OOIR: Observatory of International Research

Papers

(The median citation count of Hemoglobin is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-06-01 to 2025-06-01.)

Article	Citations
A Novel 5 kb Deletion in theβ-Globin Gene Cluster Identified in a Chinese Patient	24
Noninvasive Prenatal Diagnosis of SEA-Thalassemia by Combining 1000 Genomes Database and Relative Haplotype Dosage	16
Clinical Exome Sequencing Reveals Novel Mutations in SPTB Gene Associated with Hereditary Spherocytosis in Patients with Suspected Congenital Hemolytic Anemia	13
Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid Differentiation	12
Coexisting β-Thalassemia Trait, Gilbert Syndrome and Alpha-Globin Gene Triplication in a Child with Non-Transfusion Dependent Thalassemia Phenotype	12
The First Iranian Case of Unstable Hemoglobin Santa Ana	11
A New Case of Hb Headington (HBB: c.217A>C) Due to a New DNA Transversion, Found in a Patient with Type 2 Diabetes Mellitus	11
Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β ⁰ -Thalassemia	11
Strong Positive Dichlorophenolindophenol Precipitation Suggests Hb Dhonburi (or Hb Neapolis) (HBB: c.380T>G) Inheritance in a Couple at Risk for Severe β-Thalassemia	10
Morbidity and Mortality Associated with COVID-19 and Acute Chest Syndrome in Sickle Cell Disease Patients	9
A novel α Globin Gene Cluster Duplication, αααα³⁸⁰ Heterozygous β⁰-Thal Variant, Leading to a Blood Transfusion-Dependent Phenotype	8
ATG-Thymoglobulin Versus ATG-Fresenius for Conditioning in Thalassemia Patients Who Underwent Allogenic Stem Cell Transplantation from Matched-Sibling Donor: A Tertiary Cancer Care Center Short-Term E	8
Effect of Hydroxyurea Therapy on Growth Parameters in Older Children (6-15 Year-Old) with Sickle Cell Disease: Low Dose Versus High Dose	8
Hb Jishui [HBA1: c.225C>G, Codon 74 (GAC>GAG), Asp→Glu]: A Novel α Chain Hemoglobin Variant Detected During Hb A_1c Measurement	7
Submitting Novel Globin Gene Variants to Hemoglobin	7
Research Progress of Cell-Free Fetal DNA in Non-Invasive Prenatal Diagnosis of Thalassemia	6
High Systolic Blood Pressure, Anterior Segment Changes and Visual Impairment Independently Predict Sickle Cell Retinopathy	6
A Triple-Heterozygous β-Thalassemia Patient Demonstrated an Unusual Electrophoresis Pattern Due to a Novel β⁰ Mutation [an IVS-II-654 (C>T) mutation with a Hb Zürich-Langstrasse (HBB<	6
Gene Therapies for Hemoglobinopathies: Promises and Challenges	5
Molecular Identification and the Hematological Findings of Four Novel Variants in Globin Genes in Jiangxi Province of Southern China	5
A Review of Gene Therapies for Hemoglobinopathies	5
Identification of a β-Globin Gene Mutation with the Genotype β-28(A > G), IVS-I-5(G > A)/βCD 71/72(+A) Using Third-Generation Sequencing	5
Strengthening Health System and Community Mobilization for Sickle Cell Disease Screening and Management among Tribal Populations in India: An Interventional Study	4
Evaluation of the Function of a Rare Variant in the 3'-Untranslated Region of the β-Globin Gene	4
Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT)	4

Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a β-Thalassemia Major Phenotype	4
A 6-Year Follow-up of a Chinese Child with Homozygous β ⁰ -Thalaasemia and a Heterozygous KLF1 Mutation	4
Hypercoagulability in Sickle Cell Disease: A Thrombo-Inflammatory Mechanism	3
Point-of-Care Newborn Screening for Sickle Cell Disease at Selected Health Facilities in the Gambia	3
Polyneuropathy Associated with Age of Starting the Transfusion and Serum Ferritin Level in Iranian Patients with Thalassemia Major and Intermedia	3
Current Status of β-Thalassemic Burden in India	3
The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran	3
Rapid Identification of β-Thalassemia, Hb E, and High Hb F Determinants Using a High-Resolution Melting Analysis: Application in Prenatal Diagnosis in Southern Thailand	3
Thalassemia in Malaysia	3
The Most Common Types of 3.7 Kilobase Deletion in the Iranian Population	3
A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg, HBD : C.139G > A]	3
Fist Detection of Hb Suqian[β42(CD1) Phe→Leu, HBB:c.129T > A] in Han Chinese	3
A Rare Case of Abnormal Hemoglobin Variant Hb Mizuho: [HBB: c.206T > C β 68(E12) Leu-Pro]: A First Report in the Chinese Population	3
Hb Huadu [α124(H7)Ser→Thr (TCC>ACC), HBA2: c.373T>A]: A Novel Variant of the α-Globin Gene	3
Adherence to Iron Chelation Therapy Among Children with Beta Thalassemia Major: A Multicenter Cross-Sectional Study	3
Dynamic Viscosity of Hemoglobin Solutions Determined by Transverse Proton Magnetic Relaxation	3
First Report of Hb Youngstown in Capillary Electrophoresis and Overlapping Hb Analysis Findings with Hb Rush	3
Prediction of Heart and Liver Iron Overload in β-Thalassemia Major Patients Using Machine Learning Methods	3
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	3
Hb Ryazan: An Elongated C‐Terminal β-Chain Due to a New Frameshift Mutation, HBB: c.396delG p.Val133Trpfs*25	2
Alpha Thalassemia Major: From a Lethal to a Treatable Condition	2
Identification of a Novel Mutation in the 3′ Untranslated Region of the β-Globin Gene (HBB:c.*132C>G) in a Chinese Family	2
Iron Chelators, Such as Deferasirox, When Combined With Hydroxyurea, Provide an Additional Benefit of Iron Chelation in Patients Receiving Chronic Transfusion Therapy	2
Severe Hb H Disease Caused by Hb Zürich–Albisrieden (HBA1: c.178G>C): Another Case Report	2
A Novel 165 Kb Duplication Involving the α-Globin Gene Cluster Is Identified by Low-Pass Whole Genome Sequencing in a Chinese Thalassemia Intermedia Patient	2
Haplotype-Specific Genetic Epidemiology of Sickle Cell Anemia Patients in Accra, Ghana: Patterns, Clinical Implications, and Public Health Responses	2
The Effect of HBB: c.-121C>T Variant [–71 (C>T)] on the β-Globin Promoter: Case Series Study	2
Silent Cerebral Infarcts in Iraqi Patients with Sickle Cell Disease	2
Effect of deletions in the α-globin gene on the phenotype severity of β-thalassemia	2
Premarital Screening is Pivotal in Reducing the Births of Babies Affected with Thalassemia Major in Iraq	2
A Case of Fat Embolism Syndrome with Cerebral Involvement in Sickle Cell Anemia	2
Hb Wanjiang: A New β-Globin Chain Variant with Two Amino Acid Substitutions (HBB: c.255_264delinsTTTTTCTCAG)	2
Prevalence and Spectrum of β-Thalassemia Mutations in Baghdad, Iraq: Data from the Premarital Screening Program	2
A Novel Frameshift Mutation( HBA2 :C.337delC) Associated With α-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China	2
Ameliorating Mental Health Issues in Sickle Cell Disease Patients: A Viewpoint	2
Hb Laibin [β96(FG3)Leu→Arg; HBB: c.290T>G]: A Novel Hemoglobin Variant Described in a Chinese Family	2
Identification of a Novel Variant c.163delG in HBB Gene Resulting in a Beta Null Phenotype in a Proband with Thalassemia Intermedia	2
Hb Nivaria: A New Hemoglobin Variant with a Shortened α-Globin Chain [α139(HC1)Lys→Stop; HBA1: c.418A>T]	2
A New Hemoglobin Variant, Hb Natal (HBA1: c.423C>A), Found in a Greek Family	2
High Prevalence of Hb Riccarton Challenges HbA1c Analysis in a Danish Clinical Laboratory Using the Tosoh G11	2
The Long-Term Efficacy of Deferiprone in Thalassemia Patients With Iron Overload: Real-World Data from the Registry Database	2
Hereditary Hemolytic Anemia Due to PIEZO1 Red Blood Cell Membrane Defect	2
Spectrum of β-Thalassemia Mutations in Some Areas of Guangxi Zhuang Autonomous Region of Southern China: A Study on a Pediatric Population Aged 0–15 Years	2
Bringing Sickle Cell Disease Care Closer to Home: Feasibility and Efficacy of a Quality Improvement Initiative at a Community Hospital	2
Levels of Serum Ferritin and Hepcidin in Patients with Uncomplicated Falciparum Malaria in Hodeidah, Yemen: Considerations for Assessing Iron Status	2
Dominant β-Thalassemia Phenotype Caused by Hb Dieppe (HBB: c.383A>G): Another Case Report	2
Rare Pathogenic β⁰-Thalassemia Mutation, Codon 7 (GAG>TAG) (HBB: c.22G>T). Report of the First Two Cases in Albanian Immigrants of Northern Greece	1
The First Thai Case of Nondeletional HbH Disease Caused by Compound Heterozygosity for α-Thalassemia-1 Chiang Rai (-- ^CR ) Type Deletion with Hb Constant Spring	1
Poor Sleep Quality in Jamaican Adults With Sickle Cell Disease: Prevalence, Risk Factors, and Association With Quality of Life	1
Thalassemia Status in Cambodia	1

Prevalence and Molecular Characteristics of Hemoglobin Variants in Laibin City, Central Guangxi of Southern China	1
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)/β⁺-Thalassemia Phenotype in an Hb S T	1
Hb A ₂ -Pontedera [δ93(F9) Cys > Trp; HBD : C.282T > G]: A New δ-Globin Chain Variant Detected by Screening Tests for Hemoglobin	1
Identification of a Novel Hb H Disease with Glucose-6-Phosphate Dehydrogenase Deficiency Using Whole Genome Sequencing	1
A New Hemoglobin Variant: Hb Tangshan [ HBA1 : c.239C > T, CD79(GCG > GTG)(Ala > Val)] Detected by MALDI-TOF MS	1
Sociodemographic and Clinical Factors Predictive of Poor Health-Related Quality of Life of Children with Sickle Cell Anemia in The Gambia	1
The Effect of Single Nucleotide Polymorphisms on Clinical Phenotypes of Sabahan Transfusion-Dependent β-Thalassemia Patients with Homozygous Filipino β ⁰ -Deletion	1
Efficacy and Safety of a Dispersible Tablet of GPO-Deferasirox Monotherapy among Children with Transfusion-Dependent Thalassemia and Iron Overload	1
First Report of the 3'-Untranslated Region +1506 (A>C) [NM_000518.5: c.*32A>C] mutation on the β-Globin Gene in the Indian Population	1
Hb Lepore-Hong Kong: First Report of a Novel δ/β-Globin Gene Fusion in a Chinese Family	1
The First Compound Heterozygosity for Two Different α-Thalassemia Determinants Causes Hb Bart’s Hydrops Fetalis in a Chinese Family	1
Spectrum of β-Thalassemia and Other Hemoglobinopathies in the Saurashtra Region of Gujarat, India: Analysis of a Large Population Screening Program	1
Phenotypic Analysis of the HBA2 : C.95 G > A Mutation in China	1
An Evaluation for the Causes of Reduced Hb A₂ and the Molecular Characterization of HBD Variants in Hong Kong	1
Sickle Cell Disease in Brazil: Current Management	1
A Novel Hemoglobin Variant Hb Liaobu [α107(G14)Val→Leu, HBA2: c.322G>C] Detected by Matrix-Assisted Laser Desorption Ionization-Time-of-Flight Mass Spectrometry	1
Prevalence and Molecular Characterization of β-Thalassemia in Kirkuk Province of Northern Iraq	1
Current Status of Thalassemia in Lao People’s Democratic Republic	1
β ⁰ -Thalassemia Caused by a Novel Nonsense Mutation [ HBB: c.199A > T]	1
A Novel β-Globin Variant, Hb Odder [ HBB : C.316C > G; CD105 (Leu > Val)]	1
Perspectives of General Hematologists on a Proposed Shared Care Model for HSCT in Sickle Cell Disease	1
Existing Tubular Injury in β-Thalassemia Major Patients Receiving Iron Chelating Agents with Normal Creatinine Level in East Java, Indonesia	1
Knowledge of Sickle Cell Disease, Awareness of Sickle Cell Trait Status and Its Impact on Relationships Among Students at a Historically Black College	1
Prevalence and Management of β-Thalassemia in India	1
Detection of Hb Yulin [β13(A10)Ala→Val, HBB: c.41C>T] by Matrix-Assisted Laser Desorption Ionization-Time-of-Flight Mass Spectrometry	1
Hypersplenism Affects Growth and Haematology in HbSS: Observations from the Jamaican Birth Cohort	1
Successful Treatment of a Child with Hemoglobin Hammersmith with Hematopoietic Stem Cell Transplantation	1
Kinetic Characterisation of the R and R2 Quaternary Structures of Oxyhemoglobins Arising from Different Effects of Inositol Hexakisphosphate on Their Reactions with Ellman’s Reagent	1
Glucose-6-Phosphate Dehydrogenase Deficiency: An Overview of the Prevalence and Genetic Variants in Saudi Arabia	1
Estimating the Cost of Thalassemia Care across the World: A Thalassemia International Federation Model	1
Long-Term and Transient Calcium Channel Blockers; A Systematic Review of Their Role in the Management of Cardiomyopathy in Transfusion-Dependent Thalassemia	1
Hemoglobin β-Globin Variants In Hispanic Patients: An Institutional Experience From Dallas, Texas	1
Rare Case of Homozygosity for CYB5R3 Variant c.235C > T p.(Arg79Trp) Causing Type II Methemoglobinemia	1
Diagnosis and Treatment of Alpha Thalassemia Major	1
Noninvasive Hemoglobin Measurement Reduce Invasive Procedures in Thalassemia Patients	0
Molecular Characterization of Complex Thalassemia with Multiple Variants in β-Globin Gene Cluster and the Identification of a Novel Structural Rearrangement in γ-Globin Gene	0
Secretory Phospholipase A2 Levels Are High in Women with Sickle Cell Disease and Menstruation-Induced Vaso-Occlusive Crises	0
Elevated Plasma Atherogenic and Triglyceride-Glucose Indices: Markers of Cardiovascular Risk in Transfusion-Dependent Thalassemia	0
De Novo Occurrence of Hb Chile [β28(B10) Leu→Met] in a Korean Boy with Methemoglobinemia	0
Eight Cases of Hb Winnipeg [HBA2: c.226G>T (or HBA1)]: A Detailed Study	0
β-Thalassemia Trait Caused by SUPT5H Defects: Another Case Report	0
Analysis of Mean Corpuscular Volume and Red Cell Distribution Width in Patients with Aplastic Anemia	0
Thalidomide and Hydroxyurea in Transfusion-Dependent Thalassemia: Efficacy, Safety Profile and Impact on Quality of Life	0
Characterization and Confirmation of Mildly Unstable Hb Pontoise or α1 63(E12) Ala > Asp and Literature Review	0
Evaluating Health-Related Quality of Life in Thalassemia: Low-Dose Thalidomide vs. Standard Care—Insights from a Comparative Study	0
Evaluating Renal Glomerular Function in Beta-Thalassemia Patients Receiving Deferasirox Using Serum Cystatin-C and Creatinine: A Cross-Sectional Study	0
Factors Associated with Overt Stroke in Children and Adolescents with Sickle Cell Disease: A Retrospective Cohort Study	0
Investigation of the Distribution of Thalassemia in Children in Jiangxi Province, the People’s Republic of China	0
Hb Mizuho (HBB: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation Sequencing	0
Hb Dahua [β59(E3)Lys→Met; HBB: c.179A>T] a Novel Variant on the β-Globin Gene	0
Hb Alessandria [β37(C3)Trp→Leu; HBB: c.113G>T]: a Novel Variant on the β-Globin Chain with Slightly Increased Affinity for Oxygen Detected by Capillary Electrophoresis	0
A Novel β-Globin Variant, Hb Raklev [β 75(E19) HBB :c.227T > A (Leu→Gln)]	0
The Validation of Whole β-Globin Gene Sequencing for Detecting β-Thalassemia Mutations Found in Thailand Using Next-Generation Sequencing (NGS)	0
Dysregulated Serum Cytokine Production in Pediatric Patients with β-Thalassemia Major	0
A Novel Frameshift Mutation of HBB Causing Dominant β-Thalassemia in a Chinese Individual	0
Malaria Infection in Patients with Sickle Cell Disease in Nigeria: Association with Markers of Hyposplenism	0
Heterozygous Beta Thalassemia with Segmental Duplication of chr16p13.3 Leading to Thalassemia Intermedia Phenotype: A Report of 2 Cases with Review of Literature	0
Diagnostic Dilemma of Hemoglobinopathies Using High Performance Liquid Chromatography Alone: A Case Report from a Resource-Constrained Setting	0
Novel Insights into the Pathophysiology and Treatment of Sickle Cell Disease	0
Educational Bias in Cognitive Screening of Adults with Sickle Cell Disease: A Bilingual Multisite Observational Study	0
δβ-Thalassemia and α-Triplication: Is Genetic Retesting Worthwhile in Case of Non-Coherent Phenotype?	0
Consideration of Splenectomy in Unstable Hemoglobinopathy: A Case Report of Hb Hammersmith (HBB: c.128T>C)	0
First Case in Portugal of a Rare Hemoglobin Variant – Hb Montfermeil: Importance of Laboratory Diagnosis	0
A New α1-Globin Variant, Hb Ormylia [ HBA1 :c.63C > G; p.His21Gln]. Report of Eleven Cases in Northern Greece	0
Mutation Spectrum of β-Thalassemia in Some Ethnic Groups of North Maharashtra, India	0
A Rare Case of De Novo Beta-Thalassemia Diagnosed by Whole-Genome Sequencing in an Ethnically Danish Newborn	0
Analysis of Iron Status in Sickle Cell Disease Patients During Steady State at the Center de Recherche et de Lutte contre la Drépanocytose (CRLD) Bamako	0
Anemia in Sri Lanka: A Literature Review	0
Influence of Hemoglobin Strasbourg, a Rare High Oxygen Affinity Hemoglobin Variant, on Different Methods of HbA1c Measurement	0
Misdiagnosis of β-Thalassemia Major Due to Chinese ^G γ+( ^A γδβ) ⁰ -Thalassemia Combined with β	0
Identification of Three Families Carrying Hb Anti-Lepore Hong Kong Variant in Guangxi, China, and Analysis of Their Hematological Data	0
Eleven Cases of Hb J-Paris-I [HBA2: c.38C>A (or HBA1)]: A Stable α Chain Variant Elutes in the P3 Window on High-Performance Liquid Chromatography	0
Hemoglobinopathies and COVID-19: The Experience of a Center in Northern Greece	0
Long-Term Survival Rates of a Sickle Cell Disease Cohort in Saudi Arabia: A 2009–2023 Observational Study	0
A New Mutation, Hb A₂-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A₂ Levels	0
Genotype-Phenotype Study of β-Thalassemia Patients in Sabah	0
Detection of a Rare Mutation in the Initiation Codon of the β-Globin Gene (HBB:C.2T > C; P.Met1Thr)	0
Adherence to Iron Chelation Therapy among Adults with Thalassemia: A Systematic Review	0
The Prevalence of Obstructive Sleep Apnea and Associated Symptoms among Patients with Sickle Cell Disease: A Systematic Review and Meta-analysis	0
A Population-Oriented Genetic Scoring System to Predict Phenotype: A Pathway to Personalized Medicine in Iraqis With β-Thalassemia	0

Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis	0
Characterization of HbH Disease Caused by Compound Heterozygotes α ⁺ -Thalassemia 3.7 kb Deletion and a Large Novel α ⁰ -Thalassem	0
The Aplastic Crisis in HbSS: Observations from the Jamaican Birth Cohort	0
Update on Prevention of Hemoglobinopathies in Azerbaijan	0
Thalassemia in Viet Nam	0
First Report of an α Chain Variant [Hb Coombe Park (HBA2: c.382A>G)] from India, Coinherited with a Novel SERPINC1 Gene Mutation: A Double Whammy?	0
Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster	0
Fetal Hemoglobin H Hydrops Fetalis: Another Three Case Reports	0
Comparative Efficacy and Safety Between Deferiprone and Deferasirox with Special Reference to Serum Ferritin Level and Cardiac Function in Bengali β-Thalassemia Major Children	0
Hemoglobin Balkh, a Novel Mutation in Codon 132 of α2-Globin Gene [α132(H15) (+T) or HBA2 :C.396dup (p.Val134fs)]: A Case Report and Insight into the Pathophysiology	0
First Report of Filipino β ⁰ -Thalassemia/β-Thalassemia in a Chinese Family	0
Ethical and Clinical Considerations in the Use of Hydroxyurea in Pregnant Women with Sickle Cell Disease	0
Alloimmunization in β-Thalassemia and Sickle Cell Disease in Middle Eastern Countries: A Systemic Review	0
Dynamic Thiol-Disulfide Homeostasis in Children With β-Thalassemia Trait	0
Effect of α⁺ Thalassemia on the Severity of Plasmodium falciparum Malaria in Different Sickle Cell Genotypes in Indian Adults: A Hospital-Based Study	0
Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations	0
COVID-19 and Anemia: What Do We Know So Far?	0
Early Onset of Severe Anemia Caused by Hb Calgary ( HBB : C.194G > T): Another Case Report	0
First Reported Case of Hemoglobin H Disease Caused by the Rare α-Globin Gene Mutation ( HBA2 c.244delT) in a Chinese Family	0
Unusual Causes of β Thalassemia Trait: Discovery of another Three Novel SUPT5H Variants	0
Case Fatality Rate and Severity of COVID-19 among Patients with Sickle Cell Disease: A Systematic Review and Meta-Analysis	0
Targeted Next-Generation Sequencing Reveals a Large Novel β-Thalassemia Deletion that Removes the Entire HBB Gene	0
An Expert Overview on Therapies in Non-Transfusion-Dependent Thalassemia: Classical to Cutting Edge in Treatment	0
Quality of Life and Related Factors in β-Thalassemia Patients	0
α- and β-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh	0
Identification of a Novel 7-bp Deletion in the α-Globin Gene Cluster in One Chinese Family	0
Thalassaemia Registries: A Call for Action. A Position Statement from the Thalassaemia International Federation	0
Knowledge and Attitude toward Hemoglobinopathies in Premarital Screening Program among the General Population in the Western Region of Saudi Arabia	0
α ⁰ -Thalassemia Caused by a Novel α-Globin Gene Cluster Deletion (– ^LB ) Found in a Chinese Family	0
Thalassemia in Sri Lanka	0
Thalassemia in Indonesia	0
Thalassemia in Asia 2021 Overview of Thalassemia and Hemoglobinopathies in Bangladesh	0
Hepcidin-to-Ferritin Ratio as an Early Diagnostic Index of Iron Overload in β-Thalassemia Major Patients	0
Estradiol is Pro-Nociceptive and Associated with a Small-Fiber Neuropathy Among Premenopausal Women with Sickle Cell Disease	0
Hb Hebei [α20 (B1) His→Leu; HBA2 :C.62A > T]: A Novel Hemoglobin Variant Found during Measurement of Glycated Hemoglobin	0
The Prevalence of Hypothyroidism among Patients With β-Thalassemia: A Systematic Review and Meta-Analysis of Cross-Sectional Studies	0
Identification of a Novel 16.8Kb Deletion of the α-Globin Gene Cluster by Third-Generation Sequencing	0
Editorial	0
Thalassemia in Thailand	0
Two Novel α-Thalassemia Mutations CD 39 -C [Thr > Pro] and CD 109 ACC > CCC [Thr > Pro] Identified in Two Chinese Families: A Case Report	0
Hb Mizuho Case Report; Early Genomic Testing Facilitates a Life Changing Diagnosis	0
Thalassemia in India	0
Sickle Cell Disease and Quality of Life: An Evaluation of Reporting of Patient-Reported Outcomes in Randomized Controlled Trials	0
Celocentesis for Early Prenatal Diagnosis in Couples at-Risk for β-Thalassemia and Sicilian (δβ)⁰-Thalassemia	0
Haploidentical Hematopoietic Stem Cell Transplantation in Thalassemia	0
β-Thalassemia Intermedia Caused by the β-Globin Gene 3′ Untranslated Region: Another Case Report	0
Prevalence of Hemoglobinopathies in Premarital Screening in the Province of Nigde, Turkey	0
Characterization of Hemoglobin Malay Phenotypes in Tertiary Hospitals	0
Novel Promoter Mutation (HBB:C.-139_-138del) Associated with β-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China	0
Dominant Beta Thalassemia: A Very Rare Cause of Thalassemia in a Mediterranean Country	0
A New Hemoglobin Variant: Hb Jiujiang [α18(A16)Gly→Cys, HBA2: c.55G>T]	0
Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation ( HBB :c.336dup)	0
Hepatobiliary Manifestations in Thalassemia Patients: A Narrative Review	0
Hb Kirikiriroa [α57(E6)Gly→Cys; HBA1: c.172G>T]: A Novel Unstable α-Globin Variant with Oxidized Derivatives Interfering with Hb A_1c	0
Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D HBA1 : C.119_121delCCA Mutation and	0
Profiling of 35 Cases of Hb S/Hb E (HBB: c.20A>T/HBB: c.79G>a), Disease and Association with α-Thalassemia and β-Globin Gene Cluster Haplotypes from Odisha, India	0
Prevalence, Severity, and Determinants of Pain in Thalassemia	0
Hb A ₂ -Guangxi [δ79 (EF3) Asp→Asn, HBD : C.238G > A] and polyA + 70 ( HBD : C.*200G > A): Two No	0
Beta Globin Gene Cluster Haplotypes in Beta Thalassemia in the Kurdistan Region of Iraq	0
Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell Disease	0
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	0
A Case of Misdiagnosis Caused by the Coinheritance of Hb G-Siriraj [β7(A4)Glu→Lys; HBB: c.22G>A] and Hb H Disease	0
Venous Thromboembolism in Individuals with Sickle Cell Disease: A Narrative Review	0
Death from S. pneumoniae in HbSC Disease: Was Expanded Pneumococcal Vaccination Too Late?	0
Clinical Severity of β-Thalassemia Pediatric Patients in Myanmar	0
Description of Hb Évora (HBA2: c.106T>C) on an Unexpected Allele in a Swiss Family	0
Mutation Spectrum of β-Globin Gene in Patients with β-Thalassemia at Tidar Hospital, Magelang, Central Java, Indonesia	0
Hemoglobin Oviedo ( c.115A > G; p.T39A ): A Cause of Low Oxygen Saturation	0
Hb Kalundborg [β79(EF3)Asp→Glu; HBB: c.240C>a], a Possible Low-affinity Hemoglobin Variant Detected during Hb A_1c Measurement	0
Second Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Thalassemia Major after Graft Rejection	0
The Spectrum of α-Thalassemia Mutations in Syrian Patients	0
Development of a Quantitative Multiplex PCR to Detect Three Common Alpha Thalassemia Deletions	0
Prevalence and Associated Factors of Zinc and Vitamin D Deficiencies in Pediatric and Young Adult Patients with Non-Transfusion-Dependent Thalassemia	0
Use of Capillary Electrophoresis Migration Position for the Presumptive Identification of Hemoglobin Variants Prevalent in China	0
Pitfalls in the Diagnosis of β-Thalassemia Intermedia	0
Thalassemia in Pakistan	0
A Novel α-Globin Chain Variant, Hb Nanchang [HBA2: c.46G>A, Codon 15 (GGT>AGT) (Gly→Ser)], Detected by Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectr	0
Introduction to the Special Issue	0
Combined Gap-Polymerase Chain Reaction and Targeted Next-Generation Sequencing Improve α- and β-Thalassemia Carrier Screening in Pregnant Women in Vietnam	0
Rapid and Visual Molecular Detection of High Hb F Determinants; HPFH6, Asian Indian inv-del ( ^A γδβ) ⁰ -Thalassemia, and Thai del-	0
Updated Molecular Spectrum of β-Thalassemia Mutations in Duhok Province, Northern Iraq: Ethnic Variation and the Impact of Immigration	0
Perforated Duodenal Ulcer Associated with Deferasirox in a Child with β-Thalassemia Major	0
Thalassemia in Asia 2021 Thalassemia in Brunei Darussalam	0
Thrombosis Tendency After Splenectomy in a Danish Family With Hemoglobin Volga, and a Literature Review	0
THALASSEMIA in ASIA 2021: Thalassemia in Guangxi Province, People’s Republic of China	0
Treatment with Hydroxyurea Leads to Fetal Hemoglobin Reactivation through CA1 and LIN28B Genes: An In Vitro Study	0
Thalassemia in the Philippines	0