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

Year Number of Results
2007 1
2008 5
2009 2
2010 4
2011 2
2012 7
2013 7
2014 7
2015 10
2016 13
2017 8
2018 6
2019 4
2021 1
2022 1
2023 6
2024 2

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72 results

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Page 1
Nociception and pain in humans lacking a functional TRPV1 channel.
Katz B, Zaguri R, Edvardson S, Maayan C, Elpeleg O, Lev S, Davidson E, Peters M, Kfir-Erenfeld S, Berger E, Ghazalin S, Binshtok AM, Minke B. Katz B, et al. Among authors: edvardson s. J Clin Invest. 2023 Feb 1;133(3):e153558. doi: 10.1172/JCI153558. J Clin Invest. 2023. PMID: 36454632 Free PMC article.
SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia.
Srivastava S, Shaked HM, Gable K, Gupta SD, Pan X, Somashekarappa N, Han G, Mohassel P, Gotkine M, Doney E, Goldenberg P, Tan QKG, Gong Y, Kleinstiver B, Wishart B, Cope H, Pires CB, Stutzman H, Spillmann RC; Undiagnosed Disease Network; Sadjadi R, Elpeleg O, Lee CH, Bellen HJ, Edvardson S, Eichler F, Dunn TM. Srivastava S, et al. Among authors: edvardson s. Brain. 2023 Apr 19;146(4):1420-1435. doi: 10.1093/brain/awac460. Brain. 2023. PMID: 36718090 Free PMC article.
A loss-of-function mutation in human Oxidation Resistance 1 disrupts the spatial-temporal regulation of histone arginine methylation in neurodevelopment.
Lin X, Wang W, Yang M, Damseh N, de Sousa MML, Jacob F, Lång A, Kristiansen E, Pannone M, Kissova M, Almaas R, Kuśnierczyk A, Siller R, Shahrour M, Al-Ashhab M, Abu-Libdeh B, Tang W, Slupphaug G, Elpeleg O, Bøe SO, Eide L, Sullivan GJ, Rinholm JE, Song H, Ming GL, van Loon B, Edvardson S, Ye J, Bjørås M. Lin X, et al. Among authors: edvardson s. Genome Biol. 2023 Sep 29;24(1):216. doi: 10.1186/s13059-023-03037-1. Genome Biol. 2023. PMID: 37773136 Free PMC article.
[EXOME ANALYSIS - A GAME CHANGER IN PEDIATRICS].
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.
WiTNNess: An international natural history study of infantile-onset TNNT1 myopathy.
Strauss KA, Carson VJ, Bolettieri E, Everett M, Bollinger A, Bowser LE, Beiler K, Young M, Edvardson S, Fraenkel N, D'Amico A, Bertini E, Lingappa L, Chowdhury D, Lowes LP, Iammarino M, Alfano LN, Brigatti KW. Strauss KA, et al. Among authors: edvardson s. Ann Clin Transl Neurol. 2023 Nov;10(11):1972-1984. doi: 10.1002/acn3.51884. Epub 2023 Aug 25. Ann Clin Transl Neurol. 2023. PMID: 37632133 Free PMC article.
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.
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
72 results