Steinlein OK - Search Results

1

A Korean kindred with autosomal dominant nocturnal frontal lobe epilepsy and mental retardation.

Cho YW, Motamedi GK, Laufenberg I, Sohn SI, Lim JG, Lee H, Yi SD, Lee JH, Kim DK, Reba R, Gaillard WD, Theodore WH, Lesser RP, Steinlein OK. Cho YW, et al. Among authors: steinlein ok. Arch Neurol. 2003 Nov;60(11):1625-32. doi: 10.1001/archneur.60.11.1625. Arch Neurol. 2003. PMID: 14623738

2

Congenital myasthenic syndrome with episodic apnea in patients homozygous for a CHAT missense mutation.

Kraner S, Laufenberg I, Strassburg HM, Sieb JP, Steinlein OK. Kraner S, et al. Among authors: steinlein ok. Arch Neurol. 2003 May;60(5):761-3. doi: 10.1001/archneur.60.5.761. Arch Neurol. 2003. PMID: 12756141

3

A new Chrna4 mutation with low penetrance in nocturnal frontal lobe epilepsy.

Leniger T, Kananura C, Hufnagel A, Bertrand S, Bertrand D, Steinlein OK. Leniger T, et al. Among authors: steinlein ok. Epilepsia. 2003 Jul;44(7):981-5. doi: 10.1046/j.1528-1157.2003.61102.x. Epilepsia. 2003. PMID: 12823585 Free article.

4

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

5

Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24.

Brodtkorb E, Gu W, Nakken KO, Fischer C, Steinlein OK. Brodtkorb E, et al. Among authors: steinlein ok. Epilepsia. 2002 Mar;43(3):228-35. doi: 10.1046/j.1528-1157.2002.32001.x. Epilepsia. 2002. PMID: 11906506 Free article.

6

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.

7

Severe congenital myasthenic syndrome due to homozygosity of the 1293insG epsilon-acetylcholine receptor subunit mutation.

Sieb JP, Kraner S, Schrank B, Reitter B, Goebel TH, Tzartos SJ, Steinlein OK. Sieb JP, et al. Among authors: steinlein ok. Ann Neurol. 2000 Sep;48(3):379-83. Ann Neurol. 2000. PMID: 10976646

8

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

9

An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy.

Steinlein OK, Magnusson A, Stoodt J, Bertrand S, Weiland S, Berkovic SF, Nakken KO, Propping P, Bertrand D. Steinlein OK, et al. Hum Mol Genet. 1997 Jun;6(6):943-7. doi: 10.1093/hmg/6.6.943. Hum Mol Genet. 1997. PMID: 9175743

10

Asymmetry of long-latency auditory evoked potentials in LGI1-related autosomal dominant lateral temporal lobe epilepsy.

Brodtkorb E, Steinlein OK, Sand T. Brodtkorb E, et al. Among authors: steinlein ok. Epilepsia. 2005 Oct;46(10):1692-4. doi: 10.1111/j.1528-1167.2005.00271.x. Epilepsia. 2005. PMID: 16190946 Free article.

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