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9. Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels. Cruchaga C; Graff C; Chiang HH; Wang J; Hinrichs AL; Spiegel N; Bertelsen S; Mayo K; Norton JB; Morris JC; Goate A Arch Neurol; 2011 May; 68(5):581-6. PubMed ID: 21220649 [TBL] [Abstract][Full Text] [Related]
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12. Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study. Cash DM; Bocchetta M; Thomas DL; Dick KM; van Swieten JC; Borroni B; Galimberti D; Masellis M; Tartaglia MC; Rowe JB; Graff C; Tagliavini F; Frisoni GB; Laforce R; Finger E; de Mendonça A; Sorbi S; Rossor MN; Ourselin S; Rohrer JD; Neurobiol Aging; 2018 Feb; 62():191-196. PubMed ID: 29172163 [TBL] [Abstract][Full Text] [Related]
13. Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study. Ghidoni R; Stoppani E; Rossi G; Piccoli E; Albertini V; Paterlini A; Glionna M; Pegoiani E; Agnati LF; Fenoglio C; Scarpini E; Galimberti D; Morbin M; Tagliavini F; Binetti G; Benussi L Neurodegener Dis; 2012; 9(3):121-7. PubMed ID: 22123177 [TBL] [Abstract][Full Text] [Related]
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15. TMEM106B, the risk gene for frontotemporal dementia, is regulated by the microRNA-132/212 cluster and affects progranulin pathways. Chen-Plotkin AS; Unger TL; Gallagher MD; Bill E; Kwong LK; Volpicelli-Daley L; Busch JI; Akle S; Grossman M; Van Deerlin V; Trojanowski JQ; Lee VM J Neurosci; 2012 Aug; 32(33):11213-27. PubMed ID: 22895706 [TBL] [Abstract][Full Text] [Related]
16. Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics. Whitwell JL; Weigand SD; Boeve BF; Senjem ML; Gunter JL; DeJesus-Hernandez M; Rutherford NJ; Baker M; Knopman DS; Wszolek ZK; Parisi JE; Dickson DW; Petersen RC; Rademakers R; Jack CR; Josephs KA Brain; 2012 Mar; 135(Pt 3):794-806. PubMed ID: 22366795 [TBL] [Abstract][Full Text] [Related]
17. Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia. Wilke C; Gillardon F; Deuschle C; Hobert MA; Jansen IE; Metzger FG; Heutink P; Gasser T; Maetzler W; Blauwendraat C; Synofzik M Neurodegener Dis; 2017; 17(2-3):83-88. PubMed ID: 27760429 [TBL] [Abstract][Full Text] [Related]
18. Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutation. Bruni AC; Momeni P; Bernardi L; Tomaino C; Frangipane F; Elder J; Kawarai T; Sato C; Pradella S; Wakutani Y; Anfossi M; Gallo M; Geracitano S; Costanzo A; Smirne N; Curcio SA; Mirabelli M; Puccio G; Colao R; Maletta RG; Kertesz A; St George-Hyslop P; Hardy J; Rogaeva E Neurology; 2007 Jul; 69(2):140-7. PubMed ID: 17620546 [TBL] [Abstract][Full Text] [Related]
19. Effect of TMEM106B polymorphism on functional network connectivity in asymptomatic GRN mutation carriers. Premi E; Formenti A; Gazzina S; Archetti S; Gasparotti R; Padovani A; Borroni B JAMA Neurol; 2014 Feb; 71(2):216-21. PubMed ID: 24343233 [TBL] [Abstract][Full Text] [Related]
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