Outcome of children with hyperventilation‐induced high‐amplitude rhythmic slow activity with altered awareness von BARKER, ALEXANDER, NG, JOANNE, RITTEY, CHRISTOPHER D C, KANDLER, ROSALIND H, MORDEKAR, SANTOSH R

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Outcome of children with hyperventilation-induced high-amplitude rhythmic slow activity with altered awareness von BARKER, ALEXANDER, NG, JOANNE, RITTEY, CHRISTOPHER D C, KANDLER, ROSALIND H, MORDEKAR, SANTOSH R

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Neonatal Seizures von Rittey, Christopher D C

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A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations von MUNOT, Pinki, SAUNDERS, Dawn E, JACQUES, Thomas S, COX, Timothy C, GANESAN, Vijeya, MILEWICZ, Dianna M, REGALADO, Ellen S, OSTERGAARD, John R, BRAUN, Kees P, KERR, Timothy, LICHTENBELT, Klaske D, PHILIP, Sunny, RITTEY, Christopher

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Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection von 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

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Phenotypic Comparison of Two Scottish Families with Mutations in Different Genes Causing Autosomal Dominant Nocturnal Frontal Lobe Epilepsy von McLellan, Ailsa, Phillips, Hilary A., Rittey, Christopher, Kirkpatrick, Martin, Mulley, John C., Goudie, David, Stephenson, John B. P., Tolmie, John, Scheffer, Ingrid E., Berkovic, Samuel F., Zuberi, Sameer M.

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