E. E. Kors - Concepedia

Author

E. E. Kors

Leiden University Medical Center

Also Known As

E E Kors, E Kors, E. E. Kors, E. Kors, Esther E Kors, Esther E. Kors, Esther Kors

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

Leiden University Medical Center Leiden University Rijnland Ziekenhuis Elisabeth-TweeSteden Ziekenhuis Radboud University Medical Center

About

E. E. Kors is an author at Leiden University Medical Center specializing in medicine, neurology, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	243
2	Neurology	4	4	243
3	Social Sciences	2	2	187
4	Molecular Genetics	1	1	29
5	Molecular Medicine	1	1	27

E. E. Kors

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine E. E. Kors, Gisela M. Terwindt, F Vermeulen, Annals of Neurology	2001	358
Novel mutations in the Na<sup>+</sup>, K<sup>+</sup>‐ATPase pump gene <i>ATP1A2</i> associated with familial hemiplegic migraine and benign familial infantile convulsions Kaate R. J. Vanmolkot, E. E. Kors, Jouke‐Jan Hottenga, Annals of Neurology	2003	357
Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new <i>CACNA1A</i> mutation E. E. Kors, Atle Melberg, Kaate R. J. Vanmolkot, Neurology Neurological DisorderGeneticsSwedish FamilyEarly Onset AtaxiaEpilepsy	2004	116
Expanding the Phenotypic Spectrum of the CACNA1A Gene T666M Mutation E. E. Kors, J. Haan, Nicola Giffin, Archives of Neurology	2003	90
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 <i>ATP1A2</i> mutation Kaate R. J. Vanmolkot, Hans Stroink, Jan B. Koenderink, Annals of Neurology	2006	83
Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine Kaate R. J. Vanmolkot, E. E. Kors, Ülkü Türk Börü, European Journal of Human Genetics Molecular NeuroscienceGeneticsNeurologyNeuroscienceMedicine	2006	71
Alternating Hemiplegia of Childhood: No Mutations in the Second Familial Hemiplegic Migraine Gene<i>ATP1A2</i> E. E. Kors, Kaate R. J. Vanmolkot, J. Haan, Neuropediatrics Cluster HeadacheRare DiseasesMendelian DisorderGenetic DisorderGenetics	2004	29
Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2 Tracey D. Graves, Paola Imbrici, E. E. Kors, Neurobiology of Disease GeneticsPathologyNeurogeneticsNeurologyMedicine	2008	27

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