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

Year Number of Results
2003 1
2005 1
2007 1
2008 5
2009 2
2010 5
2011 6
2012 11
2013 7
2014 10
2015 12
2016 18
2017 10
2018 8
2019 5
2020 2
2021 4
2022 2
2023 2
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Search Results

94 results
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Page 1
Macrophage migration inhibitory factor in Nodding syndrome.
Benedek G, Abed El Latif M, Miller K, Rivkin M, Ahmed Ramadhan Lasu A, P Riek L, Lako R, Edvardson S, Arbel-Alon S, Galun E, Levite M. Benedek G, et al. Among authors: edvardson s. PLoS Negl Trop Dis. 2021 Oct 18;15(10):e0009821. doi: 10.1371/journal.pntd.0009821. eCollection 2021 Oct. PLoS Negl Trop Dis. 2021. PMID: 34662363 Free PMC article.
Delineation of the phenotype of MED17-related disease in Caucasus-Jewish families.
Fattal-Valevski A, Ben Sira L, Lerman-Sagie T, Strausberg R, Bloch-Mimouni A, Edvardson S, Kaufman R, Chernuha V, Schneebaum Sender N, Heimer G, Ben Zeev B. Fattal-Valevski A, et al. Among authors: edvardson s. Eur J Paediatr Neurol. 2021 May;32:40-45. doi: 10.1016/j.ejpn.2020.08.011. Epub 2021 Mar 5. Eur J Paediatr Neurol. 2021. PMID: 33756211
Ta-Shma A, Edvardson S, Elpeleg O, Stepensky P. Ta-Shma A, et al. Among authors: edvardson s. Harefuah. 2018 Mar;157(3):188-191. Harefuah. 2018. PMID: 29582952 Review. Hebrew.
West syndrome caused by ST3Gal-III deficiency.
Edvardson S, Baumann AM, Mühlenhoff M, Stephan O, Kuss AW, Shaag A, He L, Zenvirt S, Tanzi R, Gerardy-Schahn R, Elpeleg O. Edvardson S, et al. Epilepsia. 2013 Feb;54(2):e24-7. doi: 10.1111/epi.12050. Epub 2012 Dec 17. Epilepsia. 2013. PMID: 23252400 Free article.
Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases.
Koene S, Rodenburg RJ, van der Knaap MS, Willemsen MA, Sperl W, Laugel V, Ostergaard E, Tarnopolsky M, Martin MA, Nesbitt V, Fletcher J, Edvardson S, Procaccio V, Slama A, van den Heuvel LP, Smeitink JA. Koene S, et al. Among authors: edvardson s. J Inherit Metab Dis. 2012 Sep;35(5):737-47. doi: 10.1007/s10545-012-9492-z. Epub 2012 May 30. J Inherit Metab Dis. 2012. PMID: 22644603 Free PMC article. Review.
A Zebrafish Model for a Rare Genetic Disease Reveals a Conserved Role for FBXL3 in the Circadian Clock System.
Confino S, Dor T, Tovin A, Wexler Y, Ben-Moshe Livne Z, Kolker M, Pisanty O, Park SK, Geyer N, Reiter J, Edvardson S, Mor-Shaked H, Elpeleg O, Vallone D, Appelbaum L, Foulkes NS, Gothilf Y. Confino S, et al. Among authors: edvardson s. Int J Mol Sci. 2022 Feb 21;23(4):2373. doi: 10.3390/ijms23042373. Int J Mol Sci. 2022. PMID: 35216494 Free PMC article.
Congenital myasthenic syndrome in Israel: Genetic and clinical characterization.
Aharoni S, Sadeh M, Shapira Y, Edvardson S, Daana M, Dor-Wollman T, Mimouni-Bloch A, Halevy A, Cohen R, Sagie L, Argov Z, Rabie M, Spiegel R, Chervinsky I, Orenstein N, Engel AG, Nevo Y. Aharoni S, et al. Among authors: edvardson s. Neuromuscul Disord. 2017 Feb;27(2):136-140. doi: 10.1016/j.nmd.2016.11.014. Epub 2016 Nov 24. Neuromuscul Disord. 2017. PMID: 28024842 Free PMC article.
94 results