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 *

192 related articles for article (PubMed ID: 29349701)

  • 21. Impact of the detection of ζ-globin chains and hemoglobin Bart's using immunochromatographic strip tests for α0-thalassemia (--SEA) differential diagnosis.
    Pata S; Laopajon W; Pongpaiboon M; Thongkum W; Polpong N; Munkongdee T; Paiboonsukwong K; Fucharoen S; Tayapiwatana C; Kasinrerk W
    PLoS One; 2019; 14(10):e0223996. PubMed ID: 31661492
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Validation of the immunochromatographic strip for α-thalassemia screening: a multicenter study.
    Winichagoon P; Kumpan P; Holmes P; Finlayson J; Newbound C; Kabral A; Li B; Nuinoon M; Fawcett T; Tayapiwatana C; Kasinrerk W; Fucharoen S
    Transl Res; 2015 Jun; 165(6):689-95. PubMed ID: 25450870
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis of hemoglobin Bart's hydrops fetalis by HPLC analysis of hemoglobin in fetal blood samples.
    Sanguansermsri T; Thanaratanakorn P; Steger HF; Tongsong T; Sirivatanapa P; Wanapirak C; Sirichotiyakul S; Chanprapas P; Flatz G
    Southeast Asian J Trop Med Public Health; 2001 Mar; 32(1):180-5. PubMed ID: 11485083
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Neonatal screening for α-thalassemia by cord hemoglobin Barts: how effective is it?
    Wu MY; Xie XM; Li J; Li DZ
    Int J Lab Hematol; 2015 Oct; 37(5):649-53. PubMed ID: 25955662
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Noninvasive prenatal diagnosis for hemoglobin Bart's hydrops fetalis.
    Winichagoon P; Sithongdee S; Kanokpongsakdi S; Tantisirin P; Bernini LF; Fucharoen S
    Int J Hematol; 2005 Jun; 81(5):396-9. PubMed ID: 16158819
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Quantitative analysis of Hb Bart's in cord blood by capillary electrophoresis system.
    Munkongdee T; Pichanun D; Butthep P; Klamchuen S; Chalermpolprapa V; Winichagoon P; Svasti S; Fucharoen S
    Ann Hematol; 2011 Jul; 90(7):741-6. PubMed ID: 21188378
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Quantitation of hemoglobins Bart's, H, Portland-I, Portland-II and constant spring by anion-exchange high-performance liquid chromatography.
    Kutlar F; Gu LH; Hu H; Huisman TH
    J Chromatogr; 1989 Feb; 487(2):265-74. PubMed ID: 2722997
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Production and characterization of monoclonal antibodies against α-globin chain-containing human hemoglobins for detecting α-thalassemia disease.
    Pakdeepak K; Pata S; Chiampanichayakul S; Kasinrerk W; Tatu T
    J Immunoassay Immunochem; 2016; 37(6):564-71. PubMed ID: 27050832
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Hb Bart's Quantitative Analysis in the Screening of α-Thalassemia].
    Yi S; Wang B; Li H; Zhang H; Song JP
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2021 Dec; 29(6):1903-1906. PubMed ID: 34893131
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A Rare Case of Hemoglobin Bart's Hydrops Fetalis due to Uniparental Disomy of Chromosome 16.
    Tan YR; Tan HK
    J Med Cases; 2021 Jul; 12(7):275-279. PubMed ID: 34434471
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Co-inheritance of α
    Singha K; Srivorakun H; Fucharoen G; Fucharoen S
    Int J Lab Hematol; 2017 Oct; 39(5):508-512. PubMed ID: 28497611
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hb Bart's level in cord blood and deletions of alpha-globin genes.
    Lie-Injo LE; Solai A; Herrera AR; Nicolaisen L; Kan YW; Wan WP; Hasan K
    Blood; 1982 Feb; 59(2):370-6. PubMed ID: 6895707
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Amniotic fluid metabolomic and lipidomic alterations associated with hemoglobin Bart's diseases.
    Chen X; Chen H; Nie H; Li G; Su J; Cao X; Cao Y; Wei F
    Metabolomics; 2021 Sep; 17(9):82. PubMed ID: 34490587
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Rapid and accurate quantitation of Hb Bart's and Hb H using weak cation exchange high performance liquid chromatography: correlation with the alpha-thalassemia genotype.
    Papassotiriou I; Traeger-Synodinos J; Vlachou C; Karagiorga M; Metaxotou A; Kanavakis E; Stamoulakatou A
    Hemoglobin; 1999 Aug; 23(3):203-11. PubMed ID: 10490132
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Detection of α-thalassaemia in neonates on cord blood and dried blood spot samples by capillary electrophoresis.
    Alauddin H; Langa M; Mohd Yusoff M; Raja Sabudin RZA; Ithnin A; Abdul Razak NF; Sardi NH; Hussin NH
    Malays J Pathol; 2017 Apr; 39(1):17-23. PubMed ID: 28413201
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal diagnosis of Hb Bart's hydrops fetalis by PCR technique: Pramongkutklao experience.
    Torcharus K; Sriphaisal T; Krutvecho T; Ketupanya A; Vuthiwong C; Suwanasophon C; Noonai A
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():287-90. PubMed ID: 8629126
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Haemoglobin Bart's in Saudi Arabia.
    Pembrey ME; Weatherall DJ; Clegg JB; Bunch C; Perrine RP
    Br J Haematol; 1975 Feb; 29(2):221-34. PubMed ID: 1238097
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Potential new approaches to the management of the Hb Bart's hydrops fetalis syndrome: the most severe form of α-thalassemia.
    King AJ; Higgs DR
    Hematology Am Soc Hematol Educ Program; 2018 Nov; 2018(1):353-360. PubMed ID: 30504332
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.