Hemoglobin

Article	Citations
Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid Differentiation	32
Noninvasive Prenatal Diagnosis of SEA-Thalassemia by Combining 1000 Genomes Database and Relative Haplotype Dosage	30
Identification of a New δ chain hemoglobin Variant, Hb A2-Malay [δ46(CD5)Gly > Arg, HBD : C.139G > C;316-443A > G]	20
A Novel 5 kb Deletion in theβ-Globin Gene Cluster Identified in a Chinese Patient	19
Clinical Exome Sequencing Reveals Novel Mutations in SPTB Gene Associated with Hereditary Spherocytosis in Patients with Suspected Congenital Hemolytic Anemia	19
Strong Positive Dichlorophenolindophenol Precipitation Suggests Hb Dhonburi (or Hb Neapolis) (HBB: c.380T>G) Inheritance in a Couple at Risk for Severe β-Thalassemia	17
Morbidity and Mortality Associated with COVID-19 and Acute Chest Syndrome in Sickle Cell Disease Patients	15
The First Iranian Case of Unstable Hemoglobin Santa Ana	14
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	14
Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β 0 -Thalassemia	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	10
A Cross-Sectional Study on Pain and Quality of Life of Adult Patients with Transfusion-Dependent Thalassemia in a Tertiary Hospital In Malaysia	9
Coexisting β-Thalassemia Trait, Gilbert Syndrome and Alpha-Globin Gene Triplication in a Child with Non-Transfusion Dependent Thalassemia Phenotype	8
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<	7
A novel α Globin Gene Cluster Duplication, αααα380 Heterozygous β0-Thal Variant, Leading to a Blood Transfusion-Dependent Phenotype	7
Submitting Novel Globin Gene Variants to Hemoglobin	7
Research Progress of Cell-Free Fetal DNA in Non-Invasive Prenatal Diagnosis of Thalassemia	6
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	6
Coexistence of Mycoplasma Pneumonia and Pulmonary Embolism as a Cause of Acute Chest Syndrome in a Child with Sickle Cell Disease	6
Molecular Identification and the Hematological Findings of Four Novel Variants in Globin Genes in Jiangxi Province of Southern China	6
Gene Therapies for Hemoglobinopathies: Promises and Challenges	5
Comparison of Sickle Solubility Test with Mass Spectrometry for Hemoglobin S Confirmation	5
A 6-Year Follow-up of a Chinese Child with Homozygous β 0 -Thalaasemia and a Heterozygous KLF1 Mutation	5
A Review of Gene Therapies for Hemoglobinopathies	5
Evaluation of the Function of a Rare Variant in the 3'-Untranslated Region of the β-Globin Gene	5

Strengthening Health System and Community Mobilization for Sickle Cell Disease Screening and Management among Tribal Populations in India: An Interventional Study	5
Effect of Hydroxyurea Therapy on Growth Parameters in Older Children (6-15 Year-Old) with Sickle Cell Disease: Low Dose Versus High Dose	5
Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT)	5
Hb Huadu [α124(H7)Ser→Thr (TCC>ACC), HBA2: c.373T>A]: A Novel Variant of the α-Globin Gene	4
The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran	4
Point-of-Care Newborn Screening for Sickle Cell Disease at Selected Health Facilities in the Gambia	4
Identification of a Rare β-Globin Chain Hemoglobin Variant: HBB : C.24G > C (Glu7Asp)	4
Thalassemia in Malaysia	4
Adherence to Iron Chelation Therapy Among Children with Beta Thalassemia Major: A Multicenter Cross-Sectional Study	4
A Hemoglobin Variant, Resulting from a Novel Missense Mutation [CD 112(G14) Cys > Ser (TGT > TCT); HBB : C.338G > C], Was Discovered by MALDI-TOF MS	4
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	4
Hypercoagulability in Sickle Cell Disease: A Thrombo-Inflammatory Mechanism	4
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	4
The Risk of Rapid Deterioration of Sepsis in the Patient with Non-Transfusion-Dependent Thalassemia: A Case Report	4
Dynamic Viscosity of Hemoglobin Solutions Determined by Transverse Proton Magnetic Relaxation	3
A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg, HBD : C.139G > A]	3
Current Status of β-Thalassemic Burden in India	3
High Prevalence of Hb Riccarton Challenges HbA1c Analysis in a Danish Clinical Laboratory Using the Tosoh G11	3
The Long-Term Efficacy of Deferiprone in Thalassemia Patients With Iron Overload: Real-World Data from the Registry Database	3
Polyneuropathy Associated with Age of Starting the Transfusion and Serum Ferritin Level in Iranian Patients with Thalassemia Major and Intermedia	3
Genetically Confirmed Dual Hematologic Disorder: A Case of β-Thalassemia with Frameshift Mutation and Type 3 von Willebrand Disease in a Pediatric Patient	3
Prevalence and Spectrum of β-Thalassemia Mutations in Baghdad, Iraq: Data from the Premarital Screening Program	3
Iron Chelators, Such as Deferasirox, When Combined With Hydroxyurea, Provide an Additional Benefit of Iron Chelation in Patients Receiving Chronic Transfusion Therapy	3
Prediction of Heart and Liver Iron Overload in β-Thalassemia Major Patients Using Machine Learning Methods	3
The Most Common Types of 3.7 Kilobase Deletion in the Iranian Population	3
First Report of Hb Youngstown in Capillary Electrophoresis and Overlapping Hb Analysis Findings with Hb Rush	3
Fist Detection of Hb Suqian[β42(CD1) Phe→Leu, HBB:c.129T > A] in Han Chinese	3
Identification of a Novel Mutation in the 3′ Untranslated Region of the β-Globin Gene (HBB:c.*132C>G) in a Chinese Family	3
A Rare Hemoglobin Variant Detected for the First Time in Türkiye (Hb Iraq-Halabja): Evaluation of the Effect of Variant Hemoglobins on HbA1c Methods	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
Hereditary Hemolytic Anemia Due to PIEZO1 Red Blood Cell Membrane Defect	2
Effect of deletions in the α-globin gene on the phenotype severity of β-thalassemia	2
Sickling Disorder Caused by Co-Inheritance of Hemoglobin Maputo and Hemoglobin S: Case Report and Review of the Literature	2
Hb Ryazan: An Elongated C‐Terminal β-Chain Due to a New Frameshift Mutation, HBB: c.396delG p.Val133Trpfs*25	2
Therapeutic Response to Hydroxyurea in Beta-Thalassemia Intermedia with Rare Mutation: A Case Report	2
Identification of a Novel Variant c.163delG in HBB Gene Resulting in a Beta Null Phenotype in a Proband with Thalassemia Intermedia	2
Prevalence and Molecular Characteristics of Hemoglobin Variants in Laibin City, Central Guangxi of Southern China	2
Ameliorating Mental Health Issues in Sickle Cell Disease Patients: A Viewpoint	2
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	2
Hb Laibin [β96(FG3)Leu→Arg; HBB: c.290T>G]: A Novel Hemoglobin Variant Described in a Chinese Family	2
Hb Nivaria: A New Hemoglobin Variant with a Shortened α-Globin Chain [α139(HC1)Lys→Stop; HBA1: c.418A>T]	2
Misdiagnosis of α-Thalassemia Heterozygotes as Homozygotes Due to Base Mutations in the Primer Binding Region	2
Premarital Screening is Pivotal in Reducing the Births of Babies Affected with Thalassemia Major in Iraq	2
Severe Hb H Disease Caused by Hb Zürich–Albisrieden (HBA1: c.178G>C): Another Case Report	2
Silent Cerebral Infarcts in Iraqi Patients with Sickle Cell Disease	2
Poor Sleep Quality in Jamaican Adults With Sickle Cell Disease: Prevalence, Risk Factors, and Association With Quality of Life	2
Bringing Sickle Cell Disease Care Closer to Home: Feasibility and Efficacy of a Quality Improvement Initiative at a Community Hospital	2
A Rare Severe Hemolytic Crisis in Homozygous Hemoglobin E (HbEE)	2
Levels of Serum Ferritin and Hepcidin in Patients with Uncomplicated Falciparum Malaria in Hodeidah, Yemen: Considerations for Assessing Iron Status	2

Rare Coexistence of Hemoglobin D-Iran and Hemoglobin S in a Case from Central India	2
Encouraging Outcomes of Hematopoeitic Stem Cell Transplantation in Pediatric Sickle Cell Disease- A Decade-Long Experience from the Developing World	2
Alpha Thalassemia Major: From a Lethal to a Treatable Condition	2
A New Hemoglobin Variant, Hb Natal (HBA1: c.423C>A), Found in a Greek Family	2
Hb Wanjiang: A New β-Globin Chain Variant with Two Amino Acid Substitutions (HBB: c.255_264delinsTTTTTCTCAG)	2
Estimating the Cost of Thalassemia Care across the World: A Thalassemia International Federation Model	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
β-Thalassemia Trait Caused by a SUPT5H Defect: First Report of an Intragenic Deletion	1
Current Status of Thalassemia in Lao People’s Democratic Republic	1
Hb A 2 -Getafe [δ 132 (H10) Lys > Thr, HBD : c.88C > A]: New Mutation in the δ-Globin Gene in a Spanish Patient	1
Sociodemographic and Clinical Factors Predictive of Poor Health-Related Quality of Life of Children with Sickle Cell Anemia in The Gambia	1
Diagnosis and Treatment of Alpha Thalassemia Major	1
Nonsense Variant in the β-Spectrin Gene Causing Hereditary Spherocytosis Identified by Whole-Exome Sequencing in a Child	1
Prevalence and Molecular Characterization of β-Thalassemia in Kirkuk Province of Northern Iraq	1
δβ-Thalassemia and α-Triplication: Is Genetic Retesting Worthwhile in Case of Non-Coherent Phenotype?	1
Targeted Next-Generation Sequencing Reveals a Large Novel β-Thalassemia Deletion that Removes the Entire HBB Gene	1
Pituitary Versus Hepatic Iron Assessment in Transfusion-Dependent Thalassemia: Is Signal Intensity Ratio a Reliable Tool?	1
Identification of a Novel 7-bp Deletion in the α-Globin Gene Cluster in One Chinese Family	1
Prevalence and Management of β-Thalassemia in India	1
HbH Disease in an Elderly Man Due to Compound Heterozygosity for Deletional α-Thalassemia and Hb Dubai ( HBA2 :c.368A > 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
Spectrum of β-Thalassemia and Other Hemoglobinopathies in the Saurashtra Region of Gujarat, India: Analysis of a Large Population Screening Program	1
Hypersplenism Affects Growth and Haematology in HbSS: Observations from the Jamaican Birth Cohort	1
Identification of a Novel Hb H Disease with Glucose-6-Phosphate Dehydrogenase Deficiency Using Whole Genome Sequencing	1
A Novel Frameshift Mutation( HBA2 :C.337delC) Associated With α-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China	1
A Novel β-Globin Variant, Hb Odder [ HBB : C.316C > G; CD105 (Leu > Val)]	1
Thalassemia Status in Cambodia	1
The Effect of Single Nucleotide Polymorphisms on Clinical Phenotypes of Sabahan Transfusion-Dependent β-Thalassemia Patients with Homozygous Filipino β 0 -Deletion	1
KLF1 Knockdown Differentially Regulates γ-Globin Expression: Inhibition in K562 Cells but Reactivation in β-Thalassemia Major Erythrocytes with Erythropoiesis Disruption	1
Anemia in Sri Lanka: A Literature Review	1
Clinical Severity of β-Thalassemia Pediatric Patients in Myanmar	1
Perspectives of General Hematologists on a Proposed Shared Care Model for HSCT in Sickle Cell Disease	1
Hemoglobin β-Globin Variants In Hispanic Patients: An Institutional Experience From Dallas, Texas	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
Sickle Cell Disease in Brazil: Current Management	1
A New Hemoglobin Variant: Hb Tangshan [ HBA1 : c.239C > T, CD79(GCG > GTG)(Ala > Val)] Detected by MALDI-TOF MS	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
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
Phenotypic Analysis of the HBA2 : C.95 G > A Mutation in China	1
Long-Term and Transient Calcium Channel Blockers; A Systematic Review of Their Role in the Management of Cardiomyopathy in Transfusion-Dependent Thalassemia	1
Successful Treatment of a Child with Hemoglobin Hammersmith with Hematopoietic Stem Cell Transplantation	1
β 0 -Thalassemia Caused by a Novel Nonsense Mutation [ HBB: c.199A > T]	1
Rare Case of Homozygosity for CYB5R3 Variant c.235C > T p.(Arg79Trp) Causing Type II Methemoglobinemia	1
Efficacy and Safety of a Dispersible Tablet of GPO-Deferasirox Monotherapy among Children with Transfusion-Dependent Thalassemia and Iron Overload	1
Hemoglobin Oviedo ( c.115A > G; p.T39A ): A Cause of Low Oxygen Saturation	1
Utility of Molecular Sequencing and Hematologic Parameters for Diagnosis of α-Thalassemia: A Perspective of the National Reference Laboratory	1
Diagnostic Dilemma of Hemoglobinopathies Using High Performance Liquid Chromatography Alone: A Case Report from a Resource-Constrained Setting	1
Existing Tubular Injury in β-Thalassemia Major Patients Receiving Iron Chelating Agents with Normal Creatinine Level in East Java, Indonesia	1
The First Compound Heterozygosity for Two Different α-Thalassemia Determinants Causes Hb Bart’s Hydrops Fetalis in a Chinese Family	1
Thalassemia in Pakistan	0
Thalidomide and Hydroxyurea in Transfusion-Dependent Thalassemia: Efficacy, Safety Profile and Impact on Quality of Life	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
Thalassemia in Asia 2021 Overview of Thalassemia and Hemoglobinopathies in Bangladesh	0
Thalassemia in the Philippines	0
β-Thalassemia Intermedia Caused by the β-Globin Gene 3′ Untranslated Region: Another Case Report	0
An Expert Overview on Therapies in Non-Transfusion-Dependent Thalassemia: Classical to Cutting Edge in Treatment	0
THALASSEMIA in ASIA 2021: Thalassemia in Guangxi Province, People’s Republic of China	0
A Population-Oriented Genetic Scoring System to Predict Phenotype: A Pathway to Personalized Medicine in Iraqis With β-Thalassemia	0
Early Onset of Severe Anemia Caused by Hb Calgary ( HBB : C.194G > T): Another Case Report	0
Beta Globin Gene Cluster Haplotypes in Beta Thalassemia in the Kurdistan Region of Iraq	0
Hemoglobinopathies and COVID-19: The Experience of a Center in Northern Greece	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
Heterozygous Beta Thalassemia with Segmental Duplication of chr16p13.3 Leading to Thalassemia Intermedia Phenotype: A Report of 2 Cases with Review of Literature	0
Influence of Hemoglobin Strasbourg, a Rare High Oxygen Affinity Hemoglobin Variant, on Different Methods of HbA1c Measurement	0
Characterization of HbH Disease Caused by Compound Heterozygotes α + -Thalassemia 3.7 kb Deletion and a Large Novel α 0 -Thalassem	0
First Case in Portugal of a Rare Hemoglobin Variant – Hb Montfermeil: Importance of Laboratory Diagnosis	0
Mutation Spectrum of β-Globin Gene in Patients with β-Thalassemia at Tidar Hospital, Magelang, Central Java, Indonesia	0
Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis	0
Characterization and Confirmation of Mildly Unstable Hb Pontoise or α1 63(E12) Ala > Asp and Literature Review	0
Fetal Hemoglobin H Hydrops Fetalis: Another Three Case Reports	0
First Report of Filipino β 0 -Thalassemia/β-Thalassemia in a Chinese Family	0
When Unstable Hemoglobin Lansing Interacts with Alpha Thalassemia Along with HbS : An Interesting Case with Unique Clinical Presentation	0
Analysis of Mean Corpuscular Volume and Red Cell Distribution Width in Patients with Aplastic Anemia	0
α- and β-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh	0
Thalassemia in Indonesia	0
Long-Term Survival Rates of a Sickle Cell Disease Cohort in Saudi Arabia: A 2009–2023 Observational Study	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
α 0 -Thalassemia Caused by a Novel α-Globin Gene Cluster Deletion (– LB ) Found in a Chinese Family	0
Consideration of Splenectomy in Unstable Hemoglobinopathy: A Case Report of Hb Hammersmith (HBB: c.128T>C)	0
Characterization of Hemoglobin Malay Phenotypes in Tertiary Hospitals	0

COVID-19 and Anemia: What Do We Know So Far?	0
Clinical Implications of HbD-Punjab and HbS co-Inheritance – A Rare Case in South India	0
Prevalence and Associated Factors of Zinc and Vitamin D Deficiencies in Pediatric and Young Adult Patients with Non-Transfusion-Dependent Thalassemia	0
The Aplastic Crisis in HbSS: Observations from the Jamaican Birth Cohort	0
Prevalence, Severity, and Determinants of Pain in Thalassemia	0
Noninvasive Hemoglobin Measurement Reduce Invasive Procedures in Thalassemia Patients	0
Mutation Spectrum of β-Thalassemia in Some Ethnic Groups of North Maharashtra, India	0
HBA2 : C.4delG: A Novel Frameshift Mutation Causing α + -Thalassemia Found in a Chinese Family	0
β-Thalassemia Trait Caused by SUPT5H Defects: Another Case Report	0
Thalassemia in Thailand	0
The Prevalence of Obstructive Sleep Apnea and Associated Symptoms among Patients with Sickle Cell Disease: A Systematic Review and Meta-analysis	0
Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster	0
Dynamic Thiol-Disulfide Homeostasis in Children With β-Thalassemia Trait	0
Elevated Plasma Atherogenic and Triglyceride-Glucose Indices: Markers of Cardiovascular Risk in Transfusion-Dependent Thalassemia	0
Novel Double Heterozygosity: HBA2 : c.70G > A (Hb Chad)/ HBB : c.-78A > G and Novel Compound Heterozygosity: HBA2	0
Novel Insights into the Pathophysiology and Treatment of Sickle Cell Disease	0
Adherence to Iron Chelation Therapy among Adults with Thalassemia: A Systematic Review	0
Haploidentical Hematopoietic Stem Cell Transplantation in Thalassemia	0
Thalassemia in Viet Nam	0
Editorial	0
Misdiagnosis of β-Thalassemia Major Due to Chinese G γ+( A γδβ) 0 -Thalassemia Combined with β	0
Novel Promoter Mutation (HBB:C.-139_-138del) Associated with β-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China	0
Case Fatality Rate and Severity of COVID-19 among Patients with Sickle Cell Disease: A Systematic Review and Meta-Analysis	0
Dysregulated Serum Cytokine Production in Pediatric Patients with β-Thalassemia Major	0
Hereditary Persistence of Fetal Hemoglobin (HPFH): Detection of Unknow A γ-Globin Promoter Mutation at the C2H2 Zinc Finger Transcription Factors Binding Sites	0
Hb Mizuho Case Report; Early Genomic Testing Facilitates a Life Changing Diagnosis	0
Evaluating Health-Related Quality of Life in Thalassemia: Low-Dose Thalidomide vs. Standard Care—Insights from a Comparative Study	0
Predicting the Double Heterozygotes of HbE and α-Thalassemia-1 (Southeast Asian Type) Using RapidMiner -Generated Hematologic Algorithm	0
Evaluating Renal Glomerular Function in Beta-Thalassemia Patients Receiving Deferasirox Using Serum Cystatin-C and Creatinine: A Cross-Sectional Study	0
Estradiol is Pro-Nociceptive and Associated with a Small-Fiber Neuropathy Among Premenopausal Women with Sickle Cell Disease	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
Update on Prevention of Hemoglobinopathies in Azerbaijan	0
Educational Bias in Cognitive Screening of Adults with Sickle Cell Disease: A Bilingual Multisite Observational Study	0
A Novel β-Globin Variant, Hb Raklev [β 75(E19) HBB :c.227T > A (Leu→Gln)]	0
Investigation of the Distribution of Thalassemia in Children in Jiangxi Province, the People’s Republic of China	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
The Spectrum of α-Thalassemia Mutations in Syrian Patients	0
Treatment with Hydroxyurea Leads to Fetal Hemoglobin Reactivation through CA1 and LIN28B Genes: An In Vitro Study	0
Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell Disease	0
The Validation of Whole β-Globin Gene Sequencing for Detecting β-Thalassemia Mutations Found in Thailand Using Next-Generation Sequencing (NGS)	0
Identification of Three Families Carrying Hb Anti-Lepore Hong Kong Variant in Guangxi, China, and Analysis of Their Hematological Data	0
Celocentesis for Early Prenatal Diagnosis in Couples at-Risk for β-Thalassemia and Sicilian (δβ)0-Thalassemia	0
Genotype-Phenotype Study of β-Thalassemia Patients in Sabah	0
Venous Thromboembolism in Individuals with Sickle Cell Disease: A Narrative Review	0
A Novel Large Deletion Including the Major Regulatory Element Compounded with SEA Deletion Causing Hydrops-Fetalis-Syndrome	0
Detection of Common α-Hemoglobin Variants in Thailand by Using Real-Time PCR with High Resolution Melting Analysis	0
Hb Bart’s Disease Due to Uniparental Disomy for Chromosome 16: The Need for Clinical Vigilance in Hydropic Fetuses with Only One Parent Carrying α 0	0
A Diverse Genetic Landscape: Thalassemia Genotype Patterns in Myanmar and Cambodian Workers in Southern Thailand	0
Molecular Diagnosis and Stability Testing of Hemoglobin Phnom Penh [ HBA1 : C.353_355dup (p.Phe118_Thr119insIle)] – The First Northern Thai Case	0
De Novo Occurrence of Hb Chile [β28(B10) Leu→Met] in a Korean Boy with Methemoglobinemia	0
Secretory Phospholipase A2 Levels Are High in Women with Sickle Cell Disease and Menstruation-Induced Vaso-Occlusive Crises	0
Thalassemia in Sri Lanka	0
Hb Kirikiriroa [α57(E6)Gly→Cys; HBA1: c.172G>T]: A Novel Unstable α-Globin Variant with Oxidized Derivatives Interfering with Hb A1c	0
Thalassemia in India	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
A Novel Frameshift Mutation of HBB Causing Dominant β-Thalassemia in a Chinese Individual	0
A Retrospective Study of Unmet Blood Transfusion Needs and Status of Iron Overload in 190 Transfusion-Dependent Thalassemia Patients from Southern China	0
Hb Kalundborg [β79(EF3)Asp→Glu; HBB: c.240C>a], a Possible Low-affinity Hemoglobin Variant Detected during Hb A1c Measurement	0
Genetic Analysis and Clinical Relevance of HBA1 :c.305T > C (Leu > Pro): A Novel Variant Linked	0
Combined Gap-Polymerase Chain Reaction and Targeted Next-Generation Sequencing Improve α- and β-Thalassemia Carrier Screening in Pregnant Women in Vietnam	0
Alloimmunization in β-Thalassemia and Sickle Cell Disease in Middle Eastern Countries: A Systemic Review	0
Factors Associated with Overt Stroke in Children and Adolescents with Sickle Cell Disease: A Retrospective Cohort Study	0
Unusual Causes of β Thalassemia Trait: Discovery of another Three Novel SUPT5H Variants	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
Identification of a Patient with Transfusion-Dependent β-Thalassemia Caused by Compound Heterozygous Mutations of HBB : C.84_85insC and Common Linked Int	0
A Rare Case of De Novo Beta-Thalassemia Diagnosed by Whole-Genome Sequencing in an Ethnically Danish Newborn	0
Sickle Cell Disease and Quality of Life: An Evaluation of Reporting of Patient-Reported Outcomes in Randomized Controlled Trials	0
Hepatobiliary Manifestations in Thalassemia Patients: A Narrative Review	0
Influence of Alpha Thalassaemia on Hematological and Clinical Presentations in Patients of Sickle Cell-β-Thalassaemia with IVS I-5 (G→C) Mutation ( HBB :	0
Rapid and Visual Molecular Detection of High Hb F Determinants; HPFH6, Asian Indian inv-del ( A γδβ) 0 -Thalassemia, and Thai del-	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
Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations	0
Detection of a Rare Mutation in the Initiation Codon of the β-Globin Gene (HBB:C.2T > C; P.Met1Thr)	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
Ethical and Clinical Considerations in the Use of Hydroxyurea in Pregnant Women with Sickle Cell Disease	0
Association of Micro RNA-155 with Alloimmunization in Transfusion-Dependent Thalassemia Patients	0
Thalassaemia Registries: A Call for Action. A Position Statement from the Thalassaemia International Federation	0
Genotypic Characterization of Thalassemia in Huadu District, Guangzhou, China: A Single-Center Retrospective Study	0
First Reported Case of Hemoglobin H Disease Caused by the Rare α-Globin Gene Mutation ( HBA2 c.244delT) in a Chinese Family	0
A New α1-Globin Variant, Hb Ormylia [ HBA1 :c.63C > G; p.His21Gln]. Report of Eleven Cases in Northern Greece	0
Unraveling Hemoglobin D’s Influence: A Comprehensive Analysis of Clinicopathological Parameters in Hemoglobin D Patients	0
Thrombosis Tendency After Splenectomy in a Danish Family With Hemoglobin Volga, and a Literature Review	0
Identification of a Novel 16.8Kb Deletion of the α-Globin Gene Cluster by Third-Generation Sequencing	0
Hb A 2 -Guangxi [δ79 (EF3) Asp→Asn, HBD : C.238G > A] and polyA + 70 ( HBD : C.*200G > A): Two No	0
Thalassemia in Asia 2021 Thalassemia in Brunei Darussalam	0
Prevalence of Hemoglobinopathies in Premarital Screening in the Province of Nigde, Turkey	0
Use of Capillary Electrophoresis Migration Position for the Presumptive Identification of Hemoglobin Variants Prevalent in China	0
Death from S. pneumoniae in HbSC Disease: Was Expanded Pneumococcal Vaccination Too Late?	0
Second Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Thalassemia Major after Graft Rejection	0
Development of a Quantitative Multiplex PCR to Detect Three Common Alpha Thalassemia Deletions	0
An HBB Intron 1 Variant (c.92 + 9C > T) Suggestive of β-Thalassemia Trait	0
Hepcidin-to-Ferritin Ratio as an Early Diagnostic Index of Iron Overload in β-Thalassemia Major Patients	0
Dominant Beta Thalassemia: A Very Rare Cause of Thalassemia in a Mediterranean Country	0
Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation ( HBB :c.336dup)	0
Hb Hebei [α20 (B1) His→Leu; HBA2 :C.62A > T]: A Novel Hemoglobin Variant Found during Measurement of Glycated Hemoglobin	0