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Barriers and Facilitators to Prevention and Care of COVID-19 Infection in Cincinnati Latinx Families: a Community-Based Convergent Mixed Methods Study.
Martin KJ, Castano C, Geraghty S, Horner SR, McCann E, Beck AF, Xu Y, Gomez L, O'Dea C, Jacquez F, Clark VLP, Rule ARL. Martin KJ, et al. Among authors: mccann e. J Racial Ethn Health Disparities. 2023 Jun;10(3):1067-1085. doi: 10.1007/s40615-022-01294-7. Epub 2022 Apr 11. J Racial Ethn Health Disparities. 2023. PMID: 35411496 Free PMC article.
Thermoelectric Limitations of Graphene Nanodevices at Ultrahigh Current Densities.
Evangeli C, Swett J, Spiece J, McCann E, Fried J, Harzheim A, Lupini AR, Briggs GAD, Gehring P, Jesse S, Kolosov OV, Mol JA, Dyck O. Evangeli C, et al. Among authors: mccann e. ACS Nano. 2024 Apr 30;18(17):11153-11164. doi: 10.1021/acsnano.3c12930. Epub 2024 Apr 19. ACS Nano. 2024. PMID: 38641345
Comparison of source-location algorithms for atmospheric samplers.
Eslinger PW, Rosenthal WS, Sarathi RS, Schrom BT, McCann E. Eslinger PW, et al. Among authors: mccann e. J Environ Radioact. 2024 Mar;273:107384. doi: 10.1016/j.jenvrad.2024.107384. Epub 2024 Jan 18. J Environ Radioact. 2024. PMID: 38237240 Free article.
Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022).
Luo H, Gustavsson EK, Macpherson H, Dominik N, Zhelcheska K, Montgomery K, Anderson C, Yau WY, Efthymiou S, Turner C, DeTure M, Dickson DW, Josephs KA, Revesz T, Lashley T, Halliday G, Rowe DB, McCann E, Blair I, Lees AJ, Tienari PJ, Suomalainen A, Molina-Porcel L, Kovacs GG, Gelpi E, Hardy J, Haltia MJ, Tucci A, Jaunmuktane Z, Ryten M, Houlden H, Chen Z. Luo H, et al. Among authors: mccann e. Acta Neuropathol Commun. 2024 Jan 2;12(1):2. doi: 10.1186/s40478-023-01706-7. Acta Neuropathol Commun. 2024. PMID: 38167323 Free PMC article. No abstract available.
Validation of the novel Eosinophilic Esophagitis Impact Questionnaire.
McCann E, Chehade M, Spergel JM, Yaworsky A, Symonds T, Stokes J, Tilton ST, Sun X, Kamat S. McCann E, et al. J Patient Rep Outcomes. 2023 Nov 27;7(1):120. doi: 10.1186/s41687-023-00654-z. J Patient Rep Outcomes. 2023. PMID: 38010430 Free PMC article. Clinical Trial.
Detailed Analysis of ITPR1 Missense Variants Guides Diagnostics and Therapeutic Design.
Tolonen JP, Parolin Schnekenberg R, McGowan S, Sims D, McEntagart M, Elmslie F, Shears D, Stewart H, Tofaris GK, Dabir T, Morrison PJ, Johnson D, Hadjivassiliou M, Ellard S, Shaw-Smith C, Znaczko A, Dixit A, Suri M, Sarkar A, Harrison RE, Jones G, Houlden H, Ceravolo G, Jarvis J, Williams J, Shanks ME, Clouston P, Rankin J, Blumkin L, Lerman-Sagie T, Ponger P, Raskin S, Granath K, Uusimaa J, Conti H, McCann E, Joss S, Blakes AJM, Metcalfe K, Kingston H, Bertoli M, Kneen R, Lynch SA, Martínez Albaladejo I, Moore AP, Jones WD; Genomics England Research Consortium; Becker EBE, Németh AH. Tolonen JP, et al. Among authors: mccann e. Mov Disord. 2024 Jan;39(1):141-151. doi: 10.1002/mds.29651. Epub 2023 Nov 14. Mov Disord. 2024. PMID: 37964426 Free PMC article.
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Jeffries L, Mis EK, McWalter K, Donkervoort S, Brodsky NN, Carpier JM, Ji W, Ionita C, Roy B, Morrow JS, Darbinyan A, Iyer K, Aul RB, Banka S, Chao KR, Cobbold L, Cohen S, Custodio HM, Drummond-Borg M, Elmslie F, Finanger E, Hainline BE, Helbig I, Hewson S, Hu Y, Jackson A, Josifova D, Konstantino M, Leach ME, Mak B, McCormick D, McGee E, Nelson S, Nguyen J, Nugent K, Ortega L, Goodkin HP, Roeder E, Roy S, Sapp K, Saade D, Sisodiya SM, Stals K, Towner S, Wilson W; Deciphering Developmental Disorders; Genomics England Research Consortium; Undiagnosed Disease Network; Khokha MK, Bönnemann CG, Lucas CL, Lakhani SA. Jeffries L, et al. Genet Med. 2024 Feb;26(2):101023. doi: 10.1016/j.gim.2023.101023. Epub 2023 Nov 7. Genet Med. 2024. PMID: 37947183
314 results