Epidemiology, pathophysiology and putative genetic basis of carbamazepine- and oxcarbazepine-induced hyponatremia

Author:

Berghuis B.1,de Haan G.-J.1,van den Broek M. P. H.2,Sander J. W.13,Lindhout D.14ORCID,Koeleman B. P. C.4

Affiliation:

1. Stichting Epilepsie Instellingen Nederland (SEIN); Zwolle The Netherlands

2. Department of Clinical Pharmacy; University Medical Center Utrecht; Utrecht The Netherlands

3. UCL Institute of Neurology; NIHR UCL Hospitals Biomedical Research Centre; London UK

4. Department of Genetics; University Medical Center Utrecht; Utrecht The Netherlands

Funder

Department of Health's NIHR Biomedical Research Centre

Marvin Weil Epilepsy Research Fund

UCB

Eisai

Teva

Lundbeck

GlaxoSmithKline

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference47 articles.

1. Medical genetics: a marker for Stevens-Johnson syndrome;Chung;Nature,2004

2. Real-world efficiency of pharmacogenetic screening for carbamazepine-induced severe cutaneous adverse reactions;Chen;PLoS ONE,2014

3. Trigeminal neuralgia: its treatment with a new anticonvulsant drug (G-32883);Blom;Lancet,1962

4. Voltage clamp analysis of the inhibitory actions of diphenylhydantoin and carbamazepine on voltage-sensitive sodium channels in neuroblastoma cells;Willow;Mol Pharmacol,1985

5. Treatment of epilepsy in adults: expert opinion, 2005;Karceski;Epilepsy Behav,2005

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