These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
136 related articles for article (PubMed ID: 31379233)
21. Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in Cis. Colaco S; Trivedi A; Colah RB; Ghosh K; Nadkarni AH Hemoglobin; 2014; 38(1):24-7. PubMed ID: 24200152 [TBL] [Abstract][Full Text] [Related]
22. Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study. Kolliopoulou A; Siamoglou S; John A; Sgourou A; Kourakli A; Symeonidis A; Vlachaki E; Chalkia P; Theodoridou S; Ali BR; Katsila T; Patrinos GP; Papachatzopoulou A Hemoglobin; 2019 Jan; 43(1):27-33. PubMed ID: 31039620 [TBL] [Abstract][Full Text] [Related]
23. A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia. Jiang F; Huang LY; Chen GL; Zhou JY; Xie XM; Li DZ Hemoglobin; 2017 Jan; 41(1):59-60. PubMed ID: 28460555 [TBL] [Abstract][Full Text] [Related]
24. Alpha hemoglobin stabilizing protein: Its causal relationship with the severity of beta thalassemia. Sagar CS; Kumar R; Sharma DC; Kishor P Blood Cells Mol Dis; 2015 Aug; 55(2):104-7. PubMed ID: 26142324 [TBL] [Abstract][Full Text] [Related]
25. The Spectrum of β-Thalassemia Mutations in Hamadan Province, West Iran. Alibakhshi R; Moradi K; Aznab M; Azimi A; Shafieenia S; Biglari M Hemoglobin; 2019 Jan; 43(1):18-22. PubMed ID: 31096791 [TBL] [Abstract][Full Text] [Related]
26. First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family. Murad H; Moassas F Hemoglobin; 2019 Jan; 43(1):66-68. PubMed ID: 30843739 [TBL] [Abstract][Full Text] [Related]
27. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations. Henderson SJ; Timbs AT; McCarthy J; Gallienne AE; Proven M; Rugless MJ; Lopez H; Eglinton J; Dziedzic D; Beardsall M; Khalil MS; Old JM Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043 [TBL] [Abstract][Full Text] [Related]
28. Elevated levels of miR-210 correlate with anemia in β-thalassemia/HbE patients. Siwaponanan P; Fucharoen S; Sirankapracha P; Winichagoon P; Umemura T; Svasti S Int J Hematol; 2016 Sep; 104(3):338-43. PubMed ID: 27272941 [TBL] [Abstract][Full Text] [Related]
30. Silent β-thalassemia mutations at -101 (C>T) and -71 (C>T) and their coinheritance with the sickle cell mutation in Bahrain. Al Moamen NJ; Mahdi F; Salman E; Ahmed T; Abbas R; Al Arrayed S; Sanad H; Ahmed AA Hemoglobin; 2013; 37(4):369-77. PubMed ID: 23586372 [TBL] [Abstract][Full Text] [Related]
32. Screening for thalassemia carriers in populations with a high rate of iron deficiency: revisiting the applicability of the Mentzer Index and the effect of iron deficiency on Hb A2 levels. Amid A; Haghi-Ashtiani B; Kirby-Allen M; Haghi-Ashtiani MT Hemoglobin; 2015; 39(2):141-3. PubMed ID: 25806419 [TBL] [Abstract][Full Text] [Related]
33. Peripheral blood circular RNA circ-0008102 may serve as a novel clinical biomarker in beta-thalassemia patients. Chen M; Lv A; Zhang S; Zheng J; Lin N; Xu L; Huang H Eur J Pediatr; 2024 Mar; 183(3):1367-1379. PubMed ID: 38165465 [TBL] [Abstract][Full Text] [Related]
34. Characterization of the HBB: c.*233G > C Variant: No Evidence of a β-Thalassemic Phenotype. Smith DL; Mitui M; Park JY; Luu HS; Timmons CF Hemoglobin; 2016; 40(1):25-8. PubMed ID: 26524961 [TBL] [Abstract][Full Text] [Related]
35. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene. Panyasai S; Jaiping K; Pornprasert S Hemoglobin; 2015; 39(4):292-5. PubMed ID: 26029792 [TBL] [Abstract][Full Text] [Related]
36. Evaluation of Applying a Combination of Red Cell Indexes and Formulas to Differentiate β-Thalassemia Trait from Iron Deficiency Anemia in the Thai Population. Pornprasert S; Thongsat C; Panyachadporn U Hemoglobin; 2017 Mar; 41(2):116-119. PubMed ID: 28597705 [TBL] [Abstract][Full Text] [Related]
37. Prevalence of Thalassemia Traits and Iron Deficiency Anemia in Sindh, Pakistan. Kandhro AH; Prachayasittikul V; Isarankura Na-Ayudhya C; Nuchnoi P Hemoglobin; 2017 May; 41(3):157-163. PubMed ID: 28745572 [TBL] [Abstract][Full Text] [Related]
38. Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation. Ozkinay F; Onay H; Karaca E; Arslan E; Erturk B; Ece Solmaz A; Tekin IM; Cogulu O; Aydinok Y; Vergin C Hemoglobin; 2015; 39(4):230-4. PubMed ID: 26076395 [TBL] [Abstract][Full Text] [Related]
39. The instability of the membrane skeleton in thalassemic red blood cells. Yuan J; Bunyaratvej A; Fucharoen S; Fung C; Shinar E; Schrier SL Blood; 1995 Nov; 86(10):3945-50. PubMed ID: 7579365 [TBL] [Abstract][Full Text] [Related]
40. Association of an α-globin gene cluster duplication and heterozygous β-thalassemia in a patient with a severe thalassemia syndrome. Jiang H; Liu S; Zhang YL; Wan JH; Li R; Li DZ Hemoglobin; 2015; 39(2):102-6. PubMed ID: 25690803 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]