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

Year Number of Results
1976 1
1979 1
1981 1
1984 1
1985 1
1989 2
1990 1
1992 2
1994 1
1995 1
1996 4
1997 3
1998 5
1999 2
2000 4
2001 4
2002 1
2003 7
2004 8
2005 4
2006 5
2007 3
2008 2
2009 8
2010 6
2011 4
2012 7
2013 13
2014 9
2015 12
2016 11
2017 15
2018 8
2019 6
2020 5
2021 5
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154 results
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Page 1
Did you mean bergquist ge (2 results)?
Mutations in SCN3A cause early infantile epileptic encephalopathy.
Zaman T, Helbig I, Božović IB, DeBrosse SD, Bergqvist AC, Wallis K, Medne L, Maver A, Peterlin B, Helbig KL, Zhang X, Goldberg EM. Zaman T, et al. Ann Neurol. 2018 Apr;83(4):703-717. doi: 10.1002/ana.25188. Epub 2018 Mar 30. Ann Neurol. 2018. PMID: 29466837 Free PMC article.
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
Masnada S, Hedrich UBS, Gardella E, Schubert J, Kaiwar C, Klee EW, Lanpher BC, Gavrilova RH, Synofzik M, Bast T, Gorman K, King MD, Allen NM, Conroy J, Ben Zeev B, Tzadok M, Korff C, Dubois F, Ramsey K, Narayanan V, Serratosa JM, Giraldez BG, Helbig I, Marsh E, O'Brien M, Bergqvist CA, Binelli A, Porter B, Zaeyen E, Horovitz DD, Wolff M, Marjanovic D, Caglayan HS, Arslan M, Pena SDJ, Sisodiya SM, Balestrini S, Syrbe S, Veggiotti P, Lemke JR, Møller RS, Lerche H, Rubboli G. Masnada S, et al. Brain. 2017 Sep 1;140(9):2337-2354. doi: 10.1093/brain/awx184. Brain. 2017. PMID: 29050392 Free article.
Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes.
de Kovel CGF, Syrbe S, Brilstra EH, Verbeek N, Kerr B, Dubbs H, Bayat A, Desai S, Naidu S, Srivastava S, Cagaylan H, Yis U, Saunders C, Rook M, Plugge S, Muhle H, Afawi Z, Klein KM, Jayaraman V, Rajagopalan R, Goldberg E, Marsh E, Kessler S, Bergqvist C, Conlin LK, Krok BL, Thiffault I, Pendziwiat M, Helbig I, Polster T, Borggraefe I, Lemke JR, van den Boogaardt MJ, Møller RS, Koeleman BPC. de Kovel CGF, et al. JAMA Neurol. 2017 Oct 1;74(10):1228-1236. doi: 10.1001/jamaneurol.2017.1714. JAMA Neurol. 2017. PMID: 28806457 Free PMC article.
Resensitization to Crizotinib by the Lorlatinib ALK Resistance Mutation L1198F.
Shaw AT, Friboulet L, Leshchiner I, Gainor JF, Bergqvist S, Brooun A, Burke BJ, Deng YL, Liu W, Dardaei L, Frias RL, Schultz KR, Logan J, James LP, Smeal T, Timofeevski S, Katayama R, Iafrate AJ, Le L, McTigue M, Getz G, Johnson TW, Engelman JA. Shaw AT, et al. N Engl J Med. 2016 Jan 7;374(1):54-61. doi: 10.1056/NEJMoa1508887. Epub 2015 Dec 23. N Engl J Med. 2016. PMID: 26698910 Free PMC article. Clinical Trial.
Neurofibromatosis I and multiple sclerosis.
Bergqvist C, Hemery F, Ferkal S, Wolkenstein P. Bergqvist C, et al. Orphanet J Rare Dis. 2020 Jul 14;15(1):186. doi: 10.1186/s13023-020-01463-z. Orphanet J Rare Dis. 2020. PMID: 32664938 Free PMC article.
Genetics of inherited cardiocutaneous syndromes: a review.
Bardawil T, Khalil S, Bergqvist C, Abbas O, Kibbi AG, Bitar F, Nemer G, Kurban M. Bardawil T, et al. Open Heart. 2016 Nov 22;3(2):e000442. doi: 10.1136/openhrt-2016-000442. eCollection 2016. Open Heart. 2016. PMID: 27933191 Free PMC article. Review.
Ancestral vertebrate complexity of the opioid system.
Larhammar D, Bergqvist C, Sundström G. Larhammar D, et al. Vitam Horm. 2015;97:95-122. doi: 10.1016/bs.vh.2014.11.001. Epub 2015 Jan 23. Vitam Horm. 2015. PMID: 25677769 Review.
154 results