31:105-8.
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3. CHINCHANG W , Viprakasit V
   Further identification of Hb G-Coushatta [beta22(B4)Glu-->Ala (GAA-->GCA)] in Thailand by the polymerase chain reaction-single-strand conformation polymorphism technique and by amplification refractory mutation system-polymerase chain reaction.
   Hemoglobin. 2007;31:93-9.
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4. BUSERI FI , Shokunbi WA, Jeremiah ZA
   Plasma fibrinogen levels in Nigerian homozygous (Hb SS) sickle cell patients.
   Hemoglobin. 2007;31:89-92.
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5. BEZERRA MA , Santos MN, Araujo AS, Gomes YM, et al
   Molecular variations linked to the grouping of beta- and alpha-globin genes in neonatal patients with sickle cell disease in the State of Pernambuco, Brazil.
   Hemoglobin. 2007;31:83-8.
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6. PULIS S , Scerri CA, Wismayer PS, Galdies R, et al
   Developmental effect of the XmnI site on Ggamma-globin gene expression among newborn Hb F-Malta-I [Ggamma117(G19)His-->Arg, CAT-->CGT] heterozygotes and adult beta+ -Thalassemia homozygotes.
   Hemoglobin. 2007;31:71-82.
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7. EL-GAWHARY S , El-Shafie S, Niazi M, Aziz M, et al
   Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
   Hemoglobin. 2007;31:63-9.
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8. HUSSEIN G , Fawzy M, Serafi TE, Ismail EF, et al
   Rapid detection of beta-Thalassemia alleles in Egypt using naturally or amplified created restriction sites and direct sequencing: a step in disease control.
   Hemoglobin. 2007;31:49-62.
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9. FOULON K , Rochette J, Cadet E
   A novel beta-Thalassemic allele due to a two nucleotide deletion: beta76 (-GC).
   Hemoglobin. 2007;31:31-7.
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10. MOUMNI I , Zorai A, Daoued BB, Mosbahi I, et al
    Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation.
    Hemoglobin. 2007;31:23-9.
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11. PREHU C , Riou J, Wajcman H
    Hb Barika [alpha42(C7)Tyr-->His (alpha2)] leads to an alpha+ -Thalassemia-like syndrome.
    Hemoglobin. 2007;31:17-22.
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12. EFREMOV GD
    Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
    Hemoglobin. 2007;31:1-15.
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13. FELICE AE , Borg J, Pizzuto M, Cassar W, et al
    A review of cis-trans interplay between DNA sequences 5' to the (G)gamma- and beta-globin genes among Hb F-Malta-I heterozygotes/homozygotes and beta-thalassemia homozygotes/compound heterozygotes, and the effects of hydroxyurea on the Hb F/F-erythrocyte
    Hemoglobin. 2007;31:279-88.
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14. ZEREN F , Genc A, Curuk MA
    Preliminary data on preimplantation genetic diagnosis for hemoglobinopathies in Turkey.
    Hemoglobin. 2007;31:273-7.
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15. BOZKURT G
    Results from the north cyprus thalassemia prevention program.
    Hemoglobin. 2007;31:257-64.
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16. KUTLAR F
    Diagnostic approach to hemoglobinopathies.
    Hemoglobin. 2007;31:243-50.
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17. BASAK AN
    The molecular pathology of beta-thalassemia in Turkey: the Bogazici university experience.
    Hemoglobin. 2007;31:233-41.
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18. PETKOV GH , Efremov GD
    Molecular basis of beta-thalassemia and other hemoglobinopathies in Bulgaria: an update.
    Hemoglobin. 2007;31:225-32.
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19. KUTLAR A
    Sickle cell disease: a multigenic perspective of a single gene disorder.
    Hemoglobin. 2007;31:209-24.
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20. EFREMOV GD
    Dominantly Inherited beta-Thalassemia.
    Hemoglobin. 2007;31:193-207.
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21. GIORDANO PC , Zweegman S, Akkermans N, Arkesteijn SG, et al
    The first case of Hb Groene Hart [alpha119(H2)Pro-->Ser, CCT-->TCT (alpha1)] homozygosity confirms that a thalassemia phenotype is associated with this abnormal hemoglobin variant.
    Hemoglobin. 2007;31:179-82.
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22. PRIOR JF , Lim E, Lingam N, Raven JL, et al
    A moderately severe alpha-thalassemia condition resulting from a combination of the alpha2 polyadenylation signal (AATAAA-->AATA- -) mutation and a 3.7 Kb alpha gene deletion in an Australian family.
    Hemoglobin. 2007;31:173-7.
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23. LACAN P , Aubry M, Couprie N, Francina A, et al
    Two new beta0-thalassemic mutations: a deletion (-CC) at codon 142 or overlapping codons 142-143, and an insertion (+T) at codon 45 or overlapping codons 44-45/45-46 of the beta-globin gene.
    Hemoglobin. 2007;31:159-65.
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24. AGOUTI I , Badens C, Abouyoub A, Khattab M, et al
    Genotypic correlation between six common beta-thalassemia mutations and the XmnI polymorphism in the Moroccan population.
    Hemoglobin. 2007;31:141-9.
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25. LUO HY , Adewoye AH, Pilichowska M, Li MY, et al
    Two new alpha-thalassemia frameshift mutations.
    Hemoglobin. 2007;31:135-9.
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26. ENG B , Walker L, Nakamura LM, Hoppe C, et al
    Three new beta-globin gene promoter mutations identified through newborn screening.
    Hemoglobin. 2007;31:129-34.
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27. AL-OBAIDLI A , Hamodat M, Fawzi Z, Abu-Laban M, et al
    Molecular basis of thalassemia in Qatar.
    Hemoglobin. 2007;31:121-7.
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28. WILLIAMS JP , Scrivens JH, Green BN, Farrar LM, et al
    Hb Leeds [beta56(D7)GlyCys]: A New Hemoglobin that Aggravates Anemia in a child with beta(0)-Thalassemia Trait.
    Hemoglobin. 2007;31:367-73.
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29. LIAO C , Feng Q, Li J, Huang Y, et al
    A double heterozygote for (deltabeta)0-thalassemia and codons 41/42 (-TTCT) behaves as a homozygote for the frameshift mutation in a Chinese family.
    Hemoglobin. 2007;31:397-400.
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30. CORNUT G , Weng X, Robin L, Lavoie C, et al
    A new insertion mutation in the beta-globin gene [codons 45/46 (+A)] resulting in a beta-thalassemia minor phenotype.
    Hemoglobin. 2007;31:393-5.
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31. JEON IS , Nam KL
    Ringed sideroblasts found in a girl heterozygous for the initiation codon (ATG-->AGG) beta0-thalassemia mutation.
    Hemoglobin. 2007;31:383-6.
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32. EBERLE SE , Noguera NI, Sciuccati G, Bonduel M, et al
    Hb Alesha [beta67(E11)Val-->Met, GTG-->ATG] in an Argentinean girl.
    Hemoglobin. 2007;31:379-82.
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33. AMATO A , Cappabianca MP, Ponzini D, Rinaldi S, et al
    Hb L'Aquila [beta106(G8)Leu-->Val, CTG-->GTG]: a novel thalassemic hemoglobin variant.
    Hemoglobin. 2007;31:375-8.
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34. YOUSSRY I , Mohsen NA, Shaker OG, El-Hennawy A, et al
    Skin iron concentration: a simple, highly sensitive method for iron stores evaluation in thalassemia patients.
    Hemoglobin. 2007;31:357-65.
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35. DERAKHSHANDEH-PEYKAR P , Akhavan-Niaki H, Tamaddoni A, Ghawidel-Parsa S, et al
    Distribution of beta-thalassemia mutations in the northern provinces of Iran.
    Hemoglobin. 2007;31:351-6.
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36. KIANI AA , Mortazavi Y, Zeinali S, Shirkhani Y, et al
    The molecular analysis of beta-thalassemia mutations in Lorestan Province, Iran.
    Hemoglobin. 2007;31:343-9.
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37. KHATAMI S , Dehboneh SR, Sadeghi S, Mirzazadeh R, et al
    Globin chain synthesis is a useful complementary tool in the differential diagnosis of thalassemias.
    Hemoglobin. 2007;31:333-41.
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38. HARTEVELD CL , van Helden WC, Boxma GL, van Delft P, et al
    Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype.
    Hemoglobin. 2007;31:325-32.
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39. HARTEVELD CL , Versteegh FG, van Leer EH, Starreveld JS, et al
    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.
    Hemoglobin. 2007;31:313-23.
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40. SHEIKH-TAHA M , Koussa S, Inati A, Taher A, et al
    Febrile neutropenia and hemorrhagic stroke in a thalassemia major patient.
    Hemoglobin. 2007;31:499-501.
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41. SHIH HC , Shih MC, Chang YC, Peng CT, et al
    Hb Hekinan in a Taiwanese subject: a G-->T substitution at codon 27 of the alpha1-globin gene abolishes an HaeIII site.
    Hemoglobin. 2007;31:495-8.
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42. ATALAY A , Koyuncu H, Koseler A, Ozkan A, et al
    Hb Beograd [beta121(GH4)Glu-->Val, GAA-->GTA] in the Turkish population.
    Hemoglobin. 2007;31:491-3.
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43. MORADKHANI K , Henthorn J, Riou J, Phelan L, et al
    Hb Niigata [beta1(NA1)Val-->Leu] in a Romanian individual resulting from another nucleotide substitution than that found in the Japanese.
    Hemoglobin. 2007;31:477-82.
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44. LIAO C , Li Q, Wei J, Feng Q, et al
    Prenatal control of Hb Bart's disease in southern China.
    Hemoglobin. 2007;31:471-5.
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45. ESTEGHAMAT F , Imanian H, Azarkeivan A, Pourfarzad F, et al
    Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
    Hemoglobin. 2007;31:463-9.
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46. KOSARYAN M , Vahidshahi K, Karami H, Forootan MA, et al
    Survival of thalassemic patients referred to the Boo Ali Sina Teaching Hospital, Sari, Iran.
    Hemoglobin. 2007;31:453-62.
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47. VERMA IC , Kleanthous M, Saxena R, Fucharoen S, et al
    Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.
    Hemoglobin. 2007;31:439-52.
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48. AGOUTI I , Bennani M, Ahmed A, Barakat A, et al
    Thalassemia intermedia due to a novel mutation in the second intervening sequence of the beta-globin gene.
    Hemoglobin. 2007;31:433-8.
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49. LOPEZ BL , Flenders P, Davis-Moon L, Corbin T, et al
    Clinically significant differences in the visual analog pain scale in acute vasoocclusive sickle cell crisis.
    Hemoglobin. 2007;31:427-32.
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50. BACHIR D , Hulin A, Huet E, Habibi A, et al
    Plasma and urine hydroxyurea levels might be useful in the management of adult sickle cell disease.
    Hemoglobin. 2007;31:417-25.
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51. STEINER LA , Van Hoff J, Kutlar F, Gallagher PG, et al
    Aplastic crisis revealing the diagnosis of Hb Evans [alpha62(E11)Val-->Met, GTG-->ATG (alpha2)] in a Hispanic kindred: case report and review.
    Hemoglobin. 2007;31:409-16.
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    February 2006
52. 
    Proceedings of the 15th International Conference on Oral Chelation (ICOC) in the Treatment of Thalassemia and Other Diseases. Part 1. Taichung, Taiwan. April 22-26, 2005.
    Hemoglobin. 2006;30:63-137.
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53. MEO A , Ruggeri A, La Rosa MA, Zanghi L, et al
    Iron burden and liver fibrosis decrease during a long-term phlebotomy program and iron chelating treatment after bone marrow transplantation.
    Hemoglobin. 2006;30:131-7.
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54. PENG CT , Wu KH, Wu SF, Liang DC, et al
    Deferiprone or deferoxamine vs. combination therapy in patients with beta-thalassemia major: a case study in Taiwan.
    Hemoglobin. 2006;30:125-30.
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55. MANCUSO A , Sciarrino E, Renda MC, Maggio A, et al
    A prospective study of hepatocellular carcinoma incidence in thalassemia.
    Hemoglobin. 2006;30:119-24.
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56. PENG CT , Fucharoen S, Kontoghiorghes GJ, Tsai CH, et al
    Report on the proceedings of the 15th International Conference on Oral Chelation (ICOC) in the Treatment of Thalassemia and Other Diseases at Taichung, Taiwan, April 22-26, 2005.
    Hemoglobin. 2006;30:63-8.
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57. RUGLESS MJ , Fisher CA, Stephens AD, Amos RJ, et al
    Hb Bart's in cord blood: an accurate indicator of alpha-thalassemia.
    Hemoglobin. 2006;30:57-62.
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58. BENEITEZ D , Carrera A, Duran-Suarez JR, Paz V, et al
    Heterozygous Hb Hope [beta136(H14)Gly --> Asp] in association with heterozygous beta0-thalassemia with apparent homozygous expression, in a Spanish patient.
    Hemoglobin. 2006;30:45-9.
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59. BARDET V , Adam M, Yvart J, Wajcman H, et al
    Hb Calais [beta76(E20)Ala --> Pro]: a family study of a variant with decreased oxygen affinity.
    Hemoglobin. 2006;30:35-8.
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60. ROPERO P , Villegas A, Munoz J, Briceno O, et al
    First Spanish case of thalassemia major due to a compound heterozygosity for the IVS-II-848 (C --> A) and codon 39 (C --> T) mutations of the beta-globin gene.
    Hemoglobin. 2006;30:15-21.
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61. LI Z , Li F, Li M, Guo R, et al
    The prevalence and spectrum of thalassemia in Shenzhen, Guangdong Province, People's Republic of China.
    Hemoglobin. 2006;30:9-14.
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62. HARTEVELD CL , Jebbink MC, van der Lely N, van Delft P, et al
    Alpha-thalassemia phenotype induced by the new IVS-II-2 (T --> A) splice donor site mutation on the alpha2-globin gene.
    Hemoglobin. 2006;30:3-7.
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    January 2006
63. KONTOGHIORGHES GJ
    Iron mobilization from transferrin and non-transferrin-bound-iron by deferiprone. Implications in the treatment of thalassemia, anemia of chronic disease, cancer and other conditions.
    Hemoglobin. 2006;30:183-200.
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64. AMATO A , Pia Cappabianca M, Ponzini D, Di Biagio P, et al
    Detection of a rare beta-globin nonsense mutation [codon 59 (AAG-->TAG)] in an Italian family.
    Hemoglobin. 2006;30:405-7.
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65. EANDI EBERLE S , Noguera NI, Sciuccati G, Bonduel M, et al
    Hb Southampton [beta106(G8)Leu-->Pro, CTG-->CCG] in an Argentinean boy.
    Hemoglobin. 2006;30:401-3.
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66. LEUNG RY , Ma ES, Chan AY, Chow EY, et al
    Molecular diagnosis of a case of Hb Phnom Penh [alpha117(GH5)Phe-I1e-alpha118(H1)Thr (alpha1)].
    Hemoglobin. 2006;30:397-9.
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67. BOUVA MJ , Harteveld CL, Bakker-Verweij G, van Delft P, et al
    Ggamma -37 (A-->T): a new nondeletional hereditary persistence of fetal hemoglobin determinant associated with the rare codon 91 (+T) delta0-thalassemia.
    Hemoglobin. 2006;30:371-7.
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68. LI D , Liao C, Li J, Huang Y, et al
    Prenatal diagnosis of beta-thalassemia by reverse dot-blot hybridization in southern China.
    Hemoglobin. 2006;30:365-70.
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69. MASMAS TN , Garly ML, Lisse IM, Rodriques A, et al
    Inherited hemoglobin disorders in Guinea-Bissau, West Africa: a population study.
    Hemoglobin. 2006;30:355-64.
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70. HARTEVELD CL , Versteegh FG, Kok PJ, van Rooijen-Nijdam IH, et al
    Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
    Hemoglobin. 2006;30:349-54.
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71. 
    Proceedings of the 15th International Conference on Oral Chelation (ICOC) in the Treatment of Thalassaemia and other Diseases, part 2. Taichung, Taiwan, April 22-26, 2005.
    Hemoglobin. 2006;30:183-347.
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72. KONTOGHIORGHES GJ
    Future chelation monotherapy and combination therapy strategies in thalassemia and other conditions. comparison of deferiprone, deferoxamine, ICL670, GT56-252, L1NAll and starch deferoxamine polymers.
    Hemoglobin. 2006;30:329-47.
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73. SRICHAIRATANAKOOL S , Ounjaijean S, Thephinlap C, Khansuwan U, et al
    Iron-chelating and free-radical scavenging activities of microwave-processed green tea in iron overload.
    Hemoglobin. 2006;30:311-27.
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74. KUO HT , Peng CT, Tsai MY
    Pilot study on parental stress and behavioral adjustment to the thalassemia major disease process in children undergoing iron-chelation in western Taiwan.
    Hemoglobin. 2006;30:301-9.
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75. KUO HT , Tsai MY, Peng CT, Wu KH, et al
    Pilot study on the "quality of life" as reflected by psychosocial adjustment of children with thalassemia major undergoing iron-chelating treatment in western Taiwan.
    Hemoglobin. 2006;30:291-9.
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76. MUDIYANSE RM
    Thalassemia treatment and prevention in Uva Province, Sri Lanka: a public opinion survey.
    Hemoglobin. 2006;30:275-89.
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77. HA SY , Chik KW, Ling SC, Lee AC, et al
    A randomized controlled study evaluating the safety and efficacy of deferiprone treatment in thalassemia major patients from Hong Kong.
    Hemoglobin. 2006;30:263-74.
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78. WANG CH , Wu KH, Tsai FJ, Peng CT, et al
    Comparison of oral and subcutaneous iron chelation therapies in the prevention of major endocrinopathies in beta-thalassemia major patients.
    Hemoglobin. 2006;30:257-62.
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79. WU KH , Chang JG, Ho YJ, Wu SF, et al
    Glutathione S-transferase M1 gene polymorphisms are associated with cardiac iron deposition in patients with beta-thalassemia major.
    Hemoglobin. 2006;30:251-6.
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80. KOLNAGOU A , Kontoghiorghes GJ
    Effective combination therapy of deferiprone and deferoxamine for the rapid clearance of excess cardiac IRON and the prevention of heart disease in thalassemia. The Protocol of the International Committee on Oral Chelators.
    Hemoglobin. 2006;30:239-49.
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81. HUANG YC , Chang JS, Wu KH, Peng CT, et al
    Regression of myocardial dysfunction after switching from desferrioxamine to deferiprone therapy in beta-thalassemia major patients.
    Hemoglobin. 2006;30:229-38.
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82. KOLNAGOU A , Economides C, Eracleous E, Kontoghiorghes GJ, et al
    Low serum ferritin levels are misleading for detecting cardiac iron overload and increase the risk of cardiomyopathy in thalassemia patients. The importance of cardiac iron overload monitoring using magnetic resonance imaging T2 and T2*.
    Hemoglobin. 2006;30:219-27.
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83. WU SF , Peng CT, Wu KH, Tsai CH, et al
    Liver fibrosis and iron levels during long-term deferiprone treatment of thalassemia major patients.
    Hemoglobin. 2006;30:215-8.
    PubMed     Related articles    Abstract available
    
    
    
84. CHEN AC , Peng CT, Wu SF, Wu KH, et al
    Effect of deferiprone on liver iron overload and fibrosis in hepatitis-C-virus-infected thalassemia.
    Hemoglobin. 2006;30:209-14.
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85. BIBI A , Messaoud T, Fattoum S
    Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.
    Hemoglobin. 2006;30:175-81.
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86. LI D , Liao C, Li J, Tang X, et al
    The codon 37 (TGG-->TAG) beta(0)-thalassemia mutation found in a Chinese family.
    Hemoglobin. 2006;30:171-3.
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87. BALLAS SK , Files B, Luchtman-Jones L, Benjamin L, et al
    Secretory phospholipase A2 levels in patients with sickle cell disease and acute chest syndrome.
    Hemoglobin. 2006;30:165-70.
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88. BURNICHON N , Lacan P, Becchi M, Zanella-Cleon I, et al
    A new alpha chain hemoglobin variant: Hb Al-Hammadi Riyadh [alpha75(EF4)Asp-->Val (alpha2)].
    Hemoglobin. 2006;30:155-64.
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89. ENG B , Patterson M, Walker L, Hoppe C, et al
    Three new alpha-thalassemia point mutations ascertained through newborn screening.
    Hemoglobin. 2006;30:149-53.
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90. AL-ALLAWI NA , Jubrael JM, Hughson M
    Molecular characterization of beta-thalassemia in the Dohuk region of Iraq.
    Hemoglobin. 2006;30:479-86.
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91. POODT J , Martens HA, Walsh IB, Felix-Schollaart B, et al
    A newly identified deletion of 970 bp at the alpha-globin locus that removes the promoter region of the alpha1 gene.
    Hemoglobin. 2006;30:471-7.
    PubMed     Related articles    Abstract available
    
    
    
92. CARNLEY BP , Prior JF, Gilbert A, Lim E, et al
    The prevalence and molecular basis of hemoglobinopathies in Cambodia.
    Hemoglobin. 2006;30:463-70.
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93. PAVLOU E , Phylactides M, Kyrri A, Kalogerou E, et al
    Delta-thalassemia in Cyprus.
    Hemoglobin. 2006;30:455-62.
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94. AL-ABSI IK , Al-Subaie AM, Ameen G, Mahdi N, et al
    Association of the methylenetetrahydrofolate reductase A1298C but not the C677T single nucleotide polymorphism with sickle cell disease in Bahrain.
    Hemoglobin. 2006;30:449-53.
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95. BIBI A , Messaoud T, Beldjord C, Fattoum S, et al
    Detection of two rare beta-thalassemia alleles found in the Tunisian population: codon 47 (+A) and codons 106/107 (+G).
    Hemoglobin. 2006;30:437-47.
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96. PAPASSOTIRIOU I , Stamoulakatou A, Wajcman H, Kister J, et al
    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.
    Hemoglobin. 2006;30:409-18.
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