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Page 1
Measurement of the flux of ultrahigh energy cosmic rays from monocular observations by the High Resolution Fly's Eye experiment.
Abbasi RU, Abu-Zayyad T, Amann JF, Archbold G, Bellido JA, Belov K, Belz JW, Bergman DR, Cao Z, Clay RW, Cooper MD, Dai H, Dawson BR, Everett AA, Fedorova YA, Girard JH, Gray RC, Hanlon WF, Hoffman CM, Holzscheiter MH, Hüntemeyer P, Jones BF, Jui CC, Kieda DB, Kim K, Kirn MA, Loh EC, Manago N, Marek LJ, Martens K, Martin G, Matthews JA, Matthews JN, Meyer JR, Moore SA, Morrison P, Moosman AN, Mumford JR, Munro MW, Painter CA, Perera L, Reil K, Riehle R, Roberts M, Sarracino JS, Sasaki M, Schnetzer SR, Shen P, Simpson KM, Sinnis G, Smith JD, Sokolsky P, Song C, Springer RW, Stokes BT, Taylor SF, Thomas SB, Thompson TN, Thomson GB, Tupa D, Westerhoff S, Wiencke LR, VanderVeen TD, Zech A, Zhang X; High Resolution Fly's Eye Collaboration. Abbasi RU, et al. Among authors: morrison p. Phys Rev Lett. 2004 Apr 16;92(15):151101. doi: 10.1103/PhysRevLett.92.151101. Epub 2004 Apr 15. Phys Rev Lett. 2004. PMID: 15169276
Clinical management and outcome of head and neck paragangliomas (HNPGLs): A single centre retrospective study.
Darrat M, Lau L, Leonard C, Cooke S, Shahzad MA, McHenry C, McCance DR, Hunter SJ, Mullan K, Lindsay JR, Graham U, Bailie N, Hampton S, Rajendran S, Houghton F, Conkey D, Morrison PJ, Johnston PC. Darrat M, et al. Among authors: morrison pj. Clin Endocrinol (Oxf). 2024 May 2. doi: 10.1111/cen.15070. Online ahead of print. Clin Endocrinol (Oxf). 2024. PMID: 38696538
Connectome dysfunction in patients at clinical high risk for psychosis and modulation by oxytocin.
Davies C, Martins D, Dipasquale O, McCutcheon RA, De Micheli A, Ramella-Cravaro V, Provenzani U, Rutigliano G, Cappucciati M, Oliver D, Williams S, Zelaya F, Allen P, Murguia S, Taylor D, Shergill S, Morrison P, McGuire P, Paloyelis Y, Fusar-Poli P. Davies C, et al. Among authors: morrison p. Mol Psychiatry. 2024 Jan 19. doi: 10.1038/s41380-024-02406-x. Online ahead of print. Mol Psychiatry. 2024. PMID: 38243074
The Cerebellar Cognitive Affective/Schmahmann Syndrome Scale in Spinocerebellar Ataxias.
Selvadurai LP, Perlman SL, Ashizawa T, Wilmot GR, Onyike CU, Rosenthal LS, Shakkottai VG, Paulson HL, Subramony SH, Bushara KO, Kuo SH, Dietiker C, Geschwind MD, Nelson AB, Gomez CM, Opal P, Zesiewicz TA, Hawkins T, Yacoubian TA, Nopoulos PC, Sha SJ, Morrison PE, Figueroa KP, Pulst SM, Schmahmann JD. Selvadurai LP, et al. Among authors: morrison pe. Cerebellum. 2024 Jan 2. doi: 10.1007/s12311-023-01651-0. Online ahead of print. Cerebellum. 2024. PMID: 38165578
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: morrison pj. 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
1,046 results