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 *

109 related articles for article (PubMed ID: 23128329)

  • 1. εGγAγδβ0-thalassemia: a rare but clinically significant cause of hemolytic anemia in infants.
    Audino AN; Yeager ND
    J Pediatr Hematol Oncol; 2014 Jan; 36(1):e49-50. PubMed ID: 23128329
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Co-inheritance of β- and δ-thalassemia compromising prenatal screening in a Chinese couple seeking prevention.
    Li J; Xie XM; Zhou JY; Li DZ
    Fetal Diagn Ther; 2011; 30(1):73-6. PubMed ID: 21494010
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chronic and severe haemolytic anaemia caused by co-inheritance of beta-thalassaemia and triplicated alpha-globin genes.
    Wang C; Amato D
    Br J Haematol; 2007 Jun; 137(6):489. PubMed ID: 17408397
    [No Abstract]   [Full Text] [Related]  

  • 4. Erythrocytosis in a child due to Hb Andrew-Minneapolis [β144(HC1)Lys→Asn (AAG>AAT or AAC)] associated with a Spanish (δβ)(0)-thalassemia.
    Ropero P; González FA; Cela E; Beléndez C; Pérez B; Seri C; Fontanes E; Villegas A; Díaz-Mediavilla J
    Hemoglobin; 2013; 37(1):48-55. PubMed ID: 23215953
    [TBL] [Abstract][Full Text] [Related]  

  • 5. First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.
    Amirian A; Karimipoor M; Jafarinejad M; Taghavi M; Kordafshari A; Fathi Azar S; Mohammadi MS; Zeinali S
    Arch Iran Med; 2011 Jan; 14(1):8-11. PubMed ID: 21194254
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH.
    Blattner A; Brunner-Agten S; Ludin K; Hergersberg M; Herklotz R; Huber AR; Röthlisberger B
    Blood Cells Mol Dis; 2013 Jun; 51(1):39-47. PubMed ID: 23491071
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Congenital hemolytic anemia--hemoglobin abnormality--thalassemia].
    Fujita S
    Nihon Rinsho; 1996 Sep; 54(9):2454-9. PubMed ID: 8890578
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemia.
    Shalev H; Landau D; Pissard S; Krasnov T; Kapelushnik J; Gilad O; Broides A; Dgany O; Tamary H
    Eur J Haematol; 2013 Feb; 90(2):127-33. PubMed ID: 23206178
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of a novel δ-globin gene mutation in an Iranian family.
    Amirian A; Jafarinejad M; Kordafshari AR; Mosayyebzadeh M; Karimipoor M; Zeinali S
    Hemoglobin; 2010; 34(6):594-8. PubMed ID: 21077769
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family.
    Akbari MT; Hamid M; Izadyar M
    Ann Hematol; 2011 Mar; 90(3):349-51. PubMed ID: 20521148
    [No Abstract]   [Full Text] [Related]  

  • 11. A new form of thalassemia intermedia: Compound heterozygous beta thalassemia and hemoglobin Zurich.
    Yan CLS; Chan NCN; Lam GKS; Ng KY; Cheng CK; Li CK
    Pediatr Blood Cancer; 2019 Jun; 66(6):e27720. PubMed ID: 30900795
    [No Abstract]   [Full Text] [Related]  

  • 12. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS; He J; Zhang J; Zeng XH; Su J; Xu XH; Li SY; Chen H; Zhang YH
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine).
    Coleman MB; Lu ZH; Smith CM; Adams JG; Harrell A; Plonczynski M; Steinberg MH
    J Clin Invest; 1995 Feb; 95(2):503-9. PubMed ID: 7860732
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin gene.
    Traeger-Synodinos J; Papassotiriou I; Vrettou C; Skarmoutsou C; Stamoulakatou A; Kanavakis E
    Haematologica; 2001 Apr; 86(4):363-7. PubMed ID: 11325640
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic predisposition to β-thalassemia and sickle cell anemia in Turkey: a molecular diagnostic approach.
    Basak AN; Tuzmen S
    Methods Mol Biol; 2011; 700():291-307. PubMed ID: 21204041
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
    Carrocini GC; Ondei LS; Zamaro PJ; Bonini-Domingos CR
    Genet Mol Res; 2011 Dec; 10(4):3213-9. PubMed ID: 22194178
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Alpha and beta thalassemia.
    Muncie HL; Campbell J
    Am Fam Physician; 2009 Aug; 80(4):339-44. PubMed ID: 19678601
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Acute hemolysis in association with hepatitis B infection in a child with beta-thalassemia trait.
    Gürgey A; Yüce A; Ozbek N; Koçak N
    Turk J Pediatr; 1994; 36(3):259-62. PubMed ID: 7974818
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Thalassemia: pathophysiology of red cell changes.
    Schrier SL
    Annu Rev Med; 1994; 45():211-8. PubMed ID: 8198378
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Hereditary elliptocytosis associated with heterozygous beta-thalassemia with a hemolytic component].
    Jiménez Gonzalo FJ; de Luis Navarro J; de Blas Orlando JM; Martín Noya A
    Sangre (Barc); 1999 Oct; 44(5):391-2. PubMed ID: 10618922
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.