131 related articles for article (PubMed ID: 29614571)
1. [Clinical analysis of three cases with beta-thalassemia].
Li XY; Liu MJ; Xu LH; Xu HG; Chen HL; Fang JP
Zhonghua Er Ke Za Zhi; 2018 Apr; 56(4):294-297. PubMed ID: 29614571
[No Abstract] [Full Text] [Related]
2. A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and beta-thalassemia compound heterozygotes.
Papadakis MN; Patrinos GP; Tsaftaridis P; Loutradi-Anagnostou A
J Mol Med (Berl); 2002 Apr; 80(4):243-7. PubMed ID: 11976733
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of a case with SEA-HPFH deletion thalassemia with whole HBB gene deletion.
Ly Thi Thanh H; Le Thi Thanh H; Hoang Luong L; Huy Tran T; Liu SC; Truong HN; Ta TV; Bui TH; Tran VK
Taiwan J Obstet Gynecol; 2018 Jun; 57(3):435-441. PubMed ID: 29880180
[TBL] [Abstract][Full Text] [Related]
4. [The value of combined detection of HbA2 and HbF for the screening of thalassemia among individuals of childbearing ages].
Zhuang Q; Wang G; Wang Y; Zhuang J; Jiang Y; Huang H; Xu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jan; 39(1):16-20. PubMed ID: 34964959
[TBL] [Abstract][Full Text] [Related]
5. Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin.
Amato A; Cappabianca MP; Perri M; Zaghis I; Grisanti P; Ponzini D; Di Biagio P
Int J Lab Hematol; 2014 Feb; 36(1):13-9. PubMed ID: 23621512
[TBL] [Abstract][Full Text] [Related]
6. Fetal hemoglobin expression in the compound heterozygous state for -117 (G-->A) Agamma HPFH and IVS-1 nt 110 (G-->A) beta+ thalassemia: a case study.
Dedoussis GV; Sinopoulou K; Gyparaki M; Loutradis A
Eur J Haematol; 2000 Aug; 65(2):93-6. PubMed ID: 10966167
[TBL] [Abstract][Full Text] [Related]
7. Contrasting co-inheritance of alpha and beta mutations in delta beta thalassemia and hereditary persistence of fetal hemoglobin: a study from India.
Pandey H; Ranjan R; Singh K; Sharma A; Kishor K; Seth T; Saxena R
Hematology; 2018 Oct; 23(9):692-696. PubMed ID: 29621931
[TBL] [Abstract][Full Text] [Related]
8. [Direct genotyping of an hereditary persistence of fetal hemoglobin deletion and rapid prenatal diagnosis of the fetus at-risk for compound heterozygote of this defect with beta-thalassemia in a Chinese family].
Liu Z; Li Z; Xu X
Zhonghua Xue Ye Xue Za Zhi; 1999 Apr; 20(4):200-3. PubMed ID: 11601229
[TBL] [Abstract][Full Text] [Related]
9. [Analysis of Cut-off Value in Screening of Thalassemia by Capillary Hemoglobin Electrophoresis for Pregnant Women from Shenzhen Region of China].
Huo M; Wu WY; Liu M; Gan ZB; Mao WY; Lin RY; Liu AQ; He GR
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2016 Apr; 24(2):536-9. PubMed ID: 27151025
[TBL] [Abstract][Full Text] [Related]
10. [Molecular Epidemiological Characteristics and Differential Diagnosis of Common δβ-Thalassemia/HPFH].
Ju AP; Li N; Lin K; Huang HH; Liu SX; Jiang F
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2022 Aug; 30(4):1182-1187. PubMed ID: 35981381
[TBL] [Abstract][Full Text] [Related]
11. Combination of a triple alpha-globin gene with beta-thalassemia in a gypsy family: importance of the genetic testing in the diagnosis and search for a donor for bone marrow transplantation for one of their children.
Yus Cebrian F; Recasens Flores Mdel V; Izquierdo Álvarez S; Parra Salinas I; Rodriguez-Vigil Iturrate C
BMC Res Notes; 2016 Apr; 9():220. PubMed ID: 27080228
[TBL] [Abstract][Full Text] [Related]
12. Measurement of HbA₂ by capillary electrophoresis for diagnosing β-thalassemia/HbE disease in patients with low HbF.
Prasing W; Pornprasert S
Lab Med; 2014; 45(3):226-30. PubMed ID: 25051074
[TBL] [Abstract][Full Text] [Related]
13. Molecular characterization of a Chinese pedigree with beta-thalassemia intermedia.
Huang G; Jiang WL; Rong KB; Li YX; Luo XL; Meng JX; Yu XY
Hemoglobin; 2010 Jan; 34(2):179-83. PubMed ID: 20353356
[TBL] [Abstract][Full Text] [Related]
14. Impact of iron deficiency on hemoglobin A2% in obligate β-thalassemia heterozygotes.
Sharma P; Das R; Trehan A; Bansal D; Chhabra S; Kaur J; Marwaha RK; Varma N; Garewal G
Int J Lab Hematol; 2015 Feb; 37(1):105-11. PubMed ID: 24754744
[TBL] [Abstract][Full Text] [Related]
15. Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype.
Hariharan P; Sawant M; Gorivale M; Manchanda R; Colah R; Ghosh K; Nadkarni A
Mol Biol Rep; 2017 Oct; 44(5):413-417. PubMed ID: 28879539
[TBL] [Abstract][Full Text] [Related]
16. Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.
Fornari TA; Lanaro C; Albuquerque DM; Ferreira R; Costa FF
Exp Biol Med (Maywood); 2017 Feb; 242(3):267-274. PubMed ID: 27591578
[TBL] [Abstract][Full Text] [Related]
17. Hemoglobin F Only Syndrome at Birth: A Case of Maternal HbA2' Complicating the Diagnosis of β-Thalassemia.
Yee ME; Quarmyne MO; Segbefia C; Young AN; Zhuang L; Kutlar F
J Pediatr Hematol Oncol; 2016 Jan; 38(1):e32-4. PubMed ID: 26583619
[TBL] [Abstract][Full Text] [Related]
18. Detection of beta-thalassemia/hemoglobin E disease in samples which initially were diagnosed as homozygous hemoglobin E.
Pornprasert S; Moriyama A; Kongthai K; Waneesorn J; Jaiping K; Treesuwan K; Hattori Y
Clin Lab; 2013; 59(5-6):693-7. PubMed ID: 23865372
[TBL] [Abstract][Full Text] [Related]
19. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
Panyasai S; Fucharoen S; Surapot S; Fucharoen G; Sanchaisuriya K
Haematologica; 2004 Jul; 89(7):777-81. PubMed ID: 15257928
[TBL] [Abstract][Full Text] [Related]
20. Clinical and biological specificity of beta-thalassemia intermedia: a case report.
Girard JM; Drevin G; Brasme JF; Pissard S; Reynier P; Simard G; Denis MC
Ann Biol Clin (Paris); 2016 Dec; 74(6):688-692. PubMed ID: 27848919
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]