Gaily E - Search Results

1

PRRT2-related disorders: further PKD and ICCA cases and review of the literature.

Becker F, Schubert J, Striano P, Anttonen AK, Liukkonen E, Gaily E, Gerloff C, Müller S, Heußinger N, Kellinghaus C, Robbiano A, Polvi A, Zittel S, von Oertzen TJ, Rostasy K, Schöls L, Warner T, Münchau A, Lehesjoki AE, Zara F, Lerche H, Weber YG. Becker F, et al. Among authors: gaily e. J Neurol. 2013 May;260(5):1234-44. doi: 10.1007/s00415-012-6777-y. Epub 2013 Jan 9. J Neurol. 2013. PMID: 23299620 Review.

2

Oxcarbazepine in the treatment of early childhood epilepsy.

Gaily E, Granström ML, Liukkonen E. Gaily E, et al. J Child Neurol. 1997 Nov;12(8):496-8. doi: 10.1177/088307389701200806. J Child Neurol. 1997. PMID: 9430314

3

Oxcarbazepine in the treatment of epilepsy in children and adolescents with intellectual disability.

Gaily E, Granström ML, Liukkonen E. Gaily E, et al. J Intellect Disabil Res. 1998 Dec;42 Suppl 1:41-5. J Intellect Disabil Res. 1998. PMID: 10030431 Clinical Trial.

4

Infantile spasms: diagnosis and assessment of treatment response by video-EEG.

Gaily E, Liukkonen E, Paetau R, Rekola R, Granström ML. Gaily E, et al. Dev Med Child Neurol. 2001 Oct;43(10):658-67. doi: 10.1017/s0012162201001207. Dev Med Child Neurol. 2001. PMID: 11665822 Free article. Clinical Trial.

5

Focal and global cortical hypometabolism in patients with newly diagnosed infantile spasms.

Metsähonkala L, Gaily E, Rantala H, Salmi E, Valanne L, Aärimaa T, Liukkonen E, Holopainen I, Granström ML, Erkinjuntti M, Grönroos T, Sillanpää M. Metsähonkala L, et al. Among authors: gaily e. Neurology. 2002 Jun 11;58(11):1646-51. doi: 10.1212/wnl.58.11.1646. Neurology. 2002. PMID: 12058093

6

Two-year follow-up of intelligence after pediatric epilepsy surgery.

Korkman M, Granström ML, Kantola-Sorsa E, Gaily E, Paetau R, Liukkonen E, Boman PA, Blomstedt G. Korkman M, et al. Among authors: gaily e. Pediatr Neurol. 2005 Sep;33(3):173-8. doi: 10.1016/j.pediatrneurol.2005.04.006. Pediatr Neurol. 2005. PMID: 16139731

7

[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.

8

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

9

Dravet syndrome: new potential genetic modifiers, imaging abnormalities, and ictal findings.

Gaily E, Anttonen AK, Valanne L, Liukkonen E, Träskelin AL, Polvi A, Lommi M, Muona M, Eriksson K, Lehesjoki AE. Gaily E, et al. Epilepsia. 2013 Sep;54(9):1577-85. doi: 10.1111/epi.12256. Epub 2013 Jun 28. Epilepsia. 2013. PMID: 23808377 Free article.

10

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

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