Steinlein OK - Search Results

1

Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy.

Berkovic SF, Heron SE, Giordano L, Marini C, Guerrini R, Kaplan RE, Gambardella A, Steinlein OK, Grinton BE, Dean JT, Bordo L, Hodgson BL, Yamamoto T, Mulley JC, Zara F, Scheffer IE. Berkovic SF, et al. Among authors: steinlein ok. Ann Neurol. 2004 Apr;55(4):550-7. doi: 10.1002/ana.20029. Ann Neurol. 2004. PMID: 15048894

2

Genetics of partial epilepsies.

Berkovic SF, Steinlein OK. Berkovic SF, et al. Among authors: steinlein ok. Adv Neurol. 1999;79:375-81. Adv Neurol. 1999. PMID: 10514827 Review. No abstract available.

3

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.

Steinlein OK, Mulley JC, Propping P, Wallace RH, Phillips HA, Sutherland GR, Scheffer IE, Berkovic SF. Steinlein OK, et al. Nat Genet. 1995 Oct;11(2):201-3. doi: 10.1038/ng1095-201. Nat Genet. 1995. PMID: 7550350

4

Independent occurrence of the CHRNA4 Ser248Phe mutation in a Norwegian family with nocturnal frontal lobe epilepsy.

Steinlein OK, Stoodt J, Mulley J, Berkovic S, Scheffer IE, Brodtkorb E. Steinlein OK, et al. Epilepsia. 2000 May;41(5):529-35. doi: 10.1111/j.1528-1157.2000.tb00205.x. Epilepsia. 2000. PMID: 10802757 Free article.

5

Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel pore.

Hoda JC, Gu W, Friedli M, Phillips HA, Bertrand S, Antonarakis SE, Goudie D, Roberts R, Scheffer IE, Marini C, Patel J, Berkovic SF, Mulley JC, Steinlein OK, Bertrand D. Hoda JC, et al. Among authors: steinlein ok. Mol Pharmacol. 2008 Aug;74(2):379-91. doi: 10.1124/mol.107.044545. Epub 2008 May 2. Mol Pharmacol. 2008. PMID: 18456869

6

A potassium channel mutation in neonatal human epilepsy.

Biervert C, Schroeder BC, Kubisch C, Berkovic SF, Propping P, Jentsch TJ, Steinlein OK. Biervert C, et al. Among authors: steinlein ok. Science. 1998 Jan 16;279(5349):403-6. doi: 10.1126/science.279.5349.403. Science. 1998. PMID: 9430594

7

Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE.

Bouchardy I, Steinlein O, Combi R, Ferini-Strambi L, Gambardella A, Rudolf G, Morris MA, Picard F. Bouchardy I, et al. Neurology. 2011 Apr 5;76(14):1272-3. doi: 10.1212/WNL.0b013e31821434f0. Neurology. 2011. PMID: 21464433 No abstract available.

8

DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy.

Picard F, Makrythanasis P, Navarro V, Ishida S, de Bellescize J, Ville D, Weckhuysen S, Fosselle E, Suls A, De Jonghe P, Vasselon Raina M, Lesca G, Depienne C, An-Gourfinkel I, Vlaicu M, Baulac M, Mundwiller E, Couarch P, Combi R, Ferini-Strambi L, Gambardella A, Antonarakis SE, Leguern E, Steinlein O, Baulac S. Picard F, et al. Neurology. 2014 Jun 10;82(23):2101-6. doi: 10.1212/WNL.0000000000000488. Epub 2014 May 9. Neurology. 2014. PMID: 24814846

9

LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures.

Gu W, Brodtkorb E, Steinlein OK. Gu W, et al. Among authors: steinlein ok. Ann Neurol. 2002 Sep;52(3):364-7. doi: 10.1002/ana.10280. Ann Neurol. 2002. PMID: 12205652

10

Properties of neuronal nicotinic acetylcholine receptor mutants from humans suffering from autosomal dominant nocturnal frontal lobe epilepsy.

Bertrand S, Weiland S, Berkovic SF, Steinlein OK, Bertrand D. Bertrand S, et al. Among authors: steinlein ok. Br J Pharmacol. 1998 Oct;125(4):751-60. doi: 10.1038/sj.bjp.0702154. Br J Pharmacol. 1998. PMID: 9831911 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

161 results

Search Page