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Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
Rice G, Patrick T, Parmar R, Taylor CF, Aeby A, Aicardi J, Artuch R, Montalto SA, Bacino CA, Barroso B, Baxter P, Benko WS, Bergmann C, Bertini E, Biancheri R, Blair EM, Blau N, Bonthron DT, Briggs T, Brueton LA, Brunner HG, Burke CJ, Carr IM, Carvalho DR, Chandler KE, Christen HJ, Corry PC, Cowan FM, Cox H, D'Arrigo S, Dean J, De Laet C, De Praeter C, Dery C, Ferrie CD, Flintoff K, Frints SG, Garcia-Cazorla A, Gener B, Goizet C, Goutieres F, Green AJ, Guet A, Hamel BC, Hayward BE, Heiberg A, Hennekam RC, Husson M, Jackson AP, Jayatunga R, Jiang YH, Kant SG, Kao A, King MD, Kingston HM, Klepper J, van der Knaap MS, Kornberg AJ, Kotzot D, Kratzer W, Lacombe D, Lagae L, Landrieu PG, Lanzi G, Leitch A, Lim MJ, Livingston JH, Lourenco CM, Lyall EG, Lynch SA, Lyons MJ, Marom D, McClure JP, McWilliam R, Melancon SB, Mewasingh LD, Moutard ML, Nischal KK, Ostergaard JR, Prendiville J, Rasmussen M, Rogers RC, Roland D, Rosser EM, Rostasy K, Roubertie A, Sanchis A, Schiffmann R, Scholl-Burgi S, Seal S, Shalev SA, Corcoles CS, Sinha GP, Soler D, Spiegel R, Stephenson JB, Tacke U, Tan TY, Till M, Tolmie JL, Tomlin P, Vagnarelli F, Valente EM, Van Coster RN, Van der Aa N, Vanderver A, V… See abstract for full author list ➔ Rice G, et al. Among authors: tomlin p. Am J Hum Genet. 2007 Oct;81(4):713-25. doi: 10.1086/521373. Epub 2007 Sep 4. Am J Hum Genet. 2007. PMID: 17846997 Free PMC article.
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection.
Crow YJ, Leitch A, Hayward BE, Garner A, Parmar R, Griffith E, Ali M, Semple C, Aicardi J, Babul-Hirji R, Baumann C, Baxter P, Bertini E, Chandler KE, Chitayat D, Cau D, Déry C, Fazzi E, Goizet C, King MD, Klepper J, Lacombe D, Lanzi G, Lyall H, Martínez-Frías ML, Mathieu M, McKeown C, Monier A, Oade Y, Quarrell OW, Rittey CD, Rogers RC, Sanchis A, Stephenson JB, Tacke U, Till M, Tolmie JL, Tomlin P, Voit T, Weschke B, Woods CG, Lebon P, Bonthron DT, Ponting CP, Jackson AP. Crow YJ, et al. Among authors: tomlin p. Nat Genet. 2006 Aug;38(8):910-6. doi: 10.1038/ng1842. Epub 2006 Jul 16. Nat Genet. 2006. PMID: 16845400
Epidemiology of ticks submitted from human hosts in Alberta, Canada (2000-2019).
Kanji JN, Isaac A, Gregson D, Mierzejewski M, Shpeley D, Tomlin P, Groeschel M, Lindsay LR, Lachance L, Kowalewska-Grochowska K. Kanji JN, et al. Among authors: tomlin p. Emerg Microbes Infect. 2022 Dec;11(1):284-292. doi: 10.1080/22221751.2022.2027217. Emerg Microbes Infect. 2022. PMID: 34991433 Free PMC article. Review.
Is COVID-19 a turning point for the health workforce?
Aith F, Castilla Martínez M, Cho M, Dussault G, Harris M, Padilla M, Murphy GT, Tomlin P, Valderas JM. Aith F, et al. Among authors: tomlin p. Rev Panam Salud Publica. 2020 Sep 16;44:e102. doi: 10.26633/RPSP.2020.102. eCollection 2020. Rev Panam Salud Publica. 2020. PMID: 32952532 Free PMC article. No abstract available.
Social cognition in children with epilepsy in mainstream education.
Lew AR, Lewis C, Lunn J, Tomlin P, Basu H, Roach J, Rakshi K, Martland T. Lew AR, et al. Among authors: tomlin p. Dev Med Child Neurol. 2015 Jan;57(1):53-9. doi: 10.1111/dmcn.12613. Epub 2014 Oct 21. Dev Med Child Neurol. 2015. PMID: 25330820 Free PMC article.
114 results