Screening for hemochromatosisEDWARDS, C. Q; KUSHNER, J. P.The New England journal of medicine. 1993, Vol 328, Num 22, pp 1616-1620, issn 0028-4793Article

Primary iron overload in African AmericansWURAPA, R. K; GORDEUK, V. R; BRITTENHAM, G. M et al.The American journal of medicine. 1996, Vol 101, Num 1, pp 9-18, issn 0002-9343Article

Thermostable erythrocyte rosette-forming lymphocytes in hereditary hemochromatosis. I: Identification in peripheral bloodBRYAN, C. F; LEECH, S. H; DUCOS, R et al.Journal of clinical immunology. 1984, Vol 4, Num 2, pp 134-142, issn 0271-9142Article

Southern blood club symposium : an update on selected aspects of hemochromatosisEDWARDS, C. Q; GRIFFEN, L. M; KUSHNER, J. P et al.The American journal of the medical sciences. 1990, Vol 300, Num 4, pp 245-250, issn 0002-9629Article

HLA-linked hemochromatosis alleles in sporadic porphyria cutanea tardaEDWARDS, C. Q; GRIFFEN, L. M; GOLDGAR, D. E et al.Gastroenterology (New York, NY. 1943). 1989, Vol 97, Num 4, pp 972-981, issn 0016-5085Article

A self-controlled study of the effect of continuous subcutaneous insulin infusion on diabetic neuropathyHAUG, P. J; KELLY, T. M; CANNON, R. B et al.Journal of the neurological sciences. 1987, Vol 82, Num 1-3, pp 123-132, issn 0022-510XArticle

Mapping the locus for hereditary hemochromatosis; localization between HLA-B ABD HLA-AEDWARDS, C. Q; GRIFFEN, L. M; DADONE, M. M et al.American journal of human genetics. 1986, Vol 38, Num 6, pp 805-811, issn 0002-9297Article

Hypogonadism in hemochromatosis: reversal with iron depletionKELLY, T. M; EDWARDS, C. Q; MEIKLE, A. W et al.Annals of internal medicine. 1984, Vol 101, Num 5, pp 629-632, issn 0003-4819Article

Practice guideline development task force of the college of American pathologists : Hereditary hemochromatosisWITTE, D. L; CROSBY, W. H; EDWARDS, C. Q et al.Clinica chimica acta. 1996, Vol 245, Num 2, pp 139-200, issn 0009-8981Article

Prevalence of heterozygotes for hemochromatosis in the white population of the United StatesMCLAREN, C. E; GORDEUK, V. R; LOOKER, A. C et al.Blood. 1995, Vol 86, Num 5, pp 2021-2027, issn 0006-4971Article

Twenty-four hour variation of transferrin saturation in treated and untreated haemochromatosis homozygotesEDWARDS, C. Q; GRIFFEN, L. M; KAPLAN, J et al.Journal of internal medicine. 1989, Vol 226, Num 5, pp 373-379, issn 0954-6820Conference Paper

Increased frequency of HLA-A3 in subjects with sporadic porphyria cutanea tardaEDWARDS, C. Q; GRIFFEN, L. M; KUSHNER, J. P et al.Tissue antigens. 1988, Vol 31, Num 5, pp 250-253, issn 0001-2815Article

Proceedings/1st international conference on hemochromatosis, April 27-29, 1987, New York, NYWEINTRAUB, L. R; EDWARDS, C. Q; KRIKKER, M et al.Annals of the New York Academy of Sciences. 1988, Vol 526, issn 0077-8923, X-370 pConference Proceedings

Heterozygosity for HLA-linked hemochromatosis as a likely cause of the hepatic siderosis associated with sporadic porphyria cutanea tardaKUSHNER, J. P; EDWARDS, C. Q; DADONE, M. M et al.Gastroenterology (New York, NY. 1943). 1985, Vol 88, Num 5, pp 1232-1238, issn 0016-5085Article

Familiality of diabetes mellitusWEIRES, M. B; TAUSCH, B; HAUG, P. J et al.Experimental and clinical endocrinology & diabetes. 2007, Vol 115, Num 10, pp 634-640, issn 0947-7349, 7 p.Article

Haplotype analysis of hemochromatosis : Evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomesAJIOKA, R. S; JORDE, L. B; GRUEN, J. R et al.American journal of human genetics. 1997, Vol 60, Num 6, pp 1439-1447, issn 0002-9297Article

Iron overload in African AmericansBARTON, J. C; EDWARDS, C. Q; BERTOLI, L. F et al.The American journal of medicine. 1995, Vol 99, Num 6, pp 616-623, issn 0002-9343Article

Mapping recombinant events with molecular markers in hemochromatosis pedigreesRADISKY, E. S; AJIOKA, R. S; EDWARDS, C. Q et al.Cytogenetics and cell genetics. 1994, Vol 67, Num 2, pp 126-128, issn 0301-0171Article

Effect of insulin infusion pump use on diabetic retinopathyKELLY, T. M; SANBORN, G. E; HAUG, P. J et al.Archives of ophthalmology (1960). 1984, Vol 102, Num 8, pp 1156-1159, issn 0003-9950Article

A survey of 2,851 patients with hemochromatosis : Symptoms and response to treatmentMCDONNELL, S. M; PRESTON, B. L; JEWELL, S. A et al.The American journal of medicine. 1999, Vol 106, Num 6, pp 619-624, issn 0002-9343Article

Management of hemochromatosis : Iron overload, public health, and geneticsBARTON, J. C; MCDONNELL, S. M; ADAMS, P. C et al.Annals of internal medicine. 1998, Vol 129, Num 11, pp 932-939, issn 0003-4819Article

Screening for hemochromatosis : Phenotype versus genotypeEDWARDS, C. Q; GRIFFEN, L. M; AJIOKA, R. S et al.Seminars in hematology. 1998, Vol 35, Num 1, pp 72-76, issn 0037-1963Article

Coincidental hemochromatosis and viral hapatitisEDWARDS, C. Q; GRIFFEN, L. M; KUSHNER, J. P et al.The American journal of the medical sciences. 1991, Vol 301, Num 1, pp 50-54, issn 0002-9629Article

Comparison of stainable liver iron between symptomatic and asymptomatic hemochromatosis homozygotes and their homozygous relativesEDWARDS, C. Q; GRIFFEN, L. M; KUSHNER, J. P et al.The American journal of the medical sciences. 1991, Vol 301, Num 1, pp 44-46, issn 0002-9629Article

Prevalence of hemochromatosis among 11,065 presumably healthy blood donorsEDWARDS, C. Q; GRIFFEN, L. M; GOLDGAR, D et al.The New England journal of medicine. 1988, Vol 318, Num 21, pp 1355-1362, issn 0028-4793Article