Steinlein OK - Search Results

1

Benign familial neonatal convulsions: always benign?

Steinlein OK, Conrad C, Weidner B. Steinlein OK, et al. Epilepsy Res. 2007 Mar;73(3):245-9. doi: 10.1016/j.eplepsyres.2006.10.010. Epub 2006 Nov 28. Epilepsy Res. 2007. PMID: 17129708

2

Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2.

Dedek K, Fusco L, Teloy N, Steinlein OK. Dedek K, et al. Among authors: steinlein ok. Epilepsy Res. 2003 Apr;54(1):21-7. doi: 10.1016/s0920-1211(03)00037-8. Epilepsy Res. 2003. PMID: 12742592

3

The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions.

Steinlein OK, Villain M, Korenke C. Steinlein OK, et al. Seizure. 2012 Nov;21(9):740-2. doi: 10.1016/j.seizure.2012.07.006. Epub 2012 Aug 9. Seizure. 2012. PMID: 22877996 Free article.

4

Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions.

Biervert C, Steinlein OK. Biervert C, et al. Among authors: steinlein ok. Hum Genet. 1999 Mar;104(3):234-40. doi: 10.1007/pl00008713. Hum Genet. 1999. PMID: 10323247

5

Neonatal seizures with tonic clonic sequences and poor developmental outcome.

Schmitt B, Wohlrab G, Sander T, Steinlein OK, Hajnal BL. Schmitt B, et al. Among authors: steinlein ok. Epilepsy Res. 2005 Jul;65(3):161-8. doi: 10.1016/j.eplepsyres.2005.05.009. Epilepsy Res. 2005. PMID: 16039833

6

A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy.

Gu W, Sander T, Heils A, Lenzen KP, Steinlein OK. Gu W, et al. Among authors: steinlein ok. Epilepsy Res. 2005 Aug-Sep;66(1-3):91-8. doi: 10.1016/j.eplepsyres.2005.07.003. Epilepsy Res. 2005. PMID: 16112844

7

A novel missense mutation (N258S) in the KCNQ2 gene in a Turkish family afflicted with benign familial neonatal convulsions (BFNC).

Yalçin O, Cağlayan SH, Saltik S, Cokar O, Ağan K, Dervent A, Steinlein OK. Yalçin O, et al. Among authors: steinlein ok. Turk J Pediatr. 2007 Oct-Dec;49(4):385-9. Turk J Pediatr. 2007. PMID: 18246739

8

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

9

Mutation analysis of the potassium chloride cotransporter KCC3 (SLC12A6) in rolandic and idiopathic generalized epilepsy.

Steinlein OK, Neubauer BA, Sander T, Song L, Stoodt J, Mount DB. Steinlein OK, et al. Epilepsy Res. 2001 May;44(2-3):191-5. doi: 10.1016/s0920-1211(01)00230-3. Epilepsy Res. 2001. PMID: 11325574

10

Gene defects in idiopathic epilepsy.

Steinlein OK. Steinlein OK. Rev Neurol (Paris). 1999 Jul;155(6-7):450-3. Rev Neurol (Paris). 1999. PMID: 10472657 Review.

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