Neuropsychiatric systemic lupus erythematosus: a diagnostic challenge

Por Sommerlad, Andrew, Duncan, John, Lunn, Michael P T, Foong, Jacqueline
Publicado no BMJ Case Rep (2015)

Whippits, nitrous oxide and the dangers of legal highs

Por Thompson, Alexander G, Leite, M Isabel, Lunn, Michael P, Bennett, David L H
Publicado no Pract Neurol (2015)

Endoscopic and Open Release Similarly Safe for the Treatment of Carpal Tunnel Syndrome. A Systematic Review and Meta-Analysis

Por Vasiliadis, Haris S., Nikolakopoulou, Adriani, Shrier, Ian, Lunn, Michael P., Brassington, Ruth, Scholten, Rob J. P., Salanti, Georgia
Publicado no PLoS One (2015)

Cerebellar learning distinguishes inflammatory neuropathy with and without tremor

Por Schwingenschuh, Petra, Saifee, Tabish A., Katschnig-Winter, Petra, Reilly, Mary M., Lunn, Michael P., Manji, Hadi, Aguirregomozcorta, Maria, Schmidt, Reinhold, Bhatia, Kailash P., Rothwell, John C., Edwards, Mark J.
Publicado em 2013

Diagnosis of Neuroinvasive Astrovirus Infection in an Immunocompromised Adult With Encephalitis by Unbiased Next-Generation Sequencing

Por Naccache, Samia N., Peggs, Karl S., Mattes, Frank M., Phadke, Rahul, Garson, Jeremy A., Grant, Paul, Samayoa, Erik, Federman, Scot, Miller, Steve, Lunn, Michael P., Gant, Vanya, Chiu, Charles Y.
Publicado no Clin Infect Dis (2015)

Anti Ma2-associated myeloradiculopathy: expanding the phenotype of anti-Ma2 associated paraneoplastic syndromes

Por Murphy, Sinead M, Khan, Usman, Alifrangis, Constantine, Hazell, Steven, Hrouda, David, Blake, Julian, Ball, Joanna, Gabriel, Carolyn, Markarian, Pierre, Rees, Jeremy, Karim, Abid, Seckl, Michael J, Lunn, Michael P, Reilly, Mary M
Publicado em 2011

Diagnosing Dementia in the Clinical Setting: Can Amyloid PET Provide Additional Value Over Cerebrospinal Fluid?

Por Weston, Philip S.J., Paterson, Ross W., Dickson, John, Barnes, Anna, Bomanji, Jamshed B., Kayani, Irfan, Lunn, Michael P., Mummery, Catherine J., Warren, Jason D., Rossor, Martin N., Fox, Nick C., Zetterberg, Henrik, Schott, Jonathan M.
Publicado no J Alzheimers Dis (2016)

Glycine receptor antibodies in PERM and related syndromes: characteristics, clinical features and outcomes

Por Carvajal-González, Alexander, Leite, M. Isabel, Waters, Patrick, Woodhall, Mark, Coutinho, Ester, Balint, Bettina, Lang, Bethan, Pettingill, Philippa, Carr, Aisling, Sheerin, Una-Marie, Press, Raomand, Lunn, Michael P., Lim, Ming, Maddison, Paul, Meinck, H.-M., Vandenberghe, Wim, Vincent, Angela
Publicado em 2014

Novel Mutations Mapping to the Fourth Sodium Channel Domain of Nav1.7 Result in Variable Clinical Manifestations of Primary Erythromelalgia

Por Cregg, Roman, Laguda, Bisola, Werdehausen, Robert, Cox, James J., Linley, John E., Ramirez, Juan D., Bodi, Istvan, Markiewicz, Michael, Howell, Kevin J., Chen, Ya-Chun, Agnew, Karen, Houlden, Henry, Lunn, Michael P., Bennett, David L. H., Wood, John N., Kinali, Maria
Publicado em 2013

Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing

Por Murphy, Sinead M., Laura, Matilde, Fawcett, Katherine, Pandraud, Amelie, Liu, Yo-Tsen, Davidson, Gabrielle L, Rossor, Alexander M, Polke, James M, Castleman, Victoria, Manji, Hadi, Lunn, Michael P T, Bull, Karen, Ramdharry, Gita, Davis, Mary, Blake, Julian C, Houlden, Henry, Reilly, Mary M
Publicado em 2012

Do cerebrospinal fluid transfer methods affect measured amyloid β42, total tau, and phosphorylated tau in clinical practice?

Por Paterson, Ross W., Toombs, Jamie, Chapman, Miles D., Nicholas, Jennifer M., Heslegrave, Amanda J., Slattery, Catherine F., Foulkes, Alexander J.M., Clark, Camilla N., Lane, Christopher A.S., Weston, Philip S.J., Lunn, Michael P., Fox, Nick C., Zetterberg, Henrik, Schott, Jonathan M.
Publicado no Alzheimers Dement (Amst) (2015)

Using florbetapir positron emission tomography to explore cerebrospinal fluid cut points and gray zones in small sample sizes

Por Weston, Philip S.J., Paterson, Ross W., Modat, Marc, Burgos, Ninon, Cardoso, Manuel J., Magdalinou, Nadia, Lehmann, Manja, Dickson, John C., Barnes, Anna, Bomanji, Jamshed B., Kayani, Irfan, Cash, David M., Ourselin, Sebastien, Toombs, Jamie, Lunn, Michael P., Mummery, Catherine J., Warren, Jason D., Rossor, Martin N., Fox, Nick C., Zetterberg, Henrik, Schott, Jonathan M.
Publicado no Alzheimers Dement (Amst) (2015)

Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease

Por Pitceathly, Robert D.S., Murphy, Sinéad M., Cottenie, Ellen, Chalasani, Annapurna, Sweeney, Mary G., Woodward, Cathy, Mudanohwo, Ese E., Hargreaves, Iain, Heales, Simon, Land, John, Holton, Janice L., Houlden, Henry, Blake, Julian, Champion, Michael, Flinter, Frances, Robb, Stephanie A., Page, Rupert, Rose, Michael, Palace, Jacqueline, Crowe, Carol, Longman, Cheryl, Lunn, Michael P., Rahman, Shamima, Reilly, Mary M., Hanna, Michael G.
Publicado em 2012

Truncating and Missense Mutations in IGHMBP2 Cause Charcot-Marie Tooth Disease Type 2

Por Cottenie, Ellen, Kochanski, Andrzej, Jordanova, Albena, Bansagi, Boglarka, Zimon, Magdalena, Horga, Alejandro, Jaunmuktane, Zane, Saveri, Paola, Rasic, Vedrana Milic, Baets, Jonathan, Bartsakoulia, Marina, Ploski, Rafal, Teterycz, Pawel, Nikolic, Milos, Quinlivan, Ros, Laura, Matilde, Sweeney, Mary G., Taroni, Franco, Lunn, Michael P., Moroni, Isabella, Gonzalez, Michael, Hanna, Michael G., Bettencourt, Conceicao, Chabrol, Elodie, Franke, Andre, von Au, Katja, Schilhabel, Markus, Kabzińska, Dagmara, Hausmanowa-Petrusewicz, Irena, Brandner, Sebastian, Lim, Siew Choo, Song, Haiwei, Choi, Byung-Ok, Horvath, Rita, Chung, Ki-Wha, Zuchner, Stephan, Pareyson, Davide, Harms, Matthew, Reilly, Mary M., Houlden, Henry
Publicado no Am J Hum Genet (2014)