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LH Eunson
LH Eunson
Lecturer in Biomedical Science, University of Essex
在 Essex.ac.uk 的电子邮件经过验证
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引用次数
引用次数
年份
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
4832001
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
4401999
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
3832005
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
3382002
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
3242000
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
2722004
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
1371999
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
1212004
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
1122010
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
982000
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
952002
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
722009
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
712005
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
712004
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
632001
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
581999
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
482005
New calcium channel mutations predict aberrant RNA splicing in episodic ataxia
LH Eunson, TD Graves, MG Hanna
Neurology 65 (2), 308-310, 2005
432005
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
372008
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
342005
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