Search Results - Milward, E

Relationship between brain R2 and liver and serum iron concentrations in elderly men. by Olynyk, John, House, M., St pierre, T., Milward, E., Bruce, D.

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Clinical perspectives on hereditary hemochromatosis by Ayonrinde, O., Milward, E., Chua, A., Trinder, D., Olynyk, John

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Long-term mortality risks associated with mild anaemia in older persons: The Busselton health study by Chalmers, K., Knuiman, M., Divitini, M., Bruce, D., Olynyk, John, Milward, E.

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Changes in gene expression of cholesterol metabolism pathways in mouse models of haemochromatosis by Graham, Ross, Delima, R., Johnstone, D., Milward, E., Olynyk, John, Trinder, D.

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Serum testosterone levels correlate with haemoglobin in middle-aged and older men by Yeap, B., Beilin, J., Shi, Z., Knuiman, M., Olynyk, John, Bruce, D., Milward, E.

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The C282Y polymorphism of the hereditary hemochromatosis gene is associated with increased sex hormone-binding globulin and normal testosterone levels in men. by Yeap, B., Beilin, J., Shi, Z., Knuiman, M., Olynyk, John, Chubb, S., Bruce, D., Milward, E.

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Noncitrus Fruits as Novel Dietary Environmental Modifiers of Iron Stores in People With or Without HFE Gene Mutations by Milward, E., Baines, S., Knuiman, M., Bartholomew, H., Divitini, M., Ravine, D., Bruce, D., Olynyk, John

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Changes in Brain Transcripts Related to Alzheimer’s Disease in a Model of HFE Hemochromatosis are not Consistent with Increased Alzheimer’s Disease Risk by Johnstone, D., Graham, Ross, Trinder, D., Riveros, C., Olynyk, John, Scott, R., Moscato, P., Milward, E.

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Brain transcriptome perturbations in the transferrin receptor 2 mutant mouse support the case for brain changes in iron loading disorders, including effects relating to long-term d... by Acikyol, B., Graham, Ross, Trinder, D., House, M., Olynyk, John, Scott, R., Milward, E, Johnstone, D.

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Brain transcriptome perturbations in the Hfe -/- mouse model of genetic iron loading by Johnstone, D., Graham, Ross, Trinder, D., Delima, R., Riveros, C., Olynyk, John, Scott, R., Moscato, P., Milward, E.

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Brain Changes in Iron Loading Disorders by Milward, E., Acikyol, B., Bassett, B., Williams, E., Graham, Ross, Delima, R., Trinder, D., Olynyk, John, Johnstone, D.

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A cross sectional community study of serum iron measures and cognitive status in older adults by Milward, E., Bruce, D., Knuiman, M., Divitini, M., Cole, M., Inderjeeth, C., Clarnette, R., Maier, G., Jablensky, A., Olynyk, John

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Evaluation of Differential Normalization and Analysis Procedures for Illumina Gene Expression Microarray Data Involving Small Changes by Johnstone, D., Riveros, C., Heidari, M., Graham, Ross, Trinder, D., Berretta, R., Olynyk, John, Scott, R., Moscato, P., Milward, E.

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Hepatic iron loading in mice increases cholesterol biosynthesis. by Graham, R., Chua, A., Carter, K., Delima, R., Johnstone, D., Herbison, C., Firth, M., O’Leary, R., Milward, E., Olynyk, John, Trinder, D.

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Hepatic iron loading in mice increases cholesterol biosynthesis by Graham, Ross, Chua, A., Carter, K., Delima, R., Johnstone, D., Herbison, C., Firth, M., O'Leary, R., Milward, E., Olynyk, J., Trinder, D.

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Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age by Shi, Z., Johnstone, D., Talseth-Palmer, B., Evans, T., Spigelman, A., Groombridge, C., Milward, E., Olynyk, John, Suchy, J., Kurzawski, G., Lubinski, J., Scott, R.

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Brain iron accumulation affects myelin-related molecular systems implicated in a rare neurogenetic disease family with neuropsychiatric features by Heidari, M., Johnstone, D., Bassett, B., Graham, Ross, Chua, A., House, M., Collingwood, J., Bettencourt, C., Houlden, H., Ryten, M., Olynyk, John, Trinder, D., Milward, E.

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Pathological relationships involving iron and myelin may constitute a shared mechanism linking various rare and common brain diseases. by Heidari, M., Gerami, S., Bassett, B., Graham, Ross, Chua, A., Aryal, R., House, M., Collingwood, J., Bettencourt, C., Houlden, H., Ryten, M., Olynyk, John, Trinder, D., Johnstone, D., Milward, E.

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