Nonconvulsive status epilepticus: Epilepsy Research Foundation workshop reports
Walker, Matthew, Cross, Helen, Smith, Shelagh, Young, Camilla, Aicardi, Jean, Appleton, Richard, Aylett, Sarah, Besag, Frank, Cock, Hannah, DeLorenzo, Robert, Drislane, Franck, Duncan, John, Ferrie, Colin, Fujikawa, Denson, Gray, William, Kaplan, Peter, Koutroumanidis, Micheal, O'Regan, Mary, Plouin, Perrine, Sander, Josemir, Scott, Rod, Shorvon, Simon, Treiman, David, Wasterlain, Claude, Wieshmann, Udo
Published in Epileptic disorders (01.09.2005)
Published in Epileptic disorders (01.09.2005)
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Conference Proceeding
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection
Bonthron, David T, Goizet, Cyril, Déry, Catherine, Woods, C Geoffrey, Ali, Manir, Weschke, Bernhard, Jackson, Andrew P, Voit, Thomas, King, Mary D, Baumann, Clarisse, Till, Marianne, Quarrell, Oliver W, Crow, Yanick J, Cau, Daniel, Lacombe, Didier, Lyall, Hermione, Lanzi, Giovanni, Stephenson, John B P, Griffith, Elen, Garner, Anna, Parmar, Rekha, Lebon, Pierre, McKeown, Carole, Rogers, R Curtis, Hayward, Bruce E, Babul-Hirji, Riyana, Bertini, Enrico, Martínez-Frías, María Luisa, Monier, Anne, Leitch, Andrea, Rittey, Christopher D, Semple, Colin, Aicardi, Jean, Chitayat, David, Tolmie, John L, Ponting, Chris P, Baxter, Peter, Tacke, Uta, Mathieu, Michèle, Sanchis, Amparo, Tomlin, Pam, Oade, Yvette, Klepper, Joerg, Fazzi, Elisa, Chandler, Kate E
Published in Nature genetics (01.08.2006)
Published in Nature genetics (01.08.2006)
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Journal Article
Hemifacial spasm or subcortical epilepsy?
Arzimanoglou, Alexis A., Salefranque, Françoise, Goutières, Françoise, Aicardi, Jean
Published in Epileptic disorders (01.06.1999)
Published in Epileptic disorders (01.06.1999)
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Aicardi-Goutières syndrome: special type early-onset encephalopathy
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Book Review
Journal Article
Developmental amnesia associated with early hypoxic–ischaemic injury
Gadian, David G., Aicardi, Jean, Watkins, Kate E., Porter, David A., Mishkin, Mortimer, Vargha-Khadem, Faraneh
Published in Brain (London, England : 1878) (01.03.2000)
Published in Brain (London, England : 1878) (01.03.2000)
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Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14
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
Published in Epilepsy research (01.12.2009)
Published in Epilepsy research (01.12.2009)
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