A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy von Zuberi, S. M., Eunson, L. H., Spauschus, A., De Silva, R., Tolmie, J., Wood, N. W., McWilliam, R. C., Stephenson, J. P. B., Kullmann, D. M., Hanna, M. G.

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Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability von Eunson, L. H., Rea, R., Zuberi, S. M., Youroukos, S., Panayiotopoulos, C. P., Liguori, R., Avoni, P., McWilliam, R. C., Stephenson, J. B. P., Hanna, M. G., Kullmann, D. M., Spauschus, A.

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Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A von IMBRICI, P, EUNSON, L. H, GRAVES, T. D, BHATIA, K. P, WADIA, N. H, KULLMANN, D. M, HANNA, M. G

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Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing von Labrum, R W, Rajakulendran, S, Graves, T D, Eunson, L H, Bevan, R, Sweeney, M G, Hammans, S R, Tubridy, N, Britton, T, Carr, L J, Ostergaard, J R, Kennedy, C R, Al-Memar, A, Kullmann, D M, Schorge, S, Temple, K, Davis, M B, Hanna, M G

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A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study von Münchau, A, Valente, E M, Shahidi, G A, Eunson, L H, Hanna, M G, Quinn, N P, Schapira, A H V, Wood, N W, Bhatia, K P

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Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia von Kinali, M., Jungbluth, H., Eunson, L.H., Sewry, C.A., Manzur, A.Y., Mercuri, E., Hanna, M.G., Muntoni, F.

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

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Sodium channel gene mutations in hypokalemic periodic paralysis : An uncommon cause in the UK von DAVIES, N. P, EUNSON, L. H, SAMUEL, M, HANNA, M. G

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New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation von Pulkes, T, Liolitsa, D, Eunson, L H, Rose, M, Nelson, I P, Rahman, S, Poulton, J, Marchington, D R, Landon, D N, Debono, A G, Morgan-Hughes, J A, Hanna, M G

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Clinical, electrophysiological, and molecular genetic studies in a new family with paramyotonia congenita von Davies, N P, Eunson, L H, Gregory, R P, Mills, K R, Morrison, P J, Hanna, M G

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PAW31 Clinical and genetic spectrum of the episodic ataxias: the UK perspective von Rajakulendran, S, Labrum, R W, Graves, T D, Tomlinson, S, Eunson, L H, Davis, M B, Schorge, S, Kullmann, D M, Hanna, M G

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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 von 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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Sodium channel gene mutations in hypokalemic periodic paralysis: An uncommon cause in the UK von Davies, N. P., Eunson, L. H., Samuel, M., Hanna, M. G.

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

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New calcium channel mutations predict aberrant RNA splicing in episodic ataxia von EUNSON, Louise H, GRAVES, Tracey D, HANNA, Michael G

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Late-onset episodic ataxia type 2 due to an inframe insertion in CACNA1A von Imbrici, P, Eunson, L H, Graves, T D, Bhatia, K P, Wadia, N H, Kullmann, D M, Hanna, M G

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Nocturnal Myoclonus von Eunson, L. H.

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E.C.T von Eunson, L. H.

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Certificates for Corsets von Eunson, L. H.

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The Plebiscite von Eunson, L. H.

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