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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1991 | 1 |
1993 | 1 |
1998 | 1 |
2000 | 1 |
2008 | 1 |
2012 | 1 |
2013 | 1 |
2024 | 0 |
PubMed (cited) for id: 121201
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Benign familial neonatal convulsions caused by mutation in KCNQ3, exon 6: a European case.
Eur J Paediatr Neurol. 2013 May;17(3):308-10. doi: 10.1016/j.ejpn.2012.10.007. Epub 2012 Nov 10.
Eur J Paediatr Neurol. 2013.
PMID: 23146207
A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions.
Li H, Li N, Shen L, Jiang H, Yang Q, Song Y, Guo J, Xia K, Pan Q, Tang B.
Li H, et al.
Epilepsy Res. 2008 Mar;79(1):1-5. doi: 10.1016/j.eplepsyres.2007.12.005. Epub 2008 Feb 4.
Epilepsy Res. 2008.
PMID: 18249525
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A novel mutation of KCNQ3 (c.925T-->C) in a Japanese family with benign familial neonatal convulsions.
Hirose S, Zenri F, Akiyoshi H, Fukuma G, Iwata H, Inoue T, Yonetani M, Tsutsumi M, Muranaka H, Kurokawa T, Hanai T, Wada K, Kaneko S, Mitsudome A.
Hirose S, et al.
Ann Neurol. 2000 Jun;47(6):822-6.
Ann Neurol. 2000.
PMID: 10852552
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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, Leppert M.
Charlier C, et al.
Nat Genet. 1998 Jan;18(1):53-5. doi: 10.1038/ng0198-53.
Nat Genet. 1998.
PMID: 9425900
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Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q.
Lewis TB, Leach RJ, Ward K, O'Connell P, Ryan SG.
Lewis TB, et al.
Am J Hum Genet. 1993 Sep;53(3):670-5.
Am J Hum Genet. 1993.
PMID: 8102508
Free PMC article.
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Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneity.
Ryan SG, Wiznitzer M, Hollman C, Torres MC, Szekeresova M, Schneider S.
Ryan SG, et al.
Ann Neurol. 1991 May;29(5):469-73. doi: 10.1002/ana.410290504.
Ann Neurol. 1991.
PMID: 1859177
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