Hemoglobin

Article	Citations
Impact of COVID-19 Infection on 24 Patients with Sickle Cell Disease. One Center Urban Experience, Detroit, MI, USA	32
Prevalence and Diversity of Haplotypes of Sickle Cell Disease in the Eastern Province of Saudi Arabia	16
β-Thalassemia Major and Coronavirus-19, Mortality and Morbidity: a Systematic Review Study	14
Association between Hb A1c and Severity of COVID-19 Patients	10
Incidence Rate of COVID-19 Infection in Hemoglobinopathies: A Systematic Review and Meta-analysis	10
Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A2 Levels	9
COVID-19 in a Patient with β-Thalassemia Major and Severe Pulmonary Arterial Hypertension	9
Hematological Characteristics of β-Globin Gene Mutation –50 (G>A) (HBB: c.-100G>A) Carriers in Mainland China	9
Glucose-6-Phosphate Dehydrogenase Deficiency: An Overview of the Prevalence and Genetic Variants in Saudi Arabia	8
Thalassemia in Pakistan	8
Hb Hezhou [β64(E8)Gly→Ser; HBB: c.193G>A]: A Novel Variant on the β-Globin Gene	8
Thalassaemia Registries: A Call for Action. A Position Statement from the Thalassaemia International Federation	7
Hb Bart’s Hydrops Fetalis Syndrome and Hb H Disease Caused by Deletional Chiang Rai (– –CR) α0-Thalassemia in Two Unrelated Thai Families	7
Thalassemia in Thailand	7
Prevalence and Management of β-Thalassemia in India	7
High Prevalence of Anemia and Inherited Hemoglobin Disorders in Tribal Populations of Madhya Pradesh State, India	7
Genotype-Phenotype Correlation of β-Thalassemia in Malaysian Population: Toward Effective Genetic Counseling	7
Thalassemia in Indonesia	6
THALASSEMIA in ASIA 2021: Thalassemia in Guangxi Province, People’s Republic of China	6
The Prevention of Thalassemia Revisited: A Historical and Ethical Perspective by the Thalassemia International Federation	6
Adherence to Iron Chelation Therapy among Adults with Thalassemia: A Systematic Review	6
Hematopoietic Stem Cell Transplantation in Patients with Hemoglobinopathies	6
The Spectrum of α-Thalassemia Mutations in Kurdistan Province, West Iran	6
Thalassemia in Asia 2021 Overview of Thalassemia and Hemoglobinopathies in Bangladesh	6
Evaluation of Erythroferrone, Hepcidin, and Iron Overload Status in Iraqi Transfusion-Dependent β-Thalassemia Major Patients	6

Hb Westmead (HBA2: c.369C>G): Hematological Characteristics in Heterozygotes with and without α0-Thalassemia	6
Correlation Between Serum Ferritin and Viral Hepatitis in Thalassemia Patients	5
Quality of Life and Related Factors in β-Thalassemia Patients	5
β2-Microglobulin, Neutrophil Gelatinase-Associated Lipocalin, and Endocan Values in Evaluating Renal Functions in Patients with β-Thalassemia Major	5
Implications of Population Screening for Thalassemias and Hemoglobinopathies in Rural Areas of West Bengal, India: Report of a 10-Year Study of 287,258 Cases	5
Thalassemia in Malaysia	5
Venous Thromboembolism in Sickle Cell Disease is Associated with Neutrophilia	5
Molecular Spectrum of β-Thalassemia Mutations in Central to Eastern Thailand	5
Micromapping of Thalassemia and Hemoglobinopathies Among Laos, Khmer, Suay and Yer Ethnic Groups Residing in Lower Northeastern Thailand	5
Perforated Duodenal Ulcer Associated with Deferasirox in a Child with β-Thalassemia Major	5
Transcranial Doppler Velocities among Sickle Cell Disease Patients in Steady State	5
Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland China	5
Detection of an α-Globin Fusion Gene Using Real-Time Polymerase Chain Reaction-Based Multicolor Melting Curve	5
δ-Globin Chain Variants Associated with Decreased Hb A2 Levels: A National Reference Laboratory Experience	5
Utilization of Pneumococcal Vaccine and Penicillin Prophylaxis in Sickle Cell Disease in Three African Countries: Assessment among Healthcare Providers in SickleInAfrica	4
The Prevalence of Hypothyroidism among Patients With β-Thalassemia: A Systematic Review and Meta-Analysis of Cross-Sectional Studies	4
A Report on the Education, Employment and Marital Status of Thalassemia Patients from a Tertiary Care Center in the Middle East	4
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	4
Comparative Efficacy and Safety Between Deferiprone and Deferasirox with Special Reference to Serum Ferritin Level and Cardiac Function in Bengali β-Thalassemia Major Children	4
A Wide Spectrum Study of α-Globin Chain Variants: Cases from the UK	4
Veno-Venous Extracorporeal Membrane Oxygenation in Adult Patients with Sickle Cell Disease and Acute Chest Syndrome: a Single-Center Experience	4
Pedigree Analysis of Nonhomologous Sequence Recombination of HBA1 and HBA2 Genes	4
Molecular Genetic Analysis of α-Thalassemia in Hamadan Province, West Iran	4
Haptoglobin Genotypes Associated with Vaso-Occlusive Crisis in Sickle Cell Anemia Patients of Eastern India	4
Genetic Regulation of Redox Balance in β-Thalassemia Trait	4
Comparison of Hematopoietic Stem Cell Transplantation Results in Patients with β-Thalassemia Major from Three Different Graft Types	3
Fifteen Cases of Hb J-Meerut: The Rare Association with Hb E and/or HBA1: c.-24C>G (or HBA2) Variants	3
Hb A2-Calderdale [δ2(NA2)His→Asn; HBD: c.7C>A] and Misdiagnosis of Type 2 Diabetes Mellitus Due to Interference with Hb A1c When Using Cation Exchange High Performance	3
Thalassemia in Viet Nam	3
Detection of Paternal IVS-II-1 (G>A) (HBB: c.315+1G>A) Mutation in Cell-Free Fetal DNA Using COLD-PCR assay	3
Iron Chelators, Such as Deferasirox, When Combined With Hydroxyurea, Provide an Additional Benefit of Iron Chelation in Patients Receiving Chronic Transfusion Therapy	3
Novel α0-Thalassemia Deletion Identified in an Indian Infant with Hb H Disease	3
Distribution of HBB Gene Mutations in the Kurdish Population of Ilam Province, West Iran	3
Hemoglobinopathies and COVID-19: The Experience of a Center in Northern Greece	3
Development of the Next Generation Sequencing-Based Diagnostic Test for β-Thalassemia and its Validation in a Pashtun Family	3
Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous β-Thalassemia 3.5 kb Deletions	3
Combined Gap-Polymerase Chain Reaction and Targeted Next-Generation Sequencing Improve α- and β-Thalassemia Carrier Screening in Pregnant Women in Vietnam	3
Compound Heterozygosity for a Novel Mutation Codon 104 (–A) (HBB: c.313delA) and Codons 41/42 (–CTTT) (HBB: c.126_129delCTTT) Leading to β-Thalassemia Major in a Chinese Family	3
Pituitary Iron Deposition and Endocrine Complications in Patients with β-Thalassemia: From Childhood to Adulthood	3
Calcium Channel Blockers in Conjunction with Standard Iron-Chelating Agents for β-Thalassemia Major: Systematic Literature Search	3
Characterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis	3
Updated Molecular Spectrum of β-Thalassemia Mutations in Duhok Province, Northern Iraq: Ethnic Variation and the Impact of Immigration	3
Hb Mizuho (HBB: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation Sequencing	3
Umbilical Cord Blood Screening for the Detection of Common Deletional Mutations of α-Thalassemia in Bangladesh	3
Spectrum of β-Thalassemia and Other Hemoglobinopathies in the Saurashtra Region of Gujarat, India: Analysis of a Large Population Screening Program	3
A Study to Assess and Improve Adherence to Iron Chelation Therapy in Transfusion-Dependent Thalassemia Patients	3
Receptor Activator of Nuclear Factor κ-Β Ligand/Osteoprotegerin Axis in Adults with Hb S/β-Thalassemia and β-Thalassemia Trait	2
Hepcidin-to-Ferritin Ratio as an Early Diagnostic Index of Iron Overload in β-Thalassemia Major Patients	2
A New α Chain Variant, Hb Heilongjiang (HBA2: c.49A>C), Found During Hb A1c Measurement	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

The Trend in Timing of Prenatal Diagnosis for Thalassemia at a Chinese Tertiary Obstetric Center	2
Evaluation of the High Resolution Melting Approach for Detection of β-Thalassemia Gene Mutations	2
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	2
Thalassemia in India	2
Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia Carriers	2
Hb Manitoba [α102(G9)Ser→Arg] in Pasifika: Tongan Case Report	2
Upregulation of miR-214 Mediates Oxidative Stress in Hb H Disease via Targeting of ATF4	2
Thalassemia in Sri Lanka	2
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	2
Development of the Quality of Life Questionnaire (SF-36) for Patients with β-Thalassemia Major and β-Thalassemia Intermedia Based on Extended Rasch Analysis	2
Surrogate Markers of Subclinical Atherosclerosis and Its Associated Factors in Patients with β-Thalassemia Major	2
Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand	2
A Chinese Male with Normal Hematological Indices and High Hb A2 Levels in β-Thalassemia Trait	2
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	2
Hb S (HBB: c.20A>T) Characteristics by High Performance Liquid Chromatography in Patients with Sickle Cell Disease Receiving the Novel Agent Voxelotor	2
An Evaluation for the Causes of Reduced Hb A2 and the Molecular Characterization of HBD Variants in Hong Kong	2
XmnI Polymorphism in Sickle Cell Disease in North Morocco	2
An Autopsy Case of β-Thalassemia Major Illuminating the Pathological Spectrum of the Disease	2
Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population	2
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	2
Inner Ear Complications in Children and Adolescents with Sickle Cell Disease	2
Thalassemia in Asia 2021 Thalassemia in Brunei Darussalam	2
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	2
Heterozygosity for the Novel HBA2: c.*91_*92delTA Polyadenylation Site Variant on the α2-Globin Gene Expanding the Genetic Spectrum of α-Thalassemia in Iran	2
Hb Huadu [α124(H7)Ser→Thr (TCC>ACC), HBA2: c.373T>A]: A Novel Variant of the α-Globin Gene	1
Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations	1
Necrobiosis Lipoidica in a Patient with β-Thalassemia Major: A Case Report and Review of the Literature	1
A Case of Fat Embolism Syndrome with Cerebral Involvement in Sickle Cell Anemia	1
Clinical Severity of β-Thalassemia Pediatric Patients in Myanmar	1
Thalassemia Status in Cambodia	1
Exploration of Barriers and Facilitators to Optimal Emergency Department Care of Sickle Cell Disease: Opportunities for Patient–Physician Partnerships to Improve Care	1
Investigation of the Distribution of Thalassemia in Children in Jiangxi Province, the People’s Republic of China	1
Hb Kalundborg [β79(EF3)Asp→Glu; HBB: c.240C>a], a Possible Low-affinity Hemoglobin Variant Detected during Hb A1c Measurement	1
A Novel 5 kb Deletion in theβ-Globin Gene Cluster Identified in a Chinese Patient	1
Dysregulated Serum Cytokine Production in Pediatric Patients with β-Thalassemia Major	1
Association of Exon 14 of theSOX6Gene Sequence Variations with Response to Hydroxyurea Therapy in Patients Carrying Non Transfusion-Dependent Thalassemia	1
Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT)	1
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	1
Consideration of Splenectomy in Unstable Hemoglobinopathy: A Case Report of Hb Hammersmith (HBB: c.128T>C)	1
Hb Wanjiang: A New β-Globin Chain Variant with Two Amino Acid Substitutions (HBB: c.255_264delinsTTTTTCTCAG)	1
Total Annual Economic Burden of Patients with Sickle Cell Disease in Steady State in Greece	1
Identification and Development of a High-Risk District Model in the Prevention of β-Thalassemia in Telangana State, India	1
Hb A2-Pistoia [δ89(F5)Ser→Asn, HBD: c.269G>a]: a Novel Mutation on the δ-Globin Gene in an Italian Child	1
Estimating the Cost of Thalassemia Care across the World: A Thalassemia International Federation Model	1
A Novel Mutation at HBA1: c.349G>T Causing α-Thalassemia in a Chinese Family	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
Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn, HBB: c.[79G>A;198G>C]): A Novel β-Thalassemic Hemoglobin Variant	1
β-Thalassemia Intermedia Caused by the β-Globin Gene 3′ Untranslated Region: Another Case Report	1
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	1
Haploidentical Hematopoietic Stem Cell Transplantation in Thalassemia	1
How I Treat Acute Chest Syndrome in Asthmatic Children with Sickle Cell Disease. A Practical Review	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
Editorial	1
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	1
A Novel β0-Thalassemia Mutation,HBB: c.356_357delTT [Codon 118 (–TT)] in an Iraqi Kurd	1
Current Status of Thalassemia in Lao People’s Democratic Republic	1
β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey	1
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	1
Eight Cases of Hb Winnipeg [HBA2: c.226G>T (or HBA1)]: A Detailed Study	1
Effect of α+ Thalassemia on the Severity of Plasmodium falciparum Malaria in Different Sickle Cell Genotypes in Indian Adults: A Hospital-Based Study	1
Hb Tacoma: G>T or G>C, and Does It Matter?	1
COVID-19 and Anemia: What Do We Know So Far?	1
The Effect of Five Single Nucleotide Polymorphisms on Hb F Variation of β-Thalassemia Traits and Hematologically Normal Individuals in Southeast Turkey	1
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	1
Dominant β-Thalassemia Phenotype Caused by Hb Dieppe (HBB: c.383A>G): Another Case Report	1
Validation of Two Point of Care Devices for Hemoglobin Estimation in Blood Donors	1
Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients	1
Noninvasive Hemoglobin Measurement Reduce Invasive Procedures in Thalassemia Patients	1
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	1
Thalassemia in the Philippines	1
Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a β-Thalassemia Major Phenotype	1
A New High Affinity Hemoglobin Variant: Hb San Francisco-KP (HBB: c.104T>C)	1
Analysis of a Novel Mexican Variant of the HBB Gene Associated with β-Thalassemia Using Bioinformatic Tools	1
The Spectrum of β-Thalassemia Mutations in the Population Migration in Lebanon: A 6-Year Retrospective Study	1
In SilicoAnalysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia	1
Association of Hb Shenyang [α26(B7)Ala→Glu, GCG>GAG, HBA2: c.80C>A (or HBA1)] with Several Types of α-Thalassemia in Thailand	1
Prediction of Heart and Liver Iron Overload in β-Thalassemia Major Patients Using Machine Learning Methods	1
Missing Hb Q-India Peak in a Triple-Heterozygous Patient with Hb D-Punjab/Hb Q-India/β-Thalassemia Trait	1
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	1
Case Report of Acute Splenic Sequestration Crisis in an Adult Patient with Hb S Disease and Suspected Hereditary Persistence of Fetal Hemoglobin	1

A Rare Case of Hb H Disease and Systemic Lupus Erythematosus	1
Hb Lepore-Hong Kong: First Report of a Novel δ/β-Globin Gene Fusion in a Chinese Family	1