Hemoglobin is a journal in the English language for the communication of research and information concerning hemoglobin in humans and other species. Hemoglobin publishes articles, reviews, points of viewThe journal covers topics such as:structure, function, genetics and evolution of hemoglobinsbiochemical and biophysical properties of hemoglobin moleculescharacterization of hemoglobin disorders (variants and thalassemias),consequences and treatment of hemoglobin disordersepidemiology and prevention of hemoglobin disorders (neo-natal and adult screening)modulating factorsmethodology used for diagnosis of hemoglobin disorders
血红蛋白（Hemoglobin）是一本英语期刊，旨在交流关于人类和其他物种血红蛋白的研究和信息。血红蛋白发表文章、评论、观点该杂志涵盖的主题包括：血红蛋白的结构、功能、遗传学和进化血红蛋白分子的生化和生物物理特性血红蛋白疾病的特征（变异和地中海贫血）、血红蛋白疾病的后果和治疗流行病学和血红蛋白疾病的预防（新生儿和成人筛查）调节因素用于诊断血红蛋白疾病的方法
The Spectrum of β-Thalassemia Mutations in Hamadan Province, West Iran
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1584114
β-Thalassemia in Iran: Things Everyone Needs to Know About This Disease
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1628774
Reticulocyte Hemoglobin Equivalent (Ret-He) Combined with Red Blood Cell Distribution Width Has a Differentially Diagnostic Value for Thalassemias
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1655440
The Sub-Phenotypes of Sickle Cell Disease in Kuwait
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1610427
Detection of a Large Novel α-Thalassemia Deletion in an Autochthonous Belgian Family
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1625786
Coinheritance of Hb A2-Melbourne (HBD: c.130G>A) and Hb E (HBB: c.79G>A) in Laos and Simultaneous High Resolution Melt Detection of Hb A2-Melbourne and Hb A2-Lampang (HBD: c.142G>A) in a Single Tube
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1651332
Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-Thalassemia
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1675688
Prevalence and Risk Factors for Cardiac and Liver Iron Overload in Adults with Thalassemia in Malaysia
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1599906
Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1597732
Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15)
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1675689
Compound Heterozygosity for an Unstable Novel Hemoglobin Variant, Hb Dongguan [α52(E1)Ser→Cys (TCT>TGT); HBA1: c.158C>G], and the – –SEA (Southeast Asian) α-Thalassemia Deletion
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1680383
The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern Turkey
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1647852
Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATC or HBA2: c.3G>C)
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1686012
Barriers to the use of hydroxyurea in the management of sickle cell disease in Nigeria
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1649278
Purulent Pericarditis in Sickle Cell Disease Due to Streptococcus agalactiae; a Unique Case Report and Literature Review
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1579736
Compliance with Deferoxamine Therapy and Thyroid Dysfunction of Patients with β-Thalassemia Major in Syria
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1639517
Hb Guangxi [β65(E9)Lys→Glu (AAG>GAG); HBB: c.196A>G]: A Novel β-Globin Variant.
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1653907
Krüppel-Like Factor 1 Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1567528
Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1602052
Polymorphisms of α-Globin Genes Compromise Polymerase Chain Reaction-Based α-Thalassemia Genotyping in Three Chinese Families
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1607372
The Role of Exercise Stress Echocardiography for Determination of Subclinical Cardiac Involvement in β-Thalassemia Major
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1572620
Evaluation of the Effect of Support-Training System of Peer Group on Promotion of Self-Care in β-Thalassemia Major Patients in Southern Iran
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1651331
A Novel Human β-Globin Gene Variant [Hb London-Ontario, HBB: c.332T>G] is Associated with Transfusion-Dependent Anemia in a Patient with a Hemoglobin Electrophoresis Pattern Consistent with β-Thalassemia Trait
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1619575
Hb Milano [α109(G16)Leu→Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the α1-Globin Gene in an Italian Family
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1566138
Congenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1680384
Luspatercept: A New Kid on the Block
来源期刊：HemoglobinDOI：10.1080/03630269.2020.1719592
Job satisfaction of health care professionals in emergency medical aid in Varna district
来源期刊：HemoglobinDOI：10.14748/hem.v69i3.5939
Pattern of Thalassemia and Hemoglobinopathies in Bangladesh: A Single Center Study at the International Center for Diarrhoeal Disease Research, Bangladesh
来源期刊：HemoglobinDOI：10.1080/03630269.2020.1717763
The Effect of Blood Transfusion on Growth of Patients with Hb E/β-Thalassemia
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1692863
A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as β-Thalassemia Intermedia Due to a KLF1 Gene Mutation
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1620764
A Novel Frameshift Mutation at Codon 2 (–T) (HBB: c.9delT) and First Report of Three New β-Globin Mutations From Azerbaijan
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1657886
Necessity for preparation of the patient for upcoming clinical laboratory analysis
来源期刊：HemoglobinDOI：10.14748/hem.v71i1.6172
Instructors` and Students` Satisfaction with the Services of the Library at the Medical University - Varna
来源期刊：HemoglobinDOI：10.14748/hem.v70i4.5948
Coinheritance of Hb City of Hope (HBB: c.208G>A) and β-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (HBB: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1626741
A sickle cell disease patient with dural venous sinus thrombosis: a case report and literature review
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1651734
Iron Metabolism and Oxidative Status in Patients with Hb H Disease
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1575850
Unstable Hemoglobin Variants: The Need for Clinical Vigilance in Infants with Congenital Jaundice
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1582429
A Novel εγδβ-Thalassemia Deletion Associated with Severe Anemia at Birth and a β-Thalassemia Intermedia Phenotype Later in Life in Three Generations of a Greek Family.
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1699568
Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (– –SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart’s Hydrops Fetalis Syndrome in Thailand
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1666720
Quadrupole-Time-of-Flight Mass Spectrometric Identification of Hemoglobin Subunits α, β, γ and δ in Unknown Peaks of High Performance Liquid Chromatography of Hemoglobin in β-Thalassemias
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1632893
The Quality Management System as a Factor for the Competitiveness of the Bulgarian Pharmaceutical Manufacturers
来源期刊：HemoglobinDOI：10.14748/hem.v71i1.6051
Assessment of the impact of the particular elements in the human resources training system in A&D Pharma
来源期刊：HemoglobinDOI：10.14748/hem.v70i4.5947
Association of the CCR5Δ32 Mutant Genotype with Sickle Cell Disease in Egyptian Patients
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1680381
A De Novo Heterozygous Variant (HBB: c.379delG, p.Val127Cysfs*32) Associated with a Mild β-Thalassemia Intermedia Phenotype in a Turkish Child
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1660888
A Krüppel-Like Factor 1 Gene Mutation Ameliorates the Severity of β-Thalassemia: A Case Report
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1607373
A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1601107
Variant Curation: Overview and Challenges
来源期刊：HemoglobinDOI：10.1080/03630269.2020.1719590
Gene Therapy Getting Personal: Mutation-Specific Editing and Gene Addition Strategies for β-Thalassaemia
来源期刊：HemoglobinDOI：10.1080/03630269.2020.1719599
Anemia Severity in β-Thalassemia Correlates with Elevated Levels of microRNA-125b in Activated Phagocytic Monocytes
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1628043
Double Heterozygosity for Hb Durham-N.C. (HBB: c.344T>C) [β114(G16)Leu→Pro] and the IVS-I-110 (HBB: c.93-21G>A) Causing a Severe β-Thalassemia Phenotype
来源期刊：HemoglobinDOI：10.1080/03630269.2019.1655030
