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Items: 1 to 20 of 156

1.

Thalassemia and hemoglobinopathies in Thua Thien Hue Province, Central Vietnam.

Nguyen HV, Sanchaisuriya K, Nguyen D, Phan HT, Siridamrongvattana S, Sanchaisuriya P, Fucharoen S, Fucharoen G, Schelp FP.

Hemoglobin. 2013;37(4):333-42. doi: 10.3109/03630269.2013.790829. Epub 2013 Apr 19.

PMID:
23600535
2.

Micromapping of thalassemia and hemoglobinopathies in diferent regions of northeast Thailand and Vientiane, Laos People's Democratic Republic.

Tritipsombut J, Sanchaisuriya K, Phollarp P, Bouakhasith D, Sanchaisuriya P, Fucharoen G, Fucharoen S, Schelp FP.

Hemoglobin. 2012;36(1):47-56. doi: 10.3109/03630269.2011.637149. Epub 2011 Nov 28.

PMID:
22122810
3.

Molecular epidemiological survey of hemoglobinopathies in the Wuxi region of Jiangsu Province, eastern China.

Lin M, Han ZJ, Wang Q, Zheng L, Wang Y, Yang H, Huang Y, Lin F, Zhan XF, Lin CP, Wu JR, Luo ZY, Liu JB, Yan ZH, Zheng SY, Zheng JK, Lu M, Zhu JJ, Xie LX, Yang LY.

Hemoglobin. 2013;37(5):454-66. doi: 10.3109/03630269.2013.807285. Epub 2013 Jun 27.

PMID:
23806067
4.

Hemoglobin Constant Spring is markedly high in women of an ethnic minority group in Vietnam: a community-based survey and hematologic features.

Nguyen VH, Sanchaisuriya K, Wongprachum K, Nguyen MD, Phan TT, Vo VT, Sanchaisuriya P, Fucharoen S, Schelp FP.

Blood Cells Mol Dis. 2014 Apr;52(4):161-5. doi: 10.1016/j.bcmd.2013.12.002. Epub 2013 Dec 22.

PMID:
24368026
5.

Hemoglobinopathy carrier prevalence in the United Arab Emirates: first analysis of the Dubai Health Authority premarital screening program results.

Belhoul KM, Abdulrahman M, Alraei RF.

Hemoglobin. 2013;37(4):359-68. doi: 10.3109/03630269.2013.791627. Epub 2013 May 7.

PMID:
23647352
6.

Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy.

Siriratmanawong N, Chansri W, Singsanan S, Fucharoen G, Fucharoen S.

Hemoglobin. 2009;33(6):507-14. doi: 10.3109/03630260903343780.

PMID:
19958198
7.

Molecular lesion frequency of hemoglobin gene disorders in Taiwan.

Liu SC, Peng CT, Lin TH, Wang SJ, Shih MC, Tien N, Chang CC, Lu JJ, Lin CY.

Hemoglobin. 2011;35(3):228-36. doi: 10.3109/03630269.2011.572524.

PMID:
21599435
8.

Detection of coinherited Hb H-Constant Spring/Paksé disease and Hb E by capillary electrophoresis and high performance liquid chromatography.

Pornprasert S, Waneesorn J.

Hemoglobin. 2013;37(2):176-82. doi: 10.3109/03630269.2012.752744. Epub 2012 Dec 13.

PMID:
23234508
9.

The prevalence and molecular basis of hemoglobinopathies in Cambodia.

Carnley BP, Prior JF, Gilbert A, Lim E, Devenish R, Sing H, Sarin E, Guhadasan R, Sullivan SG, Wise CA, Bittles AH, Chan K, Wong MS, Chan V, Erber WN.

Hemoglobin. 2006;30(4):463-70.

PMID:
16987801
10.

The spectrum of α- and β-thalassemia mutations in Yunnan Province of Southwestern China.

Zhang J, Zhu BS, He J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH.

Hemoglobin. 2012;36(5):464-73.

PMID:
22943051
11.

Distribution of thalassemias and associated hemoglobinopathies identified by prenatal diagnosis in Taiwan.

Peng CT, Liu SC, Peng YC, Lin TH, Wang SJ, Le CY, Shih MC, Tien N, Lu JJ, Lin CY.

Blood Cells Mol Dis. 2013 Oct;51(3):138-41. doi: 10.1016/j.bcmd.2013.04.007. Epub 2013 May 18.

PMID:
23689197
12.

Prevalence and molecular characterization of structural hemoglobin variants in the Dongguan region of Guangdong province, southern China.

Lou JW, Wang T, Liu YH, He Y, Zhong BM, Liu JX, Zhao Y, Ye WL, Li DZ.

Hemoglobin. 2014;38(4):282-6. doi: 10.3109/03630269.2014.928779. Epub 2014 Jul 2.

PMID:
24985555
13.

Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects.

Fucharoen S, Fucharoen G.

Hemoglobin. 2012;36(1):18-24. doi: 10.3109/03630269.2011.638406. Epub 2011 Dec 6.

PMID:
22145566
14.

Hemoglobinopathy: molecular epidemiological characteristics and health effects on Hakka people in the Meizhou region, southern China.

Lin M, Wen YF, Wu JR, Wang Q, Zheng L, Liu GR, Huang Y, Yang H, Lin F, Zhan XF, Lin CP, Yang HT, Weng QQ, Huang FT, Wang Y, Yao MQ, Chen HZ, Wu DH, Zeng JB, Zeng RX, Yang H, Li GC, Lu M, Zhu JJ, Xie LX, Wang JL, Yang LY.

PLoS One. 2013;8(2):e55024. doi: 10.1371/journal.pone.0055024. Epub 2013 Feb 1.

15.

Molecular Epidemiology of Hemoglobinopathies in Cambodia.

Munkongdee T, Tanakulmas J, Butthep P, Winichagoon P, Main B, Yiannakis M, George J, Devenish R, Fucharoen S, Svasti S.

Hemoglobin. 2016 Jun;40(3):163-7. doi: 10.3109/03630269.2016.1158723.

PMID:
27117566
16.

Genetic epidemiology, hematological and clinical features of hemoglobinopathies in Iran.

Rahimi Z.

Biomed Res Int. 2013;2013:803487. doi: 10.1155/2013/803487. Epub 2013 Jun 18. Review.

17.

High prevalence of hemoglobin disorders and glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Republic of Guinea (West Africa).

Millimono TS, Loua KM, Rath SL, Relvas L, Bento C, Diakite M, Jarvis M, Daries N, Ribeiro LM, Manco L, Kaeda JS.

Hemoglobin. 2012;36(1):25-37. doi: 10.3109/03630269.2011.600491. Epub 2011 Sep 19.

PMID:
21929367
18.

Hemoglobinopathies in the Christmas Island population.

Gilbert A, Prior JF, Bennett J, Lim E, Erber WN.

Hemoglobin. 2004;28(4):357-61.

PMID:
15658194
19.

Prevalence of hemoglobinopathies in rural Bengal, India.

Dolai TK, Dutta S, Bhattacharyya M, Ghosh MK.

Hemoglobin. 2012;36(1):57-63. doi: 10.3109/03630269.2011.621007. Epub 2011 Oct 17.

PMID:
22004064
20.

Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants.

Gupta RB, Tiwary RS, Pande PL, Kutlar F, Oner C, Oner R, Huisman TH.

Hemoglobin. 1991;15(5):441-58. Review.

PMID:
1802886
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