Work

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

Year: 2006

Type: article

Study design: Case Report

Source: Annals of Neurology

DOI: 10.1002/ana.20760

Authors: K. R. J. Vanmolkot, H. Stroink, J. B. Koenderink, E. E. Kors, J. J. M. W. van den Heuvel, E. H. van den Boogerd, A. H. Stam, J. Haan, B. B. A. De Vries, G. M. Terwindt, R. R. Frants, M. D. Ferrari, A. M. J. M. van den Maagdenberg

Institutions: Leiden University Medical Center, Elisabeth-TweeSteden Ziekenhuis, Radboud University Medical Center, Rijnland Ziekenhuis

Language: English

Topic: Migraine and Headache Studies

Subfield: Psychiatry and Mental health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Migraine Trust, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, Hersenstichting

Awards: G2162484952, G6960579393

OpenAlex ID: W2145856650

FWCI: 6.573

Cites: 31

Cited by: 83

Related to: 10