Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1994 1
1999 1
2000 1
2001 2
2004 1
2005 2
2006 5
2007 3
2008 2
2009 1
2010 2
2012 2
2013 2
2014 4
2015 2
2016 4
2018 1
2019 3
2020 1
2021 3
2022 3
2023 3
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

45 results

Results by year

Filters applied: . Clear all
Page 1
Functional correlates of clinical phenotype and severity in recurrent SCN2A variants.
Berecki G, Howell KB, Heighway J, Olivier N, Rodda J, Overmars I, Vlaskamp DRM, Ware TL, Ardern-Holmes S, Lesca G, Alber M, Veggiotti P, Scheffer IE, Berkovic SF, Wolff M, Petrou S. Berecki G, et al. Commun Biol. 2022 May 30;5(1):515. doi: 10.1038/s42003-022-03454-1. Commun Biol. 2022. PMID: 35637276 Free PMC article.
Pro- and antiarrhythmic properties of a diet rich in fish oil.
Den Ruijter HM, Berecki G, Opthof T, Verkerk AO, Zock PL, Coronel R. Den Ruijter HM, et al. Among authors: berecki g. Cardiovasc Res. 2007 Jan 15;73(2):316-25. doi: 10.1016/j.cardiores.2006.06.014. Epub 2006 Jun 16. Cardiovasc Res. 2007. PMID: 16859661 Review.
SCN1A gain of function in early infantile encephalopathy.
Berecki G, Bryson A, Terhag J, Maljevic S, Gazina EV, Hill SL, Petrou S. Berecki G, et al. Ann Neurol. 2019 Apr;85(4):514-525. doi: 10.1002/ana.25438. Epub 2019 Mar 7. Ann Neurol. 2019. PMID: 30779207
Distinctive In Vitro Phenotypes in iPSC-Derived Neurons From Patients With Gain- and Loss-of-Function SCN2A Developmental and Epileptic Encephalopathy.
Mao M, Mattei C, Rollo B, Byars S, Cuddy C, Berecki G, Heighway J, Pachernegg S, Menheniott T, Apted D, Jia L, Dalby K, Nemiroff A, Mullen S, Reid CA, Maljevic S, Petrou S. Mao M, et al. Among authors: berecki g. J Neurosci. 2024 Feb 21;44(8):e0692232023. doi: 10.1523/JNEUROSCI.0692-23.2023. J Neurosci. 2024. PMID: 38148154
Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes.
Courage C, Oliver KL, Park EJ, Cameron JM, Grabińska KA, Muona M, Canafoglia L, Gambardella A, Said E, Afawi Z, Baykan B, Brandt C, di Bonaventura C, Chew HB, Criscuolo C, Dibbens LM, Castellotti B, Riguzzi P, Labate A, Filla A, Giallonardo AT, Berecki G, Jackson CB, Joensuu T, Damiano JA, Kivity S, Korczyn A, Palotie A, Striano P, Uccellini D, Giuliano L, Andermann E, Scheffer IE, Michelucci R, Bahlo M, Franceschetti S, Sessa WC, Berkovic SF, Lehesjoki AE. Courage C, et al. Among authors: berecki g. Am J Hum Genet. 2021 Apr 1;108(4):722-738. doi: 10.1016/j.ajhg.2021.03.013. Am J Hum Genet. 2021. PMID: 33798445 Free PMC article.
45 results