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Page 1
Translation initiator EIF4G1 mutations in familial Parkinson disease.
Chartier-Harlin MC, Dachsel JC, Vilariño-Güell C, Lincoln SJ, Leprêtre F, Hulihan MM, Kachergus J, Milnerwood AJ, Tapia L, Song MS, Le Rhun E, Mutez E, Larvor L, Duflot A, Vanbesien-Mailliot C, Kreisler A, Ross OA, Nishioka K, Soto-Ortolaza AI, Cobb SA, Melrose HL, Behrouz B, Keeling BH, Bacon JA, Hentati E, Williams L, Yanagiya A, Sonenberg N, Lockhart PJ, Zubair AC, Uitti RJ, Aasly JO, Krygowska-Wajs A, Opala G, Wszolek ZK, Frigerio R, Maraganore DM, Gosal D, Lynch T, Hutchinson M, Bentivoglio AR, Valente EM, Nichols WC, Pankratz N, Foroud T, Gibson RA, Hentati F, Dickson DW, Destée A, Farrer MJ. Chartier-Harlin MC, et al. Among authors: keeling bh. Am J Hum Genet. 2011 Sep 9;89(3):398-406. doi: 10.1016/j.ajhg.2011.08.009. Am J Hum Genet. 2011. PMID: 21907011 Free PMC article.
LINGO1 rs9652490 is associated with essential tremor and Parkinson disease.
Vilariño-Güell C, Ross OA, Wider C, Jasinska-Myga B, Cobb SA, Soto-Ortolaza AI, Kachergus JM, Keeling BH, Dachsel JC, Melrose HL, Behrouz B, Wszolek ZK, Uitti RJ, Aasly JO, Rajput A, Farrer MJ. Vilariño-Güell C, et al. Among authors: keeling bh. Parkinsonism Relat Disord. 2010 Feb;16(2):109-11. doi: 10.1016/j.parkreldis.2009.08.006. Epub 2009 Aug 31. Parkinsonism Relat Disord. 2010. PMID: 19720553 Free PMC article.
Characterization of DCTN1 genetic variability in neurodegeneration.
Vilariño-Güell C, Wider C, Soto-Ortolaza AI, Cobb SA, Kachergus JM, Keeling BH, Dachsel JC, Hulihan MM, Dickson DW, Wszolek ZK, Uitti RJ, Graff-Radford NR, Boeve BF, Josephs KA, Miller B, Boylan KB, Gwinn K, Adler CH, Aasly JO, Hentati F, Destée A, Krygowska-Wajs A, Chartier-Harlin MC, Ross OA, Rademakers R, Farrer MJ. Vilariño-Güell C, et al. Among authors: keeling bh. Neurology. 2009 Jun 9;72(23):2024-8. doi: 10.1212/WNL.0b013e3181a92c4c. Neurology. 2009. PMID: 19506225 Free PMC article.
MEIS1 p.R272H in familial restless legs syndrome.
Vilariño-Güell C, Chai H, Keeling BH, Young JE, Rajput A, Lynch T, Aasly JO, Uitti RJ, Wszolek ZK, Farrer MJ, Lin SC. Vilariño-Güell C, et al. Among authors: keeling bh. Neurology. 2009 Jul 21;73(3):243-5. doi: 10.1212/WNL.0b013e3181ae7c79. Neurology. 2009. PMID: 19620614 Free PMC article. No abstract available.
A case of leukocytoclastic vasculitis in a patient on dupilumab.
Bach MS, Keeling BH, Yim E. Bach MS, et al. Among authors: keeling bh. JAAD Case Rep. 2023 Sep 24;42:49-51. doi: 10.1016/j.jdcr.2023.08.048. eCollection 2023 Dec. JAAD Case Rep. 2023. PMID: 38034366 Free PMC article. No abstract available.
Cutaneous collagenous vasculopathy in a pediatric patient.
Firsowicz M, Haller CN, Soldano A, Keeling BH, Diaz LZ. Firsowicz M, et al. Among authors: keeling bh. Pediatr Dermatol. 2023 Mar;40(2):323-325. doi: 10.1111/pde.15147. Epub 2022 Oct 19. Pediatr Dermatol. 2023. PMID: 36261316
Superimposed linear atopic dermatitis treated with dupilumab.
Leszczynska MA, Trainor MA, Henkel E, Keeling BH, Diaz LZ. Leszczynska MA, et al. Among authors: keeling bh. Pediatr Dermatol. 2021 Sep;38(5):1377-1378. doi: 10.1111/pde.14695. Epub 2021 Jul 16. Pediatr Dermatol. 2021. PMID: 34272754
21 results