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Results by year

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

Year Number of Results
1980 1
1982 1
1993 2
1994 2
1995 1
1997 2
1998 2
1999 1
2000 2
2001 4
2002 8
2003 6
2004 4
2005 3
2006 6
2007 9
2008 4
2009 3
2010 9
2011 7
2012 6
2013 7
2014 7
2015 3
2016 4
2017 8
2018 6
2019 12
2020 3
2021 7
2022 3
2023 4
2024 4

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Search Results

138 results

Results by year

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Page 1
Duane Syndrome.
Barry BJ, Whitman MC, Hunter DG, Engle EC. Barry BJ, et al. Among authors: engle ec. 2007 May 25 [updated 2019 Aug 29]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2007 May 25 [updated 2019 Aug 29]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301369 Free Books & Documents. Review.
TUBB3 and KIF21A in neurodevelopment and disease.
Puri D, Barry BJ, Engle EC. Puri D, et al. Among authors: engle ec. Front Neurosci. 2023 Aug 4;17:1226181. doi: 10.3389/fnins.2023.1226181. eCollection 2023. Front Neurosci. 2023. PMID: 37600020 Free PMC article. Review.
Congenital fibrosis syndromes.
Shivaram SM, Engle EC, Petersen RA, Robb RM. Shivaram SM, et al. Among authors: engle ec. Int Ophthalmol Clin. 2001 Fall;41(4):105-13. doi: 10.1097/00004397-200110000-00011. Int Ophthalmol Clin. 2001. PMID: 11698741 Review. No abstract available.
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Tenney AP, Di Gioia SA, Webb BD, Chan WM, de Boer E, Garnai SJ, Barry BJ, Ray T, Kosicki M, Robson CD, Zhang Z, Collins TE, Gelber A, Pratt BM, Fujiwara Y, Varshney A, Lek M, Warburton PE, Van Ryzin C, Lehky TJ, Zalewski C, King KA, Brewer CC, Thurm A, Snow J, Facio FM, Narisu N, Bonnycastle LL, Swift A, Chines PS, Bell JL, Mohan S, Whitman MC, Staffieri SE, Elder JE, Demer JL, Torres A, Rachid E, Al-Haddad C, Boustany RM, Mackey DA, Brady AF, Fenollar-Cortés M, Fradin M, Kleefstra T, Padberg GW, Raskin S, Sato MT, Orkin SH, Parker SCJ, Hadlock TA, Vissers LELM, van Bokhoven H, Jabs EW, Collins FS, Pennacchio LA, Manoli I, Engle EC. Tenney AP, et al. Among authors: engle ec. Nat Genet. 2023 Jul;55(7):1149-1163. doi: 10.1038/s41588-023-01424-9. Epub 2023 Jun 29. Nat Genet. 2023. PMID: 37386251 Free PMC article.
Congenital Fibrosis of the Extraocular Muscles Overview.
Whitman MC, Jurgens JA, Hunter DG, Engle EC. Whitman MC, et al. Among authors: engle ec. 2004 Apr 27 [updated 2021 Aug 12]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2004 Apr 27 [updated 2021 Aug 12]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301522 Free Books & Documents. Review.
Human disorders of axon guidance.
Nugent AA, Kolpak AL, Engle EC. Nugent AA, et al. Among authors: engle ec. Curr Opin Neurobiol. 2012 Oct;22(5):837-43. doi: 10.1016/j.conb.2012.02.006. Epub 2012 Mar 5. Curr Opin Neurobiol. 2012. PMID: 22398400 Free PMC article. Review.
Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study.
Kuht HJ, Maconachie GDE, Han J, Kessel L, van Genderen MM, McLean RJ, Hisaund M, Tu Z, Hertle RW, Gronskov K, Bai D, Wei A, Li W, Jiao Y, Smirnov V, Choi JH, Tobin MD, Sheth V, Purohit R, Dawar B, Girach A, Strul S, May L, Chen FK, Heath Jeffery RC, Aamir A, Sano R, Jin J, Brooks BP, Kohl S, Arveiler B, Montoliu L, Engle EC, Proudlock FA, Nishad G, Pani P, Varma G, Gottlob I, Thomas MG. Kuht HJ, et al. Among authors: engle ec. Ophthalmology. 2022 Jun;129(6):708-718. doi: 10.1016/j.ophtha.2022.02.010. Epub 2022 Feb 11. Ophthalmology. 2022. PMID: 35157951 Free PMC article.
Acute ataxia in childhood.
Ryan MM, Engle EC. Ryan MM, et al. Among authors: engle ec. J Child Neurol. 2003 May;18(5):309-16. doi: 10.1177/08830738030180050901. J Child Neurol. 2003. PMID: 12822814 Review.
Human genetic disorders of axon guidance.
Engle EC. Engle EC. Cold Spring Harb Perspect Biol. 2010 Mar;2(3):a001784. doi: 10.1101/cshperspect.a001784. Cold Spring Harb Perspect Biol. 2010. PMID: 20300212 Free PMC article. Review.
138 results