메뉴 건너뛰기




Volumn 101, Issue 8, 2008, Pages 631-641

A decision analysis model for diagnostic strategies using DNA testing for hereditary haemochromatosis in at risk populations

Author keywords

[No Author keywords available]

Indexed keywords

DNA; IRON;

EID: 49149115037     PISSN: 14602725     EISSN: 14602393     Source Type: Journal    
DOI: 10.1093/qjmed/hcn070     Document Type: Article
Times cited : (7)

References (26)
  • 2
    • 0031744037 scopus 로고    scopus 로고
    • High incidence of the Cys 282 Tyr mutation in the HFE gene in the Irish population - implications for haemochromatosis
    • Murphy S, Curran MD, McDougall N, Callender ME, O'Brien CJ, Middleton D. High incidence of the Cys 282 Tyr mutation in the HFE gene in the Irish population - implications for haemochromatosis. Tissue Antigens 1998; 52:484-8.
    • (1998) Tissue Antigens , vol.52 , pp. 484-488
    • Murphy, S.1    Curran, M.D.2    McDougall, N.3    Callender, M.E.4    O'Brien, C.J.5    Middleton, D.6
  • 3
    • 49149115896 scopus 로고    scopus 로고
    • Diagnostic strategies using DNA testing for hereditary haemochromatosis: A systematic review and economic evaluation
    • in press
    • Bryant J, Cooper K, Picot J, Clegg A, Roderick P, Rosenberg W, et al Diagnostic strategies using DNA testing for hereditary haemochromatosis: A systematic review and economic evaluation. Health Technol Assess 2008 (in press).
    • (2008) Health Technol Assess
    • Bryant, J.1    Cooper, K.2    Picot, J.3    Clegg, A.4    Roderick, P.5    Rosenberg, W.6
  • 4
    • 9344224529 scopus 로고    scopus 로고
    • A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis [see comment]
    • Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis [see comment]. Nat Genet 1996; 13 399-408.
    • (1996) Nat Genet , vol.13 , pp. 399-408
    • Feder, J.N.1    Gnirke, A.2    Thomas, W.3    Tsuchihashi, Z.4    Ruddy, D.A.5    Basava, A.6
  • 5
    • 85184971965 scopus 로고    scopus 로고
    • British Committee for Standards in Haematology
    • British Society for Haematology, Oxford, Abingdon
    • British Society for Haematology. British Committee for Standards in Haematology. Guidelines on diagnosis and therapy. Genetic Haemochromatosis. Oxford, Abingdon, 2000.
    • (2000) Guidelines on diagnosis and therapy. Genetic Haemochromatosis
  • 7
    • 0037280384 scopus 로고    scopus 로고
    • Principles of good practice for decision analytic modeling in health-care evaluation: Report of the ISPOR Task Force on Good Research Practices-Modeling Studies
    • Weinstein MC, O'Brien B, Hornberger J, Jackson J, Johannesson M, McCabe C, et al. Principles of good practice for decision analytic modeling in health-care evaluation: Report of the ISPOR Task Force on Good Research Practices-Modeling Studies. Value Health 2003; 6 9-17.
    • (2003) Value Health , vol.6 , pp. 9-17
    • Weinstein, M.C.1    O'Brien, B.2    Hornberger, J.3    Jackson, J.4    Johannesson, M.5    McCabe, C.6
  • 8
    • 33646153508 scopus 로고    scopus 로고
    • Revisiting hereditary hemochromatosis: Current concepts and progress. [Review] [60 fefs]
    • Yen AW, Fancher TL, Bowlus CL. Revisiting hereditary hemochromatosis: current concepts and progress. [Review] [60 fefs]. Am J Med 2006; 119:391-9.
    • (2006) Am J Med , vol.119 , pp. 391-399
    • Yen, A.W.1    Fancher, T.L.2    Bowlus, C.L.3
  • 9
    • 0031037009 scopus 로고    scopus 로고
    • Genetic irony beyond haemochromatosis: Clinical effects of HLA-H mutations
    • Beutler E. Genetic irony beyond haemochromatosis: Clinical effects of HLA-H mutations. Lancet 1997; 349:296-7.
    • (1997) Lancet , vol.349 , pp. 296-297
    • Beutler, E.1
  • 11
    • 0036206229 scopus 로고    scopus 로고
    • Testing for haemochromatosis in a liver clinic population: Relationship between ethnic origin, HFE gene mutations, liver histology and serum iron markers [see comment]
    • Moodie SJ, Ang L, Stenner JM, Finlayson C, Khotari A, Levin GE, et al Testing for haemochromatosis in a liver clinic population: relationship between ethnic origin, HFE gene mutations, liver histology and serum iron markers [see comment]. Eur J Gastroenterol Hepatol 2002; 14:223-9.
    • (2002) Eur J Gastroenterol Hepatol , vol.14 , pp. 223-229
    • Moodie, S.J.1    Ang, L.2    Stenner, J.M.3    Finlayson, C.4    Khotari, A.5    Levin, G.E.6
  • 12
    • 0029029626 scopus 로고
    • Screening blood-donors for hereditary hemochromatosis - decision-analysis model-based on a 30-year database
    • Adams PC, Gregor JC, Kertesz AE, Valberg LS. Screening blood-donors for hereditary hemochromatosis - decision-analysis model-based on a 30-year database. Gastroenterology 1995; 109:177-88.
    • (1995) Gastroenterology , vol.109 , pp. 177-188
    • Adams, P.C.1    Gregor, J.C.2    Kertesz, A.E.3    Valberg, L.S.4
  • 13
    • 33745712799 scopus 로고    scopus 로고
    • Phenotype and HFE genotype in a population with abnormal iron markers recruited from an Endocrinology Department
    • Vantyghem MC, Fajardy I, Dhondt F, Girardot C, D'Herbomez M, Danze PM, et al. Phenotype and HFE genotype in a population with abnormal iron markers recruited from an Endocrinology Department. Eur J Endocrinol 2006; 154:835-41.
    • (2006) Eur J Endocrinol , vol.154 , pp. 835-841
    • Vantyghem, M.C.1    Fajardy, I.2    Dhondt, F.3    Girardot, C.4    D'Herbomez, M.5    Danze, P.M.6
  • 14
    • 0025877002 scopus 로고
    • Clinical presentation of hemochromatosis - a changing scene
    • Adams PC, Kertesz AE, Valberg LS. Clinical presentation of hemochromatosis - a changing scene. Am J Med 1991; 90:445-9.
    • (1991) Am J Med , vol.90 , pp. 445-449
    • Adams, P.C.1    Kertesz, A.E.2    Valberg, L.S.3
  • 15
    • 0027499440 scopus 로고
    • Rate of iron reaccumulation following iron depletion in hereditary hemochromatosis. Implications for venesection therapy
    • Adams PC, Kertesz AE, Valberg LS. Rate of iron reaccumulation following iron depletion in hereditary hemochromatosis. Implications for venesection therapy. J Clin Gastroenterol 1993; 16:207-10.
    • (1993) J Clin Gastroenterol , vol.16 , pp. 207-210
    • Adams, P.C.1    Kertesz, A.E.2    Valberg, L.S.3
  • 16
    • 33645121766 scopus 로고    scopus 로고
    • Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients
    • McCune CA, Ravine D, Carter K, Jackson HA, Hutton D, Hedderich J, et al. Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients. Gut 2006; 55:554-62.
    • (2006) Gut , vol.55 , pp. 554-562
    • McCune, C.A.1    Ravine, D.2    Carter, K.3    Jackson, H.A.4    Hutton, D.5    Hedderich, J.6
  • 18
    • 0028913123 scopus 로고
    • Indications, methods, and outcomes of percutaneous liver biopsy in England and Wales: An audit by the British Society of Gastroenterology and the Royal College of Physicians of London
    • Gilmore I, Burroughs A, Murray-Lyon IM, Williams R, Jenkins D, Hopkins A. Indications, methods, and outcomes of percutaneous liver biopsy in England and Wales: An audit by the British Society of Gastroenterology and the Royal College of Physicians of London. Gut 1995; 36 437-41.
    • (1995) Gut , vol.36 , pp. 437-441
    • Gilmore, I.1    Burroughs, A.2    Murray-Lyon, I.M.3    Williams, R.4    Jenkins, D.5    Hopkins, A.6
  • 19
    • 0034651590 scopus 로고    scopus 로고
    • Screening for hereditary hemochromatosis in siblings and children of affected patients. A cost-effectiveness analysis
    • El-Serag HB, Inadomi JM, Kowdley KV. Screening for hereditary hemochromatosis in siblings and children of affected patients. A cost-effectiveness analysis. Ann Intern Med 2000; 132:261-9.
    • (2000) Ann Intern Med , vol.132 , pp. 261-269
    • El-Serag, H.B.1    Inadomi, J.M.2    Kowdley, K.V.3
  • 20
    • 0028802963 scopus 로고
    • Screening for hemochromatosis in children of homozygotes: Prevalence and cost-effectiveness
    • Adams PC, Kertesz AE, Valberg LS. Screening for hemochromatosis in children of homozygotes: Prevalence and cost-effectiveness. Hepatology 1995; 22:1720-7.
    • (1995) Hepatology , vol.22 , pp. 1720-1727
    • Adams, P.C.1    Kertesz, A.E.2    Valberg, L.S.3
  • 21
    • 33751117755 scopus 로고    scopus 로고
    • Impact of hemochromatosis screening in patients with indeterminate results: The hemochromatosis and iron overload screening study
    • Anderson RT, Wenzel L, Walker AP, Ruggiero A, Acton RT, Hall MA, et al. Impact of hemochromatosis screening in patients with indeterminate results: The hemochromatosis and iron overload screening study. Genet Med 2006; 8:681-7.
    • (2006) Genet Med , vol.8 , pp. 681-687
    • Anderson, R.T.1    Wenzel, L.2    Walker, A.P.3    Ruggiero, A.4    Acton, R.T.5    Hall, M.A.6
  • 22
    • 0031944939 scopus 로고    scopus 로고
    • Implications of genotyping of spouses to limit investigation of children in genetic hemochromatosis
    • Adams PC. Implications of genotyping of spouses to limit investigation of children in genetic hemochromatosis. Clin Genet 1998; 53 176-8.
    • (1998) Clin Genet , vol.53 , pp. 176-178
    • Adams, P.C.1
  • 23
    • 85184967778 scopus 로고    scopus 로고
    • A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium. Gut 1997; 41:841-4.
    • A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium. Gut 1997; 41:841-4.
  • 25
    • 33749670275 scopus 로고    scopus 로고
    • Adefovir dipivoxil and pegylated interferon alfa-2a for the treatment of chronic hepatitis B: A systematic review and economic evaluation
    • Shepherd J, Jones J, Takeda A, Davidson P, Price A. Adefovir dipivoxil and pegylated interferon alfa-2a for the treatment of chronic hepatitis B: A systematic review and economic evaluation. Health Technol Assess 2006; 10:28.
    • (2006) Health Technol Assess , vol.10 , pp. 28
    • Shepherd, J.1    Jones, J.2    Takeda, A.3    Davidson, P.4    Price, A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.