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McCormack, M, Gui, Hongsheng, Ingason, Andrés, Speed, Doug, Wright, Galen EB, Zhang, Eunice J, Secolin, Rodrigo, Yasuda, Clarissa, Kwok, Maxwell, Wolking, Stefan
et al (show 2 more authors) (2017) Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Neurology, 90 (4).


Larivière, Sara, Rodríguez-Cruces, Raúl, Royer, Jessica, Caligiuri, Maria Eugenia, Gambardella, Antonio, Concha, Luis, Keller, Simon, Cendes, Fernando, Yasuda, Clarissa, Bonilha, Leonardo
et al (show 52 more authors) (2020) Network-based atrophy modelling in the common epilepsies: a worldwide ENIGMA study.


Hatton, Sean ORCID: 0000-0002-9149-8726, Huynh, Khoa, Bonilha, Leonardo, Abela, Eugenio, Alhusaini, Saud, Altmann, Andre ORCID: 0000-0002-9265-2393, Alvim, Marina KM, Balachandra, Akshara, Bartolini, Emanuele, Bender, Benjamin
et al (show 64 more authors) (2019) White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA Epilepsy study.


Altmann, Andre ORCID: 0000-0002-9265-2393, Ryten, Mina, Di Nunzio, Martina, Ravizza, Teresa ORCID: 0000-0002-9578-018X, Tolomeo, Daniele, Reynolds, Regina, Somani, Alyma, Bacigaluppi, Marco, Iori, Valentina, Micotti, Edoardo
et al (show 88 more authors) (2018) A systems-level analysis highlights microglial activation as a modifying factor in common forms of human epilepsy.

This list was generated on Mon Jun 1 04:40:23 2020 BST.