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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 3
2001 2
2002 2
2003 2
2004 2
2005 5
2006 3
2007 3
2008 3
2009 3
2010 2
2011 1
2012 3
2013 2
2014 4
2015 6
2016 1
2017 7
2018 6
2019 4
2020 2
2022 1
2023 1
2024 0

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Similar articles for PMID: 30127718

66 results

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Page 1
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability.
Campostrini G, DiFrancesco JC, Castellotti B, Milanesi R, Gnecchi-Ruscone T, Bonzanni M, Bucchi A, Baruscotti M, Ferrarese C, Franceschetti S, Canafoglia L, Ragona F, Freri E, Labate A, Gambardella A, Costa C, Gellera C, Granata T, Barbuti A, DiFrancesco D. Campostrini G, et al. Front Mol Neurosci. 2018 Aug 6;11:269. doi: 10.3389/fnmol.2018.00269. eCollection 2018. Front Mol Neurosci. 2018. PMID: 30127718 Free PMC article.
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability.
Bonzanni M, DiFrancesco JC, Milanesi R, Campostrini G, Castellotti B, Bucchi A, Baruscotti M, Ferrarese C, Franceschetti S, Canafoglia L, Ragona F, Freri E, Labate A, Gambardella A, Costa C, Rivolta I, Gellera C, Granata T, Barbuti A, DiFrancesco D. Bonzanni M, et al. Neurobiol Dis. 2018 Oct;118:55-63. doi: 10.1016/j.nbd.2018.06.012. Epub 2018 Jun 21. Neurobiol Dis. 2018. PMID: 29936235 Free article.
HCN-related channelopathies.
Baruscotti M, Bottelli G, Milanesi R, DiFrancesco JC, DiFrancesco D. Baruscotti M, et al. Pflugers Arch. 2010 Jul;460(2):405-15. doi: 10.1007/s00424-010-0810-8. Epub 2010 Mar 8. Pflugers Arch. 2010. PMID: 20213494 Review.
Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy.
Becker F, Reid CA, Hallmann K, Tae HS, Phillips AM, Teodorescu G, Weber YG, Kleefuss-Lie A, Elger C, Perez-Reyes E, Petrou S, Kunz WS, Lerche H, Maljevic S. Becker F, et al. Epilepsia Open. 2017 Aug 5;2(3):334-342. doi: 10.1002/epi4.12068. eCollection 2017 Sep. Epilepsia Open. 2017. PMID: 29588962 Free PMC article.
In Vitro Analyses of Novel HCN4 Gene Mutations.
Möller M, Silbernagel N, Wrobel E, Stallmayer B, Amedonu E, Rinné S, Peischard S, Meuth SG, Wünsch B, Strutz-Seebohm N, Decher N, Schulze-Bahr E, Seebohm G. Möller M, et al. Cell Physiol Biochem. 2018;49(3):1197-1207. doi: 10.1159/000493301. Epub 2018 Sep 7. Cell Physiol Biochem. 2018. PMID: 30196304 Free article.
A novel HCN4 mutation, G1097W, is associated with atrioventricular block.
Zhou J, Ding WG, Makiyama T, Miyamoto A, Matsumoto Y, Kimura H, Tarutani Y, Zhao J, Wu J, Zang WJ, Matsuura H, Horie M. Zhou J, et al. Circ J. 2014;78(4):938-42. doi: 10.1253/circj.cj-13-0996. Epub 2014 Jan 31. Circ J. 2014. PMID: 24492017 Free article. Clinical Trial.
66 results