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 2021-05-01 to 2025-05-01.)

Article	Citations
A Novel 5 kb Deletion in theβ-Globin Gene Cluster Identified in a Chinese Patient	23
Noninvasive Prenatal Diagnosis of SEA-Thalassemia by Combining 1000 Genomes Database and Relative Haplotype Dosage	15
Clinical Exome Sequencing Reveals Novel Mutations in SPTB Gene Associated with Hereditary Spherocytosis in Patients with Suspected Congenital Hemolytic Anemia	12
Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid Differentiation	12
Strong Positive Dichlorophenolindophenol Precipitation Suggests Hb Dhonburi (or Hb Neapolis) (HBB: c.380T>G) Inheritance in a Couple at Risk for Severe β-Thalassemia	11
First Report of Compound Heterozygosity for Hb S (HBB: c.20A>T) and Hb Haringey (HBB: c.131A>G)	11
Coexisting β-Thalassemia Trait, Gilbert Syndrome and Alpha-Globin Gene Triplication in a Child with Non-Transfusion Dependent Thalassemia Phenotype	10
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	10
Morbidity and Mortality Associated with COVID-19 and Acute Chest Syndrome in Sickle Cell Disease Patients	10
Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β ⁰ -Thalassemia	9
The First Iranian Case of Unstable Hemoglobin Santa Ana	9
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	9
Effect of Hydroxyurea Therapy on Growth Parameters in Older Children (6-15 Year-Old) with Sickle Cell Disease: Low Dose Versus High Dose	8
Submitting Novel Globin Gene Variants to Hemoglobin	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	8
Research Progress of Cell-Free Fetal DNA in Non-Invasive Prenatal Diagnosis of Thalassemia	7
Strengthening Health System and Community Mobilization for Sickle Cell Disease Screening and Management among Tribal Populations in India: An Interventional Study	6
A novel α Globin Gene Cluster Duplication, αααα³⁸⁰ Heterozygous β⁰-Thal Variant, Leading to a Blood Transfusion-Dependent Phenotype	6
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
Gene Therapies for Hemoglobinopathies: Promises and Challenges	5
High Systolic Blood Pressure, Anterior Segment Changes and Visual Impairment Independently Predict Sickle Cell Retinopathy	5
Molecular Identification and the Hematological Findings of Four Novel Variants in Globin Genes in Jiangxi Province of Southern China	5
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<	5
A Novel β⁰-Thalassemia Mutation,HBB: c.356_357delTT [Codon 118 (–TT)] in an Iraqi Kurd	4

A 6-Year Follow-up of a Chinese Child with Homozygous β ⁰ -Thalaasemia and a Heterozygous KLF1 Mutation	4
First Report of Nondeletional Hb H Disease Caused by an α2-Globin Gene Mutation: HBA2: c.184A>T	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 Huadu [α124(H7)Ser→Thr (TCC>ACC), HBA2: c.373T>A]: A Novel Variant of the α-Globin Gene	3
An Autopsy Case of β-Thalassemia Major Illuminating the Pathological Spectrum of the Disease	3
A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg, HBD : C.139G > A]	3
Polyneuropathy Associated with Age of Starting the Transfusion and Serum Ferritin Level in Iranian Patients with Thalassemia Major and Intermedia	3
Hypercoagulability in Sickle Cell Disease: A Thrombo-Inflammatory Mechanism	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
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
The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran	3
The Prevalence of HBB Mutations among the Transfusion-Dependent and Non Transfusion-Dependent Hb E/β-Thalassemia Children in a Tertiary Center of West Bengal, India	3
Thalassemia in Malaysia	3
Evaluation of the Function of a Rare Variant in the 3'-Untranslated Region of the β-Globin Gene	3
Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a β-Thalassemia Major Phenotype	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
Adherence to Iron Chelation Therapy Among Children with Beta Thalassemia Major: A Multicenter Cross-Sectional Study	3
Prediction of Heart and Liver Iron Overload in β-Thalassemia Major Patients Using Machine Learning Methods	3
Point-of-Care Newborn Screening for Sickle Cell Disease at Selected Health Facilities in the Gambia	3
Prevalence and Spectrum of β-Thalassemia Mutations in Baghdad, Iraq: Data from the Premarital Screening Program	2
Total Annual Economic Burden of Patients with Sickle Cell Disease in Steady State in Greece	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
First Report of Hb Youngstown in Capillary Electrophoresis and Overlapping Hb Analysis Findings with Hb Rush	2
Hb Laibin [β96(FG3)Leu→Arg; HBB: c.290T>G]: A Novel Hemoglobin Variant Described in a Chinese Family	2
Effect of deletions in the α-globin gene on the phenotype severity of β-thalassemia	2
Alpha Thalassemia Major: From a Lethal to a Treatable Condition	2
A New High Affinity Hemoglobin Variant: Hb San Francisco-KP (HBB: c.104T>C)	2
Iron Chelators, Such as Deferasirox, When Combined With Hydroxyurea, Provide an Additional Benefit of Iron Chelation in Patients Receiving Chronic Transfusion Therapy	2
Dynamic Viscosity of Hemoglobin Solutions Determined by Transverse Proton Magnetic Relaxation	2
Current Status of β-Thalassemic Burden in India	2
A New Hemoglobin Variant, Hb Natal (HBA1: c.423C>A), Found in a Greek Family	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
Premarital Screening is Pivotal in Reducing the Births of Babies Affected with Thalassemia Major in Iraq	2
The Long-Term Efficacy of Deferiprone in Thalassemia Patients With Iron Overload: Real-World Data from the Registry Database	2
Fist Detection of Hb Suqian[β42(CD1) Phe→Leu, HBB:c.129T > A] in Han Chinese	2
The Most Common Types of 3.7 Kilobase Deletion in the Iranian Population	2
A Case of Fat Embolism Syndrome with Cerebral Involvement in Sickle Cell Anemia	2
Hb Ryazan: An Elongated C‐Terminal β-Chain Due to a New Frameshift Mutation, HBB: c.396delG p.Val133Trpfs*25	2
Levels of Serum Ferritin and Hepcidin in Patients with Uncomplicated Falciparum Malaria in Hodeidah, Yemen: Considerations for Assessing Iron Status	2
Hb Wanjiang: A New β-Globin Chain Variant with Two Amino Acid Substitutions (HBB: c.255_264delinsTTTTTCTCAG)	2
Hb Nivaria: A New Hemoglobin Variant with a Shortened α-Globin Chain [α139(HC1)Lys→Stop; HBA1: c.418A>T]	2
Ameliorating Mental Health Issues in Sickle Cell Disease Patients: A Viewpoint	1
Elevated Hb A₂ is Not Always Indicative of β-Thalassemia	1
The Effect of HBB: c.-121C>T Variant [–71 (C>T)] on the β-Globin Promoter: Case Series Study	1
Efficacy and Safety of a Dispersible Tablet of GPO-Deferasirox Monotherapy among Children with Transfusion-Dependent Thalassemia and Iron Overload	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
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
Hemoglobin β-Globin Variants In Hispanic Patients: An Institutional Experience From Dallas, Texas	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

Diagnostic Dilemma of Hemoglobinopathies Using High Performance Liquid Chromatography Alone: A Case Report from a Resource-Constrained Setting	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
Sociodemographic and Clinical Factors Predictive of Poor Health-Related Quality of Life of Children with Sickle Cell Anemia in The Gambia	1
Phenotypic Analysis of the HBA2 : C.95 G > A Mutation in China	1
The Effect of Single Nucleotide Polymorphisms on Clinical Phenotypes of Sabahan Transfusion-Dependent β-Thalassemia Patients with Homozygous Filipino β ⁰ -Deletion	1
Spectrum of β-Thalassemia and Other Hemoglobinopathies in the Saurashtra Region of Gujarat, India: Analysis of a Large Population Screening Program	1
Identification of a Novel Hb H Disease with Glucose-6-Phosphate Dehydrogenase Deficiency Using Whole Genome Sequencing	1
Successful Treatment of a Child with Hemoglobin Hammersmith with Hematopoietic Stem Cell Transplantation	1
A New Hemoglobin Variant: Hb Tangshan [ HBA1 : c.239C > T, CD79(GCG > GTG)(Ala > Val)] Detected by MALDI-TOF MS	1
A Novel Frameshift Mutation( HBA2 :C.337delC) Associated With α-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China	1
Hb Lepore-Hong Kong: First Report of a Novel δ/β-Globin Gene Fusion in a Chinese Family	1
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	1
Diagnosis and Treatment of Alpha Thalassemia Major	1
Silent Cerebral Infarcts in Iraqi Patients with Sickle Cell Disease	1
Upregulation of miR-214 Mediates Oxidative Stress in Hb H DiseaseviaTargeting ofATF4	1
Estimating the Cost of Thalassemia Care across the World: A Thalassemia International Federation Model	1
Clinical Severity of β-Thalassemia Pediatric Patients in Myanmar	1
Thalassemia Status in Cambodia	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
A Study to Assess and Improve Adherence to Iron Chelation Therapy in Transfusion-Dependent Thalassemia Patients	1
β ⁰ -Thalassemia Caused by a Novel Nonsense Mutation [ HBB: c.199A > 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
A Novel β-Globin Variant, Hb Odder [ HBB : C.316C > G; CD105 (Leu > Val)]	1
Hypersplenism Affects Growth and Haematology in HbSS: Observations from the Jamaican Birth Cohort	1
The First Compound Heterozygosity for Two Different α-Thalassemia Determinants Causes Hb Bart’s Hydrops Fetalis in a Chinese Family	1
Hereditary Hemolytic Anemia Due to PIEZO1 Red Blood Cell Membrane Defect	1
Sickle Cell Disease in Brazil: Current Management	1
Haplotype-Specific Genetic Epidemiology of Sickle Cell Anemia Patients in Accra, Ghana: Patterns, Clinical Implications, and Public Health Responses	1
Prevalence and Molecular Characterization of β-Thalassemia in Kirkuk Province of Northern Iraq	1
Dominant β-Thalassemia Phenotype Caused by Hb Dieppe (HBB: c.383A>G): Another Case Report	1
Perspectives of General Hematologists on a Proposed Shared Care Model for HSCT in Sickle Cell Disease	1
Identification of a Novel Variant c.163delG in HBB Gene Resulting in a Beta Null Phenotype in a Proband with Thalassemia Intermedia	1
Bringing Sickle Cell Disease Care Closer to Home: Feasibility and Efficacy of a Quality Improvement Initiative at a Community Hospital	1
Existing Tubular Injury in β-Thalassemia Major Patients Receiving Iron Chelating Agents with Normal Creatinine Level in East Java, Indonesia	1
Prevalence and Molecular Characteristics of Hemoglobin Variants in Laibin City, Central Guangxi of Southern China	1
Targeted Next-Generation Sequencing Reveals a Large Novel β-Thalassemia Deletion that Removes the Entire HBB Gene	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
Long-Term and Transient Calcium Channel Blockers; A Systematic Review of Their Role in the Management of Cardiomyopathy in Transfusion-Dependent Thalassemia	1
Poor Sleep Quality in Jamaican Adults With Sickle Cell Disease: Prevalence, Risk Factors, and Association With Quality of Life	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
Glucose-6-Phosphate Dehydrogenase Deficiency: An Overview of the Prevalence and Genetic Variants in Saudi Arabia	1
An Evaluation for the Causes of Reduced Hb A₂ and the Molecular Characterization of HBD Variants in Hong Kong	1
Current Status of Thalassemia in Lao People’s Democratic Republic	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
Utilization of Pneumococcal Vaccine and Penicillin Prophylaxis in Sickle Cell Disease in Three African Countries: Assessment among Healthcare Providers in SickleInAfrica	1
Misdiagnosis of β-Thalassemia Major Due to Chinese ^G γ+( ^A γδβ) ⁰ -Thalassemia Combined with β	0
Mutation Spectrum of β-Globin Gene in Patients with β-Thalassemia at Tidar Hospital, Magelang, Central Java, Indonesia	0
A Novel Frameshift Mutation of HBB Causing Dominant β-Thalassemia in a Chinese Individual	0
Hb Kalundborg [β79(EF3)Asp→Glu; HBB: c.240C>a], a Possible Low-affinity Hemoglobin Variant Detected during Hb A_1c Measurement	0
Sickle Cell Disease and Quality of Life: An Evaluation of Reporting of Patient-Reported Outcomes in Randomized Controlled Trials	0
Educational Bias in Cognitive Screening of Adults with Sickle Cell Disease: A Bilingual Multisite Observational Study	0
Update on Prevention of Hemoglobinopathies in Azerbaijan	0
Thalassaemia Registries: A Call for Action. A Position Statement from the Thalassaemia International Federation	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
Pitfalls in the Diagnosis of β-Thalassemia Intermedia	0
Detection of the HBB: c.393T>G Mutation in Two Patients with Hypochromic Microcytic Anemia	0
Rapid and Visual Molecular Detection of High Hb F Determinants; HPFH6, Asian Indian inv-del ( ^A γδβ) ⁰ -Thalassemia, and Thai del-	0
Investigation of the Distribution of Thalassemia in Children in Jiangxi Province, the People’s Republic of China	0
Perforated Duodenal Ulcer Associated with Deferasirox in a Child with β-Thalassemia Major	0
Fetal Hemoglobin H Hydrops Fetalis: Another Three Case Reports	0
Influence of Hemoglobin Strasbourg, a Rare High Oxygen Affinity Hemoglobin Variant, on Different Methods of HbA1c Measurement	0
Introduction to the Special Issue	0
Thalidomide and Hydroxyurea in Transfusion-Dependent Thalassemia: Efficacy, Safety Profile and Impact on Quality of Life	0
Evaluating Renal Glomerular Function in Beta-Thalassemia Patients Receiving Deferasirox Using Serum Cystatin-C and Creatinine: A Cross-Sectional Study	0
Unusual Causes of β Thalassemia Trait: Discovery of another Three Novel SUPT5H Variants	0
An Expert Overview on Therapies in Non-Transfusion-Dependent Thalassemia: Classical to Cutting Edge in Treatment	0
Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell Disease	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
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
Noninvasive Hemoglobin Measurement Reduce Invasive Procedures in Thalassemia Patients	0
Hemoglobin Oviedo ( c.115A > G; p.T39A ): A Cause of Low Oxygen Saturation	0
Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation ( HBB :c.336dup)	0
Thalassemia in India	0
Malaria Infection in Patients with Sickle Cell Disease in Nigeria: Association with Markers of Hyposplenism	0
Development of a Quantitative Multiplex PCR to Detect Three Common Alpha Thalassemia Deletions	0
De Novo Occurrence of Hb Chile [β28(B10) Leu→Met] in a Korean Boy with Methemoglobinemia	0
Updated Molecular Spectrum of β-Thalassemia Mutations in Duhok Province, Northern Iraq: Ethnic Variation and the Impact of Immigration	0
Factors Associated with Overt Stroke in Children and Adolescents with Sickle Cell Disease: A Retrospective Cohort Study	0
Anemia in Sri Lanka: A Literature Review	0

First Report of Filipino β ⁰ -Thalassemia/β-Thalassemia in a Chinese Family	0
Quality of Life and Related Factors in β-Thalassemia Patients	0
Case Fatality Rate and Severity of COVID-19 among Patients with Sickle Cell Disease: A Systematic Review and Meta-Analysis	0
Incidence Rate of COVID-19 Infection in Hemoglobinopathies: A Systematic Review and Meta-analysis	0
Secretory Phospholipase A2 Levels Are High in Women with Sickle Cell Disease and Menstruation-Induced Vaso-Occlusive Crises	0
The Prevalence of Obstructive Sleep Apnea and Associated Symptoms among Patients with Sickle Cell Disease: A Systematic Review and Meta-analysis	0
Thalassemia in Asia 2021 Overview of Thalassemia and Hemoglobinopathies in Bangladesh	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
First Reported Case of Hemoglobin H Disease Caused by the Rare α-Globin Gene Mutation ( HBA2 c.244delT) in a Chinese Family	0
Genotype-Phenotype Study of β-Thalassemia Patients in Sabah	0
Adherence to Iron Chelation Therapy among Adults with Thalassemia: A Systematic Review	0
Correlation Between Serum Ferritin and Viral Hepatitis in Thalassemia Patients	0
A Population-Oriented Genetic Scoring System to Predict Phenotype: A Pathway to Personalized Medicine in Iraqis With β-Thalassemia	0
Celocentesis for Early Prenatal Diagnosis in Couples at-Risk for β-Thalassemia and Sicilian (δβ)⁰-Thalassemia	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
A New α1-Globin Variant, Hb Ormylia [ HBA1 :c.63C > G; p.His21Gln]. Report of Eleven Cases in Northern Greece	0
Novel Promoter Mutation (HBB:C.-139_-138del) Associated with β-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China	0
Consideration of Splenectomy in Unstable Hemoglobinopathy: A Case Report of Hb Hammersmith (HBB: c.128T>C)	0
A New Hemoglobin Variant: Hb Jiujiang [α18(A16)Gly→Cys, HBA2: c.55G>T]	0
Identification of Three Families Carrying Hb Anti-Lepore Hong Kong Variant in Guangxi, China, and Analysis of Their Hematological Data	0
Prevalence, Severity, and Determinants of Pain in Thalassemia	0
A Rare Case of De Novo Beta-Thalassemia Diagnosed by Whole-Genome Sequencing in an Ethnically Danish Newborn	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
Early Onset of Severe Anemia Caused by Hb Calgary ( HBB : C.194G > T): Another Case Report	0
Ethical and Clinical Considerations in the Use of Hydroxyurea in Pregnant Women with Sickle Cell Disease	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
The Spectrum of β-Thalassemia Mutations in the Population Migration in Lebanon: A 6-Year Retrospective Study	0
Prevalence and Associated Factors of Zinc and Vitamin D Deficiencies in Pediatric and Young Adult Patients with Non-Transfusion-Dependent Thalassemia	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
Hemoglobinopathies and COVID-19: The Experience of a Center in Northern Greece	0
Novel Insights into the Pathophysiology and Treatment of Sickle Cell Disease	0
Thalassemia in Sri Lanka	0
Hb Tacoma: G>T or G>C, and Does It Matter?	0
Hb Mizuho (HBB: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation Sequencing	0
Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis	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
δβ-Thalassemia and α-Triplication: Is Genetic Retesting Worthwhile in Case of Non-Coherent Phenotype?	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
β-Thalassemia Intermedia Caused by the β-Globin Gene 3′ Untranslated Region: Another Case Report	0
Knowledge and Attitude toward Hemoglobinopathies in Premarital Screening Program among the General Population in the Western Region of Saudi Arabia	0
Mutation Spectrum of β-Thalassemia in Some Ethnic Groups of North Maharashtra, India	0
Thalassemia in Viet Nam	0
The Validation of Whole β-Globin Gene Sequencing for Detecting β-Thalassemia Mutations Found in Thailand Using Next-Generation Sequencing (NGS)	0
Alloimmunization in β-Thalassemia and Sickle Cell Disease in Middle Eastern Countries: A Systemic Review	0
Thalassemia in Thailand	0
Long-Term Survival Rates of a Sickle Cell Disease Cohort in Saudi Arabia: A 2009–2023 Observational Study	0
COVID-19 and Anemia: What Do We Know So Far?	0
Hb Mizuho Case Report; Early Genomic Testing Facilitates a Life Changing Diagnosis	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
Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster	0
Dominant Beta Thalassemia: A Very Rare Cause of Thalassemia in a Mediterranean Country	0
Prolonged QTc Interval in Nigerian Children with Sickle Cell Anemia	0
α- and β-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh	0
Haploidentical Hematopoietic Stem Cell Transplantation in Thalassemia	0
Dysregulated Serum Cytokine Production in Pediatric Patients with β-Thalassemia Major	0
Eight Cases of Hb Winnipeg [HBA2: c.226G>T (or HBA1)]: A Detailed Study	0
The Spectrum of α-Thalassemia Mutations in Syrian Patients	0
Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations	0
Thalassemia in Indonesia	0
Prevalence of Hemoglobinopathies in Premarital Screening in the Province of Nigde, Turkey	0
α ⁰ -Thalassemia Caused by a Novel α-Globin Gene Cluster Deletion (– ^LB ) Found in a Chinese Family	0
Hb Dahua [β59(E3)Lys→Met; HBB: c.179A>T] a Novel Variant on the β-Globin Gene	0
Estradiol is Pro-Nociceptive and Associated with a Small-Fiber Neuropathy Among Premenopausal Women with Sickle Cell Disease	0
Characterization and Confirmation of Mildly Unstable Hb Pontoise or α1 63(E12) Ala > Asp and Literature Review	0
The Prevalence of Hypothyroidism among Patients With β-Thalassemia: A Systematic Review and Meta-Analysis of Cross-Sectional Studies	0
Analysis of Mean Corpuscular Volume and Red Cell Distribution Width in Patients with Aplastic Anemia	0
The Aplastic Crisis in HbSS: Observations from the Jamaican Birth Cohort	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
Treatment with Hydroxyurea Leads to Fetal Hemoglobin Reactivation through CA1 and LIN28B Genes: An In Vitro Study	0
Hepatobiliary Manifestations in Thalassemia Patients: A Narrative Review	0
Thalassemia in Asia 2021 Thalassemia in Brunei Darussalam	0
Description of Hb Évora (HBA2: c.106T>C) on an Unexpected Allele in a Swiss Family	0
Elevated Plasma Atherogenic and Triglyceride-Glucose Indices: Markers of Cardiovascular Risk in Transfusion-Dependent Thalassemia	0
Identification of a Novel 16.8Kb Deletion of the α-Globin Gene Cluster by Third-Generation Sequencing	0
Evaluating Health-Related Quality of Life in Thalassemia: Low-Dose Thalidomide vs. Standard Care—Insights from a Comparative Study	0
Thrombosis Tendency After Splenectomy in a Danish Family With Hemoglobin Volga, and a Literature Review	0
Hepcidin-to-Ferritin Ratio as an Early Diagnostic Index of Iron Overload in β-Thalassemia Major Patients	0
Editorial	0
Detection of a Rare Mutation in the Initiation Codon of the β-Globin Gene (HBB:C.2T > C; P.Met1Thr)	0
Use of Capillary Electrophoresis Migration Position for the Presumptive Identification of Hemoglobin Variants Prevalent in China	0
Identification of a Novel 7-bp Deletion in the α-Globin Gene Cluster in One Chinese Family	0
β-Thalassemia Trait Caused by SUPT5H Defects: Another Case Report	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
Venous Thromboembolism in Individuals with Sickle Cell Disease: A Narrative Review	0
Beta Globin Gene Cluster Haplotypes in Beta Thalassemia in the Kurdistan Region of Iraq	0
Thalassemia in Pakistan	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
Hb A₂-Calderdale [δ2(NA2)His→Asn; HBD: c.7C>A] and Misdiagnosis of Type 2 Diabetes Mellitus Due to Interference with Hb A_1c When Using Cation Exchange High Performance	0
A Novel β-Globin Variant, Hb Raklev [β 75(E19) HBB :c.227T > A (Leu→Gln)]	0
Combined Gap-Polymerase Chain Reaction and Targeted Next-Generation Sequencing Improve α- and β-Thalassemia Carrier Screening in Pregnant Women in Vietnam	0
Characterization of Hemoglobin Malay Phenotypes in Tertiary Hospitals	0
Dynamic Thiol-Disulfide Homeostasis in Children With β-Thalassemia Trait	0
Death from S. pneumoniae in HbSC Disease: Was Expanded Pneumococcal Vaccination Too Late?	0
Thalassemia in the Philippines	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