Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients

Por Schottlaender, Lucia V., Bettencourt, Conceição, Kiely, Aoife P., Chalasani, Annapurna, Neergheen, Viruna, Holton, Janice L., Hargreaves, Iain, Houlden, Henry
Publicado no PLoS One (2016)

α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson’s disease and multiple system atrophy?

Por Kiely, Aoife P., Asi, Yasmine T., Kara, Eleanna, Limousin, Patricia, Ling, Helen, Lewis, Patrick, Proukakis, Christos, Quinn, Niall, Lees, Andrew J., Hardy, John, Revesz, Tamas, Houlden, Henry, Holton, Janice L.
Publicado em 2013

Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation

Por Kiely, Aoife P., Ling, Helen, Asi, Yasmine T., Kara, Eleanna, Proukakis, Christos, Schapira, Anthony H., Morris, Huw R., Roberts, Helen C., Lubbe, Steven, Limousin, Patricia, Lewis, Patrick A., Lees, Andrew J., Quinn, Niall, Hardy, John, Love, Seth, Revesz, Tamas, Houlden, Henry, Holton, Janice L.
Publicado no Mol Neurodegener (2015)

A 6.4MB duplication of the alpha-synuclein locus causing fronto-temporal dementia and parkinsonism - phenotype-genotype correlations

Por Kara, Eleanna, Kiely, Aoife P, Proukakis, Christos, Giffin, Nicola, Love, Seth, Hehir, Jason, Rantell, Khadija, Pandraud, Amelie, Hernandez, Dena G, Nacheva, Elizabeth, Pittman, Alan M, Nalls, Mike A, Singleton, Andrew B, Revesz, Tamas, Bhatia, Kailash P, Quinn, Niall, Hardy, John, Holton, Janice L, Houlden, Henry
Publicado no JAMA Neurol (2014)