Gaily E - Search Results

1

Castrén M, Gaily E, Tengström C, Lähdetie J, Archer H, Ala-Mello S. Castrén M, et al. Among authors: gaily e. Eur J Paediatr Neurol. 2011 Jan;15(1):65-9. doi: 10.1016/j.ejpn.2010.04.005. Epub 2010 May 20. Eur J Paediatr Neurol. 2011. PMID: 20493745

2

Long-term outcome in pyridoxine-responsive infantile epilepsy.

Riikonen R, Mankinen K, Gaily E. Riikonen R, et al. Among authors: gaily e. Eur J Paediatr Neurol. 2015 Nov;19(6):647-51. doi: 10.1016/j.ejpn.2015.08.001. Epub 2015 Aug 18. Eur J Paediatr Neurol. 2015. PMID: 26310861

3

Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia.

Schwarz N, Hahn A, Bast T, Müller S, Löffler H, Maljevic S, Gaily E, Prehl I, Biskup S, Joensuu T, Lehesjoki AE, Neubauer BA, Lerche H, Hedrich UBS. Schwarz N, et al. Among authors: gaily e. J Neurol. 2016 Feb;263(2):334-343. doi: 10.1007/s00415-015-7984-0. Epub 2015 Dec 8. J Neurol. 2016. PMID: 26645390

4

Psychomotor development in children of mothers with epilepsy.

Granström ML, Gaily E. Granström ML, et al. Among authors: gaily e. Neurology. 1992 Apr;42(4 Suppl 5):144-8. Neurology. 1992. PMID: 1374167

5

Minor anomalies in children of mothers with epilepsy.

Gaily E, Granström ML. Gaily E, et al. Neurology. 1992 Apr;42(4 Suppl 5):128-31. Neurology. 1992. PMID: 1574168

6

Normal intelligence in children with prenatal exposure to carbamazepine.

Gaily E, Kantola-Sorsa E, Hiilesmaa V, Isoaho M, Matila R, Kotila M, Nylund T, Bardy A, Kaaja E, Granström ML. Gaily E, et al. Neurology. 2004 Jan 13;62(1):28-32. doi: 10.1212/wnl.62.1.28. Neurology. 2004. PMID: 14718692

7

Pregnancy registries in epilepsy: a consensus statement on health outcomes.

Meador KJ, Pennell PB, Harden CL, Gordon JC, Tomson T, Kaplan PW, Holmes GL, French JA, Hauser WA, Wells PG, Cramer JA; HOPE Work Group. Meador KJ, et al. Neurology. 2008 Sep 30;71(14):1109-17. doi: 10.1212/01.wnl.0000316199.92256.af. Epub 2008 Aug 13. Neurology. 2008. PMID: 18703463 Review.

8

Clinical and genetic spectrum of SCN2A-associated episodic ataxia.

Schwarz N, Bast T, Gaily E, Golla G, Gorman KM, Griffiths LR, Hahn A, Hukin J, King M, Korff C, Miranda MJ, Møller RS, Neubauer B, Smith RA, Smol T, Striano P, Stroud B, Vaccarezza M, Kluger G, Lerche H, Fazeli W. Schwarz N, et al. Among authors: gaily e. Eur J Paediatr Neurol. 2019 May;23(3):438-447. doi: 10.1016/j.ejpn.2019.03.001. Epub 2019 Mar 7. Eur J Paediatr Neurol. 2019. PMID: 30928199

9

[Current prospects of genetics in epilepsy diagnostics--when and what?].

Uusimaa J, Gaily E, Ignatius J, Lehesjoki AE. Uusimaa J, et al. Among authors: gaily e. Duodecim. 2009;125(22):2521-30. Duodecim. 2009. PMID: 20095121 Review. Finnish.

10

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

Liao Y, Anttonen AK, Liukkonen E, Gaily E, Maljevic S, Schubert S, Bellan-Koch A, Petrou S, Ahonen VE, Lerche H, Lehesjoki AE. Liao Y, et al. Among authors: gaily e. Neurology. 2010 Oct 19;75(16):1454-8. doi: 10.1212/WNL.0b013e3181f8812e. Neurology. 2010. PMID: 20956790

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