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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2016 | 1 |
2020 | 1 |
2021 | 3 |
2023 | 1 |
2024 | 1 |
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Page 1
Conflict of Interest Disclosures.
Global Spine J. 2023 May;13(2_suppl):568S-591S. doi: 10.1177/21925682231173597.
Global Spine J. 2023.
PMID: 37222100
Free PMC article.
No abstract available.
Seasonal influence of tuberculosis diagnosis in Rwanda.
Uwamahoro D, Beeman A, Sharma VK, Henry MB, Garbern SC, Becker J, Harfouche FD, Rogers AP, Kendric K, Guptill M.
Uwamahoro D, et al.
Trop Med Health. 2021 May 12;49(1):36. doi: 10.1186/s41182-021-00328-w.
Trop Med Health. 2021.
PMID: 33980306
Free PMC article.
Item in Clipboard
Pushing the Limits of Minimally Invasive Spine Surgery-From Preoperative to Intraoperative to Postoperative Management.
Drossopoulos PN, Sharma A, Ononogbu-Uche FC, Tabarestani TQ, Bartlett AM, Wang TY, Huie D, Gottfried O, Blitz J, Erickson M, Lad SP, Bullock WM, Shaffrey CI, Abd-El-Barr MM.
Drossopoulos PN, et al.
J Clin Med. 2024 Apr 20;13(8):2410. doi: 10.3390/jcm13082410.
J Clin Med. 2024.
PMID: 38673683
Free PMC article.
Review.
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Prevalence and drug use correlates of extra-medical use of prescription medications for sleep among adults in the United States: Results of the 2015-2018 National Survey on Drug Use and Health.
Lopez-Quintero C, Warren T, Falise A, Sharma V, Bares C, Oshri A.
Lopez-Quintero C, et al.
Pharmacol Biochem Behav. 2021 May;204:173169. doi: 10.1016/j.pbb.2021.173169. Epub 2021 Mar 6.
Pharmacol Biochem Behav. 2021.
PMID: 33684453
Free PMC article.
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Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science.
Schoch K, Esteves C, Bican A, Spillmann R, Cope H, McConkie-Rosell A, Walley N, Fernandez L, Kohler JN, Bonner D, Reuter C, Stong N, Mulvihill JJ, Novacic D, Wolfe L, Abdelbaki A, Toro C, Tifft C, Malicdan M, Gahl W, Liu P, Newman J, Goldstein DB, Hom J, Sampson J, Wheeler MT; Undiagnosed Diseases Network; Cogan J, Bernstein JA, Adams DR, McCray AT, Shashi V.
Schoch K, et al.
Genet Med. 2021 Feb;23(2):259-271. doi: 10.1038/s41436-020-00984-z. Epub 2020 Oct 23.
Genet Med. 2021.
PMID: 33093671
Free PMC article.
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De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype.
Shashi V, Pena LD, Kim K, Burton B, Hempel M, Schoch K, Walkiewicz M, McLaughlin HM, Cho M, Stong N, Hickey SE, Shuss CM; Undiagnosed Diseases Network; Freemark MS, Bellet JS, Keels MA, Bonner MJ, El-Dairi M, Butler M, Kranz PG, Stumpel CT, Klinkenberg S, Oberndorff K, Alawi M, Santer R, Petrovski S, Kuismin O, Korpi-Heikkilä S, Pietilainen O, Aarno P, Kurki MI, Hoischen A, Need AC, Goldstein DB, Kortüm F.
Shashi V, et al.
Am J Hum Genet. 2016 Oct 6;99(4):991-999. doi: 10.1016/j.ajhg.2016.08.017. Epub 2016 Sep 29.
Am J Hum Genet. 2016.
PMID: 27693232
Free PMC article.
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