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Articles published in Hemoglobin

Retrieve available abstracts of 135 articles:
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    November 2021
  1. MELVIN RG, Liederman Z, Arya S, Rotin L, et al
    A Case of Fat Embolism Syndrome with Cerebral Involvement in Sickle Cell Anemia.
    Hemoglobin. 2021 Nov 8:1-5. doi: 10.1080/03630269.2021.1990081.
    PubMed     Abstract available

  2. DEHURY S, Mohanty PK, Patel S, Meher S, et al
    Profiling of 35 Cases of Hb S/Hb E (HBB: c.20A>T/HBB: c.79G>a), Disease and Association with alpha-Thalassemia and beta-Globin Gene Cluster Haplotypes from Odisha, India.
    Hemoglobin. 2021;45:380-386.
    PubMed     Abstract available

  3. CHAN NCN, Wong THY, Cheng KCK, Chan NPH, et al
    An Evaluation for the Causes of Reduced Hb A2 and the Molecular Characterization of HBD Variants in Hong Kong.
    Hemoglobin. 2021;45:387-391.
    PubMed     Abstract available

  4. HAGHPANAH S, Hosseini-Bensenjan M, Sayadi M, Karimi M, et al
    Incidence Rate of COVID-19 Infection in Hemoglobinopathies: A Systematic Review and Meta-analysis.
    Hemoglobin. 2021;45:371-379.
    PubMed     Abstract available

  5. FARRA C, Abdouni L, Souaid M, Awwad J, et al
    The Spectrum of beta-Thalassemia Mutations in the Population Migration in Lebanon: A 6-Year Retrospective Study.
    Hemoglobin. 2021;45:365-370.
    PubMed     Abstract available

  6. TSITSIKAS DA, Kamal M, Braimoh A, Benson S, et al
    Hb S (HBB: c.20A>T) Characteristics by High Performance Liquid Chromatography in Patients with Sickle Cell Disease Receiving the Novel Agent Voxelotor.
    Hemoglobin. 2021;45:355-357.
    PubMed     Abstract available

  7. ALIYEVA G, Abdulalimov E, Asadov C, Mammadova T, et al
    First Report of beta-Thalassemia Intermedia in a Patient Compound Heterozygous for -92 (C>T) and Codons 36/37 (-T) Mutations.
    Hemoglobin. 2021;45:347-348.
    PubMed     Abstract available

    September 2021
  8. HUANG LF, Yu LL, Nikuze L, Singh S, et al
    Spectrum of beta-Thalassemia Mutations in Some Areas of Guangxi Zhuang Autonomous Region of Southern China: A Study on a Pediatric Population Aged 0-15 Years.
    Hemoglobin. 2021;45:318-321.
    PubMed     Abstract available

    Glucose-6-Phosphate Dehydrogenase Deficiency: An Overview of the Prevalence and Genetic Variants in Saudi Arabia.
    Hemoglobin. 2021;45:287-295.
    PubMed     Abstract available

  10. YADAV DD, Jamwal M, Singh N, Sharma R, et al
    Hb Mizuho (HBB: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation Sequencing.
    Hemoglobin. 2021;45:338-340.
    PubMed     Abstract available

  11. RUENGDIT C, Punyamung M, Khamphikham P, Pongpunyayuen P, et al
    Multiplex Quantitative Real-Time Polymerase Chain Reaction and High-Resolution Melting Analysis for Identification of a Couple At-Risk of Having a Newborn with Severe Thalassemia.
    Hemoglobin. 2021;45:309-313.
    PubMed     Abstract available

  12. TRUTTMANN R, Schmidt A, Hartmann B, Rusch S, et al
    Description of Hb Evora (HBA2: c.106T>C) on an Unexpected Allele in a Swiss Family.
    Hemoglobin. 2021;45:314-317.
    PubMed     Abstract available

  13. ZAHRA A, Ragab A, Al-Abboh H, Ismaiel A, et al
    Perforated Duodenal Ulcer Associated with Deferasirox in a Child with beta-Thalassemia Major.
    Hemoglobin. 2021;45:335-337.
    PubMed     Abstract available

  14. CHEN HQ, Wu LS, Jiang F, Li DZ, et al
    Dominant beta-Thalassemia Phenotype Caused by Hb Dieppe (HBB: c.383A>G): Another Case Report.
    Hemoglobin. 2021;45:329-331.
    PubMed     Abstract available

  15. SEN A, Seenappa V, Chakrabarti P, Dolai TK, et al
    First Report of the 3'-Untranslated Region +1506 (A>C) [NM_000518.5: c.*32A>C] mutation on the beta-Globin Gene in the Indian Population.
    Hemoglobin. 2021;45:325-328.
    PubMed     Abstract available

  16. DELICOU S, Aggeli K, Magganas K, Patsourakos D, et al
    Acute Chest Syndrome in Sickle Cell Disease: Clinical Presentation and Outcomes. The Experience of a Single Thalassemia and Sickle Cell Unit in a University Hospital.
    Hemoglobin. 2021;45:303-308.
    PubMed     Abstract available

  17. HAGHPANAH S, Hosseini-Bensenjan M, Sayadi M, Karimi M, et al
    The Prevalence of Hypothyroidism among Patients With beta-Thalassemia: A Systematic Review and Meta-Analysis of Cross-Sectional Studies.
    Hemoglobin. 2021;45:275-286.
    PubMed     Abstract available

  18. KHALIL MSM, Timbs AT, Henderson SJ, Schuh A, et al
    Eleven Cases of Hb J-Paris-I [HBA2: c.38C>A (or HBA1)]: A Stable alpha Chain Variant Elutes in the P3 Window on High-Performance Liquid Chromatography.
    Hemoglobin. 2021;45:322-324.
    PubMed     Abstract available

  19. TRIPATHY I, Panja A, Dolai TK, Mallick AK, et al
    Comparative Efficacy and Safety Between Deferiprone and Deferasirox with Special Reference to Serum Ferritin Level and Cardiac Function in Bengali beta-Thalassemia Major Children.
    Hemoglobin. 2021;45:296-302.
    PubMed     Abstract available

    July 2021
  20. ATROSHI SD, Al-Allawi NAS, Eissa AA
    Updated Molecular Spectrum of beta-Thalassemia Mutations in Duhok Province, Northern Iraq: Ethnic Variation and the Impact of Immigration.
    Hemoglobin. 2021;45:239-244.
    PubMed     Abstract available

  21. PERERA S, Allen A, Rees DC, Premawardhena A, et al
    Pitfalls in the Diagnosis of beta-Thalassemia Intermedia.
    Hemoglobin. 2021;45:265-268.
    PubMed     Abstract available

  22. KHALIL MSM, Timbs AT, Henderson SJ, Schuh A, et al
    Eight Cases of Hb Winnipeg [HBA2: c.226G>T (or HBA1)]: A Detailed Study.
    Hemoglobin. 2021;45:256-258.
    PubMed     Abstract available

  23. ETEMAD K, Mohseni P, Aghighi M, Bahadorimonfared A, et al
    Quality of Life and Related Factors in beta-Thalassemia Patients.
    Hemoglobin. 2021;45:245-249.
    PubMed     Abstract available

  24. UCUCU S, Karabiyik T, Azik FM
    IVS-II-16 (G>C) (HBB: c.315+16G>C) or IVS-II-666 (C>T) (HBB: c.316-185C>T) Mutations Trigger an Hb S (HBB: c.20A>T)/beta(+)-Thalassemia Phenotype in an Hb S Trait Patient.
    Hemoglobin. 2021;45:225-227.
    PubMed     Abstract available

  25. IDRIS IM, Yusuf AA, Gwarzo DH, Kurawa MS, et al
    High Systolic Blood Pressure, Anterior Segment Changes and Visual Impairment Independently Predict Sickle Cell Retinopathy.
    Hemoglobin. 2021;45:228-233.
    PubMed     Abstract available

  26. MARTIN G, Grimholt RM, Le D, Bechensteen AG, et al
    Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a beta-Thalassemia Major Phenotype.
    Hemoglobin. 2021;45:215-219.
    PubMed     Abstract available

  27. RAFAT M, Allamehzadeh Z, Shekari M, Afsa M, et al
    The Effect of HBB: c.-121C>T Variant [-71 (C>T)] on the beta-Globin Promoter: Case Series Study.
    Hemoglobin. 2021;45:234-238.
    PubMed     Abstract available

  28. JIANG F, Tang XW, Li J, Zhou JY, et al
    Hb Lepore-Hong Kong: First Report of a Novel delta/beta-Globin Gene Fusion in a Chinese Family.
    Hemoglobin. 2021;45:220-224.
    PubMed     Abstract available

    June 2021
  29. ANAH MU, Nlemadim AC, Uzomba CI, Ineji EO, et al
    Prolonged QTc Interval in Nigerian Children with Sickle Cell Anemia.
    Hemoglobin. 2021 Jun 10:1-6. doi: 10.1080/03630269.2021.1937207.
    PubMed     Abstract available

    May 2021
  30. ZHAO Q, Zhao SM, Zhang X, Chen SP, et al
    Detection of the HBB: c.393T>G Mutation in Two Patients with Hypochromic Microcytic Anemia.
    Hemoglobin. 2021 May 25:1-4. doi: 10.1080/03630269.2021.1929307.
    PubMed     Abstract available

  31. BROWN BJ, Madu A, Sangeda RZ, Nkya S, et al
    Utilization of Pneumococcal Vaccine and Penicillin Prophylaxis in Sickle Cell Disease in Three African Countries: Assessment among Healthcare Providers in SickleInAfrica.
    Hemoglobin. 2021;45:163-170.
    PubMed     Abstract available

  32. TSOLAKIDIS V, Vlachaki E, Papaioannou M, Pantelidou D, et al
    Total Annual Economic Burden of Patients with Sickle Cell Disease in Steady State in Greece.
    Hemoglobin. 2021;45:143-149.
    PubMed     Abstract available

  33. MOORE JA, Pullon BM, Wang D, Brennan SO, et al
    Hb Tacoma: G>T or G>C, and Does It Matter?
    Hemoglobin. 2021;45:203-206.
    PubMed     Abstract available

  34. SOOD R, Rastogi P, Bansal D, Das R, et al
    An Autopsy Case of beta-Thalassemia Major Illuminating the Pathological Spectrum of the Disease.
    Hemoglobin. 2021;45:180-185.
    PubMed     Abstract available

  35. ATROSHI SD, Al-Allawi N, Chui DHK, Najmabadi H, et al
    A Novel beta(0)-Thalassemia Mutation, HBB: c.356_357delTT [Codon 118 (-TT)] in an Iraqi Kurd.
    Hemoglobin. 2021;45:212-214.
    PubMed     Abstract available

  36. SAENSUWANNA A, Penglong T, Srinoun K
    Upregulation of miR-214 Mediates Oxidative Stress in Hb H Disease via Targeting of ATF4.
    Hemoglobin. 2021;45:197-202.
    PubMed     Abstract available

  37. RUJEERAPAIBOON N, Tantiworawit A, Piriyakhuntorn P, Rattanathammethee T, et al
    Correlation Between Serum Ferritin and Viral Hepatitis in Thalassemia Patients.
    Hemoglobin. 2021;45:175-179.
    PubMed     Abstract available

  38. THEPPORNPITAK K, Trakarnsanga B, Lauhasurayotin S, Poparn H, et al
    A Study to Assess and Improve Adherence to Iron Chelation Therapy in Transfusion-Dependent Thalassemia Patients.
    Hemoglobin. 2021;45:171-174.
    PubMed     Abstract available

  39. LUO LP, Ma L, Lin SB, Huang JG, et al
    Elevated Hb A2 is Not Always Indicative of beta-Thalassemia.
    Hemoglobin. 2021;45:186-190.
    PubMed     Abstract available

  40. SAHA J, Panja A, Nayek K
    The Prevalence of HBB Mutations among the Transfusion-Dependent and Non Transfusion-Dependent Hb E/beta-Thalassemia Children in a Tertiary Center of West Bengal, India.
    Hemoglobin. 2021;45:157-162.
    PubMed     Abstract available

  41. TIAN Q, Lei YL, Xu LL, Li DZ, et al
    First Report of Nondeletional Hb H Disease Caused by an alpha2-Globin Gene Mutation: HBA2: c.184A>T.
    Hemoglobin. 2021;45:210-211.
    PubMed     Abstract available

    March 2021
  42. ALIMOHAMMADI-BIDHENDI S, Azadmehr S, Razipour M, Zeinali S, et al
    Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and alpha-Major Regulatory Element Haplotype Analysis in Iran.
    Hemoglobin. 2021 Mar 27:1-4. doi: 10.1080/03630269.2021.1882482.
    PubMed     Abstract available

  43. OGU UO, Reyes Gil M, Tolu SS, Acharya SA, et al
    First Report of Compound Heterozygosity for Hb S (HBB: c.20A>T) and Hb Haringey (HBB: c.131A>G).
    Hemoglobin. 2021;45:136-139.
    PubMed     Abstract available

  44. YIN Z, Hao Y, Huang X, Chen X, et al
    A Novel Mutation at HBA1: c.349G>T Causing alpha-Thalassemia in a Chinese Family.
    Hemoglobin. 2021;45:94-96.
    PubMed     Abstract available

  45. MARTINEZ VILLEGAS O, Mendoza-Melendez D, Trueba-Gomez R, Rosenfeld-Mann F, et al
    Analysis of a Novel Mexican Variant of the HBB Gene Associated with beta-Thalassemia Using Bioinformatic Tools.
    Hemoglobin. 2021;45:87-93.
    PubMed     Abstract available

  46. INATI A, Al Alam C, El Ojaimi C, Hamad T, et al
    Clinical Features and Outcome of Sickle Cell Disease in a Tertiary Center in Northern Lebanon: A Retrospective Cohort Study in a Local, Hospital-Associated Registry.
    Hemoglobin. 2021;45:80-86.
    PubMed     Abstract available

  47. PANICHCHOB P, Iamdeelert P, Wongsariya P, Wongsariya P, et al
    Molecular Spectrum of beta-Thalassemia Mutations in Central to Eastern Thailand.
    Hemoglobin. 2021;45:97-102.
    PubMed     Abstract available

  48. SHARIFI F, Safizadeh H, Bahrampour A
    Development of the Quality of Life Questionnaire (SF-36) for Patients with beta-Thalassemia Major and beta-Thalassemia Intermedia Based on Extended Rasch Analysis.
    Hemoglobin. 2021;45:119-123.
    PubMed     Abstract available

  49. ZARDKHONI SZ, Moghaddam AG, Rad F, Ghatee MA, et al
    Serum Zinc Level in beta-Thalassemia Major: A Retrospective Study in Southwest Iran.
    Hemoglobin. 2021;45:103-106.
    PubMed     Abstract available

  50. ZHAO YL, Lin QF, He XW, Li YQ, et al
    Hb Hezhou [beta64(E8)Gly-->Ser; HBB: c.193G>A]: A Novel Variant on the beta-Globin Gene.
    Hemoglobin. 2021;45:133-135.
    PubMed     Abstract available

  51. SOLTANI D, Fakhrzadeh H, Sharifi F, Mahmoudi MJ, et al
    Surrogate Markers of Subclinical Atherosclerosis and Its Associated Factors in Patients with beta-Thalassemia Major.
    Hemoglobin. 2021;45:107-111.
    PubMed     Abstract available

  52. COLAH RB, Nadkarni AH, Gorakshakar AC, Sawant PM, et al
    The Changing Trends in Prenatal Diagnosis of Hemoglobinopathies in India: The Quest of a Single Center to Reduce the Burden of Disease over Three Decades.
    Hemoglobin. 2021;45:112-118.
    PubMed     Abstract available

  53. RUENGDIT C, Khamphikham P, Jinorose N, Pornprasert S, et al
    Hb Bart's Hydrops Fetalis Syndrome and Hb H Disease Caused by Deletional Chiang Rai (- -(CR)) alpha(0)-Thalassemia in Two Unrelated Thai Families.
    Hemoglobin. 2021;45:75-79.
    PubMed     Abstract available

  54. WANG RY, Jiang F, Xu LL, Li DZ, et al
    Mild alpha-Thalassemia Caused by a Mosaic alpha-Globin Gene Mutation.
    Hemoglobin. 2021;45:140-141.
    PubMed     Abstract available

    January 2021
  55. MEHER S, Mohanty PK, Patel S, Das K, et al
    Haptoglobin Genotypes Associated with Vaso-Occlusive Crisis in Sickle Cell Anemia Patients of Eastern India.
    Hemoglobin. 2021 Jan 3:1-7. doi: 10.1080/03630269.2020.1801459.
    PubMed     Abstract available

  56. ZAFARI M, Rad MTS, Mohseni F, Nikbakht N, et al
    beta-Thalassemia Major and Coronavirus-19, Mortality and Morbidity: a Systematic Review Study.
    Hemoglobin. 2021;45:1-4.
    PubMed     Abstract available

  57. CHEN X, Lin Z, Hu J, Chen S, et al
    Report of Two Novel Thalassemia Variants, HBB: c.181delG and HBA1: c.121_126delAAGACC, in Chinese Individuals.
    Hemoglobin. 2021;45:52-55.
    PubMed     Abstract available

  58. LIU L, Sun Y, Chen S, Yu C, et al
    Identification of Two Novel Thalassemia Variants, HBA1: c.263delA and HBA2: c.376dupC, in Chinese Individuals.
    Hemoglobin. 2021;45:49-51.
    PubMed     Abstract available

  59. AL-ZUHAIRY SH, Darweesh MA, Othman MA
    Relation of Serum Ferritin Level with Serum Hepcidin and Fucose Levels in Children with beta-Thalassemia Major.
    Hemoglobin. 2021;45:69-73.
    PubMed     Abstract available

  60. BALLAS SK, Riddick-Burden G, Congdon-Martin E
    Determinants of the Outcome of the Transition of Children with Sickle Cell Disease to Adult Programs.
    Hemoglobin. 2021;45:62-65.
    PubMed     Abstract available

  61. TARIQ A, Khurshid S, Sajjad M
    Evaluation of the High Resolution Melting Approach for Detection of beta-Thalassemia Gene Mutations.
    Hemoglobin. 2021;45:20-24.
    PubMed     Abstract available

  62. LIN QY, Chen DY, Kong S, Liu WQ, et al
    A Rare Case of Hb H Disease and Systemic Lupus Erythematosus.
    Hemoglobin. 2021;45:66-68.
    PubMed     Abstract available

  63. WANG WJ, Ding ZX, Zhang HM, Tao TT, et al
    Identification of a Novel beta-Thalassemia Mutation at Codon 130 (+T) (HBB: c.391insT) in Han Chinese.
    Hemoglobin. 2021;45:46-48.
    PubMed     Abstract available

  64. GOLLAMUDI J, Sarvepalli S, Vadaparti Binf A, Alin T, et al
    Venous Thromboembolism in Sickle Cell Disease is Associated with Neutrophilia.
    Hemoglobin. 2021;45:56-59.
    PubMed     Abstract available

  65. SIGAL IR, Ciunci CA
    Case Report of Acute Splenic Sequestration Crisis in an Adult Patient with Hb S Disease and Suspected Hereditary Persistence of Fetal Hemoglobin.
    Hemoglobin. 2021;45:60-61.
    PubMed     Abstract available

  66. DOULGERAKI A, Fragodimitri C, Athanasopoulou H, Drakaki K, et al
    Chronic Hemolysis May Adversely Affect Skeletal Health. A Cross-Sectional Study of a Pediatric Population.
    Hemoglobin. 2021;45:30-36.
    PubMed     Abstract available

  67. AYDOGDU S, Toret E, Aksoy BA, Aydin MF, et al
    Comparison of Hematopoietic Stem Cell Transplantation Results in Patients with beta-Thalassemia Major from Three Different Graft Types.
    Hemoglobin. 2021;45:25-29.
    PubMed     Abstract available

  68. ANGASTINIOTIS M, Petrou M, Loukopoulos D, Modell B, et al
    The Prevention of Thalassemia Revisited: A Historical and Ethical Perspective by the Thalassemia International Federation.
    Hemoglobin. 2021;45:5-12.
    PubMed     Abstract available

  69. LIEDERMAN Z, Quartey NK, Ward R, Papadakos J, et al
    Exploration of Barriers and Facilitators to Optimal Emergency Department Care of Sickle Cell Disease: Opportunities for Patient-Physician Partnerships to Improve Care.
    Hemoglobin. 2021;45:13-19.
    PubMed     Abstract available

    November 2020
  70. CHOURASIA S, Kumar R, Singh MPSS, Vishwakarma C, et al
    High Prevalence of Anemia and Inherited Hemoglobin Disorders in Tribal Populations of Madhya Pradesh State, India.
    Hemoglobin. 2020 Nov 22:1-10. doi: 10.1080/03630269.2020.1848859.
    PubMed     Abstract available

    July 2020
  71. BALANCHIVADZE N, Kudirka AA, Askar S, Almadhoun K, et al
    Impact of COVID-19 Infection on 24 Patients with Sickle Cell Disease. One Center Urban Experience, Detroit, MI, USA.
    Hemoglobin. 2020;44:284-289.
    PubMed     Abstract available

    May 2020
  72. PINTO VM, Derchi GE, Bacigalupo L, Pontali E, et al
    COVID-19 in a Patient with beta-Thalassemia Major and Severe Pulmonary Arterial Hypertension.
    Hemoglobin. 2020;44:218-220.
    PubMed     Abstract available

    March 2020
  73. TERAN MM, Monaco ME, Lazarte SS, Haro C, et al
    Genetic Regulation of Redox Balance in beta-Thalassemia Trait.
    Hemoglobin. 2020;44:122-127.
    PubMed     Abstract available

  74. AL-ALI AK, Alsulaiman A, Alzahrani AJ, Obeid OT, et al
    Prevalence and Diversity of Haplotypes of Sickle Cell Disease in the Eastern Province of Saudi Arabia.
    Hemoglobin. 2020;44:78-81.
    PubMed     Abstract available

  75. AZIMI A, Tahmasebi S, Moradi K, Nejati P, et al
    Severe alpha-Thalassemia Due to Compound Heterozygosity for Hb Adana (alpha59 Gly>Asp) (HBA1: c.179G > A) and Codon 127 (A > T) (HBA2: c.382A > T) in an Iranian Family.
    Hemoglobin. 2020;44:139-142.
    PubMed     Abstract available

  76. HORRI-NACEUR A, Timson DJ
    In Silico Analysis of the Effects of Point Mutations on alpha-Globin: Implications for alpha-Thalassemia.
    Hemoglobin. 2020;44:89-103.
    PubMed     Abstract available

  77. SAMHA L, Sirdah MM, Reading NS, Karmi B, et al
    Molecular Understanding of Severe Cases of beta-Thalassemia in the Nablus Region, West Bank, Palestine.
    Hemoglobin. 2020;44:128-130.
    PubMed     Abstract available

  78. AKSU T, Coskun C, Kuskonmaz B, Unal S, et al
    Hb H Disease Diagnosed During Adolescent Pregnancy.
    Hemoglobin. 2020;44:137-138.
    PubMed     Abstract available

  79. AZARKEIVAN A, Cohan N, Niazkar HR, Azizi A, et al
    Hb S (HBB: c.20A>T) and alpha- and beta-Thalassemia Coinheritance in Iranian Patients.
    Hemoglobin. 2020;44:109-112.
    PubMed     Abstract available

  80. HALDER R, Sundaram UKD, Veetil KK, Rath A, et al
    Concomitant Existence of Paroxysmal Nocturnal Hemoglobinuria in a Patient with Hb E (HBB: c.79G>A) Trait.
    Hemoglobin. 2020;44:134-136.
    PubMed     Abstract available

  81. JIANG F, Xu LL, Chen GL, Zhou JY, et al
    Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland China.
    Hemoglobin. 2020;44:86-88.
    PubMed     Abstract available

  82. MANCO L, Bento C, Relvas L, Cunha E, et al
    Multi-Locus Models to Address Hb F Variability in Portuguese beta-Thalassemia Carriers.
    Hemoglobin. 2020;44:113-117.
    PubMed     Abstract available

  83. AL-NOOD HA, Al-Nood RM, Ghanem NS, Al-Hadi AM, et al
    Effect of the Hydoxyurea in Yemeni Transfusion-Dependent beta-Thalassemia Patients.
    Hemoglobin. 2020;44:104-108.
    PubMed     Abstract available

  84. ALASHKAR F, Herbstreit F, Carpinteiro A, Baum J, et al
    Veno-Venous Extracorporeal Membrane Oxygenation in Adult Patients with Sickle Cell Disease and Acute Chest Syndrome: a Single-Center Experience.
    Hemoglobin. 2020;44:71-77.
    PubMed     Abstract available

  85. CHEN YJ, Li YQ, Liu Q, Tang LY, et al
    A Chinese Male with Normal Hematological Indices and High Hb A2 Levels in beta-Thalassemia Trait.
    Hemoglobin. 2020;44:131-133.
    PubMed     Abstract available

    January 2020
  86. SEMKIU KM, Oliveira JL, Nguyen PL, Porter TR, et al
    Hb F-Wentzville [(G)gamma24(B6)Gly-->Glu; HBG2: c.74G>A, p.Gly25Glu]: An Unstable (G)gamma-Globin Variant Associated with Neonatal Hemolytic Anemia.
    Hemoglobin. 2020 Jan 27:1-3. doi: 10.1080/03630269.2020.1716002.
    PubMed     Abstract available

  87. SARIHI R, Amirizadeh N, Oodi A, Azarkeivan A, et al
    Distribution of Red Blood Cell Alloantibodies Among Transfusion-Dependent beta-Thalassemia Patients in Different Population of Iran: Effect of Ethnicity.
    Hemoglobin. 2020;44:31-36.
    PubMed     Abstract available

  88. BELISARIO AR, Carneiro-Proietti AB, Sabino EC, Araujo A, et al
    Hb S/beta-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics.
    Hemoglobin. 2020;44:1-9.
    PubMed     Abstract available

  89. MASHON RS, Das R, Dhawan R, Kakkar N, et al
    Hb Rush (HBB: c.304G>C): A Rare Variant Hemoglobin Mimicking the Hb S (HBB: c.20A>T) Variant on High Performance Liquid Chromatography.
    Hemoglobin. 2020;44:64-66.
    PubMed     Abstract available

  90. MIR SA, Alshehri BM, Alaidarous M, Banawas SS, et al
    Prevalence of Hemoglobinopathies (beta-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma'ah, Saudi Arabia.
    Hemoglobin. 2020;44:47-50.
    PubMed     Abstract available

  91. NAZ S, Rehman SU, Shakeel M, Rehman H, et al
    Molecular Heterogeneity of beta-Thalassemia in the Kohat Region, Khyber Pakhtunkhwa Province, Pakistan.
    Hemoglobin. 2020;44:37-41.
    PubMed     Abstract available

  92. AL-RIYAMI AZ, Daar S, Kindi SA, Madhani AA, et al
    alpha-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region.
    Hemoglobin. 2020;44:20-26.
    PubMed     Abstract available

  93. ROPERO P, Arbeteta J, Nieto JM, Gonzalez FA, et al
    Nondeletional alpha-Thalassemia: Two New Mutations on the alpha2 Gene.
    Hemoglobin. 2020;44:17-19.
    PubMed     Abstract available

  94. VAN GAMMEREN AJ, Pelkmans L, Endschot CCWV, Roelofsen-de Beer RJAC, et al
    An Unusual Compound Heterozygosity for Hb O-Arab (HBB: c.364G>A) and Hb D-Los Angeles (HBB: c.364G>C).
    Hemoglobin. 2020;44:61-63.
    PubMed     Abstract available

  95. LUO H, Zou Y, Liu Y
    A Novel beta-Thalassemia Mutation [IVS-I-6 (T>G), HBB: c.92+6T>G] in a Chinese Family.
    Hemoglobin. 2020;44:55-57.
    PubMed     Abstract available

  96. CHEN X, Luo S, Huang J, Yuan D, et al
    Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare alpha-Thalassemia Gene HBA2: c.1A>G Mutation.
    Hemoglobin. 2020;44:51-54.
    PubMed     Abstract available

  97. SAKAMOTO A, Nakadate H, Tada K, Yamashiro Y, et al
    A Japanese Family with the Unstable Hb Sydney (HBB: c.203T>C) Variant and Persistent Low Hemoglobin Oxygen Saturation.
    Hemoglobin. 2020;44:58-60.
    PubMed     Abstract available

  98. SHOUJAA A, Moasses F, Mukhalalaty Y, Murad H, et al
    Genotype/Phenotype Correlation of beta-Thalassemia in Syrian Patients: A Cross-Sectional Study.
    Hemoglobin. 2020;44:42-46.
    PubMed     Abstract available

  99. SAJADPOUR Z, Amini-Farsani Z, Motovali-Bashi M, Yadollahi M, et al
    Association between Different Polymorphic Markers and beta-Thalassemia Intermedia in Central Iran.
    Hemoglobin. 2020;44:27-30.
    PubMed     Abstract available

    December 2019
  100. MAKIS A, Georgiou I, Traeger-Synodinos J, Storino MR, et al
    A Novel epsilongammadeltabeta-Thalassemia Deletion Associated with Severe Anemia at Birth and a beta-Thalassemia Intermedia Phenotype Later in Life in Three Generations of a Greek Family.
    Hemoglobin. 2019 Dec 12:1-4. doi: 10.1080/03630269.2019.1699568.
    PubMed     Abstract available

    October 2019
  101. JIANG H, Jiang F, Li J, Tang F, et al
    Congenital Nonspherocytic Hemolytic Anemia Caused by Kruppel-Like Factor 1 Gene Variants: Another Case Report.
    Hemoglobin. 2019 Oct 23:1-4. doi: 10.1080/03630269.2019.1680384.
    PubMed     Abstract available

    May 2019
  102. ADEYEMO TA, Diaku-Akinwunmi IN, Ojewunmi OO, Bolarinwa AB, et al
    Barriers to the use of hydroxyurea in the management of sickle cell disease in Nigeria.
    Hemoglobin. 2019;43:188-192.
    PubMed     Abstract available

  103. CANNATA M, Cassara F, Vinciguerra M, Licari P, et al
    Double Heterozygosity for Hb Durham-N.C. (HBB: c.344T>C) [beta114(G16)Leu-->Pro] and the IVS-I-110 (HBB: c.93-21G>A) Causing a Severe beta-Thalassemia Phenotype.
    Hemoglobin. 2019;43:210-213.
    PubMed     Abstract available

  104. SAFAEI S, Abedi H, Parand S, Karimi M, et al
    Evaluation of the Effect of Support-Training System of Peer Group on Promotion of Self-Care in beta-Thalassemia Major Patients in Southern Iran.
    Hemoglobin. 2019;43:198-203.
    PubMed     Abstract available

  105. WANG MK, Shergill R, Jefkins M, Cheung J, et al
    A sickle cell disease patient with dural venous sinus thrombosis: a case report and literature review.
    Hemoglobin. 2019;43:193-197.
    PubMed     Abstract available

  106. YILMAZ S
    The Spectrum of beta-Thalassemia Mutations in Siirt Province, Southeastern Turkey.
    Hemoglobin. 2019;43:174-181.
    PubMed     Abstract available

  107. BORGES E, Tchonhi C, Couto CSB, Gomes V, et al
    Unusual beta-Globin Haplotype Distribution in Newborns from Bengo, Angola.
    Hemoglobin. 2019;43:149-154.
    PubMed     Abstract available

  108. YASSOUF MY, Alquobaili F, Kabalan Y, Mukhalalaty Y, et al
    Compliance with Deferoxamine Therapy and Thyroid Dysfunction of Patients with beta-Thalassemia Major in Syria.
    Hemoglobin. 2019;43:218-221.
    PubMed     Abstract available

  109. HASAN KN, Sufian A, Mazumder AK, Khaleque MA, et al
    A Novel Pathogenic beta-Thalassemia Mutation Identified at Codon 8 (HBB: c.27delG) in a Bangladeshi Family Acquired De Novo.
    Hemoglobin. 2019;43:162-165.
    PubMed     Abstract available

  110. ABDULLAH UYH, Ibrahim HM, Mahmud NB, Salleh MZ, et al
    Quadrupole-Time-of-Flight Mass Spectrometric Identification of Hemoglobin Subunits alpha, beta, gamma and delta in Unknown Peaks of High Performance Liquid Chromatography of Hemoglobin in beta-Thalassemias.
    Hemoglobin. 2019;43:182-187.
    PubMed     Abstract available

  111. HADIPOUR DEHSHAL M, Tabrizi Namini M, Hantoushzadeh R, Yousefi Darestani S, et al
    beta-Thalassemia in Iran: Things Everyone Needs to Know About This Disease.
    Hemoglobin. 2019;43:166-173.
    PubMed     Abstract available

    March 2019
  112. MORADI K, Aznab M, Tahmasebi S, Dastafkan Z, et al
    The Spectrum of alpha-Thalassemia Mutations in the Lak Population of Iran.
    Hemoglobin. 2019;43:107-111.
    PubMed     Abstract available

  113. JIT BP, Mohanty PK, Pradhan A, Purohit P, et al
    Erythrocyte cAMP in Determining Frequency of Acute Pain Episodes in Sickle Cell Disease Patients from Odisha State, India.
    Hemoglobin. 2019;43:88-94.
    PubMed     Abstract available

  114. ZHOU JY, Jiang F, Li J, Chen GL, et al
    Coinheritance of Hb City of Hope (HBB: c.208G>A) and beta-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (HBB: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization.
    Hemoglobin. 2019;43:145-147.
    PubMed     Abstract available

  115. HEIREMAN L, Luyckx A, Schynkel K, Dheedene A, et al
    Detection of a Large Novel alpha-Thalassemia Deletion in an Autochthonous Belgian Family.
    Hemoglobin. 2019;43:112-115.
    PubMed     Abstract available

  116. YANG K, Ren Q, Wu Y, Zhou Y, et al
    A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as beta-Thalassemia Intermedia Due to a KLF1 Gene Mutation.
    Hemoglobin. 2019;43:140-144.
    PubMed     Abstract available

  117. NGIM CF, Lee MY, Othman N, Lim SM, et al
    Prevalence and Risk Factors for Cardiac and Liver Iron Overload in Adults with Thalassemia in Malaysia.
    Hemoglobin. 2019;43:95-100.
    PubMed     Abstract available

  118. ADEKILE AD, Al-Sherida S, Marouf R, Mustafa N, et al
    The Sub-Phenotypes of Sickle Cell Disease in Kuwait.
    Hemoglobin. 2019;43:83-87.
    PubMed     Abstract available

  119. SUN M, Lou J, Zhag Y, Fu Y, et al
    Polymorphisms of alpha-Globin Genes Compromise Polymerase Chain Reaction-Based alpha-Thalassemia Genotyping in Three Chinese Families.
    Hemoglobin. 2019;43:101-106.
    PubMed     Abstract available

  120. XIE XM, Liu YN, Li J, Jiang F, et al
    A Kruppel-Like Factor 1 Gene Mutation Ameliorates the Severity of beta-Thalassemia: A Case Report.
    Hemoglobin. 2019;43:137-139.
    PubMed     Abstract available

    January 2019
  121. AZIMI A, Nejati P, Tahmasebi S, Alimoradi S, et al
    Characterization of the IVS-II-821 (A>C) (HBB: c.316-30A>C) Mutation in a beta-Thalassemia Phenotype in Iran.
    Hemoglobin. 2019;43:23-26.
    PubMed     Abstract available

  122. NUINOON M, Thipthara O, Fucharoen S
    Compound Heterozygote for a Novel Elongated C-Terminal beta-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous alpha-Thalassemia-2.
    Hemoglobin. 2019;43:52-55.
    PubMed     Abstract available

  123. JIANG F, Li J, Zhou JY, Liao C, et al
    Regulatory Single Nucleotide Polymorphism rs368698783 (G>A): a Genetic Modifier of Hb F Production Only under Erythropoietic Stress Characteristic for beta-Globin Chain Deficiency?
    Hemoglobin. 2019;43:73-75.
    PubMed     Abstract available

  124. ALIBAKHSHI R, Moradi K, Aznab M, Azimi A, et al
    The Spectrum of beta-Thalassemia Mutations in Hamadan Province, West Iran.
    Hemoglobin. 2019;43:18-22.
    PubMed     Abstract available

  125. CURCIO C, Giannone V, Benzoni E, Cesaretti C, et al
    Hb Milano [alpha109(G16)Leu-->Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the alpha1-Globin Gene in an Italian Family.
    Hemoglobin. 2019;43:4-6.
    PubMed     Abstract available

  126. SU Q, Chen S, Wu L, Tian R, et al
    Severe Thalassemia Caused by Hb Zunyi [beta147(HC3)Stop-->Gln; HBB: c.442T>C)] on the beta-Globin Gene.
    Hemoglobin. 2019;43:7-11.
    PubMed     Abstract available

  127. PARSAEE M, Pouraliakbar H, Azarkeivan A, Ghadrdoost B, et al
    The Role of Exercise Stress Echocardiography for Determination of Subclinical Cardiac Involvement in beta-Thalassemia Major.
    Hemoglobin. 2019;43:34-37.
    PubMed     Abstract available

  128. AGBUDUWE C, Rugless M, Asba N, Proven M, et al
    Severe Drug-Induced Hemolysis in a Patient with Compound Heterozygosity for Hb Peterborough (HBB: c.334G>T) and Hb Lepore-Boston-Washington (NG_000007.3: g.63632_71046del).
    Hemoglobin. 2019;43:56-59.
    PubMed     Abstract available

  129. KOLLIOPOULOU A, Siamoglou S, John A, Sgourou A, et al
    Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in beta-Thalassemia Intermedia: A Validation Cohort Study.
    Hemoglobin. 2019;43:27-33.
    PubMed     Abstract available

  130. INTASAI N, Phasit A, Panyasai S, Pornprasert S, et al
    A Case Report of Compound Heterozygosity for beta(0)/beta(+)-Thalassemia Resulting from under Diagnosed beta-Thalassemia Found in a Hb A'2 Sample.
    Hemoglobin. 2019;43:63-65.
    PubMed     Abstract available

  131. YAO X, Xu LH, Xu HG, Li XY, et al
    Iron Metabolism and Oxidative Status in Patients with Hb H Disease.
    Hemoglobin. 2019;43:38-41.
    PubMed     Abstract available

  132. BHAT A, Neculiseanu E, Tam EL, Gendy A, et al
    Purulent Pericarditis in Sickle Cell Disease Due to Streptococcus agalactiae; a Unique Case Report and Literature Review.
    Hemoglobin. 2019;43:1-3.
    PubMed     Abstract available

  133. MURAD H, Moassas F
    First Report on the Coinheritance of alpha-Thalassemia and a Rare beta-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family.
    Hemoglobin. 2019;43:66-68.
    PubMed     Abstract available

  134. ZHAO Y, Lou J, Sun M, Fu Y, et al
    Hb H Disease Results from Compound Heterozygosity of - -(SEA) and -alpha(MAL3.5) in a Chinese Family.
    Hemoglobin. 2019;43:69-72.
    PubMed     Abstract available

  135. TAMADDONI A, Khabaz Astaneh S, Tabaripour R, Akhavan-Niaki H, et al
    Kruppel-Like Factor 1 Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with beta-Thalassemia Intermedia.
    Hemoglobin. 2019;43:12-17.
    PubMed     Abstract available

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