메뉴 건너뛰기




Volumn 178, Issue 1, 2009, Pages 39-42

Haemochromatosis gene frequency in a control and diabetic Irish population

Author keywords

Control; Diabetic; Haemochromatosis; Irish population

Indexed keywords

DNA; HFE PROTEIN, HUMAN; HLA ANTIGEN CLASS 1; MEMBRANE PROTEIN;

EID: 61849098857     PISSN: 00211265     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11845-008-0248-6     Document Type: Article
Times cited : (7)

References (14)
  • 1
    • 0001089987 scopus 로고    scopus 로고
    • EASL International Consensus Conference on Haemochromatosis, Part II. Expert document
    • doi: 10.1016/S0168-8278(01)80874-6
    • Adams P, Brissot P, Powell LW (2000) EASL International Consensus Conference on Haemochromatosis, Part II. Expert document. J Hepatol 33(3):487-496. doi: 10.1016/S0168-8278(01)80874-6
    • (2000) J Hepatol , vol.33 , Issue.3 , pp. 487-496
    • Adams, P.1    Brissot, P.2    Powell, L.W.3
  • 2
    • 2542560427 scopus 로고    scopus 로고
    • Hereditary hemochromatosis - A new look at an old disease
    • doi: 10.1056/NEJMra031573
    • Pietrangelo A (2004) Hereditary hemochromatosis-a new look at an old disease. N Engl J Med 350:2383-2397. doi: 10.1056/NEJMra031573
    • (2004) N Engl J Med , vol.350 , pp. 2383-2397
    • Pietrangelo, A.1
  • 4
    • 0032451161 scopus 로고    scopus 로고
    • Hemochromatosis in Ireland and HFE
    • doi: 10.1006/bcmd.1998.0211
    • Ryan E, O'Keane C, Crowe J (1998) Hemochromatosis in Ireland and HFE. Blood Cells Mol Dis 24(20):428-432. doi: 10.1006/bcmd.1998.0211
    • (1998) Blood Cells Mol Dis , vol.24 , Issue.20 , pp. 428-432
    • Ryan, E.1    O'Keane, C.2    Crowe, J.3
  • 6
    • 0001257976 scopus 로고
    • Idiopathic hemochromatosis, an iron storage disease
    • Finch SC, Finch CA (1955) Idiopathic hemochromatosis, an iron storage disease. Medicine 34:381-430
    • (1955) Medicine , vol.34 , pp. 381-430
    • Finch, S.C.1    Finch, C.A.2
  • 7
    • 0035960427 scopus 로고    scopus 로고
    • Prevalence of hereditary haemochromatosis in late-onset type 1 diabetes mellitus: A retrospective study
    • doi: 10.1016/S0140-6736(01)06526-6
    • Ellervik C, Mandrup-Poulsen T, Nordestgaard BG et al (2001) Prevalence of hereditary haemochromatosis in late-onset type 1 diabetes mellitus: A retrospective study. Lancet 358(9291):1405-1409. doi: 10.1016/ S0140-6736(01)06526-6
    • (2001) Lancet , vol.358 , Issue.9291 , pp. 1405-1409
    • Ellervik, C.1    Mandrup-Poulsen, T.2    Nordestgaard, B.G.3
  • 8
    • 0037298439 scopus 로고    scopus 로고
    • A search for association between hereditary haemochromatosis HFE gene mutations and type 2 diabetes mellitus in a Polish population
    • Malecki MT, Klupa T, Walus M, Czogala W, Greenlaw P, Sieradzki J (2003) A search for association between hereditary haemochromatosis HFE gene mutations and type 2 diabetes mellitus in a Polish population. Med Sci Monit 9(2):BR91-BR95
    • (2003) Med Sci Monit , vol.9 , Issue.2
    • Malecki, M.T.1    Klupa, T.2    Walus, M.3    Czogala, W.4    Greenlaw, P.5    Sieradzki, J.6
  • 9
    • 28444449032 scopus 로고    scopus 로고
    • Clinical aspects of hemochromatosis
    • doi: 10.1055/s-2005-923310
    • O'Neill J, Powell L (2005) Clinical aspects of hemochromatosis. Semin Liver Dis 25(4):381-391. doi: 10.1055/s-2005-923310
    • (2005) Semin Liver Dis , vol.25 , Issue.4 , pp. 381-391
    • O'Neill, J.1    Powell, L.2
  • 10
    • 0042131687 scopus 로고    scopus 로고
    • Evidence that the Cys282Tyr mutation of the HFE gene originated from a population in Southern Scandinavia and spread with the Vikings
    • doi: 10.1034/j.1399-0004.2003.00083.x
    • Milman N, Pedersen P (2003) Evidence that the Cys282Tyr mutation of the HFE gene originated from a population in Southern Scandinavia and spread with the Vikings. Clin Genet 64(1):36-47. doi: 10.1034/ j.1399-0004.2003.00083.x
    • (2003) Clin Genet , vol.64 , Issue.1 , pp. 36-47
    • Milman, N.1    Pedersen, P.2
  • 11
    • 0034896126 scopus 로고    scopus 로고
    • Haemochromatosis gene mutations in Finns, Swedes and Swedish Saamis
    • doi: 10.1159/000053362
    • Beckman L, Sjoberg K, Eriksson S, Beckman L (2001) Haemochromatosis gene mutations in Finns, Swedes and Swedish Saamis. Hum Hered 52(2):110-112. doi: 10.1159/000053362
    • (2001) Hum Hered , vol.52 , Issue.2 , pp. 110-112
    • Beckman, L.1    Sjoberg, K.2    Eriksson, S.3    Beckman, L.4
  • 12
    • 0036839568 scopus 로고    scopus 로고
    • Mild iron overload in patients carrying the HFE S65C gene mutation: A retrospective study in patients with suspected iron overload and healthy controls
    • doi: 10.1136/gut.51.5.723
    • Holmstrom P, Marmur J, Eggertsen G, Gafvels M, Stal P (2002) Mild iron overload in patients carrying the HFE S65C gene mutation: A retrospective study in patients with suspected iron overload and healthy controls. Gut 51:723-730. doi: 10.1136/gut.51.5.723
    • (2002) Gut , vol.51 , pp. 723-730
    • Holmstrom, P.1    Marmur, J.2    Eggertsen, G.3    Gafvels, M.4    Stal, P.5
  • 13
    • 0033039405 scopus 로고    scopus 로고
    • A survey of 2,851 patients with hemochromatosis: Symptoms and response to treatment
    • doi: 10.1016/S0002-9343(99)00120-5
    • McDonnell SM, Preston BL, Jewell SA et al (1999) A survey of 2,851 patients with hemochromatosis: Symptoms and response to treatment. Am J Med 106(6):619-624. doi: 10.1016/S0002-9343(99)00120-5
    • (1999) Am J Med , vol.106 , Issue.6 , pp. 619-624
    • McDonnell, S.M.1    Preston, B.L.2    Jewell, S.A.3
  • 14
    • 38349079861 scopus 로고    scopus 로고
    • Iron-overload-related disease in HFE hereditary hemochromatosis
    • doi: 10.1056/NEJMoa073286
    • Allen KJ, Gurrin LC, Constantine CC et al (2008) Iron-overload-related disease in HFE hereditary hemochromatosis. N Engl J Med 358:211-230. doi: 10.1056/NEJMoa073286
    • (2008) N Engl J Med , vol.358 , pp. 211-230
    • Allen, K.J.1    Gurrin, L.C.2    Constantine, C.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.