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Volumn 32, Issue 2, 2005, Pages 123-130

Alpha-thalassaemia and population health in Southeast Asia

Author keywords

Genetic counselling; Hb Barts hydrops fetalis; Hb H disease; Prenatal diagnosis

Indexed keywords

GLOBIN; HEMOGLOBIN H;

EID: 22344439232     PISSN: 03014460     EISSN: None     Source Type: Journal    
DOI: 10.1080/03014460500075084     Document Type: Conference Paper
Times cited : (38)

References (28)
  • 2
    • 0035057577 scopus 로고    scopus 로고
    • Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?
    • Chan LC, Ma SK, Chan AY, Ha SY, Waye JS, Lau YL, Chui DH. 2001. Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia? J Clin Pathol 54:317-320.
    • (2001) J Clin Pathol , vol.54 , pp. 317-320
    • Chan, L.C.1    Ma, S.K.2    Chan, A.Y.3    Ha, S.Y.4    Waye, J.S.5    Lau, Y.L.6    Chui, D.H.7
  • 4
    • 0035139122 scopus 로고    scopus 로고
    • Sickle cell disease: No longer a single gene disorder
    • Chui DHK, Dover GJ. 2001. Sickle cell disease: No longer a single gene disorder. Curr Opin Pediatr 13:22-27.
    • (2001) Curr Opin Pediatr , vol.13 , pp. 22-27
    • Chui, D.H.K.1    Dover, G.J.2
  • 5
    • 0032055871 scopus 로고    scopus 로고
    • Hydrops fetalis caused by α-thalassemia: An emerging health care problem
    • Chui DHK, Waye JS. 1998. Hydrops fetalis caused by α-thalassemia: An emerging health care problem. Blood 91:2213-2222.
    • (1998) Blood , vol.91 , pp. 2213-2222
    • Chui, D.H.K.1    Waye, J.S.2
  • 6
    • 0037305250 scopus 로고    scopus 로고
    • Hemoglobin H disease: Not necessarily a benign disorder
    • Chui DHK, Fucharoen S, Chan V. 2003. Hemoglobin H disease: Not necessarily a benign disorder. Blood 101:791-800.
    • (2003) Blood , vol.101 , pp. 791-800
    • Chui, D.H.K.1    Fucharoen, S.2    Chan, V.3
  • 7
    • 0037190608 scopus 로고    scopus 로고
    • Prenatal exclusion of β thalassaemia major by examination of maternal plasma
    • Chiu RW, Lau TK, Leung TN, Chow KC, Chui DH, Lo YM. 2002. Prenatal exclusion of β thalassaemia major by examination of maternal plasma. Lancet 360:998-1000.
    • (2002) Lancet , vol.360 , pp. 998-1000
    • Chiu, R.W.1    Lau, T.K.2    Leung, T.N.3    Chow, K.C.4    Chui, D.H.5    Lo, Y.M.6
  • 8
    • 2942579453 scopus 로고    scopus 로고
    • Molecular diagnosis of haemoglobin disorders
    • Clark BE, Thein SL. 2004. Molecular diagnosis of haemoglobin disorders. Clin Lab Haematol 26:159-176.
    • (2004) Clin Lab Haematol , vol.26 , pp. 159-176
    • Clark, B.E.1    Thein, S.L.2
  • 10
    • 0002029882 scopus 로고    scopus 로고
    • Molecular genetics of the human globin genes
    • Steinberg MH, Forget BG, Higgs DR, Nagel RL, editors. Cambridge: Cambridge University Press
    • Forget BG. 2001. Molecular genetics of the human globin genes. In: Steinberg MH, Forget BG, Higgs DR, Nagel RL, editors. Disorders of haemoglobin; genetics, pathophysiology, and clinical management. Cambridge: Cambridge University Press, pp 117-130.
    • (2001) Disorders of Haemoglobin; Genetics, Pathophysiology, and Clinical Management , pp. 117-130
    • Forget, B.G.1
  • 12
    • 0001916646 scopus 로고    scopus 로고
    • Molecular mechanisms of α thalassemia
    • Steinberg MH, Forget BG, Higgs DR, Nagel RL, editors. Cambridge: Cambridge University Press
    • Higgs DR. 2001. Molecular mechanisms of α thalassemia. In: Steinberg MH, Forget BG, Higgs DR, Nagel RL, editors. Disorders of haemoglobin; genetics, pathophysiology, and clinical management. Cambridge: Cambridge University Press, pp 405-430.
    • (2001) Disorders of Haemoglobin; Genetics, Pathophysiology, and Clinical Management , pp. 405-430
    • Higgs, D.R.1
  • 13
    • 0001916646 scopus 로고    scopus 로고
    • Clinical and laboratory features of the α-thalassaemia syndromes
    • Steinberg MH, Forget BG, Higgs DR, Nagel RL, editors. Cambridge: Cambridge University Press
    • Higgs DR, Bowden DK. 2001. Clinical and laboratory features of the α-thalassaemia syndromes. In: Steinberg MH, Forget BG, Higgs DR, Nagel RL, editors. Disorders of haemoglobin; genetics, pathophysiology, and clinical management. Cambridge: Cambridge University Press, pp 431-469.
    • (2001) Disorders of Haemoglobin; Genetics, Pathophysiology, and Clinical Management , pp. 431-469
    • Higgs, D.R.1    Bowden, D.K.2
  • 14
    • 0030857933 scopus 로고    scopus 로고
    • The risk of α-thalassaemia in offspring of β-thalassaemia carriers in Hong Kong
    • Lam YH, Ghosh A, Tang MH, Chan V. 1997a. The risk of α-thalassaemia in offspring of β-thalassaemia carriers in Hong Kong. Prenat Diagn 17:733-736.
    • (1997) Prenat Diagn , vol.17 , pp. 733-736
    • Lam, Y.H.1    Ghosh, A.2    Tang, M.H.3    Chan, V.4
  • 15
    • 0030940684 scopus 로고    scopus 로고
    • Second-trimester hydrops fetalis in pregnancies affected by homozygous α-thalassaemia-1
    • Lam YH, Ghosh A, Tang MHY, Lee CP, Sin SY. 1997b. Second-trimester hydrops fetalis in pregnancies affected by homozygous α-thalassaemia-1. Prenat Diagn 17:267-269.
    • (1997) Prenat Diagn , vol.17 , pp. 267-269
    • Lam, Y.H.1    Ghosh, A.2    Tang, M.H.Y.3    Lee, C.P.4    Sin, S.Y.5
  • 16
    • 14744267781 scopus 로고    scopus 로고
    • Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood
    • Lau ET, Kwok YK, Chui DHK et al. 2005. Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood. Prenat Diagn 25:123-128.
    • (2005) Prenat Diagn , vol.25 , pp. 123-128
    • Lau, E.T.1    Kwok, Y.K.2    Chui, D.H.K.3
  • 17
    • 0030905118 scopus 로고    scopus 로고
    • Prevalence and genotypes of α- And β-thalassemia carriers in Hong Kong - Implications for population screening
    • Lau YL, Chan LC, Chan YY, Ha SY, Yeung CY, Waye JS, Chui DH. 1997. Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong - Implications for population screening. N Engl J Med 336:1298-1301.
    • (1997) N Engl J Med , vol.336 , pp. 1298-1301
    • Lau, Y.L.1    Chan, L.C.2    Chan, Y.Y.3    Ha, S.Y.4    Yeung, C.Y.5    Waye, J.S.6    Chui, D.H.7
  • 18
    • 0038618800 scopus 로고    scopus 로고
    • The simultaneous presence of or- And β-thalassaemia alleles: A pitfall of thalassaemia screening
    • Law HY, Chee MK, Tan GP, Ng IS. 2003. The simultaneous presence of or- and β-thalassaemia alleles: A pitfall of thalassaemia screening. Community Genet 6:14-21.
    • (2003) Community Genet , vol.6 , pp. 14-21
    • Law, H.Y.1    Chee, M.K.2    Tan, G.P.3    Ng, I.S.4
  • 20
    • 0035543925 scopus 로고    scopus 로고
    • Hb Dartmouth [α66(E15)Leu→Pro (α2) (CTG→CCG)] : A novel α2-globin gene mutation associated with severe neonatal anemia when inherited in trans with Southeast Asian α-thalassemia-1
    • McBride KL, Snow K, Kubik KS, Fairbanks VF, Hoyer JD, Fairweather RB, Chaffee S, Edwards WH. 2001. Hb Dartmouth [α66(E15)Leu→Pro (α2) (CTG→CCG)] : A novel α2-globin gene mutation associated with severe neonatal anemia when inherited in trans with Southeast Asian α-thalassemia-1. Hemoglobin 25:375-382.
    • (2001) Hemoglobin , vol.25 , pp. 375-382
    • McBride, K.L.1    Snow, K.2    Kubik, K.S.3    Fairbanks, V.F.4    Hoyer, J.D.5    Fairweather, R.B.6    Chaffee, S.7    Edwards, W.H.8
  • 21
    • 9644287956 scopus 로고    scopus 로고
    • Want the world to know? Publish here
    • Savla U, Hawley J. 2004. Want the world to know? Publish here. J Clin Invest 114, 602.
    • (2004) J Clin Invest , vol.114 , pp. 602
    • Savla, U.1    Hawley, J.2
  • 22
    • 0035412399 scopus 로고    scopus 로고
    • A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia
    • Tan ASC, Quah TC, Low PS, Chong SS. 2001. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia. Blood 98:250-251.
    • (2001) Blood , vol.98 , pp. 250-251
    • Tan, A.S.C.1    Quah, T.C.2    Low, P.S.3    Chong, S.S.4
  • 26
    • 0033708636 scopus 로고    scopus 로고
    • Homozygous Hb Sallanches [α104(G11)Cys→Tyr] in a Pakistani child with Hb H disease
    • Waye JS, Walker L, Chui DHK, Lafferty J, Kirby M. 2000. Homozygous Hb Sallanches [α104(G11)Cys→Tyr] in a Pakistani child with Hb H disease. Hemoglobin 24:355-357.
    • (2000) Hemoglobin , vol.24 , pp. 355-357
    • Waye, J.S.1    Walker, L.2    Chui, D.H.K.3    Lafferty, J.4    Kirby, M.5
  • 27
    • 0035320886 scopus 로고    scopus 로고
    • Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias
    • Weatherall DJ. 2001. Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias. Nat Rev Genet 2:245-255.
    • (2001) Nat Rev Genet , vol.2 , pp. 245-255
    • Weatherall, D.J.1
  • 28
    • 2442556148 scopus 로고    scopus 로고
    • The prevalence and spectrum of α and β thalassaemia in Guangdong Province: Implications for the future health burden and population screening
    • Xu XM, Zhou YQ, Luo GX, Liao C, Zhou M, Chen PY, Lu JP, Jia SQ, Xiao GF, Shen X, et al. 2004. The prevalence and spectrum of α and β thalassaemia in Guangdong Province: Implications for the future health burden and population screening. J Clin Pathol 57:517-522.
    • (2004) J Clin Pathol , vol.57 , pp. 517-522
    • Xu, X.M.1    Zhou, Y.Q.2    Luo, G.X.3    Liao, C.4    Zhou, M.5    Chen, P.Y.6    Lu, J.P.7    Jia, S.Q.8    Xiao, G.F.9    Shen, X.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.