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129 related items for PubMed ID: 32567375
1. Variability of clinical syndromes and cerebral glucose metabolism in symptomatic frontotemporal lobar degeneration associated with progranulin mutations. Licata A, Grimmer T, Winkelmann J, Wagner M, Goldhardt O, Riedl L, Roßmeier C, Yakushev I, Diehl-Schmid J. Amyotroph Lateral Scler Frontotemporal Degener; 2020 Aug; 21(5-6):389-395. PubMed ID: 32567375 [Abstract] [Full Text] [Related]
2. Assessing network degeneration and phenotypic heterogeneity in genetic frontotemporal lobar degeneration by decoding FDG-PET. Corriveau-Lecavalier N, Barnard LR, Przybelski SA, Gogineni V, Botha H, Graff-Radford J, Ramanan VK, Forsberg LK, Fields JA, Machulda MM, Rademakers R, Gavrilova RH, Lapid MI, Boeve BF, Knopman DS, Lowe VJ, Petersen RC, Jack CR, Kantarci K, Jones DT. Neuroimage Clin; 2024 Aug; 41():103559. PubMed ID: 38147792 [Abstract] [Full Text] [Related]
3. A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms. Puoti G, Lerza MC, Ferretti MG, Bugiani O, Tagliavini F, Rossi G. J Alzheimers Dis; 2014 Aug; 42(3):939-47. PubMed ID: 25024321 [Abstract] [Full Text] [Related]
4. Brain progranulin expression in GRN-associated frontotemporal lobar degeneration. Chen-Plotkin AS, Xiao J, Geser F, Martinez-Lage M, Grossman M, Unger T, Wood EM, Van Deerlin VM, Trojanowski JQ, Lee VM. Acta Neuropathol; 2010 Jan; 119(1):111-22. PubMed ID: 19649643 [Abstract] [Full Text] [Related]
5. The neuroimaging signature of frontotemporal lobar degeneration associated with Granulin mutations: an effective connectivity study. Premi E, Grassi M, Gazzina S, Paghera B, Pepe D, Archetti S, Padovani A, Borroni B. J Nucl Med; 2013 Jul; 54(7):1066-71. PubMed ID: 23687363 [Abstract] [Full Text] [Related]
6. Autosomal Dominant Frontotemporal Lobar Degeneration in a Filipino Family with Progranulin Mutation. Dominguez J, Ng A, Yu J, Guevarra AC, Daroy ML, Alfon A, Catindig JA, Dizon M, Santiago J, Del Moral MC, Yu J, Jamerlan A, Ligsay A, Bagyinszky E, An SS, Kim S. Dement Geriatr Cogn Disord; 2020 Jul; 49(6):557-564. PubMed ID: 33486486 [Abstract] [Full Text] [Related]
7. Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration. Chiang HH, Forsell C, Lilius L, Öijerstedt L, Thordardottir S, Shanmugarajan K, Westerlund M, Nennesmo I, Thonberg H, Graff C. Eur J Hum Genet; 2013 Nov; 21(11):1260-5. PubMed ID: 23463024 [Abstract] [Full Text] [Related]
8. Rare exonic variant affects GRN splicing and contributes to frontotemporal lobar degeneration. Wauters E, Gossye H, Frydas A, Sieben A, Van Broeckhoven C. Neurobiol Aging; 2023 Oct; 130():61-69. PubMed ID: 37459659 [Abstract] [Full Text] [Related]
9. A novel frameshift GRN mutation results in frontotemporal lobar degeneration with a distinct clinical phenotype in two siblings: case report and literature review. Hosaka T, Ishii K, Miura T, Mezaki N, Kasuga K, Ikeuchi T, Tamaoka A. BMC Neurol; 2017 Sep 15; 17(1):182. PubMed ID: 28915852 [Abstract] [Full Text] [Related]
10. Serum progranulin levels in patients with frontotemporal lobar degeneration and Alzheimer's disease: detection of GRN mutations in a Spanish cohort. Antonell A, Gil S, Sánchez-Valle R, Balasa M, Bosch B, Prat MC, Chiollaz AC, Fernández M, Yagüe J, Molinuevo JL, Lladó A. J Alzheimers Dis; 2012 Sep 15; 31(3):581-91. PubMed ID: 22647257 [Abstract] [Full Text] [Related]
11. Anterior brain glucose hypometabolism predates dementia in progranulin mutation carriers. Jacova C, Hsiung GY, Tawankanjanachot I, Dinelle K, McCormick S, Gonzalez M, Lee H, Sengdy P, Bouchard-Kerr P, Baker M, Rademakers R, Sossi V, Stoessl AJ, Feldman HH, Mackenzie IR. Neurology; 2013 Oct 08; 81(15):1322-31. PubMed ID: 24005336 [Abstract] [Full Text] [Related]
12. Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration. Piaceri I, Pradella S, Cupidi C, Nannucci S, Polito C, Bagnoli S, Tedde A, Smirne N, Anfossi M, Gallo M, Bernardi L, Colao R, Maletta R, Bruni AC, Sorbi S, Nacmias B. J Alzheimers Dis; 2014 Oct 08; 40(3):679-85. PubMed ID: 24503614 [Abstract] [Full Text] [Related]
13. Serum C-Peptide, Visfatin, Resistin, and Ghrelin are Altered in Sporadic and GRN-Associated Frontotemporal Lobar Degeneration. Zanardini R, Benussi L, Fostinelli S, Saraceno C, Ciani M, Borroni B, Padovani A, Binetti G, Ghidoni R. J Alzheimers Dis; 2018 Oct 08; 61(3):1053-1060. PubMed ID: 29226876 [Abstract] [Full Text] [Related]
14. Clinical and Neuroimaging Aspects of Familial Frontotemporal Lobar Degeneration Associated with MAPT and GRN Mutations. Boeve BF, Rosen H. Adv Exp Med Biol; 2021 Oct 08; 1281():77-92. PubMed ID: 33433870 [Abstract] [Full Text] [Related]
15. A Novel Loss-of-Function GRN Mutation p.(Tyr229*): Clinical and Neuropathological Features. Kuuluvainen L, Pöyhönen M, Pasanen P, Siitonen M, Rummukainen J, Tienari PJ, Paetau A, Myllykangas L. J Alzheimers Dis; 2017 Oct 08; 55(3):1167-1174. PubMed ID: 27767988 [Abstract] [Full Text] [Related]
16. Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia. van Swieten JC, Heutink P. Lancet Neurol; 2008 Oct 08; 7(10):965-74. PubMed ID: 18771956 [Abstract] [Full Text] [Related]
17. Progranulin gene (GRN) promoter methylation is increased in patients with sporadic frontotemporal lobar degeneration. Galimberti D, D'Addario C, Dell'osso B, Fenoglio C, Marcone A, Cerami C, Cappa SF, Palazzo MC, Arosio B, Mari D, Maccarrone M, Bresolin N, Altamura AC, Scarpini E. Neurol Sci; 2013 Jun 08; 34(6):899-903. PubMed ID: 22797721 [Abstract] [Full Text] [Related]
18. Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutations. Sakae N, Roemer SF, Bieniek KF, Murray ME, Baker MC, Kasanuki K, Graff-Radford NR, Petrucelli L, Van Blitterswijk M, Rademakers R, Dickson DW. Ann Clin Transl Neurol; 2019 Sep 08; 6(9):1782-1796. PubMed ID: 31448566 [Abstract] [Full Text] [Related]
19. Astroglial toxicity promotes synaptic degeneration in the thalamocortical circuit in frontotemporal dementia with GRN mutations. Marsan E, Velmeshev D, Ramsey A, Patel RK, Zhang J, Koontz M, Andrews MG, de Majo M, Mora C, Blumenfeld J, Li AN, Spina S, Grinberg LT, Seeley WW, Miller BL, Ullian EM, Krummel MF, Kriegstein AR, Huang EJ. J Clin Invest; 2023 Mar 15; 133(6):. PubMed ID: 36602862 [Abstract] [Full Text] [Related]
20. Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy. Bagnoli S, Piaceri I, Tedde A, Piacentini S, Nannucci S, Bracco L, Sorbi S, Nacmias B. Cell Mol Neurobiol; 2012 Jan 15; 32(1):13-6. PubMed ID: 21800185 [Abstract] [Full Text] [Related] Page: [Next] [New Search]