Search Results - Liolitsa, D

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  1. 1
    Type 2 diabetes mellitus, cognitive impairment and dementia

    Type 2 diabetes mellitus, cognitive impairment and dementia by Stewart, R., Liolitsa, D.

    Published in Diabetic medicine
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  2. 2
    Genetic variability in the insulin signalling pathway may contribute to the risk of late onset Alzheimer's disease

    Genetic variability in the insulin signalling pathway may contribute to the risk of late onset Alzheimer's disease by Liolitsa, D, Powell, J, Lovestone, S

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  3. 3
    New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation

    New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation by Pulkes, T, Liolitsa, D, Eunson, L H, Rose, M, Nelson, I P, Rahman, S, Poulton, J, Marchington, D R, Landon, D N, Debono, A G, Morgan-Hughes, J A, Hanna, M G

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  4. 4
    Mitochondrial disease: mutations and mechanisms

    Mitochondrial disease: mutations and mechanisms by McKenzie, Matthew, Liolitsa, Danae, Hanna, Michael G

    Published in Neurochemical research
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  5. 5
    Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease

    Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease by ABRAHAM, Richard, MYERS, Amanda, KWON, Jennifer M, PETERSEN, Ronald C, TANGALOS, Eric, NORTON, Joanne, MORRIS, John C, BULLOCK, Roger, LIOLITSA, Danae, LOVESTONE, Simon, HARDY, John, GOATE, Alison, WAVRANT-DEVRIEZE, Fabienne, O'DONOVAN, Michael, WILLIAMS, Julie, OWEN, Michael J, JONES, Lesley, HAMSHERE, Marian L, THOMAS, Hollie V, MARSHALL, Helen, COMPTON, Danielle, SPURLOCK, Gillian, TURIC, Dragana, HOOGENDOORN, Bastiaan

    Published in Human genetics
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  6. 6
    New phenotypic diversity associated with the mitochondrial tRNASer(UCN) gene mutation

    New phenotypic diversity associated with the mitochondrial tRNASer(UCN) gene mutation by Pulkes, T., Liolitsa, D., Eunson, L.H., Rose, M., Nelson, I.P., Rahman, S., Poulton, J., Marchington, D.R., Landon, D.N., Debono, A.G., Morgan-Hughes, J.A., Hanna, M.G.

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  7. 7
    New phenotypic diversity associated with the mitochondrial tRNA Ser(UCN) gene mutation

    New phenotypic diversity associated with the mitochondrial tRNA Ser(UCN) gene mutation by Pulkes, T., Liolitsa, D., Eunson, L.H., Rose, M., Nelson, I.P., Rahman, S., Poulton, J., Marchington, D.R., Landon, D.N., Debono, A.G., Morgan-Hughes, J.A., Hanna, M.G.

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