L. H. Eunson - Concepedia

Concepedia

Author

L. H. Eunson

University College London

Also Known As

L Eunson, L H Eunson, L. H. Eunson, L.H. Eunson, LOUISE EUNSON, Louise Eunson, Louise H Eunson, Louise H. Eunson

25

Publications

1.9K

Citations

17

H-Index

46

Concepts

All Affiliations

University College London National Hospital for Neurology and Neurosurgery Royal Hospital for Children St Thomas' Hospital

LH

About

L. H. Eunson is an author at University College London specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	1.4K
2	Social Sciences	5	5	844
3	Health Sciences	1	1	45
4	Natural Sciences	1	1	33
5	Biology	1	1	33

L. H. Eunson

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16

Publications

1.9K

Citations

16

H-Index

	Year	Citations
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel Anne Jouvenceau, L. H. Eunson, Alexander Spauschus, The Lancet ChannelopathiesNeurophysiologyNeuroanatomyMedicinePhysiology	2001	383
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data Naheed L. Khan, Shushant Jain, John Lynch, Brain Motor DysfunctionNeurological DisorderCorticobasal DegenerationGeneticsPathology	2005	319
Functional Downregulation of P2X<sub>3</sub>Receptor Subunit in Rat Sensory Neurons Reveals a Significant Role in Chronic Neuropathic and Inflammatory Pain J. Elaine Barclay, Sadhana Patel, Gabriele Dorn, Journal of Neuroscience	2002	256
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability L. H. Eunson, Ruth Rea, Sameer M. Zuberi, Annals of Neurology GeneticsMolecular GeneticsDisease Gene IdentificationSocial SciencesType 1	2000	255
The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS Teeratorn Pulkes, L. H. Eunson, Victor Patterson, Annals of Neurology GeneticsPathologyMolecular GeneticsDisease Gene IdentificationGenomics	1999	118
Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy Sanjeev Rajakulendran, Tracey D. Graves, Robyn Labrum, The Journal of Physiology GeneticsDisease Gene IdentificationSynaptic SignalingSocial SciencesP/q Calcium Channel	2010	106
Variable K<sup>+</sup> channel subunit dysfunction in inherited mutations of <i>KCNA1</i> Ruth Rea, Alexander Spauschus, L. H. Eunson, The Journal of Physiology	2002	75
Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia Maria Kinali, Heinz Jungbluth, L. H. Eunson, Neuromuscular Disorders HypertonicityChannelopathiesNeurophysiologyPhysiologySevere Neuromyotonia	2004	64
Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing Robyn Labrum, Sanjeev Rajakulendran, Tracey D. Graves, Journal of Medical Genetics	2009	63
Sodium channel gene mutations in hypokalemic periodic paralysis: An uncommon cause in the UK Nigel P. Davies, L. H. Eunson, Marcus A. Samuel, Neurology Electrolyte DisorderMuscle FunctionExon 12Periodic ParalysisMuscle Physiology	2001	45

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