A 9-month retrospective evaluation of the aetiology and management of patients presenting with encephalitis/meningoencephalitis at a South London hospital

由 Bharucha, Tehmina, Nashef, Lina, Moran, Nick, Watkins, Sue, Brown, David, Zuckerman, Mark
發表在 Epidemiol Infect (2020)

Motor evoked potential polyphasia: A novel endophenotype of idiopathic generalized epilepsy

由 Chowdhury, Fahmida A., Pawley, Adam D., Ceronie, Bryan, Nashef, Lina, Elwes, Robert D.C., Richardson, Mark P.
發表在 Neurology (2015)

Analysis of rare copy number variation in absence epilepsies

由 Addis, Laura, Rosch, Richard E., Valentin, Antonio, Makoff, Andrew, Robinson, Robert, Everett, Kate V., Nashef, Lina, Pal, Deb K.
發表在 Neurol Genet (2016)

Cortical excitability correlates with seizure control and epilepsy duration in chronic epilepsy

由 Pawley, Adam D., Chowdhury, Fahmida A., Tangwiriyasakul, Chayanin, Ceronie, Bryan, Elwes, Robert D. C., Nashef, Lina, Richardson, Mark. P.
發表在 Ann Clin Transl Neurol (2017)

Array comparative genomic hybridization: Results from an adult population with drug-resistant epilepsy and co-morbidities

由 Galizia, Elizabeth C., Srikantha, Maithili, Palmer, Rodger, Waters, Jonathan J., Lench, Nicholas, Ogilvie, Caroline Mackie, Kasperavičiūtė, Dalia, Nashef, Lina, Sisodiya, Sanjay M.
出版 2012

Revealing a Brain Network Endophenotype in Families with Idiopathic Generalised Epilepsy

由 Chowdhury, Fahmida A., Woldman, Wessel, FitzGerald, Thomas H. B., Elwes, Robert D. C., Nashef, Lina, Terry, John R., Richardson, Mark P.
出版 2014

Investigation of Glutamine and GABA Levels in Patients With Idiopathic Generalized Epilepsy Using MEGAPRESS

由 Chowdhury, Fahmida A., O’Gorman, Ruth L., Nashef, Lina, Elwes, Robert D., Edden, Richard A., Murdoch, James B., Barker, Gareth J., Richardson, Mark P.
發表在 J Magn Reson Imaging (2014)

Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14

由 Chioza, Barry A., Aicardi, Jean, Aschauer, Harald, Brouwer, Oebele, Callenbach, Petra, Covanis, Athanasios, Dooley, Joseph M., Dulac, Olivier, Durner, Martina, Eeg-Olofsson, Orvar, Feucht, Martha, Friis, Mogens Laue, Guerrini, Renzo, Kjeldsen, Marianne Juel, Nabbout, Rima, Nashef, Lina, Sander, Thomas, Sirén, Auli, Wirrell, Elaine, McKeigue, Paul, Robinson, Robert, Gardiner, R. Mark, Everett, Kate V.
出版 2009

Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy

由 Leu, Costin, Balestrini, Simona, Maher, Bridget, Hernández-Hernández, Laura, Gormley, Padhraig, Hämäläinen, Eija, Heggeli, Kristin, Schoeler, Natasha, Novy, Jan, Willis, Joseph, Plagnol, Vincent, Ellis, Rachael, Reavey, Eleanor, O'Regan, Mary, Pickrell, William O., Thomas, Rhys H., Chung, Seo-Kyung, Delanty, Norman, McMahon, Jacinta M., Malone, Stephen, Sadleir, Lynette G., Berkovic, Samuel F., Nashef, Lina, Zuberi, Sameer M., Rees, Mark I., Cavalleri, Gianpiero L., Sander, Josemir W., Hughes, Elaine, Helen Cross, J., Scheffer, Ingrid E., Palotie, Aarno, Sisodiya, Sanjay M.
發表在 EBioMedicine (2015)