E
Eija Gaily
Researcher at University of Helsinki
Publications - 55
Citations - 3094
Eija Gaily is an academic researcher from University of Helsinki. The author has contributed to research in topics: Epilepsy & Epilepsy surgery. The author has an hindex of 32, co-authored 54 publications receiving 2822 citations. Previous affiliations of Eija Gaily include Boston Children's Hospital & Helsinki University Central Hospital.
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Journal ArticleDOI
Maternal use of antiepileptic drugs and the risk of major congenital malformations : A joint European prospective study of human teratogenesis associated with maternal epilepsy
E. B. Samren,C M van Duijn,S Koch,V K Hiilesmaa,H. Klepel,A H Bardy,G B Mannagetta,A W Deichl,Eija Gaily,Marja-Liisa Granström,H. Meinardi,D. E. Grobbee,A. Hofman,D. Janz,Dick Lindhout +14 more
TL;DR: The objective was to quantify the risks of intrauterine antiepileptic drug (AED) exposure in monotherapy and poly‐therapy and to assess the importance of knowing the carrier and removal status of these drugs.
Journal ArticleDOI
Normal intelligence in children with prenatal exposure to carbamazepine
Eija Gaily,E. Kantola-Sorsa,Vilho Hiilesmaa,M. Isoaho,Riitta Matila,M. Kotila,T. Nylund,A. Bardy,Erja Kaaja,M. L. Granström +9 more
TL;DR: Caramazepine monotherapy with maternal serum levels within the reference range does not impair intelligence in prenatally exposed offspring, but exposures to polytherapy and to valproate during pregnancy were associated with significantly reduced verbal intelligence.
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Valproate in the treatment of epilepsy in girls and women of childbearing potential
Torbjörn Tomson,Anthony G Marson,Anthony G Marson,Paul Boon,Maria Paola Canevini,Athanasios Covanis,Eija Gaily,Reetta Kälviäinen,Eugen Trinka +8 more
TL;DR: This document provides guidance on the use of valproate in girls and women of childbearing age from a joint Task Force of the Commission on European Affairs and the International League Against Epilepsy, following strengthened warnings from the Coordination Group for Mutual Recognition and Decentralised Procedures‐Human.
Journal ArticleDOI
SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain.
Y Liao,Anna-Kaisa Anttonen,Elina Liukkonen,Eija Gaily,Snezana Maljevic,Simone Schubert,A Bellan-Koch,Steven Petrou,V. E. Ahonen,Holger Lerche,Anna-Elina Lehesjoki +10 more
TL;DR: A neuronal hyperexcitability resulting in seizures and other episodic symptoms extending the spectrum of SCN2A-associated phenotypes can explain the later onset of episodic ataxia.
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Minor anomalies in offspring of epileptic mothers
TL;DR: Several minor anomalies previously regarded as typical of fetal hydantoin syndrome were shown to be genetically linked to epilepsy, and only hypertelorism and digital hypoplasia were associated with phenytoin exposure.