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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 26303193)

  • 1. Phenotype and Genotype in a Cohort of 312 Adult Patients with Nontransfusion-Dependent Thalassemia in Northeast Thailand.
    Prayalaw P; Teawtrakul N; Jetsrisuparb A; Pongudom S; Fucharoen G; Fucharoen S
    Acta Haematol; 2016; 135(1):15-20. PubMed ID: 26303193
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic heterogeneity of hemoglobin AEBart's disease: a large cohort data from a single referral center in northeast Thailand.
    Chaibunruang A; Karnpean R; Fucharoen G; Fucharoen S
    Blood Cells Mol Dis; 2014 Apr; 52(4):176-80. PubMed ID: 24314747
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia in Northeast Thailand.
    Yamsri S; Pakdee N; Fucharoen G; Sanchaisuriya K; Fucharoen S
    Acta Haematol; 2016; 136(4):233-239. PubMed ID: 27710960
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The diverse molecular basis and hematological features of Hb H and AEBart's diseases in Northeast Thailand.
    Boonsa S; Sanchaisuriya K; Fucharoen G; Wiangnon S; Jetsrisuparb A; Fucharoen S
    Acta Haematol; 2004; 111(3):149-54. PubMed ID: 15034236
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Molecular Characterization of Hb H and AEBart’s Diseases in Thai Children: Phramongkutklao Hospital Experiences.
    Boonyawat B; Photia A; Monsereenusorn C; Rujkijyanont P; Traivaree C
    J Med Assoc Thai; 2017 Feb; 100(2):167-74. PubMed ID: 29916623
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.
    Charoenkwan P; Teerachaimahit P; Sanguansermsri T
    Hemoglobin; 2014; 38(5):335-8. PubMed ID: 25238043
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A large cohort of β(+)-thalassemia in Thailand: molecular, hematological and diagnostic considerations.
    Yamsri S; Singha K; Prajantasen T; Taweenan W; Fucharoen G; Sanchaisuriya K; Fucharoen S
    Blood Cells Mol Dis; 2015 Feb; 54(2):164-9. PubMed ID: 25471338
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular basis of Hb H and AEBart's diseases in the Lao People's Democratic Republic.
    Singha K; Srivorakun H; Fucharoen G; Fucharoen S
    Int J Lab Hematol; 2020 Feb; 42(1):23-27. PubMed ID: 31693295
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.
    Prakobkaew N; Fucharoen S; Fuchareon G; Siriratmanawong N
    Eur J Haematol; 2014 Jan; 92(1):73-9. PubMed ID: 24112054
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular understanding of Indian untransfused thalassemia intermedia.
    Nadkarni A; Dabke P; Colah R; Ghosh K
    Int J Lab Hematol; 2015 Dec; 37(6):791-6. PubMed ID: 26226914
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-beta-thalassemia in Northeast Thailand.
    Nuntakarn L; Fucharoen S; Fucharoen G; Sanchaisuriya K; Jetsrisuparb A; Wiangnon S
    Blood Cells Mol Dis; 2009; 42(1):32-5. PubMed ID: 18951049
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular and clinical features of Hb H disease in northern Thailand.
    Charoenkwan P; Taweephon R; Sae-Tung R; Thanarattanakorn P; Sanguansermsri T
    Hemoglobin; 2005; 29(2):133-40. PubMed ID: 15921165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. A large cohort of Hb H disease in northeast Thailand: A molecular revisited, diverse genetic interactions and identification of a novel mutation.
    Singha K; Tepakhan W; Yamsri S; Chaibunruang A; Srivorakun H; Pansuwan A; Fucharoen G; Fucharoen S
    Clin Chim Acta; 2024 Jul; 561():119830. PubMed ID: 38914363
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interaction between Hb E and Hb Yala (HBB:c.129delT); a novel frameshift beta globin gene mutation, resulting in Hemoglobin E/β
    Ekwattanakit S; Riolueang S; Viprakasit V
    Hematology; 2018 Mar; 23(2):117-121. PubMed ID: 28768465
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular basis of thalassemia intermedia in Iran.
    Akbari MT; Izadi P; Izadyar M; Kyriacou K; Kleanthous M
    Hemoglobin; 2008; 32(5):462-70. PubMed ID: 18932071
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic factors affecting clinical severity in beta-thalassemia syndromes.
    Winichagoon P; Fucharoen S; Chen P; Wasi P
    J Pediatr Hematol Oncol; 2000; 22(6):573-80. PubMed ID: 11132233
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and hematological features of codon 17, A-T mutation of beta-thalassemia in Thai patients.
    Laosombat V; Wongchanchailert M; Sattayasevana B; Wiriyasateinkul A; Fucharoen S
    Eur J Haematol; 2001 Feb; 66(2):126-9. PubMed ID: 11168520
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
    Viprakasit V; Ekwattanakit S; Chalaow N; Riolueang S; Wijit S; Tanyut P; Chat-Uthai N; Tachavanich K
    Acta Haematol; 2014; 131(2):88-94. PubMed ID: 24081251
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.