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Page 1
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.
Vollstedt EJ, Schaake S, Lohmann K, Padmanabhan S, Brice A, Lesage S, Tesson C, Vidailhet M, Wurster I, Hentati F, Mirelman A, Giladi N, Marder K, Waters C, Fahn S, Kasten M, Brüggemann N, Borsche M, Foroud T, Tolosa E, Garrido A, Annesi G, Gagliardi M, Bozi M, Stefanis L, Ferreira JJ, Correia Guedes L, Avenali M, Petrucci S, Clark L, Fedotova EY, Abramycheva NY, Alvarez V, Menéndez-González M, Jesús Maestre S, Gómez-Garre P, Mir P, Belin AC, Ran C, Lin CH, Kuo MC, Crosiers D, Wszolek ZK, Ross OA, Jankovic J, Nishioka K, Funayama M, Clarimon J, Williams-Gray CH, Camacho M, Cornejo-Olivas M, Torres-Ramirez L, Wu YR, Lee-Chen GJ, Morgadinho A, Pulkes T, Termsarasab P, Berg D, Kuhlenbäumer G, Kühn AA, Borngräber F, de Michele G, De Rosa A, Zimprich A, Puschmann A, Mellick GD, Dorszewska J, Carr J, Ferese R, Gambardella S, Chase B, Markopoulou K, Satake W, Toda T, Rossi M, Merello M, Lynch T, Olszewska DA, Lim SY, Ahmad-Annuar A, Tan AH, Al-Mubarak B, Hanagasi H, Koziorowski D, Ertan S, Genç G, de Carvalho Aguiar P, Barkhuizen M, Pimentel MMG, Saunders-Pullman R, van de Warrenburg B, Bressman S, Toft M, Appel-Cresswell S, Lang AE, Skorvanek M, Boon AJW, Krüger R, Sammler EM, Tu… See abstract for full author list ➔ Vollstedt EJ, et al. Among authors: clark l. Mov Disord. 2023 Feb;38(2):286-303. doi: 10.1002/mds.29288. Epub 2023 Jan 24. Mov Disord. 2023. PMID: 36692014
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17.
Clark LN, Poorkaj P, Wszolek Z, Geschwind DH, Nasreddine ZS, Miller B, Li D, Payami H, Awert F, Markopoulou K, Andreadis A, D'Souza I, Lee VM, Reed L, Trojanowski JQ, Zhukareva V, Bird T, Schellenberg G, Wilhelmsen KC. Clark LN, et al. Proc Natl Acad Sci U S A. 1998 Oct 27;95(22):13103-7. doi: 10.1073/pnas.95.22.13103. Proc Natl Acad Sci U S A. 1998. PMID: 9789048 Free PMC article.
Comparison of tau spread in people with Down syndrome versus autosomal-dominant Alzheimer's disease: a cross-sectional study.
Wisch JK, McKay NS, Boerwinkle AH, Kennedy J, Flores S, Handen BL, Christian BT, Head E, Mapstone M, Rafii MS, O'Bryant SE, Price JC, Laymon CM, Krinsky-McHale SJ, Lai F, Rosas HD, Hartley SL, Zaman S, Lott IT, Tudorascu D, Zammit M, Brickman AM, Lee JH, Bird TD, Cohen A, Chrem P, Daniels A, Chhatwal JP, Cruchaga C, Ibanez L, Jucker M, Karch CM, Day GS, Lee JH, Levin J, Llibre-Guerra J, Li Y, Lopera F, Roh JH, Ringman JM, Supnet-Bell C, van Dyck CH, Xiong C, Wang G, Morris JC, McDade E, Bateman RJ, Benzinger TLS, Gordon BA, Ances BM; Alzheimer's Biomarker Consortium-Down syndrome; Dominantly Inherited Alzheimer Network. Wisch JK, et al. Lancet Neurol. 2024 May;23(5):500-510. doi: 10.1016/S1474-4422(24)00084-X. Lancet Neurol. 2024. PMID: 38631766
Molecular genetic analysis of Lubag.
Wilhelmsen KC, Moskowitz CB, Weeks DE, Neystat M, Nygaard TG, Clark L, Dancoup M, Sobrevega EE, Rosales R, Gamez GL, Pacioles O, Perez M, Fahn S. Wilhelmsen KC, et al. Among authors: clark l. Adv Neurol. 1998;78:341-8. Adv Neurol. 1998. PMID: 9750931 No abstract available.
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q.
Ikeuchi T, Sanpei K, Takano H, Sasaki H, Tashiro K, Cancel G, Brice A, Bird TD, Schellenberg GD, Pericak-Vance MA, Welsh-Bohmer KA, Clark LN, Wilhelmsen K, Tsuji S. Ikeuchi T, et al. Among authors: clark ln. Genomics. 1998 Apr 15;49(2):321-6. doi: 10.1006/geno.1998.5266. Genomics. 1998. PMID: 9598323
Tau mutations in frontotemporal dementia.
Wilhelmsen KC, Clark LN, Miller BL, Geschwind DH. Wilhelmsen KC, et al. Among authors: clark ln. Dement Geriatr Cogn Disord. 1999;10 Suppl 1:88-92. doi: 10.1159/000051221. Dement Geriatr Cogn Disord. 1999. PMID: 10436349 Review.
From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.
Nasreddine ZS, Loginov M, Clark LN, Lamarche J, Miller BL, Lamontagne A, Zhukareva V, Lee VM, Wilhelmsen KC, Geschwind DH. Nasreddine ZS, et al. Among authors: clark ln. Ann Neurol. 1999 Jun;45(6):704-15. doi: 10.1002/1531-8249(199906)45:6<704::aid-ana4>3.0.co;2-x. Ann Neurol. 1999. PMID: 10360762
Assay precision and risk of misclassification at rule-out cut-offs for high-sensitivity cardiac troponin.
Kavsak PA, Mills NL, Clark L, Ko DT, Sharif S, Chen-Tournoux A, Friedman SM, Belley-Cote EP, Worster A, Cox J, Thiruganasambandamoorthy V, Lou A, Taher J, Scheuermeyer F, McCudden C, Abramson BL, Eintracht S, Shea JL, Yip PM, Huang Y, Chen M, Tsui AKY, Thorlacius L, Aakre KM, Raizman JE, Fung AWS, Humphries KH, Arnoldo S, Bhayana V, Djiana R, Beriault DR, St-Cyr J, Booth RA, Blank DW, Sivilotti MLA, Jaffe AS. Kavsak PA, et al. Among authors: clark l. Can J Cardiol. 2024 May 13:S0828-282X(24)00361-1. doi: 10.1016/j.cjca.2024.05.007. Online ahead of print. Can J Cardiol. 2024. PMID: 38750895 No abstract available.
2,864 results