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BMJ
Volumn 322, Issue 7293, 2001, Pages 1061-
Screening for familial hypercholesterolaemia
Author keywords

[No Author keywords available]
Indexed keywords

CLINICAL FEATURE; COST EFFECTIVENESS ANALYSIS; DIAGNOSTIC ACCURACY; EARLY DIAGNOSIS; FAMILIAL HYPERCHOLESTEROLEMIA; FAMILY STUDY; GENETIC RISK; GENETIC SCREENING; HUMAN; LETTER; PRIORITY JOURNAL;
EID: 0035962371     PISSN: 09598138     EISSN: 14685833     Source Type: Journal    
DOI: 10.1136/bmj.322.7293.1061/a     Document Type: Letter
Times cited : (6)
References (10)
  • 1
    • 0034676774 scopus 로고    scopus 로고
    • Outcome of case finding among relatives of patients with known heterozygous familial hypercholesterolaemia
    • (16 December.)
    • Bhatnagar D, Morgan J, Siddiq S, Mackness MI, Miller JP, Durrington PN. Outcome of case finding among relatives of patients with known heterozygous familial hypercholesterolaemia. BMJ 2000; 321: 1497–1500. (16 December.)
    • (2000) BMJ , vol.321 , pp. 1497-1500
    • Bhatnagar, D.1    Morgan, J.2    Siddiq, S.3    Mackness, M.I.4    Miller, J.P.5    Durrington, P.N.6
  • 2
    • 0035852415 scopus 로고    scopus 로고
    • Familial hypercholesterolaemia is underdiagnosed after AMI
    • (13 January.)
    • Dorsch MF, Lawrance RA, Durham NP, Hall AS. Familial hypercholesterolaemia is underdiagnosed after AMI. BMJ 2001; 322: 111. (13 January.)
    • (2001) BMJ , vol.322 , pp. 111
    • Dorsch, M.F.1    Lawrance, R.A.2    Durham, N.P.3    Hall, A.S.4
  • 3
    • 0034662322 scopus 로고    scopus 로고
    • Extent of underdiagnosis of familial hypercholesterolaemia in routine practice: prospective registry study
    • Neil HAW, Hammond T, Huxley R, Matthews DR, Humphries SE. Extent of underdiagnosis of familial hypercholesterolaemia in routine practice: prospective registry study. BMJ 2000; 321: 148.
    • (2000) BMJ , vol.321 , pp. 148
    • Neil, H.A.W.1    Hammond, T.2    Huxley, R.3    Matthews, D.R.4    Humphries, S.E.5
  • 4
    • 0031688024 scopus 로고    scopus 로고
    • Mutations in the low-density lipoprotein receptor gene in Chinese familial hypercholesterolemia patients
    • Mak YT, Pang CP, Tomlinson B, Zhang J, Chan YS, Mak TW, et al. Mutations in the low-density lipoprotein receptor gene in Chinese familial hypercholesterolemia patients. Arterioscl Throm Vas 1998; 18: 1600–1605.
    • (1998) Arterioscl Throm Vas , vol.18 , pp. 1600-1605
    • Mak, Y.T.1    Pang, C.P.2    Tomlinson, B.3    Zhang, J.4    Chan, Y.S.5    Mak, T.W.6
  • 5
    • 0027449252 scopus 로고
    • Documented need for more effective diagnosis and treatment of familial hypercholesterolemia according to data from 502 heterozygotes in Utah
    • Williams RR, Schumacher MC, Barlow GK, Hunt SC, Ware JL, Pratt M, Latham BD. Documented need for more effective diagnosis and treatment of familial hypercholesterolemia according to data from 502 heterozygotes in Utah. Am J Cardiol 1993; 72: 18D–24D.
    • (1993) Am J Cardiol , vol.72 , pp. 18D-24D
    • Williams, R.R.1    Schumacher, M.C.2    Barlow, G.K.3    Hunt, S.C.4    Ware, J.L.5    Pratt, M.6    Latham, B.D.7
  • 6
    • 0034676774 scopus 로고    scopus 로고
    • Outcome of case finding among relatives of patients with known heterozygous familial hypercholesterolaemia
    • (16 December.)
    • Bhatnagar D, Morgan J, Siddiq S, Mackness MI, Miller JP, Durrington PN. Outcome of case finding among relatives of patients with known heterozygous familial hypercholesterolaemia. BMJ 2000; 321: 1497–1500. (16 December.)
    • (2000) BMJ , vol.321 , pp. 1497-1500
    • Bhatnagar, D.1    Morgan, J.2    Siddiq, S.3    Mackness, M.I.4    Miller, J.P.5    Durrington, P.N.6
  • 7
    • 0025944056 scopus 로고
    • Steering Committee, Simon Broome Register Group. Risk of fatal coronary heart disease in familial hypercholesterolaemia
    • Steering Committee, Simon Broome Register Group. Risk of fatal coronary heart disease in familial hypercholesterolaemia. BMJ 1991; 303: 893–896.
    • (1991) BMJ , vol.303 , pp. 893-896
  • 8
    • 0032759131 scopus 로고    scopus 로고
    • Mutation screening and genotype:phenotype correlation in familial hypercholesterolaemia
    • Graham CA, McClean E, Ward AJM, Beattie ED, Martin S, O'Kane M, et al. Mutation screening and genotype:phenotype correlation in familial hypercholesterolaemia. Atherosclerosis 1999; 147: 309–316.
    • (1999) Atherosclerosis , vol.147 , pp. 309-316
    • Graham, C.A.1    McClean, E.2    Ward, A.J.M.3    Beattie, E.D.4    Martin, S.5    O'Kane, M.6
  • 9
    • 24644453476 scopus 로고    scopus 로고
    • A cryptic splice mutation (ivs 12+11 c>g) in the ldlr gene in five families with familial hypercholesterolaemia
    • Kirk CW, Graham CA, Lyttle K, Beattie ED, Nicholls DP. A cryptic splice mutation (ivs 12+11 c>g) in the ldlr gene in five families with familial hypercholesterolaemia. J Med Genet 2000; 37(suppl 1):S73.
    • (2000) J Med Genet , vol.37 , Issue.1 , pp. S73
    • Kirk, C.W.1    Graham, C.A.2    Lyttle, K.3    Beattie, E.D.4    Nicholls, D.P.5
  • 10
    • 0030048642 scopus 로고    scopus 로고
    • A novel single base deletion in the LDLR gene (211delG): effect on serum lipid profiles and the influence of other genetic polymorphisms in the ACE, APOE and APOB genes
    • Ward AJ, O'Kane M, Nicholls DP, Young IS, Nevin NC, Graham CA. A novel single base deletion in the LDLR gene (211delG): effect on serum lipid profiles and the influence of other genetic polymorphisms in the ACE, APOE and APOB genes. Atherosclerosis 1996; 120: 83–91.
    • (1996) Atherosclerosis , vol.120 , pp. 83-91
    • Ward, A.J.1    O'Kane, M.2    Nicholls, D.P.3    Young, I.S.4    Nevin, N.C.5    Graham, C.A.6

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.