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Articles published in Hemoglobin

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Single Articles


    June 2017
  1. PORNPRASERT S, Thongsat C, Panyachadporn U
    Evaluation of Applying a Combination of Red Cell Indexes and Formulas to Differentiate beta-Thalassemia Trait from Iron Deficiency Anemia in the Thai Population.
    Hemoglobin. 2017 Jun 9:1-4. doi: 10.1080/03630269.2017.1323763.
    PubMed     Text format     Abstract available


    April 2017
  2. WAH ST, Yi YS, Khin AA, Plabplueng C, et al
    Prevalence of Anemia and Hemoglobin Disorders Among School Children in Myanmar.
    Hemoglobin. 2017 Apr 2:1-6. doi: 10.1080/03630269.2017.1289103.
    PubMed     Text format     Abstract available


    November 2016
  3. MAINOU M, Kotsiafti A, Klonizakis P, Soulountsi V, et al
    A Case of Fatal Agranulocytosis That Developed in a Patient with beta-Thalassemia Major Treated with Deferiprone.
    Hemoglobin. 2016;40:435-437.
    PubMed     Text format     Abstract available


  4. GORELLO P, Arcioni F, Palmieri A, Barbanera Y, et al
    The Molecular Spectrum of beta- and alpha-Thalassemia Mutations in Non-Endemic Umbria, Central Italy.
    Hemoglobin. 2016;40:371-376.
    PubMed     Text format     Abstract available


  5. LEE HH, Mak AS, Kou KO, Poon CF, et al
    An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Kruppel-like Factor 1 mutations.
    Hemoglobin. 2016;40:431-434.
    PubMed     Text format     Abstract available


  6. GARCIA-MORIN M, Lopez-Sanguos C, Vazquez P, Alvarez T, et al
    Lactate Dehydrogenase: A Marker of the Severity of Vaso-Occlusive Crisis in Children with Sickle Cell Disease Presenting at the Emergency Department.
    Hemoglobin. 2016;40:388-391.
    PubMed     Text format     Abstract available


  7. LAI Y, Chen Y, Chen B, Zheng H, et al
    Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang beta-Thalassemia Intermedia Patients.
    Hemoglobin. 2016;40:405-410.
    PubMed     Text format     Abstract available


  8. JIANG H, Yan JM, Zhou JY, Li DZ, et al
    Hb Alesha [beta67(E11)Val-->Met (GTG>ATG); HBB: c.202G > A] Found in a Chinese Girl.
    Hemoglobin. 2016;40:420-421.
    PubMed     Text format     Abstract available


  9. BHATTACHARYYA KK, Chatterjee T, Mondal UB
    A comprehensive screening program for beta-thalassemia and other hemoglobinopathies in the Hooghly District of West Bengal, India, dealing with 21 137 cases.
    Hemoglobin. 2016;40:396-399.
    PubMed     Text format     Abstract available


  10. KURTOGLU A, Karakus V, Erkal O, Kurtoglu E, et al
    beta-Thalassemia gene mutations in Antalya, Turkey: results from a single centre study.
    Hemoglobin. 2016;40:392-395.
    PubMed     Text format     Abstract available


  11. MEJRI A, Mansri M, Hadj Fredj S, Ouali F, et al
    First description of the rs45496295 polymorphism of the C/EBPE gene in beta-thalassemia intermedia patients.
    Hemoglobin. 2016;40:411-416.
    PubMed     Text format     Abstract available


  12. PULE GD, Ngo Bitoungui VJ, Chetcha Chemegni B, Kengne AP, et al
    Studies of novel variants associated with Hb F in Sardinians and Tanzanians in sickle cell disease patients from Cameroon.
    Hemoglobin. 2016;40:377-380.
    PubMed     Text format     Abstract available


  13. ZHAO L, Qing J, Liang Y, Chen Z, et al
    A novel compound heterozygosity in Southern China: IVS-II-5 (G > C) and IVS-II-672 (A > C).
    Hemoglobin. 2016;40:428-430.
    PubMed     Text format     Abstract available


  14. CHAN NC, Lau KM, Cheng KC, Chan NP, et al
    A Multi-locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese beta-thalassemia Carriers.
    Hemoglobin. 2016;40:400-404.
    PubMed     Text format     Abstract available


    September 2016
  15. JORGENSEN DR, Rosano C, Novelli EM
    Can Neuroimaging Markers of Vascular Pathology Explain Cognitive Performance in Adults with Sickle Cell Anemia? A Review of the Literature.
    Hemoglobin. 2016.
    PubMed     Text format     Abstract available


  16. GALLAGHER PG, Maksimova Y, Schulz VP, Forget BG, et al
    Mutation in a Highly Conserved COOH-Terminal Residue of Kruppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous beta-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype.
    Hemoglobin. 2016;40:361-364.
    PubMed     Text format     Abstract available


  17. WAYE JS, Eng B, Hanna M, Hohenadel BA, et al
    Novel Mutation of the Translation Initiation Codon of the alpha1-Globin Gene (ATG>AAG or HBA1:c.2T>A).
    Hemoglobin. 2016;40:369-370.
    PubMed     Text format     Abstract available


  18. LIM YC, Tan KM, Chong SS, Rajendran J, et al
    A Patient with beta-Thalassemia Intermedia Secondary to Homozygosity for a Polyadenylation Signal Mutation (AATAAA > AATAGA) (HBB: C.*112A > G) on the beta-Globin Gene.
    Hemoglobin. 2016;40:359-360.
    PubMed     Text format     Abstract available


  19. PANJA A, Chowdhury P, Basu A
    Hb Midnapore [beta53(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.
    Hemoglobin. 2016;40:300-303.
    PubMed     Text format     Abstract available


  20. DERAKHSHAN SM, Khaniani MS, Afkhami F, PourFeizi AH, et al
    Molecular Study of Deletional and Nondeletional Mutations on the alpha-Globin Locus in the Azeri Population of Northwestern Iran.
    Hemoglobin. 2016;40:319-322.
    PubMed     Text format     Abstract available


  21. LOOVERS HM, Tamminga N, Mulder AB, Tamminga RY, et al
    Clinical Course of Two Children with Unstable Hemoglobins: The Effect of Hydroxyurea Therapy.
    Hemoglobin. 2016;40:341-344.
    PubMed     Text format     Abstract available


  22. YANG X, Yan JM, Li J, Xie XM, et al
    Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (- -SEA/) Deletion.
    Hemoglobin. 2016;40:353-355.
    PubMed     Text format     Abstract available


  23. PULTE D, Lovett PB, Axelrod D, Crawford A, et al
    Comparison of Emergency Department Wait Times in Adults with Sickle Cell Disease Versus Other Painful Etiologies.
    Hemoglobin. 2016;40:330-334.
    PubMed     Text format     Abstract available


  24. YERUVA SL, Paul Y, Oneal P, Nouraie M, et al
    Renal Failure in Sickle Cell Disease: Prevalence, Predictors of Disease, Mortality and Effect on Length of Hospital Stay.
    Hemoglobin. 2016;40:295-299.
    PubMed     Text format     Abstract available


  25. ITALIA K, Dabke P, Sawant P, Nadkarni A, et al
    Hb E-beta-Thalassemia in Five Indian States.
    Hemoglobin. 2016;40:310-315.
    PubMed     Text format     Abstract available


  26. DING ZY, Shen GS, Zhang S, He PY, et al
    Epidemiology of Hemoglobinopathies in the Huzhou Region, Zhejiang Province, Southeast China.
    Hemoglobin. 2016;40:304-309.
    PubMed     Text format     Abstract available


  27. WARD R, Taha KM
    Patient Involvement as Experts in the Development and Assessment of a Smartphone App as a Patient Education Tool for the Management of Thalassemia and Iron Overload Syndromes.
    Hemoglobin. 2016;40:323-329.
    PubMed     Text format     Abstract available


  28. ZAREI T, Dehbozorgian J, Imanifard J, Setoodegan F, et al
    A Number of Cases in Iran Presenting with Coinheritance of Hemoglobin-H Disease and Beta-Thalassemia Minor.
    Hemoglobin. 2016;40:316-318.
    PubMed     Text format     Abstract available


  29. TORRES LS, Okumura JV, Belini-Junior E, Oliveira RG, et al
    Phenotypic Diversity of Sickle Cell Disease in Patients with a Double Heterozygosity for Hb S and Hb D-Punjab.
    Hemoglobin. 2016;40:356-358.
    PubMed     Text format     Abstract available


  30. WANG XY, Lin MX, Lin M
    A novel 6.3 kb deletion and the Rare 27.6 kb Deletion Causing alpha+-Thalassemia in two Chinese Patients.
    Hemoglobin. 2016;40:365-368.
    PubMed     Text format     Abstract available


  31. ORTS JA, Zuniga A, Bello Y, Fabregat AB, et al
    Hb A1c Determination by Capillary Electrophoresis is an Efficient Method for Detecting beta-Thalassemias and Hemoglobin Variants.
    Hemoglobin. 2016;40:335-340.
    PubMed     Text format     Abstract available


    August 2016
  32. DARVISHI KHEZRI H, Emami Zeydi A, Sharifi H, Jalali H, et al
    Is Vitamin C Supplementation in Patients with beta-Thalassemia Major Beneficial or Detrimental?
    Hemoglobin. 2016;40:293-4.
    PubMed     Text format     Abstract available


  33. SOLER AM, Schelotto M, de Oliveira Mota N, Dorta Ferreira R, et al
    The -(alpha)(5.2) Deletion Detected in a Uruguayan Family: First Case Report in the Americas.
    Hemoglobin. 2016;40:289-92.
    PubMed     Text format     Abstract available


  34. PONGJANTHARASATIEN K, Banyatsuppasin W, Pounsawat S, Jindadamrongwech S, et al
    Occurrence of the - -(SEA), - -(THAI) and - -(FIL) alpha-Thalassemia-1 Carriers from a 7-Year Study at Ramathibodi Hospital, Bangkok, Thailand.
    Hemoglobin. 2016;40:283-4.
    PubMed     Text format     Abstract available


  35. HE S, Lin L, Wei Y, Chen B, et al
    Identification of a Novel beta-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family.
    Hemoglobin. 2016;40:277-9.
    PubMed     Text format     Abstract available


  36. YANG Y, Li DZ, He P
    A Program on Noninvasive Prenatal Diagnosis of alpha-Thalassemia in Mainland China: A Cost-Benefit Analysis.
    Hemoglobin. 2016;40:247-9.
    PubMed     Text format     Abstract available


  37. BILGEN T, Canatan D, Delibas S, Keser I, et al
    A Novel Mutation in the Promoter Region of the beta-Globin Gene: HBB: c.-127G > C.
    Hemoglobin. 2016;40:280-2.
    PubMed     Text format     Abstract available


  38. VINCIGUERRA M, Passarello C, Leto F, Crivello A, et al
    Coinheritance of a Rare Nucleotide Substitution on the beta-Globin Gene and Other Known Mutations in the Globin Clusters: Management in Genetic Counseling.
    Hemoglobin. 2016;40:231-5.
    PubMed     Text format     Abstract available


  39. YANG Y, Li DZ, He P
    Hb Dapu (HBA2: c.52G > T): A Novel Nondeletional alpha-Thalassemia Mutation.
    Hemoglobin. 2016;40:264-6.
    PubMed     Text format     Abstract available


  40. MEHER S, Dehury S, Mohanty PK, Patel S, et al
    Hb Tianshui (HBB: C.119A > G) in Compound Heterozygosity with Hb S (HBB: C.20A > T) from Odisha, India.
    Hemoglobin. 2016;40:270-2.
    PubMed     Text format     Abstract available


  41. KARIMI M, Jooya P, Haghpanah S, Mokhtari M, et al
    Evaluation of the Relationship Between Hb F Levels and Nucleated Red Blood Cells with Morbidity in Non Transfusion-Dependent Thalassemia Patients.
    Hemoglobin. 2016;40:250-6.
    PubMed     Text format     Abstract available


  42. SINGH MP, Gupta RB, Yadav R, Sharma RK, et al
    Prevalence of alpha(+)-Thalassemia in the Scheduled Tribe and Scheduled Caste Populations of Damoh District in Madhya Pradesh, Central India.
    Hemoglobin. 2016;40:285-8.
    PubMed     Text format     Abstract available


    June 2016
  43. BOUCHER MO, Chui DH, Woda BA, Newburger PE, et al
    Mild Microcytic Anemia in an Infant with a Compound Heterozygosity for Hb C (HBB: c.19G > A) and Hb Osu Christiansborg (HBB: c.157G > A).
    Hemoglobin. 2016;40:208-9.
    PubMed     Text format     Abstract available


  44. BELISARIO AR, Sales RR, Silva CM, Velloso-Rodrigues C, et al
    The Natural History of Hb S/Hereditary Persistence of Fetal Hemoglobin in 13 Children from the State of Minas Gerais, Brazil.
    Hemoglobin. 2016;40:215-9.
    PubMed     Text format     Abstract available


  45. YAN JM, Zhou JY, Xie XM, Li J, et al
    A New delta-Globin Gene Variant: Hb A2-Fengshun [delta121(GH4)Glu-->Lys (HBD: c.364G > A)].
    Hemoglobin. 2016;40:213-4.
    PubMed     Text format     Abstract available


  46. BUI THI KIM L, Phu Chi D, Hoang Thanh C
    Spectrum of Common alpha-Globin Deletion Mutations in the Southern Region of Vietnam.
    Hemoglobin. 2016;40:206-7.
    PubMed     Text format     Abstract available


  47. JIANG H, Yan JM, Li J, Xie XM, et al
    Diagnostic Dilemma of Hb Perth [beta32(B14)Leu-->Pro; HBB: c.98T > C] in Mainland China.
    Hemoglobin. 2016;40:202-5.
    PubMed     Text format     Abstract available


  48. PARMEGGIANI G, Gualandi F, Selvatici R, Rimessi P, et al
    A Family with gamma-Thalassemia and High Hb A2 Levels.
    Hemoglobin. 2016;40:187-90.
    PubMed     Text format     Abstract available


  49. MIRI-MOGHADDAM E, Bahrami S, Naderi M, Bazi A, et al
    Molecular Characterization of beta-Thalassemia Intermedia in Southeast Iran.
    Hemoglobin. 2016;40:173-8.
    PubMed     Text format     Abstract available


  50. MUNKONGDEE T, Tanakulmas J, Butthep P, Winichagoon P, et al
    Molecular Epidemiology of Hemoglobinopathies in Cambodia.
    Hemoglobin. 2016;40:163-7.
    PubMed     Text format     Abstract available


  51. MAXIMO C, Olalla Saad ST, Thome E, Queiroz AM, et al
    Amputations in Sickle Cell Disease: Case Series and Literature Review.
    Hemoglobin. 2016;40:150-5.
    PubMed     Text format     Abstract available


  52. YUZBASIOGLU ARIYUREK S, Yildiz SM, Yalin AE, Guzelgul F, et al
    Hemoglobinopathies in the Cukurova Region and Neighboring Provinces.
    Hemoglobin. 2016;40:168-72.
    PubMed     Text format     Abstract available


  53. ZHENG CY, Minniti CP, Chaitowitz MH
    Sickle Cell Crisis Complicated by Synthetic Cannabinoid Abuse: A Case Report.
    Hemoglobin. 2016;40:220-2.
    PubMed     Text format     Abstract available


  54. DIVOKA M, Partschova M, Kucerova J, Mojzikova R, et al
    Molecular Characterization of beta-Thalassemia in the Czech and Slovak Populations: Mediterranean, Asian and Unique Mutations.
    Hemoglobin. 2016;40:156-62.
    PubMed     Text format     Abstract available


  55. ZHOU JY, Yan JM, Li J, Li DZ, et al
    First Case of a Compound Heterozygosity for Two Nondeletional alpha-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze.
    Hemoglobin. 2016;40:210-2.
    PubMed     Text format     Abstract available


  56. HAN L, Su H, Wu H, Jiang W, et al
    Molecular Epidemiological Survey of Glucose-6-Phosphate Dehydrogenase Deficiency and Thalassemia in Uygur and Kazak Ethnic Groups in Xinjiang, Northwest China.
    Hemoglobin. 2016;40:179-86.
    PubMed     Text format     Abstract available


  57. LI J, Yan JM, Xie XM, Zhou JY, et al
    Consequences of Delayed Prenatal Diagnosis of beta-Thalassemia in Mainland China.
    Hemoglobin. 2016;40:191-3.
    PubMed     Text format     Abstract available


    January 2016
  58. HE Y, Zhao Y, Lou JW, Liu YH, et al
    Fetal Anemia and Hydrops Fetalis Associated with Homozygous Hb Constant Spring (HBA2: c.427T > C).
    Hemoglobin. 2016.
    PubMed     Text format     Abstract available


  59. WU MY, Li DZ
    The Codon 35 (A > G) (HBB: c.107A > G) at the alpha-beta Chain Interface of the beta-Globin Gene: A Silent Mutation?
    Hemoglobin. 2016;40:56-8.
    PubMed     Text format     Abstract available


  60. KORDAFSHARI A, Amirian A, Zeinali S, Valaei A, et al
    Molecular Characterization of delta-Thalassemia in Iran.
    Hemoglobin. 2016;40:44-7.
    PubMed     Text format     Abstract available


  61. GATIN L, Rogier de Mare A, Mary P, Vialle R, et al
    Osteonecrosis of the Femoral Head: A Proposed New Treatment in Homozygous Sickle Cell Disease.
    Hemoglobin. 2016;40:1-9.
    PubMed     Text format     Abstract available


  62. YANG Y, He P, Li DZ
    Analysis of Fetal Blood: Is There Still a Role for Prenatal Diagnosis of Thalassemia?
    Hemoglobin. 2016;40:29-31.
    PubMed     Text format     Abstract available


  63. GHARTEY-KWANSAH G, Boampong JN, Aboagye B, Afoakwah R, et al
    The Prevalence of alpha-Thalassemia and Its Relation to Plasmodium falciparum Infection in Patients Presenting to Clinics in Two Distinct Ecological Zones in Ghana.
    Hemoglobin. 2016;40:32-7.
    PubMed     Text format     Abstract available


  64. UGRIN M, Stojiljkovic M, Zukic B, Klaassen K, et al
    Functional Analysis of an (A)gamma-Globin Gene Promoter Variant (HBG1: g.-225_-222delAGCA) Underlines Its Role in Increasing Fetal Hemoglobin Levels Under Erythropoietic Stress.
    Hemoglobin. 2016;40:48-52.
    PubMed     Text format     Abstract available


  65. SURAPOLCHAI P, Sirachainan N, So CC, Hongeng S, et al
    Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses.
    Hemoglobin. 2016;40:70-3.
    PubMed     Text format     Abstract available


  66. AU PK, Kan AS, Tang MH, Leung KY, et al
    A Fetus with Hb Bart's Disease Due to Maternal Uniparental Disomy for Chromosome 16.
    Hemoglobin. 2016;40:66-9.
    PubMed     Text format     Abstract available


  67. WU MY, Li DZ
    First Detection of the -27 (A > G) (HBB: c.-77A > G) Mutation of the beta-Globin Gene in a Chinese Family.
    Hemoglobin. 2016;40:59-60.
    PubMed     Text format     Abstract available


  68. FARASHI S, Vakili S, Garous NF, Ashki M, et al
    Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 Gene.
    Hemoglobin. 2016;40:38-43.
    PubMed     Text format     Abstract available


  69. SMITH DL, Mitui M, Park JY, Luu HS, et al
    Characterization of the HBB: c.*233G > C Variant: No Evidence of a beta-Thalassemic Phenotype.
    Hemoglobin. 2016;40:25-8.
    PubMed     Text format     Abstract available


  70. SILVA AN, Cardoso GL, Cunha DA, Diniz IG, et al
    The Spectrum of beta-Thalassemia Mutations in a Population from the Brazilian Amazon.
    Hemoglobin. 2016;40:20-4.
    PubMed     Text format     Abstract available


  71. AKINBAMI AO, Campbell AD, Han ZJ, Luo HY, et al
    Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.
    Hemoglobin. 2016;40:64-5.
    PubMed     Text format     Abstract available


  72. SMELTZER MP, Nolan VG, Yu X, Nottage KA, et al
    Distance from an Urban Sickle Cell Center and its Effects on Routine Healthcare Management and Rates of Hospitalization.
    Hemoglobin. 2016;40:10-5.
    PubMed     Text format     Abstract available


  73. LI YQ, Ye LH, Mo Y
    Hb Matera (HBB: c.167 T > A): A Second Case Detected in a Pregnant Chinese Woman by the Capillary Electrophoresis Method.
    Hemoglobin. 2016;40:125-6.
    PubMed     Text format     Abstract available


  74. KHOSRAVI A, Jalali-Far M, Saki N, Hosseini H, et al
    Evaluation of alpha-Globin Gene Mutations Among Different Ethnic Groups in Khuzestan Province, Southwest Iran.
    Hemoglobin. 2016;40:113-7.
    PubMed     Text format     Abstract available


  75. ZHENG X, Lin M, Yang H, Pan MC, et al
    Molecular Epidemiological Characterization and Health Burden of Thalassemias in the Chaoshan Region, People's Republic of China.
    Hemoglobin. 2016;40:138-42.
    PubMed     Text format     Abstract available


  76. OLIVEIRA A, Warcel D, Huntley N, Eleftheriou P, et al
    Symptomatic Erythrocytosis Due to Homozygosity for Hb Luton [HBA2: c.269A>T (or HBA1)] and alpha-Thalassemia: A Clinical Update.
    Hemoglobin. 2016;40:127-9.
    PubMed     Text format     Abstract available


  77. FARASHI S, Rad F, Shahmohammadi B, Imanian H, et al
    First Report of a Dominantly Inherited beta-Thalassemia Caused by a Novel Elongated beta-Globin Chain.
    Hemoglobin. 2016;40:102-7.
    PubMed     Text format     Abstract available


  78. ALKHALDI SM, Khatatbeh MM, Berggren VE, Taha HA, et al
    Knowledge and Attitudes Toward Mandatory Premarital Screening Among University Students in North Jordan.
    Hemoglobin. 2016;40:118-24.
    PubMed     Text format     Abstract available


  79. CHERRY L, Calo C, Talmaci R, Perrin P, et al
    beta-Thalassemia Haplotypes in Romania in the Context of Genetic Mixing in the Mediterranean Area.
    Hemoglobin. 2016;40:85-96.
    PubMed     Text format     Abstract available


  80. COLLIER AB 3RD, Coon LM, Monteleone P, Umaru S, et al
    A Novel beta-Globin Chain Hemoglobin Variant, Hb Allentown [beta137(H15)Val-->Trp (GTG>TGG) HBB: c.412_413delinsTG, p.Val138Trp], Associated with Low Oxygen Saturation, Intermittent Aplastic Crises and Splenomegaly.
    Hemoglobin. 2016;40:130-3.
    PubMed     Text format     Abstract available


  81. HENDERSON SJ, Timbs AT, McCarthy J, Gallienne AE, et al
    Ten Years of Routine alpha- and beta-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Hemoglobin. 2016;40:75-84.
    PubMed     Text format     Abstract available


    July 2015
  82. SOUZA RA, Carlos AM, Souza BM, Rodrigues CV, et al
    alpha-Thalassemia: Genotypic Profile Associated with Ethnicity and Hematological Differentiation of Iron Deficiency Anemia in the Region of Uberaba, Minas Gerais, Brazil.
    Hemoglobin. 2015.
    PubMed     Text format     Abstract available


    May 2015
  83. UNAL S, Chui DH, Gumruk F
    Fanconi's Anemia Effect or Sickle Cell Anemia Effect: That is the Question.
    Hemoglobin. 2015.
    PubMed     Text format     Abstract available


    January 2015
  84. ZAKER-KANDJANI B, Namdar-Aligoodarzi P, Azarkeivan A, Najmabadi H, et al
    Mutation screening of the Kruppel-like factor 1 gene using single-strand conformational polymorphism in a cohort of Iranian beta-thalassemia patients.
    Hemoglobin. 2015;39:24-9.
    PubMed     Text format     Abstract available


  85. PERERA PS, Silva I, Hapugoda M, Wickramarathne MN, et al
    Rare hemoglobin variants: Hb G-Szuhu (HBB: c.243C>G), Hb G-Coushatta (HBB: c.68A>C) and Hb Mizuho (HBB: c.206T>C) in Sri Lankan families.
    Hemoglobin. 2015;39:62-5.
    PubMed     Text format     Abstract available


  86. HERRERA MA, De La Fuente-Gonzalo F, Gonzalez FA, Nieto JM, et al
    Identification of a novel mutation in the beta-globin gene 3' untranslated region (HBB: c.*+118A > G) in Spain.
    Hemoglobin. 2015;39:30-5.
    PubMed     Text format     Abstract available


  87. WIJARNPREECHA K, Kumfu S, Chattipakorn SC, Chattipakorn N, et al
    Cardiomyopathy associated with iron overload: how does iron enter myocytes and what are the implications for pharmacological therapy?
    Hemoglobin. 2015;39:9-17.
    PubMed     Text format     Abstract available


  88. GHALLYAN N, Donald T, Broad D, Johnson S, et al
    Hb Feilding [beta12(A9)Thr --> Pro; HBB: c.37A>C]: a novel unstable beta-globin chain variant.
    Hemoglobin. 2015;39:49-51.
    PubMed     Text format     Abstract available


  89. GHERGHEREHCHI R, Habibzadeh A
    Insulin resistance and beta cell function in patients with beta-thalassemia major.
    Hemoglobin. 2015;39:69-73.
    PubMed     Text format     Abstract available


  90. UNAL S, Chui DH, Luo HY, Okur H, et al
    The first report of a homozygous codons 9/10 (+T) beta-thalassemia mutation in a Turkish patient.
    Hemoglobin. 2015;39:66-8.
    PubMed     Text format     Abstract available


  91. LIU S, Chen L, Zhang X, Li J, et al
    Primer-introduced restriction analysis polymerase chain reaction method for non-invasive prenatal testing of beta-thalassemia.
    Hemoglobin. 2015;39:18-23.
    PubMed     Text format     Abstract available


  92. KUMAR R, Sagar C, Sharma D, Kishor P, et al
    beta-globin genes: mutation hot-spots in the global thalassemia belt.
    Hemoglobin. 2015;39:1-8.
    PubMed     Text format     Abstract available


  93. LI J, Li R, Li DZ
    Identification of nondeletional alpha-thalassemia in a prenatal screening program by reverse dot-blot in southern China.
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  94. KATTAMIS A, Delaporta P, Fylaktou I, Vrettou C, et al
    Hb Souli, a 6 bp in-frame deletion on the HBA2 gene (HBA2: c.[41-46delCCTGGG]) leads to alpha-thalassemia intermedia, when in trans to a single alpha-globin gene deletion.
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  95. BOUDRAHEM-ADDOUR N, Izem-Meziane M, Bouguerra K, Nadjem N, et al
    Oxidative status and plasma lipid profile in beta-thalassemia patients.
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  96. BALLAS SK, Vichinsky EP
    Is the medical home for adult patients with sickle cell disease a reality or an illusion?
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  97. AMID A, Haghi-Ashtiani B, Kirby-Allen M, Haghi-Ashtiani MT, et al
    Screening for thalassemia carriers in populations with a high rate of iron deficiency: revisiting the applicability of the Mentzer Index and the effect of iron deficiency on Hb A2 levels.
    Hemoglobin. 2015;39:141-3.
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  98. SALLER E, Dutly F, Frischknecht H
    Two novel alpha2 gene mutations causing altered amino acid sequences produce a mild (Hb Kinshasa, HBA2: c.428A > T) and severe (HBA2: c.342-345insCC) alpha-thalassemia phenotype.
    Hemoglobin. 2015;39:144-6.
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  99. KHAN J, Ahmad N, Siraj S, Hoti N, et al
    Genetic determinants of beta-thalassemia intermedia in Pakistan.
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  100. ERAZO BM, Ramirez GA, Cerrato LE, Pinto LJ, et al
    Prevalence of Hb S (HHB: c.20A > T) in a Honduran population of African descent.
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  101. SHERIEF LM, Kamal NM, Abdelrahman HM, Hassan BA, et al
    First report of acute lymphoblastic leukemia in an Egyptian child with beta-thalassemia major.
    Hemoglobin. 2015;39:127-9.
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  102. JIANG H, Liu S, Zhang YL, Wan JH, et al
    Association of an alpha-globin gene cluster duplication and heterozygous beta-thalassemia in a patient with a severe thalassemia syndrome.
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  103. NITTA T, Kawano F, Yamashiro Y, Takagi F, et al
    A new Kruppel-like factor 1 mutation (c.947G > A or p.C316Y) in humans causes beta-thalassemia minor.
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  104. HASSAN SM, Harteveld CL, Bakker E, Giordano PC, et al
    Broader spectrum of beta-thalassemia mutations in Oman: regional distribution and comparison with neighboring countries.
    Hemoglobin. 2015;39:107-10.
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  105. DAS S, Mashon RS
    Coinheritance of Hb D-Punjab and beta-thalassemia: diagnosis and implications in prenatal diagnosis.
    Hemoglobin. 2015;39:138-40.
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  106. LI Z, Li L, Yao Y, Li N, et al
    A novel promoter mutation (HBB: c.-75G>T) was identified as a cause of beta(+)-thalassemia.
    Hemoglobin. 2015;39:115-20.
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  107. MOAYEDI ESFAHANI BA, Reisi N, Mirmoghtadaei M
    Evaluating the safety and efficacy of silymarin in beta-thalassemia patients: a review.
    Hemoglobin. 2015;39:75-80.
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  108. CAKIR U, Demircioglu F
    Prevalence of Depression in Patients with beta-Thalassemia as Assessed by the Beck's Depression Inventory [Hemoglobin. 2014;38(4):289-291].
    Hemoglobin. 2015;39:451.
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  109. LEE HW, Han SM, Yang Y, Lin TH, et al
    Thalassemia Phenotypes and Genotypes in Taiwan: A Retrospective Study Based on Thalassemia Screening of Young Men for Military Conscription.
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  110. FARASHI S, Bayat N, Faramarzi Garous N, Ashki M, et al
    Interaction of an alpha-Globin Gene Triplication with beta-Globin Gene Mutations in Iranian Patients with beta-Thalassemia Intermedia.
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  111. VLACHAKI E, Neokleous N, Paspali D, Vetsiou E, et al
    Evaluation of Mental Health and Physical Pain in Patients with beta-Thalassemia Major in Northern Greece.
    Hemoglobin. 2015;39:169-72.
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  112. FARASHI S, Faramarzi Garous N, Zeinali F, Vakili S, et al
    A 21 Nucleotide Duplication on the alpha1- and alpha2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease.
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  113. SHAMOON RP, Al-Allawi NA, Cappellini MD, Di Pierro E, et al
    Molecular Basis of beta-Thalassemia Intermedia in Erbil Province of Iraqi Kurdistan.
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  114. OBAID JM, Abo El-Nazar SY, Ghanem AM, El-Hadidi AS, et al
    Compensation of CD55 Underexpression on Red Blood Cells of beta-Thalassemia Major Patients.
    Hemoglobin. 2015;39:184-9.
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  115. WAYE JS, Eng B, Hanna M, Hohenadel BA, et al
    alpha(+)-Thalassemia Due to a Frameshift Mutation of the alpha2-Globin Gene [codons 55/56 (+T) or HBA2: c.168dup].
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  116. HE S, Zheng C, Meng D, Chen R, et al
    Hb H Hydrops Fetalis Syndrome Caused by Association of the - -(SEA) Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family.
    Hemoglobin. 2015;39:216-9.
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  117. PORNPRASERT S, Saoboontan S, Punyamung M
    Detection of Hb Constant Spring (HBA2: c.427T>C) Heterozygotes in Combination with beta-Thalassemia or Hb E Trait by Capillary Electrophoresis.
    Hemoglobin. 2015;39:211-5.
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  118. CHEN B, Huang P, Yi S, Chen Q, et al
    First Detection of a Splice Site beta-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family.
    Hemoglobin. 2015;39:207-8.
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  119. JONASSAINT CR, Shah N, Jonassaint J, De Castro L, et al
    Usability and Feasibility of an mHealth Intervention for Monitoring and Managing Pain Symptoms in Sickle Cell Disease: The Sickle Cell Disease Mobile Application to Record Symptoms via Technology (SMART).
    Hemoglobin. 2015;39:162-8.
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  120. MUSZLAK M, Pissard S, Badens C, Chamouine A, et al
    Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
    Hemoglobin. 2015;39:156-61.
    PubMed     Text format     Abstract available


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