Statin-associated weakness in myasthenia gravis: a case report

Por Keogh, Michael J, Findlay, John M, Leach, Simon, Bowen, John
Publicado em 2010

Neuroferritinopathy: a new inborn error of iron metabolism

Por Keogh, Michael J., Jonas, Patricia, Coulthard, Alan, Chinnery, Patrick F., Burn, John
Publicado em 2012

Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB

Por Keogh, Michael J., Pyle, Angela, Daud, Daniyal, Griffin, Helen, Douroudis, Konstantinos, Eglon, Gail, Miller, James, Horvath, Rita, Chinnery, Patrick F.
Publicado no Neurology (2015)

Specific interaction of hepatitis C virus glycoproteins with mannan binding lectin inhibits virus entry

Por Brown, Kristelle S., Keogh, Michael J., Owsianka, Ania M., Adair, Richard, Patel, Arvind H., Arnold, James N., Ball, Jonathan K., Sim, Robert B., Tarr, Alexander W., Hickling, Timothy P.
Publicado no Protein Cell (2010)

HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development

Por Lindsay, Susan J., Xu, Yaobo, Lisgo, Steven N., Harkin, Lauren F., Copp, Andrew J., Gerrelli, Dianne, Clowry, Gavin J., Talbot, Aysha, Keogh, Michael J., Coxhead, Jonathan, Santibanez-Koref, Mauro, Chinnery, Patrick F.
Publicado no Front Neuroanat (2016)

Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource

Por Keogh, Michael J., Wei, Wei, Wilson, Ian, Coxhead, Jon, Ryan, Sarah, Rollinson, Sara, Griffin, Helen, Kurzawa-Akanbi, Marzena, Santibanez-Koref, Mauro, Talbot, Kevin, Turner, Martin R., McKenzie, Chris-Anne, Troakes, Claire, Attems, Johannes, Smith, Colin, Al Sarraj, Safa, Morris, Chris M., Ansorge, Olaf, Pickering-Brown, Stuart, Ironside, James W., Chinnery, Patrick F.
Publicado no Genome Res (2017)

Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains

Por Wei, Wei, Keogh, Michael J., Wilson, Ian, Coxhead, Jonathan, Ryan, Sarah, Rollinson, Sara, Griffin, Helen, Kurzawa-Akinibi, Marzena, Santibanez-Koref, Mauro, Talbot, Kevin, Turner, Martin R., McKenzie, Chris-Anne, Troakes, Claire, Attems, Johannes, Smith, Colin, Al Sarraj, Safa, Morris, Christopher M., Ansorge, Olaf, Pickering-Brown, Stuart, Ironside, James W., Chinnery, Patrick F
Publicado no Acta Neuropathol Commun (2017)

Erratum to: Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains

Por Wei, Wei, Keogh, Michael J., Wilson, Ian, Coxhead, Jonathan, Ryan, Sarah, Rollinson, Sara, Griffin, Helen, Kurzawa-Akanbi, Marzena, Santibanez-Koref, Mauro, Talbot, Kevin, Turner, Martin R., McKenzie, Chris-Anne, Troakes, Claire, Attems, Johannes, Smith, Colin, Al Sarraj, Safa, Morris, Christopher M., Ansorge, Olaf, Pickering-Brown, Stuart, Ironside, James W., Chinnery, Patrick F
Publicado no Acta Neuropathol Commun (2017)

LRRK2 exonic variants and risk of multiple system atrophy

Por Heckman, Michael G., Schottlaender, Lucia, Soto-Ortolaza, Alexandra I., Diehl, Nancy N., Rayaprolu, Sruti, Ogaki, Kotaro, Fujioka, Shinsuke, Murray, Melissa E., Cheshire, William P., Uitti, Ryan J., Wszolek, Zbigniew K., Farrer, Matthew J., Sailer, Anna, Singleton, Andrew B., Chinnery, Patrick F., Keogh, Michael J., Gentleman, Steve M., Holton, Janice L., Aoife, Kiely, Mann, David M.A., Al-Sarraj, Safa, Troakes, Claire, Dickson, Dennis W., Houlden, Henry, Ross, Owen A.
Publicado no Neurology (2014)