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

Year Number of Results
1980 1
1982 1
1984 1
1987 1
1988 1
1990 1
1993 1
1995 2
1996 1
1998 1
2000 1
2001 1
2002 2
2006 1
2007 3
2009 1
2011 1
2012 1
2014 1
2015 1
2021 3
2022 0
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25 results
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Page 1
Hyperammonemia in the ICU.
Clay AS, Hainline BE. Clay AS, et al. Among authors: hainline be. Chest. 2007 Oct;132(4):1368-78. doi: 10.1378/chest.06-2940. Chest. 2007. PMID: 17934124 Review.
Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia.
Muir AM, Gardner JF, van Jaarsveld RH, de Lange IM, van der Smagt JJ, Wilson GN, Dubbs H, Goldberg EM, Zitano L, Bupp C, Martinez J, Srour M, Accogli A, Alhakeem A, Meltzer M, Gropman A, Brewer C, Caswell RC, Montgomery T, McKenna C, McKee S, Powell C, Vasudevan PC, Brady AF, Joss S, Tysoe C, Noh G, Tarnopolsky M, Brady L, Zafar M, Schrier Vergano SA, Murray B, Sawyer L, Hainline BE, Sapp K, DeMarzo D, Huismann DJ, Wentzensen IM, Schnur RE, Monaghan KG, Juusola J, Rhodes L, Dobyns WB, Lecoquierre F, Goldenberg A, Polster T, Axer-Schaefer S, Platzer K, Klöckner C, Hoffman TL, MacArthur DG, O'Leary MC, VanNoy GE, England E, Varghese VC, Mefford HC. Muir AM, et al. Among authors: hainline be. Genet Med. 2021 May;23(5):881-887. doi: 10.1038/s41436-020-01076-8. Epub 2021 Jan 20. Genet Med. 2021. PMID: 33473207 Free PMC article.
Management of a pregnancy complicated by pompe disease.
Weida J, Hainline BE, Bodkin C, Williams MK. Weida J, et al. Among authors: hainline be. Case Rep Obstet Gynecol. 2012;2012:137861. doi: 10.1155/2012/137861. Epub 2012 Dec 10. Case Rep Obstet Gynecol. 2012. PMID: 23304582 Free PMC article.
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.
Goodman LD, Cope H, Nil Z, Ravenscroft TA, Charng WL, Lu S, Tien AC, Pfundt R, Koolen DA, Haaxma CA, Veenstra-Knol HE, Wassink-Ruiter JSK, Wevers MR, Jones M, Walsh LE, Klee VH, Theunis M, Legius E, Steel D, Barwick KES, Kurian MA, Mohammad SS, Dale RC, Terhal PA, van Binsbergen E, Kirmse B, Robinette B, Cogné B, Isidor B, Grebe TA, Kulch P, Hainline BE, Sapp K, Morava E, Klee EW, Macke EL, Trapane P, Spencer C, Si Y, Begtrup A, Moulton MJ, Dutta D, Kanca O; Undiagnosed Diseases Network, Wangler MF, Yamamoto S, Bellen HJ, Tan QK. Goodman LD, et al. Among authors: hainline be. Am J Hum Genet. 2021 Sep 2;108(9):1669-1691. doi: 10.1016/j.ajhg.2021.06.019. Epub 2021 Jul 26. Am J Hum Genet. 2021. PMID: 34314705
1H NMR metabolomics study of age profiling in children.
Gu H, Pan Z, Xi B, Hainline BE, Shanaiah N, Asiago V, Gowda GA, Raftery D. Gu H, et al. Among authors: hainline be. NMR Biomed. 2009 Oct;22(8):826-33. doi: 10.1002/nbm.1395. NMR Biomed. 2009. PMID: 19441074 Free PMC article.
An atypical case of Canavan disease with stroke-like presentation.
Delaney KE, Kralik SF, Hainline BE, Golomb MR. Delaney KE, et al. Among authors: hainline be. Pediatr Neurol. 2015 Feb;52(2):218-21. doi: 10.1016/j.pediatrneurol.2014.10.019. Epub 2014 Oct 25. Pediatr Neurol. 2015. PMID: 25497124
Pyruvate carboxylase deficiency--insights from liver transplantation.
Nyhan WL, Khanna A, Barshop BA, Naviaux RK, Precht AF, Lavine JE, Hart MA, Hainline BE, Wappner RS, Nichols S, Haas RH. Nyhan WL, et al. Among authors: hainline be. Mol Genet Metab. 2002 Sep-Oct;77(1-2):143-9. doi: 10.1016/s1096-7192(02)00123-3. Mol Genet Metab. 2002. PMID: 12359142
25 results