209 related articles for article (PubMed ID: 10716259)
1. Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy.
Di Maria E; Tabaton M; Vigo T; Abbruzzese G; Bellone E; Donati C; Frasson E; Marchese R; Montagna P; Munoz DG; Pramstaller PP; Zanusso G; Ajmar F; Mandich P
Ann Neurol; 2000 Mar; 47(3):374-7. PubMed ID: 10716259
[TBL] [Abstract][Full Text] [Related]
2. The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases.
Morris HR; Janssen JC; Bandmann O; Daniel SE; Rossor MN; Lees AJ; Wood NW
J Neurol Neurosurg Psychiatry; 1999 May; 66(5):665-7. PubMed ID: 10209184
[TBL] [Abstract][Full Text] [Related]
3. A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration.
Higgins JJ; Litvan I; Nee LE; Loveless JM
Neurology; 1999 Jan; 52(2):404-6. PubMed ID: 9932968
[TBL] [Abstract][Full Text] [Related]
4. Relationship between frontotemporal dementia and corticobasal degeneration/progressive supranuclear palsy.
Kertesz A; Munoz D
Dement Geriatr Cogn Disord; 2004; 17(4):282-6. PubMed ID: 15178937
[TBL] [Abstract][Full Text] [Related]
5. Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration.
Pittman AM; Myers AJ; Abou-Sleiman P; Fung HC; Kaleem M; Marlowe L; Duckworth J; Leung D; Williams D; Kilford L; Thomas N; Morris CM; Dickson D; Wood NW; Hardy J; Lees AJ; de Silva R
J Med Genet; 2005 Nov; 42(11):837-46. PubMed ID: 15792962
[TBL] [Abstract][Full Text] [Related]
6. Key emerging issues in progressive supranuclear palsy and corticobasal degeneration.
Josephs KA
J Neurol; 2015 Mar; 262(3):783-8. PubMed ID: 25701010
[TBL] [Abstract][Full Text] [Related]
7. Does corticobasal degeneration exist? A clinicopathological re-evaluation.
Ling H; O'Sullivan SS; Holton JL; Revesz T; Massey LA; Williams DR; Paviour DC; Lees AJ
Brain; 2010 Jul; 133(Pt 7):2045-57. PubMed ID: 20584946
[TBL] [Abstract][Full Text] [Related]
8. VEGF haplotypes are associated with increased risk to progressive supranuclear palsy and corticobasal syndrome.
Borroni B; Del Bo R; Goldwurm S; Archetti S; Bonvicini C; Agosti C; Bigni B; Papetti A; Ghezzi S; Sacilotto G; Pezzoli G; Gennarelli M; Bresolin N; Comi GP; Padovani A
J Alzheimers Dis; 2010; 21(1):87-94. PubMed ID: 20413880
[TBL] [Abstract][Full Text] [Related]
9. Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.
Kouri N; Ross OA; Dombroski B; Younkin CS; Serie DJ; Soto-Ortolaza A; Baker M; Finch NCA; Yoon H; Kim J; Fujioka S; McLean CA; Ghetti B; Spina S; Cantwell LB; Farlow MR; Grafman J; Huey ED; Ryung Han M; Beecher S; Geller ET; Kretzschmar HA; Roeber S; Gearing M; Juncos JL; Vonsattel JPG; Van Deerlin VM; Grossman M; Hurtig HI; Gross RG; Arnold SE; Trojanowski JQ; Lee VM; Wenning GK; White CL; Höglinger GU; Müller U; Devlin B; Golbe LI; Crook J; Parisi JE; Boeve BF; Josephs KA; Wszolek ZK; Uitti RJ; Graff-Radford NR; Litvan I; Younkin SG; Wang LS; Ertekin-Taner N; Rademakers R; Hakonarsen H; Schellenberg GD; Dickson DW
Nat Commun; 2015 Jun; 6():7247. PubMed ID: 26077951
[TBL] [Abstract][Full Text] [Related]
10. Analysis of PITX3 gene in patients with multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration.
Jamrozik Z; Berdynski M; Zekanowski C; Baranczyk-Kuzma A; Sławek J; Kuzma-Kozakiewicz M; Maruszak A; Kwiecinski H
Ann Clin Lab Sci; 2013; 43(2):151-3. PubMed ID: 23694789
[TBL] [Abstract][Full Text] [Related]
11. Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting.
Scaravilli T; Tolosa E; Ferrer I
Mov Disord; 2005 Aug; 20 Suppl 12():S21-8. PubMed ID: 16092076
[TBL] [Abstract][Full Text] [Related]
12. Novel haplotypes in 17q21 are associated with progressive supranuclear palsy.
Pastor P; Ezquerra M; Perez JC; Chakraverty S; Norton J; Racette BA; McKeel D; Perlmutter JS; Tolosa E; Goate AM
Ann Neurol; 2004 Aug; 56(2):249-58. PubMed ID: 15293277
[TBL] [Abstract][Full Text] [Related]
13. Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype.
Houlden H; Baker M; Morris HR; MacDonald N; Pickering-Brown S; Adamson J; Lees AJ; Rossor MN; Quinn NP; Kertesz A; Khan MN; Hardy J; Lantos PL; St George-Hyslop P; Munoz DG; Mann D; Lang AE; Bergeron C; Bigio EH; Litvan I; Bhatia KP; Dickson D; Wood NW; Hutton M
Neurology; 2001 Jun; 56(12):1702-6. PubMed ID: 11425937
[TBL] [Abstract][Full Text] [Related]
14. Recent advances in the understanding of tau protein and movement disorders.
Arvanitakis Z; Wszolek ZK
Curr Opin Neurol; 2001 Aug; 14(4):491-7. PubMed ID: 11470966
[TBL] [Abstract][Full Text] [Related]
15. Role of the tau gene region chromosome inversion in progressive supranuclear palsy, corticobasal degeneration, and related disorders.
Webb A; Miller B; Bonasera S; Boxer A; Karydas A; Wilhelmsen KC
Arch Neurol; 2008 Nov; 65(11):1473-8. PubMed ID: 19001166
[TBL] [Abstract][Full Text] [Related]
16. Diffusion tensor magnetic resonance imaging for single subject diagnosis in neurodegenerative diseases.
Sajjadi SA; Acosta-Cabronero J; Patterson K; Diaz-de-Grenu LZ; Williams GB; Nestor PJ
Brain; 2013 Jul; 136(Pt 7):2253-61. PubMed ID: 23729473
[TBL] [Abstract][Full Text] [Related]
17. Clinical and pathologic evidence of corticobasal degeneration and progressive supranuclear palsy in familial tauopathy.
Tuite PJ; Clark HB; Bergeron C; Bower M; St George-Hyslop P; Mateva V; Anderson J; Knopman DS
Arch Neurol; 2005 Sep; 62(9):1453-7. PubMed ID: 16157754
[TBL] [Abstract][Full Text] [Related]
18. Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration.
Sanchez-Contreras M; Heckman MG; Tacik P; Diehl N; Brown PH; Soto-Ortolaza AI; Christopher EA; Walton RL; Ross OA; Golbe LI; Graff-Radford N; Wszolek ZK; Dickson DW; Rademakers R
Mov Disord; 2017 Jan; 32(1):115-123. PubMed ID: 27709685
[TBL] [Abstract][Full Text] [Related]
19. Association of an extended haplotype in the tau gene with progressive supranuclear palsy.
Baker M; Litvan I; Houlden H; Adamson J; Dickson D; Perez-Tur J; Hardy J; Lynch T; Bigio E; Hutton M
Hum Mol Genet; 1999 Apr; 8(4):711-5. PubMed ID: 10072441
[TBL] [Abstract][Full Text] [Related]
20. [Genetic background of corticobasal syndrome].
Doi H; Tanaka F
Rinsho Shinkeigaku; 2013; 53(11):1026-8. PubMed ID: 24291868
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]