List of works by Snežana Maljević

Antisense oligonucleotide therapy reduces seizures and extends life span in an SCN2A gain-of-function epilepsy model

scientific article published in 2021

Gain-of-function HCN2 variants in genetic epilepsy.

scientific article published on 24 October 2017

Models for discovery of targeted therapy in genetic epileptic encephalopathies

scientific article published on 25 July 2017

Molecular analysis of the A322D mutation in the GABA receptor alpha-subunit causing juvenile myoclonic epilepsy

scientific article

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

scientific article (publication date: April 2003)

Mutations in GABRB3: From febrile seizures to epileptic encephalopathies.

scientific article published on 4 January 2017

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.

scientific article

Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

article

SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain ⬇️

scientific article published on October 19, 2010

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