Search Results - Bahlo, M.

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  1. 1
    Natural history of HFE simple heterozygosity for C282Y and H63D: A prospective 12-year study

    Natural history of HFE simple heterozygosity for C282Y and H63D: A prospective 12-year study by Zaloumis, S., Allen, K., Bertalli, N., Turkovic, L., Delatycki, M., Nicoll, A., Mclaren, C., English, D., Hopper, J., Giles, G., Anderson, G., Olynyk, John, Powell, L., Gurrin, L., Bahlo, M., Vulpe, C., Forrest, S., Fletcher, A.

    Published 2015
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  2. 2
    HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women

    HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women by Warne, C., Zaloumis, S., Bertalli, N., Delatycki, M., Nicoll, A., McLaren, C., Hopper, J., Giles, G., Anderson, G., Olynyk, John, Powell, L., Allen, K., Gurrin, L., Bahlo, M., Fletcher, A., Forrest, S., Osborne, N., Vulpe, C., Turkovic, L.

    Published 2017
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  3. 3
    Iron-overload-related disease in HFE hereditary hemochromatosis

    Iron-overload-related disease in HFE hereditary hemochromatosis by Allen, K., Gurrin, L., Constantine, C., Osborne, N., Delatycki, M., Nicoll, A., McLaren, C., Bahlo, M., Nisselle, A., Vulpe, C., Anderson, G., Southey, M., Giles, G., English, D., Hopper, J., Olynyk, John, Powell, L., Gertig, D.

    Published 2008
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  4. 4
    Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3

    Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3 by Sim, J., Scerri, T., Fanjul-Fernández, M., Riseley, J., Gillies, G., Pope, K., Van Roozendaal, H., Heng, Julian, Mandelstam, S., McGillivray, G., Macgregor, D., Kannan, L., Maixner, W., Harvey, A., Amor, D., Delatycki, M., Crino, P., Bahlo, M., Lockhart, P., Leventer, R.

    Published 2016
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  5. 5
    HFE C282Y/H63D Compound Heterozygotes Are at Low Risk of Hemochromatosis-Related Morbidity

    HFE C282Y/H63D Compound Heterozygotes Are at Low Risk of Hemochromatosis-Related Morbidity by Gurrin, L., Bertalli, N., Dalton, G., Osborne, N., Constantine, C., McLaren, C., English, D., Gertig, D., Delatycki, M., Nicoll, A., Southey, M., Hopper, J., Giles, G., Anderson, G., Olynyk, John, Powell, L., Allen, K., Bahlo, M., Vulpe, C., Forrest, S., Fletcher, A.

    Published 2009
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  6. 6
    A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis

    A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis by Constantine, C., Anderson, G., Vulpe, C., McLaren, C., Bahlo, M., Yeap, H., Gertig, D., Osborne, N., Bertalli, N., Beckman, K., Chen, V., Matak, P., McKie, A., Delatycki, M., Olynyk, John, English, D., Southey, M., Giles, G., Hopper, J., Allen, K., Gurrin, L.

    Published 2009
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