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 *

104 related articles for article (PubMed ID: 25158816)

  • 1. Beta thalassaemia intermedia due to silent alpha globin gene quadruplication in an infant.
    So CC; Chiang AK; Kan A; Lee V; Ng E
    Pathology; 2014 Oct; 46(6):570-2. PubMed ID: 25158816
    [No Abstract]   [Full Text] [Related]  

  • 2. Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia.
    Sollaino MC; Paglietti ME; Perseu L; Giagu N; Loi D; Galanello R
    Haematologica; 2009 Oct; 94(10):1445-8. PubMed ID: 19794088
    [TBL] [Abstract][Full Text] [Related]  

  • 3. α-globin gene quadruplication and heterozygous β-thalassemia: a not so rare cause of thalassemia intermedia.
    Origa R; Sollaino MC; Borgna-Pignatti C; Piga A; Feliu Torres A; Masile V; Galanello R
    Acta Haematol; 2014; 131(3):162-4. PubMed ID: 24217654
    [No Abstract]   [Full Text] [Related]  

  • 4. Beta thalassaemia intermedia due to co-inheritance of three unique alpha globin cluster duplications characterised by next generation sequencing analysis.
    Clark B; Shooter C; Smith F; Brawand D; Steedman L; Oakley M; Rushton P; Rooks H; Wang X; Drousiotou A; Kyrri A; Hadjigavriel M; Will A; Fisher C; Higgs DR; Phylipsen M; Harteveld C; Kleanthous M; Thein SL
    Br J Haematol; 2018 Jan; 180(1):160-164. PubMed ID: 27469621
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes.
    Farashi S; Vakili S; Faramarzi Garous N; Ashki M; Imanian H; Azarkeivan A; Najmabadi H
    Expert Rev Hematol; 2015 Oct; 8(5):693-8. PubMed ID: 26343893
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Thalassaemia intermedia caused by coinheritance of a β-thalassaemia mutation and a de novo duplication of α-globin genes in the paternal allele.
    Pang D; Shang X; Cai D; Zhu F; Cheng Y; Zhong J; Yi S; Zhang Q; Xu X
    Br J Haematol; 2019 Aug; 186(4):620-624. PubMed ID: 31124576
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association of an α-globin gene cluster duplication and heterozygous β-thalassemia in a patient with a severe thalassemia syndrome.
    Jiang H; Liu S; Zhang YL; Wan JH; Li R; Li DZ
    Hemoglobin; 2015; 39(2):102-6. PubMed ID: 25690803
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Heterozygous β thalassemia with triplication of the α globin gene].
    Constanço MC; Rocha P; Bento C; Silva HM
    Acta Med Port; 2011; 24(4):633-6. PubMed ID: 22521023
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The carrier frequency of α-globin gene triplication in an Iranian population with normal or borderline hematological parameters.
    Moosavi SF; Amirian A; Zarbakhsh B; Kordafshari A; Mirzahoseini H; Zeinali S; Karimipoor M
    Hemoglobin; 2011; 35(4):323-30. PubMed ID: 21797699
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia.
    Farashi S; Bayat N; Faramarzi Garous N; Ashki M; Montajabi Niat M; Vakili S; Imanian H; Zeinali S; Najmabadi H; Azarkeivan A
    Hemoglobin; 2015; 39(3):201-6. PubMed ID: 26084319
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Alpha globin gene duplications in beta thalassemia patients with intact beta globin gene.
    Faà V; Masala M; Cao A; Rosatelli MC
    Blood Cells Mol Dis; 2010 Mar; 44(3):156-8. PubMed ID: 20117028
    [No Abstract]   [Full Text] [Related]  

  • 13. Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genes.
    Mehta PR; Upadhye DS; Sawant PM; Gorivale MS; Nadkarni AH; Shanmukhaiah C; Ghosh K; Colah RB
    Ann Hematol; 2015 Dec; 94(12):1953-8. PubMed ID: 26319530
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Moderate-severe beta-thalassemia intermedia phenotype caused by sextuplicated alpha-globin gene allele in two beta-thalassemia carriers.
    Achour A; Knijnenburg J; Koopmann T; Raz A; Tischkowitz M; Coates TD; Baas F; Harteveld CL
    Am J Hematol; 2024 Aug; 99(8):1655-1658. PubMed ID: 38817045
    [No Abstract]   [Full Text] [Related]  

  • 15. Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri Lanka.
    Perera S; Allen A; Silva I; Hapugoda M; Wickramarathne MN; Wijesiriwardena I; Allen S; Rees D; Efremov DG; Fisher CA; Weatherall DJ; Premawardhena A
    Sci Rep; 2019 Jul; 9(1):10116. PubMed ID: 31300739
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Silent carrier beta-thalassaemia due to a severe beta-globin mutation interacting with other genetic elements.
    Rund D; Filon D; Oppenheim A; Abramov A
    Eur J Pediatr; 1993 Jul; 152(7):574-6. PubMed ID: 8354316
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patients.
    Harteveld CL; Refaldi C; Cassinerio E; Cappellini MD; Giordano PC
    Blood Cells Mol Dis; 2008; 40(3):312-6. PubMed ID: 18249014
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Analyzing 5'HS3 and 5'HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutations.
    Neishabury M; Azarkeivan A; Oberkanins C; Abedini SS; Zamani S; Najmabadi H
    Blood Cells Mol Dis; 2011 Mar; 46(3):201-5. PubMed ID: 21232998
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Thalassemia Intermedia Caused by 16p13.3 Sectional Duplication in a β-Thalassemia Heterozygous Child.
    Liu S; Jiang H; Wu MY; Zhang YL; Li DZ
    Pediatr Hematol Oncol; 2015; 32(5):349-53. PubMed ID: 26086873
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.