| Molecular Spectrum of - and -Thalassemia Mutations in a Large Ethnic Hakka Population in Southern China |
7 |
| A Novel beta-Thalassemia Mutation in a Chinese family: IVS-II-203-205 (TCT > CC) (HBB: c.315+203TCT > CC) |
5 |
| The Spectrum of alpha-Thalassemia Mutations in the Lak Population of Iran |
4 |
| BCL11A Down-Regulation Induces -Globin in Human -Thalassemia Major Erythroid Cells |
4 |
| Successful Outcome of Hyperhemolysis in Sickle Cell Disease following Multiple Lines of Treatment: The Role of Complement Inhibition |
4 |
| Efficacy of the National Thalassaemia and Sickle Cell Disease Prevention Programme in Northern Greece: 15-Year Experience, Practice and Policy Gaps for Natives and Migrants |
3 |
| The Spectrum of beta-Thalassemia Mutations in Hamadan Province, West Iran |
3 |
| beta-Thalassemia in Iran: Things Everyone Needs to Know About This Disease |
3 |
| The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the Literature |
3 |
| Prevalence and Characteristics of Priapism in Sickle Cell Disease |
3 |
| Hb Nouakchott [114(GH2)ProLeu; HBA1: c.344C > T], A Second and Third Case Described in Two Unrelated Dutch Families |
2 |
| Hepatocellular Carcinoma in a -Thalassemia Intermedia Patient: Yet Another Case in the Expanding Epidemic |
2 |
| Erythrocyte cAMP in Determining Frequency of Acute Pain Episodes in Sickle Cell Disease Patients from Odisha State, India |
2 |
| Assessment of Peripheral Neuropathy in Patients with -Thalassemia via Electrophysiological Study: Reevaluation in the Era of Iron Chelators |
2 |
| Various -Thalassemia Genotype Combinations of the Saudi-Type Polyadenylation Signal Mutation ((T-Saudi)) in the Population of Bahrain: An Update of Genotype-Phenotype Analyses |
2 |
| Atrial fibrillation in -thalassemia Major Patients: Diagnosis, Management and Therapeutic Options |
2 |
| Coinheritance of Hb A(2)-Melbourne (HBD: c.130G>A) and Hb E (HBB: c.79G>A) in Laos and Simultaneous High Resolution Melt Detection of Hb A(2)-Melbourne and Hb A(2)-Lampang (HBD: c.142G>A) in a Single Tube |
2 |
| The Sub-Phenotypes of Sickle Cell Disease in Kuwait |
2 |
| Purulent Pericarditis in Sickle Cell Disease Due to Streptococcus agalactiae; a Unique Case Report and Literature Review |
2 |
| Compound Heterozygote for a Novel Elongated C-Terminal beta-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G > A) with Heterozygous alpha-Thalassemia-2 |
2 |
| Barriers to the use of hydroxyurea in the management of sickle cell disease in Nigeria |
2 |
| Detection of Hb A(2) and Hb Constant Spring (HBA2: c.427T>C) by Capillary Electrophoresis in a Patient with Hb H-Hb CS Disease |
1 |
| Detection of a Large Novel alpha-Thalassemia Deletion in an Autochthonous Belgian Family |
1 |
| Results of Coexistence of beta-Thalassemia Minor in Hb H Disease Patients |
1 |
| Hb Sichuan [alpha 67(E16)Thr -> Ile, HBA2: c.203C>T]: A Novel Hemoglobin Variant That Can Be Detected by Glycated Hemoglobin Electrophoresis |
1 |
| Quality of Life of Pakistani Children with beta-Thalassemia Major |
1 |
| Quality of Life and Depression in Turkish Patients with beta-Thalassemia Major: A Cross-Sectional Study |
1 |
| Unusual beta-Globin Haplotype Distribution in Newborns from Bengo, Angola |
1 |
| First Identification of the 3.5kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the -Globin Gene Cluster in a Chinese Family |
1 |
| Codon 14 (+T) (HBB: c.44_45insT): a Rare -Thalassemia Mutation Reported Only in Azerbaijan |
1 |
| First Report of a Coincidental Discovery of Hb Shimonoseki [54(E3)GlnArg, HBA2: c.164A > G (or HBA1)] in a Greek Family |
1 |
| Awareness and Attitude of University Students About Screening and Testing for Hemoglobinopathies: Case Study of the Aseer Region, Saudi Arabia |
1 |
| Prevalence of -Thalassemia in the Egyptian Population |
1 |
| Frequency of -Globin Gene Triplications and Coinheritance with -Globin Gene Mutations in the Iranian Population |
1 |
| Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia |
1 |
| Compound Heterozygosity of -Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India |
1 |
| Molecular Characterization of -Thalassemia Mutations Via the Amplification Refractory Mutation System-Polymerase Chain Reaction Method at the North Waziristan Agency, Pakistan |
1 |
| Study on the Role of Polymorphisms of the SOX-6 and MYB Genes and Fetal Hemoglobin Levels in Sicilian Patients with -Thalassemia and Sickle Cell Disease |
1 |
| Preventable Severe Thalassemia among Children |
1 |
| Analysis of Gene Mutation Types of - and -Thalassemia in Fuzhou, Fujian Province in China |
1 |
| Development of Visual Detection of -Thalassemia-1 (the - -(SEA) Deletion) Using pH-Sensitive Loop-Mediated Isothermal Amplification |
1 |
| A Simple Whole-Blood Polymerase Chain Reaction without DNA Extraction for Thalassemia Diagnosis |
1 |
| Molecular and Hematological Characterization of Two Novel -Globin Gene Mutations Found in Chinese Individuals |
1 |
| Compound Heterozygosity for Hb Adana (HBA2: c.179G > A) and the -alpha(3.7)/alpha alpha Thalassemia Deletion in Greece: Clinical Phenotype and Genetic Counseling |
1 |
| delta-Thalassemia with Complete Absence of Hb A(2) in a Chinese Family |
1 |
| Life-Threatening Drug-Induced Liver Injury in a Patient with -Thalassemia Major and Severe Iron Overload on Polypharmacy |
1 |
| Hb Hubei [114(GH2)ProHis, HBA1: c.344C > A]: A Novel Hemoglobin Variant of the 1-Globin Chain |
1 |
| o Unstable Hemoglobin Variants: The Need for Clinical Vigilance in Infants with Congenital Jaundice |
1 |
| Hb Moscva [24(B6)GlyAsp (GGT > GAT), HBB: c.74G > A]: An Unstable Hemoglobin Newly Detected as a De Novo Mutation in a Mauritanian Patient |
1 |
| Psychological Factors Associated with Episodic Chelation Adherence in Thalassemia |
1 |
