Genetic variation of CACNA1H in idiopathic generalized epilepsy von Heron, Sarah E., Phillips, Hilary A., Mulley, John C., Mazarib, Aziz, Neufeld, Miriam Y., Berkovic, Samuel F., Scheffer, Ingrid E.

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The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene von Bhalla, Kavita, Phillips, Hilary A, Crawford, Joanna, McKenzie, Olivia L D, Mulley, John C, Eyre, Helen, Gardner, Alison E, Kremmidiotis, Gabriel, Callen, David F

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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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Familial Partial Epilepsy with Variable Foci: Clinical Features and Linkage to Chromosome 22q12 von Berkovic, Samuel F., Serratosa, Jose M., Phillips, Hilary A., Xiong, Lan, Andermann, Eva, Díaz‐Otero, Fernando, Gómez‐Garre, Pilar, Martín, Mercedes, Fernández‐Bullido, Yolanda, Andermann, Frederick, Lopes‐Cendes, Iscia, Dubeau, Francois, Desbiens, Richard, Scheffer, Ingrid E., Wallace, Robyn H., Mulley, John C., Pandolfo, Massimo

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Sodium-channel defects in benign familial neonatal-infantile seizures von Heron, Sarah E, Crossland, Kathryn M, Andermann, Eva, Phillips, Hilary A, Hall, Allison J, Bleasel, Andrew, Shevell, Michael, Mercho, Suha, Seni, Marie-Helene, Guiot, Marie-Christine, Mulley, John C, Berkovic, Samuel F, Scheffer, Ingrid E

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CHRNB2 Is the Second Acetylcholine Receptor Subunit Associated with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy von Phillips, Hilary A., Favre, Isabelle, Kirkpatrick, Martin, Zuberi, Sameer M., Goudie, David, Heron, Sarah E., Scheffer, Ingrid E., Sutherland, Grant R., Berkovic, Samuel F., Bertrand, Daniel, Mulley, John C.

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Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability von Derry, Christopher P., Heron, Sarah E., Phillips, Fiona, Howell, Stephen, MacMahon, Jacinta, Phillips, Hilary A., Duncan, John S., Mulley, John C., Berkovic, Samuel F., Scheffer, Ingrid E.

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A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy von Steinlein, Ortrud K, Mulley, John C, Propping, Peter, Wallace, Robyn H, Phillips, Hilary A, Sutherland, Grant R, Scheffer, Ingrid E, Berkovic, Samuel F

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Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel pore von Hoda, Jean-Charles, Gu, Wenli, Friedli, Marc, Phillips, Hilary A, Bertrand, Sonia, Antonarakis, Stylianos E, Goudie, David, Roberts, Richard, Scheffer, Ingrid E, Marini, Carla, Patel, Jayesh, Berkovic, Samuel F, Mulley, John C, Steinlein, Ortrud K, Bertrand, Daniel

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Bringing French to Life: Creative activities for 5-11 von Watts, Catherine, Phillips, Hilary

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Bringing German to Life: Creative activities for 5-11 von Watts, Catherine, Phillips, Hilary

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Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel β1 subunit gene SCN1B von WALLACE, R. H, WANG, D. W, BERKOVIC, S. F, MULLEY, J. C, SINGH, R, SCHEFFER, I. E, GEORGE, A. L, PHILLIPS, H. A, SAAR, K, REIS, A, JOHNSON, E. W, SUTHERLAND, G. R

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Febrile seizures and generalized epilepsy associated with a mutation in the Na + -channel ß1 subunit gene SCN1B von Mulley, John C, Wallace, Robyn H, Wang, Dao W, Singh, Rita, Scheffer, Ingrid E, George, Alfred L, Phillips, Hilary A, Saar, Kathrin, Reis, Andre, Johnson, Eric W, Sutherland, Grant R, Berkovic, Samuel F

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Incidence and origin of null alleles in the (AC)n microsatellite markers von CALLEN, D. F, THOMPSON, A. D, YANG SHEN, PHILLIPS, H. A, RICHARDS, R. I, MULLEY, J. C, SUTHERLAND, G. R

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Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2 von Scheffer, Ingrid E., Phillips, Hilary A., O'Brien, Catherine E., Saling, Michael M., Wrennall, Jacqueline A., Wallace, Robyn H., Mulley, John C., Berkovic, Samuel F.

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Human Nocturnal Frontal Lobe Epilepsy: Pharmocogenomic Profiles of Pathogenic Nicotinic Acetylcholine Receptor β-Subunit Mutations outside the Ion Channel Pore von Jean-Charles Hoda, Wenli Gu, Marc Friedli, Hilary A. Phillips, Sonia Bertrand, Stylianos E. Antonarakis, David Goudie, Richard Roberts, Ingrid E. Scheffer, Carla Marini, Jayesh Patel, Samuel F. Berkovic, John C. Mulley, Ortrud K. Steinlein, Daniel Bertrand

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Sodium-channel defects in benign femilial neonatal-infantile seizures von Heron, Sarah E, Crossland, Kathryn M, Andermann, Eva, Phillips, Hilary A

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Localization of craniosynostosis Adelaide type to 4p16 von Hollway, Georgina E., Phillips, Hilary A., Adès, Lesley C., Haan, Eric A., Mulley, John C.

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SSCP variants within the α4 subunit of the neuronal nicotinic acetylcholine receptor gene von Phillips, Hilary A., Mulley, John C.

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A cysteine endopeptidase from barley malt which degrades hordein von Phillips, Hilary A., Wallace, William

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