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

Year Number of Results
1993 1
1994 3
2002 1
2003 3
2004 3
2005 2
2006 1
2011 1
2012 2
2013 1
2015 2
2017 1
2018 2
2019 1
2020 2
2021 0
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25 results
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Page 1
FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants.
Mitter D, Pringsheim M, Kaulisch M, Plümacher KS, Schröder S, Warthemann R, Abou Jamra R, Baethmann M, Bast T, Büttel HM, Cohen JS, Conover E, Courage C, Eger A, Fatemi A, Grebe TA, Hauser NS, Heinritz W, Helbig KL, Heruth M, Huhle D, Höft K, Karch S, Kluger G, Korenke GC, Lemke JR, Lutz RE, Patzer S, Prehl I, Hoertnagel K, Ramsey K, Rating T, Rieß A, Rohena L, Schimmel M, Westman R, Zech FM, Zoll B, Malzahn D, Zirn B, Brockmann K. Mitter D, et al. Among authors: conover e. Genet Med. 2018 Jan;20(1):98-108. doi: 10.1038/gim.2017.75. Epub 2017 Jun 29. Genet Med. 2018. PMID: 28661489
Einstein's milestones.
Conover E. Conover E. Science. 2015 Mar 6;347(6226):1085, 1087-8, 1092 passim. doi: 10.1126/science.347.6226.1085. Science. 2015. PMID: 25745160 No abstract available.
Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice.
Pringsheim M, Mitter D, Schröder S, Warthemann R, Plümacher K, Kluger G, Baethmann M, Bast T, Braun S, Büttel HM, Conover E, Courage C, Datta AN, Eger A, Grebe TA, Hasse-Wittmer A, Heruth M, Höft K, Kaindl AM, Karch S, Kautzky T, Korenke GC, Kruse B, Lutz RE, Omran H, Patzer S, Philippi H, Ramsey K, Rating T, Rieß A, Schimmel M, Westman R, Zech FM, Zirn B, Ulmke PA, Sokpor G, Tuoc T, Leha A, Staudt M, Brockmann K. Pringsheim M, et al. Among authors: conover e. Ann Clin Transl Neurol. 2019 Mar 3;6(4):655-668. doi: 10.1002/acn3.735. eCollection 2019 Apr. Ann Clin Transl Neurol. 2019. PMID: 31019990 Free PMC article.
Hazardous exposures during pregnancy.
Conover E. Conover E. J Obstet Gynecol Neonatal Nurs. 1994 Jul-Aug;23(6):524-32. doi: 10.1111/j.1552-6909.1994.tb01916.x. J Obstet Gynecol Neonatal Nurs. 1994. PMID: 7965259 Review.
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