271 related articles for article (PubMed ID: 18710411)
1. Hematological features and molecular lesions of hemoglobin gene disorders in Taiwanese patients.
Lin HJ; Shih MC; Peng CT; Liu TC; Chen KW; Shih HC; Chang JG
Int J Lab Hematol; 2010 Feb; 32(1 Pt 2):1-7. PubMed ID: 18710411
[TBL] [Abstract][Full Text] [Related]
2. Distribution of thalassemias and associated hemoglobinopathies identified by prenatal diagnosis in Taiwan.
Peng CT; Liu SC; Peng YC; Lin TH; Wang SJ; Le CY; Shih MC; Tien N; Lu JJ; Lin CY
Blood Cells Mol Dis; 2013 Oct; 51(3):138-41. PubMed ID: 23689197
[TBL] [Abstract][Full Text] [Related]
3. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].
Indrák K; Divoký V; Brabec V; Indráková J; Svobodová M; Huisman TH
Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425
[TBL] [Abstract][Full Text] [Related]
4. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E
Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
[TBL] [Abstract][Full Text] [Related]
5. Molecular lesion frequency of hemoglobin gene disorders in Taiwan.
Liu SC; Peng CT; Lin TH; Wang SJ; Shih MC; Tien N; Chang CC; Lu JJ; Lin CY
Hemoglobin; 2011; 35(3):228-36. PubMed ID: 21599435
[TBL] [Abstract][Full Text] [Related]
6. Dominantly Inherited beta-Thalassemia.
Efremov GD
Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
[TBL] [Abstract][Full Text] [Related]
7. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand.
Yamsri S; Sanchaisuriya K; Fucharoen G; Sae-Ung N; Fucharoen S
Blood Cells Mol Dis; 2011 Aug; 47(2):120-4. PubMed ID: 21664157
[TBL] [Abstract][Full Text] [Related]
8. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
Efremov GD
Hemoglobin; 2007; 31(1):1-15. PubMed ID: 17365000
[TBL] [Abstract][Full Text] [Related]
9. Cord blood screening for alpha-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: correlation with genotypes and hematologic parameters.
Charoenkwan P; Taweephol R; Sirichotiyakul S; Tantiprabha W; Sae-Tung R; Suanta S; Sakdasirisathaporn P; Sanguansermsri T
Blood Cells Mol Dis; 2010 Jun; 45(1):53-7. PubMed ID: 20299254
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
Siriratmanawong N; Pinmuang-Ngam C; Fucharoen G; Fucharoen S
Fetal Diagn Ther; 2007; 22(4):264-8. PubMed ID: 17369692
[TBL] [Abstract][Full Text] [Related]
11. Molecular epidemiological study of alpha- and beta-thalassemia in Sihui city.
Tan JR; Li WJ; Ma JY; Mo QH; Li LY; Jia SQ; Lao XW; Li LY; He RQ; Xu XM
Di Yi Jun Yi Da Xue Xue Bao; 2003 Jul; 23(7):716-9. PubMed ID: 12865230
[TBL] [Abstract][Full Text] [Related]
12. Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects.
Fucharoen S; Fucharoen G
Hemoglobin; 2012; 36(1):18-24. PubMed ID: 22145566
[TBL] [Abstract][Full Text] [Related]
13. Hemoglobinopathies mimicking Hb S/beta-thalassemia: Hb S/S with alpha-thalassemia and Hb S/Volga.
Luo HY; Heeney M; Wang WC; Eung SH; Ware RE; Steinberg MH; Chui DH
Am J Hematol; 2006 May; 81(5):361-5. PubMed ID: 16628724
[TBL] [Abstract][Full Text] [Related]
14. Molecular mechanisms of thalassemia in southeast Asia.
Winichagoon P; Fucharoen S; Wilairat P; Fukumaki Y
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():235-40. PubMed ID: 8629113
[TBL] [Abstract][Full Text] [Related]
15. Molecular characterization of beta-thalassemia mutations in Guadeloupe.
Romana M; Keclard L; Guillemin G; Lavocat E; Saint-Martin C; Berchel C; Mérault G
Am J Hematol; 1996 Dec; 53(4):228-33. PubMed ID: 8948659
[TBL] [Abstract][Full Text] [Related]
16. Silent thalassemias: genotypes and phenotypes.
Bianco I; Cappabianca MP; Foglietta E; Lerone M; Deidda G; Morlupi L; Grisanti P; Ponzini D; Rinaldi S; Graziani B
Haematologica; 1997; 82(3):269-80. PubMed ID: 9234571
[TBL] [Abstract][Full Text] [Related]
17. Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.
Verma IC; Kleanthous M; Saxena R; Fucharoen S; Winichagoon P; Raizuddin S; Khan SN; Akbari MT; Izadyar M; Kotea N; Old JM; Ioannou PA; Khan B
Hemoglobin; 2007; 31(4):439-52. PubMed ID: 17994378
[TBL] [Abstract][Full Text] [Related]
18. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
Srivorakun H; Fucharoen G; Sae-Ung N; Sanchaisuriya K; Ratanasiri T; Fucharoen S
Eur J Haematol; 2009 Jul; 83(1):57-65. PubMed ID: 19226360
[TBL] [Abstract][Full Text] [Related]
19. Clinical phenotypes and genotypes diagnosis of thalassemia in children.
Torcharus K; Sriphaisal T; Krutvecho T; Suwanasophon C; Intarapakawong J
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():275-7. PubMed ID: 8629123
[TBL] [Abstract][Full Text] [Related]
20. [A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].
Li Q; Li LY; Mo QH
Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jan; 28(1):16-9. PubMed ID: 18227017
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]