Author

Esther E. Kors

Observed names: E E Kors, E Kors, E. E. Kors, E. Kors, Esther De Theije‐Kors, Esther E Kors, Esther Kors, Esther de Theije-Kors, Kors, E.

Institution: Leiden University

Observed institutions: Leiden University, Uppsala University Hospital, Leiden University Medical Center, Erasmus MC, Rijnland Ziekenhuis, Neurology, Inc

OpenAlex ID: A5111660922

Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

2001 · Esther E. Kors, Gisela M. Terwindt, et al. · Annals of Neurology · 361

Novel mutations in the Na+, K+‐ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions

2003 · Kaate R. J. Vanmolkot, Esther E. Kors, et al. · Annals of Neurology · 359

Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation

2004 · E. E. Kors, A. Melberg, et al. · Neurology · 117

Expanding the Phenotypic Spectrum of the CACNA1A Gene T666M Mutation

2003 · E. E. Kors, J. Haan, et al. · Archives of Neurology · 91

Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation

2006 · K. R. J. Vanmolkot, H. Stroink, et al. · Annals of Neurology · 83

Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine

2006 · Kaate R J Vanmolkot, Esther E Kors, et al. · European Journal of Human Genetics · 73

Recent findings in headache genetics

2004 · Esther E Kors, Kaate RJ Vanmolkot, et al. · Current Opinion in Neurology · 57

Migraine genetics: An update

2005 · J. Haan, E. E. Kors, et al. · Current Pain and Headache Reports · 54

Calcium channel mutations and migraine

2002 · Esther E. Kors, Arn M.J.M. van den Maagdenberg, et al. · Current Opinion in Neurology · 40

Episodic ataxia type 2

2002 · A. M. J. M. van den Maagdenberg, E. E. Kors, et al. · Journal of Neurology · 39

Alternating Hemiplegia of Childhood: No Mutations in the Second Familial Hemiplegic Migraine GeneATP1A2

2004 · E. E. Kors, K. R. J. Vanmolkot, et al. · Neuropediatrics · 29

Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2

2008 · Tracey D. Graves, Paola Imbrici, et al. · Neurobiology of Disease · 28

Migraine genetics

2003 · Esther Kors, Joost Haan, et al. · Current Pain and Headache Reports · 27

Genetics of primary headaches

1999 · Esther E. Kors, Joost Haan, et al. · Current Opinion in Neurology · 21

Toward a molecular genetic classification of familial hemiplegic migraine

2004 · Joost Haan, Esther E. Kors, et al. · Current Pain and Headache Reports · 11

Hemiplegic and Basilar‐type Migraine: Epidemiology, Genetics, and Mechanisms

2006 · Esther De Theije‐Kors, Joost Haan · Headache Currents · 3

Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine.

2003 · G Terwindt, E Kors, et al. · Headache The Journal of Head and Face Pain · 3

Single-fiber EMG in familial hemiplegic migraine [5] (multiple letters)

2005 · Jean Schoenen, Anna Ambrosini, et al. · 1

[From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene].

2004 · E E Kors, K R J Vanmolkot, et al. · PubMed · 1

Cefalea en racimos

2009 · J. A Van Vliet, J Haan, et al. · Acta Médica Costarricense

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Quiz Page November 2008

2008 · Joke I Roodnat, Esther de Theije-Kors, et al. · American Journal of Kidney Diseases

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Works count: 24

Citation count: 1,398

H-index: 14

I10-index: 15