Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intolerance
Pulkes, T, Liolitsa, D, Wills, A J, Hargreaves, I, Heales, S, Hanna, M G
Published in Neurology (22.03.2005)
Published in Neurology (22.03.2005)
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Journal Article
New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation
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
Published in Neuromuscular disorders : NMD (01.05.2005)
Published in Neuromuscular disorders : NMD (01.05.2005)
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Journal Article
Association study of the 5-HT2A receptor gene polymorphism, T102C and essential hypertension
LIOLITSA, D, POWELL, J. F, PRINCE, M, LOVESTONE, S
Published in Journal of human hypertension (01.05.2001)
Published in Journal of human hypertension (01.05.2001)
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Conference Proceeding
Journal Article
Mitochondrial disease: mutations and mechanisms
McKenzie, Matthew, Liolitsa, Danae, Hanna, Michael G
Published in Neurochemical research (01.03.2004)
Published in Neurochemical research (01.03.2004)
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Journal Article
Variation in DCP1 , encoding ACE, is associated with susceptibility to Alzheimer disease
Owen, Michael J, Kehoe, Patrick G, Russ, Carsten, McIlroy, Stephen, Williams, Hywel, Holmans, Peter, Holmes, Clive, Liolitsa, Danae, Vahidassr, Djamil, Powell, John, McGleenon, Bronagh, Liddell, Malcolm, Plomin, Robert, Dynan, Kevin, Williams, Nigel, Neal, Jim, Cairns, Nigel J, Wilcock, Gordon, Passmore, Peter, Lovestone, Simon, Williams, Julie
Published in Nature genetics (01.01.1999)
Published in Nature genetics (01.01.1999)
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Journal Article
Classical mitochondrial phenotypes without mtDNA mutations: the possible role of nuclear genes
Pulkes, Teeratorn, Liolitsa, Danae, Nelson, Isabelle P, Hanna, Michael G
Published in Neurology (28.10.2003)
Published in Neurology (28.10.2003)
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Journal Article
Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease
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 (01.12.2001)
Published in Human genetics (01.12.2001)
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Journal Article
New phenotypic diversity associated with the mitochondrial tRNASer(UCN) gene mutation
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.
Published in Neuromuscular disorders : NMD (01.05.2005)
Published in Neuromuscular disorders : NMD (01.05.2005)
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Journal Article
Association study of the 5-HT(2A) receptor gene polymorphism, T102C and essential hypertension
Liolitsa, D, Powell, J F, Prince, M, Lovestone, S
Published in Journal of human hypertension (01.05.2001)
Get full text
Published in Journal of human hypertension (01.05.2001)
Journal Article
New phenotypic diversity associated with the mitochondrial tRNA Ser(UCN) gene mutation
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.
Published in Neuromuscular disorders : NMD (2005)
Published in Neuromuscular disorders : NMD (2005)
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Journal Article