Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1B von WALLACE, R. H, SCHEFFER, I. E, PARASIVAM, G, BARNETT, S, WALLACE, G. B, SUTHERLAND, G. R, BERKOVIC, S. F, MULLEY, J. C

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Inhibition of cardiac voltage‐gated sodium channels by grape polyphenols von Wallace, C H R, Baczkó, I, Jones, L, Fercho, M, Light, P E

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Sodium channel α1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms von WALLACE, R. H, HODGSON, B. L, YAMAMOTO, T, ANDERMANN, E, MULLEY, J. C, BERKOVIC, S. F, SCHEFFER, I. E, GRINTON, B. E, GARDINER, R. M, ROBINSON, R, RODRIGUEZ-CASERO, V, SADLEIR, L, MORGAN, J, HARKIN, L. A, DIBBENS, L. M

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LGI1 mutations in temporal lobe epilepsies von BERKOVIC, S. F, IZZILLO, P, KORCZYN, A. D, SCHEFFER, I. E, MULLEY, J. C, MCMAHON, J. M, HARKIN, L. A, MCINTOSH, A. M, PHILLIPS, H. A, BRIELLMANN, R. S, WALLACE, R. H, MAZARIB, A, NEUFELD, M. Y

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X-linked myoclonic epilepsy with spasticity and intellectual disability: Mutation in the homeobox gene ARX von SCHEFFER, I. E, WALLACE, R. H, PHILLIPS, F. L, HEWSON, P, REARDON, K, PARASIVAM, G, STROMME, P, BERKOVIC, S. F, GECZ, J, MULLEY, J. C

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The incidence of deep vein thrombosis and pulmonary embolism following cast immobilisation and early functional bracing of Tendo Achilles rupture without thromboprophylaxis von Heyes, G. J., Tucker, A., Michael, A. L. R., Wallace, R. G. H.

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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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Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21 von Wallace, R H, Berkovic, S F, Howell, R A, Sutherland, G R, Mulley, J C

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Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy von Lower, Karen M, Lütcherath, Viggo, Gécz, Jozef, Frints, Suzanna G.M, Partington, Michael, Strømme, Petter, Scheffer, Ingrid E, Gedeon, Ági K, Lewis, Suzanne M.E, Turner, Gillian, Fryns, Jean-Pierre, Sutherland, Grant R, Wallace, Robyn H, Mangelsdorf, Marie E, Shaw, Marie A, Mulley, John C, Bruyere, Helene

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Erratum to: The incidence of deep vein thrombosis and pulmonary embolism following cast immobilisation and early functional bracing of Tendo Achilles rupture without thromboprophyl... von Heyes, G. J., Tucker, A., Michael, A. L. R., Wallace, R. G. H.

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Generalized epilepsy with febrile seizures plus–associated sodium channel β1 subunit mutations severely reduce beta subunit–mediated modulation of sodium channel function von Xu, R, Thomas, E.A, Gazina, E.V, Richards, K.L, Quick, M, Wallace, R.H, Harkin, L.A, Heron, S.E, Berkovic, S.F, Scheffer, I.E, Mulley, J.C, Petrou, S

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Neuronal Sodium-Channel alpha 1-Subunit Mutations in Generalized Epilepsy with Febrile Seizures Plus von Wallace, R H, Scheffer, I E, Barnett, S, Richards, M, Dibbens, L, Desai, R R, Lerman-Sagie, T, Lev, D, Mazarib, A, Brand, N, Ben-Zeev, B, Goikhman, I, Singh, R, Kremmidiotis, G

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Generalized epilepsy with febrile seizures plus-associated sodium channel beta 1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function von Xu, R, Thomas, E A, Gazina, E V, Richards, K L, Quick, M, Wallace, R H, Harkin, LA, Heron, SE, Berkovic, S F, Scheffer, I E, Mulley, J C, Petrou, S

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A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy von Steinlein, O K, Mulley, J C, Propping, P, Wallace, R H, Phillips, H A, Sutherland, G R, Scheffer, I E, Berkovic, S F

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Somatic mutations in GLI3 can cause hypothalamic hamartoma and gelastic seizures von Wallace, R H, Freeman, J L, Shouri, M R, Izzillo, P A, Rosenfeld, J V, Mulley, J C, Harvey, A S, Berkovic, S F

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Constitutively active adenosine monophosphate-activated protein kinase regulates voltage-gated sodium channels in ventricular myocytes von LIGHT, Peter E, WALLACE, Catriona H. R, DYCK, Jason R. B

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A Negative Search for a Paramyxoviral Etiology of Paget's Disease of Bone: Molecular, Immunological, and Ultrastructural Studies in U.K. Patients von Helfrich, M. H., Hobson, R. P., Grabowski, P. S., Zurbriggen, A., Cosby, S. L., Dickson, G. R., Fraser, W. D., Ooi, C. G., Selby, P. L., Crisp, A. J., Wallace, R. G. H., Kahn, S., Ralston, S. H.

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A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome von Bassuk, Alexander G., Wallace, Robyn H., Buhr, Aimee, Buller, Andrew R., Afawi, Zaid, Shimojo, Masahito, Miyata, Shingo, Chen, Shan, Gonzalez-Alegre, Pedro, Griesbach, Hilary L., Wu, Shu, Nashelsky, Marcus, Vladar, Eszter K., Antic, Dragana, Ferguson, Polly J., Cirak, Sebahattin, Voit, Thomas, Scott, Matthew P., Axelrod, Jeffrey D., Gurnett, Christina, Daoud, Azhar S., Kivity, Sara, Neufeld, Miriam Y., Mazarib, Aziz, Straussberg, Rachel, Walid, Simri, Korczyn, Amos D., Slusarski, Diane C., Berkovic, Samuel F., El-Shanti, Hatem I.

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Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations von Scheffer, Ingrid E., Harkin, Louise A., Grinton, Bronwyn E., Dibbens, Leanne M., Turner, Samantha J., Zielinski, Marta A., Xu, Ruwei, Jackson, Graeme, Adams, Judith, Connellan, Mary, Petrou, Steven, Wellard, R. Mark, Briellmann, Regula S., Wallace, Robyn H., Mulley, John C., Berkovic, Samuel F.

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The non-operative functional management of patients with a rupture of the tendo Achillis leads to low rates of re-rupture von WALLACE, R. G. H, HEYES, G. J, MICHAEL, A. L. R

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