Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease von Sandhu, Kam, Flintoff, Kaledas, Chatfield, Mark D., Dixon, Jeannette L., Ramm, Louise E., Ramm, Grant A., Powell, Lawrie W., Subramaniam, V. Nathan, Wallace, Daniel F.

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Clinical cofactors and hepatic fibrosis in hereditary hemochromatosis: The role of diabetes mellitus von Wood, Marnie J., Powell, Lawrie W., Dixon, Jeannette L., Ramm, Grant A.

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Excess alcohol greatly increases the prevalence of cirrhosis in hereditary hemochromatosis von Fletcher, Linda M., Dixon, Jeannette L., Purdie, David M., Powell, Lawrie W., Crawford, Darrell H.G.

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Steatosis Is a Cofactor in Liver Injury in Hemochromatosis von Powell, Elizabeth E., Ali, Azmat, Clouston, Andrew D., Dixon, Jeannette L., Lincoln, Douglas J., Purdie, David M., Fletcher, Linda M., Powell, Lawrie W., Jonsson, Julie R.

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The Clinical Relevance of Compound Heterozygosity for the C282Y and H63D Substitutions in Hemochromatosis von Walsh, Alissa, Dixon, Jeannette L., Ramm, Grant A., Hewett, David G., Lincoln, Douglas J., Anderson, Gregory J., Subramaniam, V. Nathan, Dodemaide, Julian, Cavanaugh, Juleen A., Bassett, Mark L., Powell, Lawrie W.

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Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis von Wallace, Daniel F., Pedersen, Palle, Dixon, Jeannette L., Stephenson, Peter, Searle, Jeffrey W., Powell, Lawrie W., Subramaniam, V. Nathan

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Transforming growth factor-β and toll-like receptor-4 polymorphisms are not associated with fibrosis in haemochromatosis von Wood, Marnie J, Powell, Lawrie W, Dixon, Jeannette L, Subramaniam, V Nathan, Ramm, Grant A

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Should HFE p.C282Y homozygotes with moderately elevated serum ferritin be treated? A randomised controlled trial comparing iron reduction with sham treatment (Mi-iron) von Ong, Sim Yee, Dolling, Lara, Dixon, Jeannette L, Nicoll, Amanda J, Gurrin, Lyle C, Wolthuizen, Michelle, Wood, Erica M, Anderson, Greg J, Ramm, Grant A, Allen, Katrina J, Olynyk, John K, Crawford, Darrell, Kava, Jennifer, Ramm, Louise E, Gow, Paul, Durrant, Simon, Powell, Lawrie W, Delatycki, Martin B

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A novel mutation in ferroportin implicated in iron overload von Wallace, Daniel F, Dixon, Jeannette L, Ramm, Grant A, Anderson, Gregory J, Powell, Lawrie W, Subramaniam, V. Nathan

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Changing epidemiology of invasive pneumococcal disease in central Australia prior to conjugate vaccine: A 16-year study von Torzillo, Paul J, Morey, Frances, Gratten, Mike, Murphy, Denise, Matters, Rex, Dixon, Jeannette

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Regression of Fibrosis Stage With Treatment Reduces Long-Term Risk of Liver Cancer in Patients With Hemochromatosis Caused by Mutation in HFE von Bardou-Jacquet, Edouard, Morandeau, Emilie, Anderson, Gregory J., Ramm, Grant A., Ramm, Louise E., Morcet, Jeff, Bouzille, Guillaume, Dixon, Jeannette, Clouston, Andrew D., Lainé, Fabrice, Turlin, Bruno, Powell, Lawrie W., Deugnier, Yves M.

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Hemojuvelin (HJV)-associated hemochromatosis: analysis of HJV and HFE mutations and iron overload in three families von Wallace, DF, Dixon, JL, Ramm, GA, Anderson, GJ, Powell, LW, Subramaniam, N

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Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y von Wallace, Daniel F., Walker, Ann P., Pietrangelo, Antonello, Clare, Michael, Bomford, Adrian B., Dixon, Jeannette L., Powell, Lawrie W., Subramaniam, V.Nathan, Dooley, James S.

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Role of early case detection by screening relatives of patients with HFE-associated hereditary haemochromatosis von Powell, Lawrie W., Dixon, Jeannette L., Hewett, David G.

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A novel mutation in ferroportin implicated in iron overlord von WALLACE, Daniel F, DIXON, Jeannette L, RAMM, Grant A, ANDERSON, Gregory J, POWELL, Lawrie W, NATHAN SUBRAMANIAM, V

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Psychological Adjustment and Knowledge About Hereditary Hemochromatosis in a Clinic‐Based Sample: A Prospective Study von Meiser, Bettina, Dunn, Stewart, Dixon, Jeannette, Powell, Lawrie W.

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Etiology of acute lower respiratory tract infection in Central Australian Aboriginal children von TORZILLO, PAUL, DIXON, JEANNETTE, MANNING, KATHY, HUTTON, SUE, GRATTEN, MIKE, HUESTON, LINDA, LEINONEN, MAIJA, MOREY, FRAN, FORSYTHE, SIMON, NUM, RICHARD, ERLICH, JOHN, ASCHE, VAL, CUNNINGHAM, ANTHONY, RILEY, IAN

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1056 Rats of iron accumulation in untreated subjects homozygous for the C282Y hemochromatosis mutation: relevance to disease penetrance von Powell, Lawrie W., Dixon, Jeannette L., Hewett, David G., Purdie, David M., Ramm, Grant A., Anderson, Greg J., Subramaniam, Nathan, Fletcher, Linda M., Crawford, Darrell H., Cavanaugh, Juleen A., Bassett, Mark L.

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1059 The clinical relevance of compound heterozygosity for the hemochromatosis mutations (C282Y/H63D) von Hewett, David G., Dixon, Jeannette L., Purdie, David M., Ramm, Grant A., Anderson, Greg J., Subramaniam, Nathan, Fletcher, Linda M., Crawford, Darrell H., Cavanaugh, Juleen A., Bassett, Mark L., Powell, Lawrie W.

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Moral Intelligence in a Sample of Incarcerated Females von WATT, MARGO C., FRAUSIN, SILVIA, DIXON, JEANNETTE, NIMMO, SANDRA

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