Research Publications

Adams, P.C., Speechley, M., & Kertesz, A. (1991). Long Term Survival Analysis in Hereditary Hemochromatosis. American Gastroenterology, 101, 368-372.

Adams, P.C. (1996, April). Hemochromatosis: Iron Overload. Medicine North America, 43-46.

Adams, P.C. & Speechely, M. (1996). The Effect of Arthritis on the Quality of Life in Hereditary Hemochromatosis. The Journal of Rheumatology, 23(4), 707-710.

Adams, P.C. & Valberg, L.S. (1996). Evolving Expression of Hereditary Hemochromatosis. Seminars in Liver Disease, 16(1), 47-54.

Adams, P.C., Deugnier, Y., Moirand, R., & Brissot, P. (1997, January). The Relationship Between Iron Overload, Clinical Symptoms and Age in 410 Patients with Genetic Hemochromatosis. Hepatology, 25(1), 162-166.

Adams, P.C. (1998, July 28). Hemochromatosis: clinical implications of genetic testing. Canadian Medical Association Journal, 159, 156-158.

Adams, P.C. (1998). Hemochromatosis: new insights in pathogenesis and diagnosis following the discovery of the gene. Critical Reviews in Clinical Laboratory Sciences, 35(3), 239-273.

Adams, P.C., Kertesz, A.E., McLaren, C.E., Barr, R., Bamford, A., & Charkrabarti, S. (2000). Population screening for hemochromatosis: a comparison of unbound iron-binding capacity, transferrin saturation, and C282Y genotyping in 5,211 voluntary blood donors. Hepatology, 31(5), 1160-4.

Bacon, B.R. (1997). The Elusive Hemochromatosis Gene and Other Reports on Iron Metabolism, Progress. American Liver Foundation.

Bacon, B.R. (1997). Diagnosis and Management of Hemochromatosis. Gastroenterology, 113, 995-999.

Bacon, B.R. & Sadiq, S.A. (1997). Hereditary Hemochromatosis: Presentation and Diagnosis in the 1990's. American Journal of Gastroenterology, 92(5), 784-789.

Bacon, B.R. (1998). Iron overload states. Clinics in Liver Disease, 2(1), 63-75.

Bacon, B.R., Powell, L.W., Adams, P.C., Kresina, T.F., & Hoofnagle, J.H. (1999). Molecular Medicine and Hemochromatosis: At the Crossroads. Gastroenterology, 116, 193-207.

Barton, J.C., McDonnell, S.M., Adams, P.C., Brissot, P., Powell, L.W., Edwards, C.Q., Cook, J.C., Kowdley, K.V. & Hemochromatosis Management Working Group. (1998, December 1). Supplement; diagnosis and management; Management of Hemochromatosis. Annals of Internal Medicine, 129, 932-939.

Barton, J.C., McDonnell, S.M., Adams, P.C., Brissot, P., Powell, L.W., Edwards, C.Q., Cook, J.C., Kowdley, K.V. & Hemochromatosis Management Working Group. (1998). Management of Hemochromatosis. Annals of Internal Medicine, 129(11), 932-939.

Barton, J.C., Grindon, A.J., Barton, N.H., & Bertoli, L.F. (1999, June). Hemochromatosis probands as blood donors. Transfusion, 39, 578-585.

Bassett, M.L., Halliday, J.W., & Powell, L.W. (1980). Hemochromatosis - Newer Concepts: Diagnosis and Management. Year Book Medical Publishers, 6-44.

Becker, G. (2001). Type 2 Diabetes. pp. 96 and 142.

Borwein, S.T., Ghent, P.R., Flanagan, P.R., Chamberlain, M.J., & Valberg, L.S. (1983). Genetic and Phenotypic Expression of Hemochromatosis in Canadians. Clinical and Investigative Medicine, 6(3), 171-179.

Bothwell, T. H., Charlton, R. W., Motulsky, A. G., Stanbury, J., et al. (1983). Idiopathic Hemochromatosis: the metabolic basis of inherited disease. New York, NY: McGraw Hill.

Bothwell, T.H., Charlton, R.W., & Motulsky, A.G. (1995). Hemochromatosis. In Scriver, C.R. [et al.] (Eds.), The Metabolic and Molecular Bases of Inherited Disease. (2nd ed., pp. 2237-2269). New York, NY: McGraw Hill, Health Professions Division.

Bulaj, Z.J., Griffen, L.M., Jorde, L.B., Edwards, C.Q., Kushner, J.P. (1996). Clinical and Biochemical Abnormalities in People Heterozygous for Hemochromatosis. New England Journal of Medicine, 335(24), 1799-1805.

Burke, W., Thomson, E., Khoury, M.J., McDonnell, S.M., Press, N., Adams, P.C., Barton, J.C., Beutler, E., Brittenham, G., Buchanan, A., Wright, C.E., Cogswell, M.E., Meslin, E.M., Motulsky, A.G., Powell, L.W., Sigal, E., Wilfond, B.S., Collins, F.S. (1998). Consensus Statement on Hereditary Hemochromatosis-Gene Discovery and Its Implications for Population-Based Screening. The Journal of the American Medical Association. 280-2, 172-178.

Callender, S.T., Marney, S.R., & Warner, G.T. (1970). Eggs and iron absorption. British Journal of Haemotology, 19, 657-665.

Chopra, S. (2001). Liver Book: A Comprehensive Guide to Diagnosis, Treatment and Recovery. Lightening Source, Inc.

Corwin, Q.E., et al. (1977, July). Hereditary Hemochromatosis: diagnosis in siblings and children. New England Journal of Medicine, 7-12.

Cox, T.M. (1980). Prevalence of the Hemochromatosis gene. New England Journal Medicine, 302, 695-696.

Crawford, D.H. & Hickman, P. (2000). Screening for hemochromatosis [editorial]. Hepatology, 31(5), 1192-1193.

Crawford, R. (1990). The Iron Elephant (1st ed.). Glyndon, MD: Vida Publishing, Inc.

Crawford, R. (2000) The Iron Elephant (2nd ed.). Glyndon, MD: Vida Publishing, Inc.

Creighton, S. & Hayden, M. (1984, October). Hemochromatosis in B.C. BC Medical Journal, 26(10), 613-614.

Crosby, W.H. (1986, October). Hemochromatosis - Treatment to Alleviate Injury. Archives of Internal Medicine, 46, 1910-1911.

Dadone, M. M., et al. (1982). Hereditary Hemochromatosis. American Journal of Clinical Pathology, 78, 196-207.

Davis, J.G. (1998). Population screening for hemochromatosis: the evolving role of genetic analysis [editorial]. Annals of Internal Medicine, 129(11), 905-908.

Disler, P.B., Lynch, S.R., Charlton, R.W., Torrance, J.D., Bothwell, T.H., Walker, R.B., & Mayet. F. (1975). The effect of tea on iron absorption: Gut. 16, 193-200.

Emery, T. (1991, May). Iron and Your Health: Facts and Fallacies. CRC Press.

Everson, G.T., & Weinberg H. (2003). Living with Hemochromatosis. Long Island City, NY: Hatherleigh Press.

Feder, J.N., Gnirke, A., Thomas, W., Tsuchihashi, Z., Ruddy, D.A., Basava, A., Dormishian, F., et al. (1996, August). A novel MHC Class I-like gene is mutated in patients with hereditary haemochromatosis. Nature Genetics, 13, 399-408.

Garrison, C. (2001). Cooking with Less Iron. Nashville, TN: Cumberland House Publishing Inc.

Jeffrey, G. & Adams, P.C. (1999, June). Blood from patients with hereditary Hemochromatosis - a wasted resource? Transfusion, 39, 549-550.

Kaikov, Y., Wadsworth, L.D, Hassall, E., Dimmick, J.E., & Rogers, P.C.J. (1992, July). Primary Hemochromatosis in Children: Report of Three Newly Diagnosed Cases and Review of the Pediatric Literature. Pediatrics, 90, 37-42.

Kassen, B.O., Hayden, M.R., Busser, J.R., Ensworth, S.G., & Ross, J.S. (1993, January). Hemochromatosis. BC Medical Journal, 35(1), 31-33.

Lauffer, R.B. (1991). Iron and Your Heart. St. Marten’s Press.

Levstik, M. & Adams, P.C. (1998, January-February). Eligibility and Exclusion of Hemochromatosis Patients as Voluntary Blood Donors. Canadian Journal of Gastroenterology, 12(1), 61-63.

Maxwell, M.W. (1980). Blood, pure and eloquent. New York, NY: McGraw-Hill Book Company.

McDonnell, S.M., Preston, B.L., Jewell, S.A., Barton, J.C., Edwards, C.Q., Adams, P.C., & Yip R. (1999). A survey of 2,851 patients with Hemochromatosis: symptoms and response to treatment. American Journal of Medicine, 106, 619-624.

McDonnell, S.M., Preston, B.L., Grindon, A.J., Barton, J.C., Edwards, C.Q., & Adams, P.C. (1999, June). A survey of phlebotomy among persons with Hemochromatosis. Transfusion 39, 651-656.

Milder, S.M., Cook, J.D., Stray, S., & Firch, C.A. (1980). Idiopathic Hemochromatosis, an interim report: Medicine. 59(1).

Meyer, Ballot, Bothwell et al. (1987). The HLA linked iron loading gene in an Afrikaner population. British Journal of Medical Genetics. 24, 348-356.

Moirand, R., Adams, P.C., Bicheler, V., Brissot, P., & Deugnier, Y. (1997, July). Clinical Features of Genetic Hemochromatosis in Women Compared with Men. Annals of Internal Medicine, 127(2), 105-110.

Motulsky, A.G. (1979). Genetics of Hemochromatosis. New England Journal Medicine, 301, 1291.

Motulsky, A.G., Powell, L.W., Sigal, E., Wilfond, B.S., & Collins, F.S. (1998). Consensus Statement on Hereditary Hemochromatosis-Gene Discovery and Its Implications for Population-Based Screening. The Journal of the American Medical Association. 280-282, 172-178.

National Centre for Biotechnology Information. (n.d.) *235200 Hemochromatosis; HFE. Online Medelian Inheritance in Man.

Natow, A.B & Heslin, J. (1993). The Iron Counter. New York, NY: Pocket Books.

Niederau, C., Fischer, R., Pürschel, A., Stremmel, W., Häussinger, D., & Strohmeyer, G. (1996). Long-term Survival in Patients with Hereditary Hemochromatosis. Gastroenterology, 110(4), 1107-1119.

Olynyk, J.K., Cullen, D.J., Aquilia, S., Rossi, E., Summerville, L., & Powell, L.W. (1999). A population-based study of the clinical expression of the hemochromatosis gene. New England Journal of Medicine. 341(10), 718-724.

Parker, J.N. (2002, July). The Official Patient’s Sourcebook on Hemochromatosis. ICON Group International, Inc.

Powell, L.W., George, D.K., McDonnell, S.M., & Kowdley, K.V. (1998). Diagnosis of hemochromatosis. Annals of Internal Medicine, 129(11), 925-931.

Powell, L.W. (1996). Hemochromatosis: The Impact of Early Diagnosis and Therapy. Gastroenterology, 110(4), 1304-1307.

Rajantie, et al. (1893). Scandinavian Journal of Haematology, 31, 20-22.

Robinson, A. (1995). Iron: A Double-Edged Sword. Fairview, TN: The Arthritis Trust of America.

Rochette, J., Pointon, J.J., Fisher, C.A., Perera, G., Arambepola, M., Arichchi, D.S., et al. (1999). Multicentric origin of hemochromatosis gene (HFE) mutations. American Journal of Human Genetics, 64(4), 1056-1062.

Sacher, RA. (1999, June). Hemochromatosis and blood donors: a perspective. Transfusion, 39, 551-554.

Saddi, R., & Feingold, J. (1974). Idiopathic Hemochromatosis: an autosomal recessive disease. Clinical Genetics, 5, 234-241.

Sardi, B. (1991). The Iron Time Bomb.

Sheldon, J.H. (1935). Hemochromatosis. New York, NY: Oxford University Press.

Simon, M., Bourel, M., et al. (1977). Idiopathic Hemochromatosis: Demonstration of recessive transmission and early detection by family HLA typing. New England Journal of Medicine, 297, 1017-1021.

Tavill, AS. (1999). Clinical implications of the hemochromatosis gene [editorial]. New England Journal of Medicine, 341(10), 755-757.

Warder, M. (2000). The Bronze Killer. Delta, BC, Canada: Imperani Publishers.

Whittington, C.A. (2001). Ironic Health. Abbotsford, BC, Canada: Cinori Publishing Inc.

Witte, D.L., Crosby, W.H., Edwards, C.Q., Fairbanks, V.F., & Mitros, F.A. (1996). Hereditary Hemochromatosis. Clinica Chimica Acta, 245, 139-200.