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

Year Number of Results
1979 1
1980 1
1982 1
1984 1
1991 1
1993 2
1994 1
1995 2
2003 1
2004 1
2013 4
2014 6
2015 7
2016 8
2017 5
2018 2
2019 2
2020 4
2021 1
2022 4
2023 0
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41 results
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Page 1
Maternal 15q Duplication Syndrome.
Lusk L, Vogel-Farley V, DiStefano C, Jeste S. Lusk L, et al. 2016 Jun 16 [updated 2021 Jul 15]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2016 Jun 16 [updated 2021 Jul 15]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 27308687 Free Books & Documents. Review.
PACS1 Neurodevelopmental Disorder.
Lusk L, Smith S, Martin C, Taylor C, Chung W. Lusk L, et al. 2020 Jul 16. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2020 Jul 16. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 32672908 Free Books & Documents. Review.
Dynamic mapping of human cortical development during childhood through early adulthood.
Gogtay N, Giedd JN, Lusk L, Hayashi KM, Greenstein D, Vaituzis AC, Nugent TF 3rd, Herman DH, Clasen LS, Toga AW, Rapoport JL, Thompson PM. Gogtay N, et al. Among authors: lusk l. Proc Natl Acad Sci U S A. 2004 May 25;101(21):8174-9. doi: 10.1073/pnas.0402680101. Epub 2004 May 17. Proc Natl Acad Sci U S A. 2004. PMID: 15148381 Free PMC article.
Predicting birth weight in fetuses with gastroschisis.
Zaki MN, Lusk LA, Overcash RT, Rao R, Truong YN, Liebowitz M, Porto M. Zaki MN, et al. Among authors: lusk la. J Perinatol. 2018 Feb;38(2):122-126. doi: 10.1038/jp.2017.171. Epub 2017 Dec 21. J Perinatol. 2018. PMID: 29266095
Adherence to and outcomes of a University-Consortium gastroschisis pathway.
DeUgarte DA, Calkins KL, Guner Y, Kim J, Kling K, Kramer K, Lee H, Lusk L, Saadai P, Uy C, Rottkamp C; University of California Fetal Consortium. DeUgarte DA, et al. Among authors: lusk l. J Pediatr Surg. 2020 Jan;55(1):45-48. doi: 10.1016/j.jpedsurg.2019.09.048. Epub 2019 Oct 27. J Pediatr Surg. 2020. PMID: 31704046
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature.
Priestley JRC, Pace LM, Sen K, Aggarwal A, Alves CAPF, Campbell IM, Cuddapah SR, Engelhardt NM, Eskandar M, Jolín García PC, Gropman A, Helbig I, Hong X, Gowda VK, Lusk L, Trapane P, Srinivasan VM, Suwannarat P, Ganetzky RD. Priestley JRC, et al. Among authors: lusk l. Mol Genet Metab Rep. 2022 Nov 16;33:100931. doi: 10.1016/j.ymgmr.2022.100931. eCollection 2022 Dec. Mol Genet Metab Rep. 2022. PMID: 36420423 Free PMC article.
A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism.
Parthasarathy S, Ruggiero SM, Gelot A, Soardi FC, Ribeiro BFR, Pires DEV, Ascher DB, Schmitt A, Rambaud C, Represa A, Xie HM, Lusk L, Wilmarth O, McDonnell PP, Juarez OA, Grace AN, Buratti J, Mignot C, Gras D, Nava C, Pierce SR, Keren B, Kennedy BC, Pena SDJ, Helbig I, Cuddapah VA. Parthasarathy S, et al. Among authors: lusk l. Am J Hum Genet. 2022 Dec 1;109(12):2253-2269. doi: 10.1016/j.ajhg.2022.11.002. Epub 2022 Nov 21. Am J Hum Genet. 2022. PMID: 36413998
Peak performance.
Lusk LT. Lusk LT. RDH. 1994 Mar;14(3):32, 37-8. RDH. 1994. PMID: 8041911 No abstract available.
41 results