Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel A Jouvenceau, LH Eunson, A Spauschus, V Ramesh, SM Zuberi, ... The Lancet 358 (9284), 801-807, 2001 | 483 | 2001 |
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy SM Zuberi, LH Eunson, A Spauschus, R De Silva, J Tolmie, NW Wood, ... Brain 122 (5), 817-825, 1999 | 440 | 1999 |
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data NL Khan, S Jain, JM Lynch, N Pavese, P Abou-Sleiman, JL Holton, ... Brain 128 (12), 2786-2796, 2005 | 383 | 2005 |
Functional downregulation of P2X3 receptor subunit in rat sensory neurons reveals a significant role in chronic neuropathic and inflammatory pain J Barclay, S Patel, G Dorn, G Wotherspoon, S Moffatt, L Eunson, ... Journal of neuroscience 22 (18), 8139-8147, 2002 | 338 | 2002 |
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability LH Eunson, R Rea, SM Zuberi, S Youroukos, CP Panayiotopoulos, ... Annals of Neurology: Official Journal of the American Neurological …, 2000 | 324 | 2000 |
Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia P Imbrici, SL Jaffe, LH Eunson, NP Davies, C Herd, R Robertson, ... Brain 127 (12), 2682-2692, 2004 | 272 | 2004 |
The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS T Pulkes, L Eunson, V Patterson, A Siddiqui, NW Wood, IP Nelson, ... Annals of neurology 46 (6), 916-919, 1999 | 137 | 1999 |
Striatal and cortical pre‐and postsynaptic dopaminergic dysfunction in sporadic parkin‐linked parkinsonism C Scherfler, NL Khan, N Pavese, L Eunson, E Graham, AJ Lees, ... Brain 127 (6), 1332-1342, 2004 | 121 | 2004 |
Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy S Rajakulendran, TD Graves, RW Labrum, D Kotzadimitriou, L Eunson, ... The Journal of physiology 588 (11), 1905-1913, 2010 | 112 | 2010 |
A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study A Münchau, EM Valente, GA Shahidi, LH Eunson, MG Hanna, NP Quinn, ... Journal of Neurology, Neurosurgery & Psychiatry 68 (5), 609-614, 2000 | 98 | 2000 |
Variable K+ channel subunit dysfunction in inherited mutations of KCNA1 R Rea, A Spauschus, LH Eunson, MG Hanna, DM Kullmann The Journal of physiology 538 (1), 5-23, 2002 | 95 | 2002 |
Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing RW Labrum, S Rajakulendran, TD Graves, LH Eunson, R Bevan, ... Journal of medical genetics 46 (11), 786-791, 2009 | 72 | 2009 |
Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A P Imbrici, LH Eunson, TD Graves, KP Bhatia, NH Wadia, DM Kullmann, ... Neurology 65 (6), 944-946, 2005 | 71 | 2005 |
Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia M Kinali, H Jungbluth, LH Eunson, CA Sewry, AY Manzur, E Mercuri, ... Neuromuscular Disorders 14 (10), 689-693, 2004 | 71 | 2004 |
Sodium channel gene mutations in hypokalemic periodic paralysis: an uncommon cause in the UK NP Davies, LH Eunson, M Samuel, MG Hanna Neurology 57 (7), 1323-1325, 2001 | 63 | 2001 |
Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy A Spauschus, L Eunson, MG Hanna, DM Kullmann Annals of the New York Academy of Sciences 868 (1), 442-446, 1999 | 58 | 1999 |
Parkin disease in a Brazilian kindred: manifesting heterozygotes and clinical follow‐up over 10 years NL Khan, W Horta, L Eunson, E Graham, JO Johnson, S Chang, M Davis, ... Movement disorders 20 (4), 479-484, 2005 | 48 | 2005 |
New calcium channel mutations predict aberrant RNA splicing in episodic ataxia LH Eunson, TD Graves, MG Hanna Neurology 65 (2), 308-310, 2005 | 43 | 2005 |
Premature stop codons in a facilitating EF-hand splice variant of CaV2. 1 cause episodic ataxia type 2 TD Graves, P Imbrici, EE Kors, GM Terwindt, LH Eunson, RR Frants, ... Neurobiology of disease 32 (1), 10-15, 2008 | 37 | 2008 |
New phenotypic diversity associated with the mitochondrial tRNASer (UCN) gene mutation T Pulkes, D Liolitsa, LH Eunson, M Rose, IP Nelson, S Rahman, J Poulton, ... Neuromuscular Disorders 15 (5), 364-371, 2005 | 34 | 2005 |