157 related articles for article (PubMed ID: 22521023)
1. [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]
2. 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]
3. 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]
4. 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]
5. [Molecular diagnosis in a Korean family with thalassemia intermedia due to co-inheritance of triplicated alpha-globin genes (alphaalpha/alphaalphaalpha(anti 3.7)) and beta-thalassemia trait (IVS-II-1 G-->A)].
Chen M; Han JY; Sun Q; Kim IH; Ren Z; Huang S; Zeng Y
Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):195-7. PubMed ID: 11876981
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. [Thalassemia intermedia caused by interaction of IVS-1 1(G--A) mutation in the beta-globin gene and heterozygotic triplication in the alpha-globin gene].
Martínez-López J; Galán García P; del Río E; Baiget M; Gilsanz Rodríguez F
Rev Clin Esp; 1998 Mar; 198(3):153-5. PubMed ID: 9586437
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Thalassemia intermedia as a result of heterozygosis for beta 0 -thalassemia and alpha alpha alpha anti-3,7 genotype in a Brazilian patient.
Kimura EM; Grignoli CR; Pinheiro VR; Costa FF; Sonati MF
Braz J Med Biol Res; 2003 Jun; 36(6):699-701. PubMed ID: 12792697
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. The carriage rates of ααα
Long J; Liu E
Gene; 2021 Feb; 768():145296. PubMed ID: 33181251
[TBL] [Abstract][Full Text] [Related]
14. Frequency of alpha-globin gene triplications and their interaction with beta-thalassemia mutations.
Giordano PC; Bakker-Verwij M; Harteveld CL
Hemoglobin; 2009; 33(2):124-31. PubMed ID: 19373588
[TBL] [Abstract][Full Text] [Related]
15. [Molecular diagnosis of beta-thalassemia intermedia].
Chen J; Liu W; Chen M
Zhonghua Yi Xue Za Zhi; 1997 Aug; 77(8):575-8. PubMed ID: 9772460
[TBL] [Abstract][Full Text] [Related]
16. 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]
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. [The first case of thalassemia intermedia in Spain due to the interaction of 3 alpha genes with beta-thalassemia minor].
Villegas A; López Rubio M; Sánchez J; González A; Pérez Clausell C; Sal del Río A; del Potro E; Valverde F; Espinós D
Rev Clin Esp; 1993 Apr; 192(6):268-70. PubMed ID: 8497721
[TBL] [Abstract][Full Text] [Related]
19. Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 beta-thalassemia.
Fallah MS; Zadeh-Vakili A; Aleyasin SA; Mahdian R; Karimipour M; Raeisi M; Jamali S; Ebrahimi A; Fooladi P; Naderi M; Baysal E; Zeinali S
Blood Cells Mol Dis; 2009; 43(2):158-60. PubMed ID: 19577494
[No Abstract] [Full Text] [Related]
20. Phenotypes of individuals with a beta thal classical allele associated either with a beta thal silent allele or with alpha globin gene triplication.
Bianco I; Lerone M; Foglietta E; Deidda G; Cappabianca MP; Morlupi L; Ponzini D; Grisanti P; Di Biagio P; Amato A; Mezzabotta M; Graziani B
Haematologica; 1997; 82(5):513-25. PubMed ID: 9407714
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]