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Primary Care - Clinics in Office Practice
Volumn 31, Issue 3, 2004, Pages 767-770
Clinical consult: Iron overload - Hereditary hemochromatosis
Author keywords

[No Author keywords available]
Indexed keywords

ADULT; ANAMNESIS; ANEMIA; ARTICLE; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC PROCEDURE; DIFFERENTIAL DIAGNOSIS; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC SCREENING; HEALTH BEHAVIOR; HEMOCHROMATOSIS; HETEROZYGOSITY; HUMAN; IRON OVERLOAD; MALE; PHLEBOTOMY; PRIMARY MEDICAL CARE; PRIORITY JOURNAL; SKIN PIGMENTATION;
EID: 4344634687     PISSN: 00954543     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pop.2004.04.007     Document Type: Review
Times cited : (7)
References (8)
  • 1
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    • Practice guideline development task force of the College of American Pathologists: Hereditary hemochromatosis
    • Witte D.L., Crosby W.H., Edwards C.Q., Fairbanks V.F., Mitros F.A. Practice guideline development task force of the College of American Pathologists: hereditary hemochromatosis. Clin Chim Acta. 245:1996;139-200
    • (1996) Clin Chim Acta , vol.245 , pp. 139-200
    • Witte, D.L.1    Crosby, W.H.2    Edwards, C.Q.3    Fairbanks, V.F.4    Mitros, F.A.5
  • 2
    • 0029827481 scopus 로고    scopus 로고
    • Clinical and biochemical abnormalities in people heterozygous for hemochromatosis
    • Bulaj Z.J., Griffen L.M., Jorde L.B., Edwards C.Q., Kushner J.P. Clinical and biochemical abnormalities in people heterozygous for hemochromatosis. N Engl J Med. 335:1996;1799-1805
    • (1996) N Engl J Med , vol.335 , pp. 1799-1805
    • Bulaj, Z.J.1    Griffen, L.M.2    Jorde, L.B.3    Edwards, C.Q.4    Kushner, J.P.5
  • 3
    • 9344224529 scopus 로고    scopus 로고
    • A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
    • Feder J.N., Gnirke A., Thomas W., et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet. 13:1996;399-408
    • (1996) Nat Genet , vol.13 , pp. 399-408
    • Feder, J.N.1    Gnirke, A.2    Thomas, W.3
  • 4
    • 0030221927 scopus 로고    scopus 로고
    • Mutation analysis in hereditary hemochromatosis
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    • (1996) Blood Cells Mol Dis , vol.22 , pp. 187-194
    • Beutler, E.1    Gelbart, T.2    West, C.3
  • 5
    • 0032401727 scopus 로고    scopus 로고
    • Management of hemochromatosis. Hemochromatosis Management Working Group
    • Barton J.C., McDonnell S.M., Adams P.C., et al. Management of hemochromatosis. Hemochromatosis Management Working Group. Ann Intern Med. 129:1998;932-939
    • (1998) Ann Intern Med , vol.129 , pp. 932-939
    • Barton, J.C.1    McDonnell, S.M.2    Adams, P.C.3
  • 6
    • 0031936407 scopus 로고    scopus 로고
    • Distribution of transferrin saturation in an Australian population: Relevance to the early diagnosis of hemochromatosis
    • McLaren C.E., McLachlan G.J., Halliday J.W., et al. Distribution of transferrin saturation in an Australian population: relevance to the early diagnosis of hemochromatosis. Gastroenterology. 114:1998;543-549
    • (1998) Gastroenterology , vol.114 , pp. 543-549
    • McLaren, C.E.1    McLachlan, G.J.2    Halliday, J.W.3
  • 7
    • 0035038147 scopus 로고    scopus 로고
    • Diagnosis and mangagement of hemochromatosis
    • Tavill A.S. Diagnosis and mangagement of hemochromatosis. Hepatology. 33:2001;1321-1328
    • (2001) Hepatology , vol.33 , pp. 1321-1328
    • Tavill, A.S.1

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.