SCOPUS 정보 검색 플랫폼

Volumn 343, Issue 21, 2000, Pages 1529-1535

Disease-related conditions in relatives of patients with hemochromatosis

(8) Bulaj, Zaneta J a Ajioka, Richard S a Phillips, John D a LaSalle, Bernard A a Jorde, Lynn B a Griffen, Linda M a Edwards, Corwin Q b Kushner, James P a

a UNIVERSITY OF UTAH SCHOOL OF MEDICINE (United States)

b LDS HOSPITAL (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOTRANSFERASE; HLA ANTIGEN; TRANSFERRIN;

ADULT; AMINOTRANSFERASE BLOOD LEVEL; ARTHROPATHY; ARTICLE; CLINICAL FEATURE; DISEASE ASSOCIATION; FEMALE; GENE MUTATION; GENOTYPE; HEMOCHROMATOSIS; HOMOZYGOSITY; HUMAN; IRON OVERLOAD; LIVER CIRRHOSIS; LIVER FIBROSIS; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RELATIVE; SIBLING; SYMPTOM; TRANSFERRIN BLOOD LEVEL;

ADULT; FAMILY; FEMALE; HEMOCHROMATOSIS; HOMOZYGOTE; HUMANS; IRON OVERLOAD; LIVER CIRRHOSIS; MALE; MIDDLE AGED; PREVALENCE; TRANSAMINASES; TRANSFERRIN;

EID: 0034707120 PISSN: 00284793 EISSN: None Source Type: Journal
DOI: 10.1056/NEJM200011233432104 Document Type: Article

Times cited : (189)

References (24)

1
- 0002890398
- Hemochromatosis
- Lee GR, Foerster J, Lukens J, Paraskevas F, Greer JP, Rodgers GM, eds. Wintrobe's clinical hematology. 10th ed. Vol. 1. Baltimore: Lippincott Williams and Wilkins
- (1999) , pp. 1056-1070
- Edwards, C.Q.¹

2
- 0000702937
- Hemochromatosis
- Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic and molecular bases of inherited disease. 7th ed. Vol. 2. New York: McGraw-Hill
- (1995) , pp. 2237-2269
- Bothwell, T.H.¹ Charlton, R.W.² Motulsky, A.G.³

3
- 9344224529
- A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
- (1996) Nat Genet , vol.13 , pp. 399-408
- Feder, J.N.¹ Gnirke, A.² Thomas, W.³

4
- 0020147627
- Hereditary haemochromatosis
- (1982) Clin Haematol , vol.11 , pp. 411-435
- Edwards, C.Q.¹ Dadone, M.M.² Skolnick, M.H.³ Kushner, J.P.⁴

5
- 0030876559
- Clinical features of genetic hemochromatosis in women compared with men
- (1997) Ann Intern Med , vol.127 , pp. 105-110
- Moirand, R.¹ Adams, P.C.² Bicheler, V.³ Brissot, P.⁴ Deugnier, Y.⁵

6
- 0033039405
- A survey of 2,851 patients with hemochromatosis: Symptoms and response to treatment
- (1999) Am J Med , vol.106 , pp. 619-624
- McDonnell, S.M.¹ Preston, B.L.² Jewell, S.A.³

7
- 0023901798
- Prevalence of hemochromatosis among 11,065 presumably healthy blood donors
- (1988) N Engl J Med , vol.318 , pp. 1355-1362
- Edwards, C.Q.¹ Griffen, L.M.² Goldgar, D.³ Drummond, C.⁴ Skolnick, M.H.⁵ Kushner, J.P.⁶

8
- 0033517343
- A population-based study of the clinical expression of the hemochromatosis gene
- (1999) N Engl J Med , vol.341 , pp. 718-724
- Olynyk, J.K.¹ Cullen, D.J.² Aquilia, S.³ Rossi, E.⁴ Summerville, L.⁵ Powell, L.W.⁶

9
- 0025877002
- Clinical presentation of hemochromatosis: A changing scene
- (1991) Am J Med , vol.90 , pp. 445-449
- Adams, P.C.¹ Kertesz, A.E.² Valberg, L.S.³

10
- 0019765753
- Hereditary hemochromatosis: Contributions of genetic analyses
- (1981) Prog Hematol , vol.12 , pp. 43-71
- Edwards, C.Q.¹ Skolnick, M.H.² Kushner, J.P.³

11
- 0029827481
- Clinical and biochemical abnormalities in people heterozygous for hemochromatosis
- (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

12
- 0019952842
- Hereditary hemochromatosis: Analysis of laboratory expression of the disease by genotype in 18 pedigrees
- (1982) Am J Clin Pathol , vol.78 , pp. 196-207
- Dadone, M.M.¹ Kushner, J.P.² Edwards, C.Q.³ Bishop, D.T.⁴ Skolnick, M.H.⁵

13
- 0017681652
- Hereditary hemochromatosis: Diagnosis in siblings and children
- (1977) N Engl J Med , vol.297 , pp. 7-13
- Edwards, C.Q.¹ Carroll, M.² Bray, P.³ Cartwright, G.E.⁴

14
- 39149136945
- Hepatic pathology in relatives of patients with haemochromatosis
- (1962) J Pathol Bacteriol , vol.84 , pp. 53-64
- Scheuer, P.J.¹ Williams, R.² Muir, A.R.³

15
- 0034161367
- Hemochromatosis genes and other factors contributing to the pathogenesis of porphyria cutanea tarda
- (2000) Blood , vol.95 , pp. 1565-1571
- Bulaj, Z.J.¹ Phillips, J.D.² Ajioka, R.S.³

16
- 0028806153
- Chronic hepatitis: An update on terminology and reporting
- (1995) Am J Surg Pathol , vol.19 , pp. 1409-1417
- Batts, K.P.¹ Ludwig, J.²

17
- 0007239451
- PROPHET. Cambridge, Mass.: Bolt Beranek and Newman, (software)
- (1997)

18
- 0003425407
- New York: John Wiley
- Biostatistics: A foundation for analysis in the health sciences. 7th ed. , pp. 1999
- Daniel, W.W.¹

19
- 0031707469
- Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosis
- (1998) Gastroenterology , vol.115 , pp. 929-936
- Guyader, D.¹ Jacquelinet, C.² Moirand, R.³

20
- 0002916049
- Screening for hemochromatosis
- Barton J, Edwards C, eds. Hemochromatosis: genetics, pathophysiology, diagnosis and treatment. Cambridge, England: Cambridge University Press
- (2000) , pp. 519-524
- Witte, D.¹

21
- 0034056799
- Population screening for hemochromatosis: A comparison of unbound iron-binding capacity, transferrin saturation, and C282Y genotyping in 5,211 voluntary blood donors
- (2000) Hepatology , vol.31 , pp. 1160-1164
- Adams, P.C.¹ Kertesz, A.E.² McLaren, C.E.³ Barr, R.⁴ Bamford, A.⁵ Chakrabarti, S.⁶

22
- 0027319493
- Screening for hemochromatosis
- (1993) N Engl J Med , vol.328 , pp. 1616-1620
- Edwards, C.Q.¹ Kushner, J.P.²

23
- 0029353515
- Dissociation between tissue iron concentrations and transferrin saturation among inbred mouse strains
- (1995) J Lab Clin Med , vol.126 , pp. 128-136
- Leboeuf, R.C.¹ Tolson, D.² Heinecke, J.W.³

24
- 0033168767
- The C282Y mutation causing hereditary hemochromatosis does not produce a null allele
- (1999) Blood , vol.94 , pp. 9-11
- Levy, J.E.¹ Montross, L.K.² Cohen, D.E.³ Fleming, M.D.⁴ Andrews, N.C.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.