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Items: 18

1.

An Aγ-globin G->A gene polymorphism associated with β039 thalassemia globin gene and high fetal hemoglobin production.

Breveglieri G, Bianchi N, Cosenza LC, Gamberini MR, Chiavilli F, Zuccato C, Montagner G, Borgatti M, Lampronti I, Finotti A, Gambari R.

BMC Med Genet. 2017 Aug 29;18(1):93. doi: 10.1186/s12881-017-0450-3.

2.

Klf10 Gene, a Secondary Modifier and a Pharmacogenomic Biomarker of Hydroxyurea Treatment Among Patients With Hemoglobinopathies.

Elalfy MS, El Sherif NH, Kamal TM, Aly NH.

J Pediatr Hematol Oncol. 2017 Apr;39(3):e155-e162. doi: 10.1097/MPH.0000000000000762.

PMID:
28085748
3.

Association of Xmn1 -158 γG variant with severity and HbF levels in β-thalassemia major and sickle cell anaemia.

Dadheech S, Jain S, Madhulatha D, Sharma V, Joseph J, Jyothy A, Munshi A.

Mol Biol Rep. 2014 May;41(5):3331-7. doi: 10.1007/s11033-014-3195-5. Epub 2014 Feb 2.

PMID:
24488321
4.

Gγ-Xmn I polymorphism: a significant determinant of β-thalassemia treatment without blood transfusion.

Ansari SH, Shamsi TS, Munzir S, Khan MT, Erum S, Perveen K, Farzana T, Ashraf M, Mehboob T, Moinuddin M.

J Pediatr Hematol Oncol. 2013 May;35(4):e153-6. doi: 10.1097/MPH.0b013e31827e8662.

PMID:
23389500
5.

Prevalence of Xmnl Gγ polymorphism in Egyptian patients with β-thalassemia major.

Tantawy AA, Andrawes NG, Ismaeil A, Kamel SA, Emam W.

Ann Saudi Med. 2012 Sep-Oct;32(5):487-91. doi: 10.5144/0256-4947.2012.487.

6.

Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion.

Danjou F, Anni F, Perseu L, Satta S, Dessì C, Lai ME, Fortina P, Devoto M, Galanello R.

Haematologica. 2012 Jul;97(7):989-93. doi: 10.3324/haematol.2011.053504. Epub 2012 Jan 22.

7.

Hydroxyurea-induced hematological response in transfusion-independent beta-thalassemia intermedia: case series and review of literature.

Ehsani MA, Hedayati-Asl AA, Bagheri A, Zeinali S, Rashidi A.

Pediatr Hematol Oncol. 2009 Nov;26(8):560-5. doi: 10.3109/08880010903271671. Review.

PMID:
19954365
8.

Clinical observation on YiSuiShengXueGranule on treating 156 patients with beta-thalassemia major and the molecular mechanism study.

Fang S, Wu Z, Zhang X, Liu Y, Wang W, Chai L, Cai H, Yi J, Wang L, Chen Y, Lv X, Huang Y, Wang R, Chen P.

Biol Pharm Bull. 2007 Nov;30(11):2084-7.

9.

Genotypic correlation between six common beta-thalassemia mutations and the XmnI polymorphism in the Moroccan population.

Agouti I, Badens C, Abouyoub A, Khattab M, Sayah F, Barakat A, Bennani M.

Hemoglobin. 2007;31(2):141-9.

PMID:
17486495
10.

Two beta-globin cluster-linked polymorphic loci in thalassemia patients of variable levels of fetal hemoglobin.

Bandyopadhyay S, Mondal BC, Sarkar P, Chandra S, Das MK, Dasgupta UB.

Eur J Haematol. 2005 Jul;75(1):47-53.

PMID:
15946310
11.

Response to hydroxyurea treatment in Iranian transfusion-dependent beta-thalassemia patients.

Yavarian M, Karimi M, Bakker E, Harteveld CL, Giordano PC.

Haematologica. 2004 Oct;89(10):1172-8.

12.

Asymptomatic homozygous deletional beta(0)-thalassemia in an African individual.

Faustino P, Reis AB, Feliciano H, Ferrão L, Pereira P, Picanço I, Miranda A, Seixas T, Romão L, Júnior EC, Lavinha J.

Am J Hematol. 2002 Jul;70(3):232-6.

13.

The role of heterocellular hereditary persistence of fetal haemoglobin in beta(0)-thalassaemia intermedia.

Chang YP, Littera R, Garau R, Smith KD, Dover GJ, Iannelli S, Cacace E, Contu L.

Br J Haematol. 2001 Sep;114(4):899-906.

PMID:
11564083
14.

[Current views of thalassemia intermedia].

Longinotti M, Dore F, Oggiano L, Pardini S, Pistidda P, Guiso L, Frogheri L, Bonfigli S, Murineddu M, Rimini E.

Recenti Prog Med. 1992 Apr;83(4):233-40. Review. Italian.

PMID:
1626119
15.

Homozygous beta-thalassemia without anemia.

Safaya S, Rieder RF, Dowling CE, Kazazian HH Jr, Adams JG 3rd.

Blood. 1989 Jan;73(1):324-8.

16.

Biochemical and molecular aspects of beta-thalassemia types in northern Sardinia.

Masala B, Manca L, Gallisai D, Stangoni A, Lanclos KD, Kutlar F, Yang KG, Huisman TH.

Hemoglobin. 1988;12(5-6):661-71.

PMID:
3209410
18.

Polymorphism of foetal haemoglobin in the Sardinian beta +-thalassaemia.

Masala B, Formato M, Manca L, Demuro P, Gallisai D, Dore F, Longinotti M.

Acta Haematol. 1986;76(4):208-11.

PMID:
2437750

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