Variable K+ channel subunit dysfunction in inherited mutations of KCNA1 by Rea, Ruth, Spauschus, Alexander, Eunson, Louise H., Hanna, Michael G., Kullmann, Dimitri M.

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Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2 by Graves, Tracey D, Imbrici, Paola, Kors, Esther E, Terwindt, Gisela M, Eunson, Louise H, Frants, Rune R, Haan, Joost, Ferrari, Michel D, Goadsby, Peter J, Hanna, Michael G, van den Maagdenberg, Arn M J M, Kullmann, Dimitri M

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Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data by Khan, Naheed L., Jain, Shushant, Lynch, John M., Pavese, Nicola, Abou-Sleiman, Patrick, Holton, Janice L., Healy, Daniel G., Gilks, William P., Sweeney, Mary G., Ganguly, Milan, Gibbons, Vaneesha, Gandhi, Sonia, Vaughan, Jenny, Eunson, Louise H., Katzenschlager, Regina, Gayton, Juliet, Lennox, Graham, Revesz, Tamas, Nicholl, David, Bhatia, Kailash P., Quinn, Niall, Brooks, David, Lees, Andrew J., Davis, Mary B., Piccini, Paola, Singleton, Andrew B., Wood, Nicholas W.

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Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel by Jouvenceau, Anne, Eunson, Louise H, Spauschus, Alexander, Ramesh, Venkataswaran, Zuberi, Sameer M, Kullmann, Dimitri M, Hanna, Michael G

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Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia by Imbrici, Paola, Jaffe, Stephen L., Eunson, Louise H., Davies, Nicholas P., Herd, Colin, Robertson, Robert, Kullmann, Dimitri M., Hanna, Michael G.

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Premature stop codons in a facilitating EF-hand splice variant of CaV 2.1 cause episodic ataxia type 2 by Graves, Tracey D, Imbrici, Paola, Kors, Esther E, Terwindt, Gisela M, Eunson, Louise H, Frants, Rune R, Haan, Joost, Ferrari, Michel D, Goadsby, Peter J, Hanna, Michael G, van den Maagdenberg, Arn M.J.M, Kullmann, Dimitri M

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Premature stop codons in a facilitating EF-hand splice variant of Ca sub(V)2.1 cause episodic ataxia type 2 by Graves, Tracey D, Imbrici, Paola, Kors, Esther E, Terwindt, Gisela M, Eunson, Louise H, Frants, Rune R, Haan, Joost, Ferrari, Michel D, Goadsby, Peter J, Hanna, Michael G, Van den Maagdenberg, Arn MJM, Kullmann, Dimitri M

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Premature stop codons in a facilitating EF-hand splice variant of Ca V2.1 cause episodic ataxia type 2 by Graves, Tracey D., Imbrici, Paola, Kors, Esther E., Terwindt, Gisela M., Eunson, Louise H., Frants, Rune R., Haan, Joost, Ferrari, Michel D., Goadsby, Peter J., Hanna, Michael G., van den Maagdenberg, Arn M.J.M., Kullmann, Dimitri M.

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Dysfunction of the brain calcium channel Ca sub(V)2.1 in absence epilepsy and episodic ataxia by Imbrici, Paola, Jaffe, Stephen L, Eunson, Louise H, Davies, Nicholas P, Herd, Colin, Robertson, Robert, Kullmann, Dimitri M, Hanna, Michael G

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