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223 related items for PubMed ID: 29226876

  • 1. 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; 61(3):1053-1060. PubMed ID: 29226876
    [Abstract] [Full Text] [Related]

  • 2. 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
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  • 3. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.
    Pottier C, Zhou X, Perkerson RB, Baker M, Jenkins GD, Serie DJ, Ghidoni R, Benussi L, Binetti G, López de Munain A, Zulaica M, Moreno F, Le Ber I, Pasquier F, Hannequin D, Sánchez-Valle R, Antonell A, Lladó A, Parsons TM, Finch NA, Finger EC, Lippa CF, Huey ED, Neumann M, Heutink P, Synofzik M, Wilke C, Rissman RA, Slawek J, Sitek E, Johannsen P, Nielsen JE, Ren Y, van Blitterswijk M, DeJesus-Hernandez M, Christopher E, Murray ME, Bieniek KF, Evers BM, Ferrari C, Rollinson S, Richardson A, Scarpini E, Fumagalli GG, Padovani A, Hardy J, Momeni P, Ferrari R, Frangipane F, Maletta R, Anfossi M, Gallo M, Petrucelli L, Suh E, Lopez OL, Wong TH, van Rooij JGJ, Seelaar H, Mead S, Caselli RJ, Reiman EM, Noel Sabbagh M, Kjolby M, Nykjaer A, Karydas AM, Boxer AL, Grinberg LT, Grafman J, Spina S, Oblak A, Mesulam MM, Weintraub S, Geula C, Hodges JR, Piguet O, Brooks WS, Irwin DJ, Trojanowski JQ, Lee EB, Josephs KA, Parisi JE, Ertekin-Taner N, Knopman DS, Nacmias B, Piaceri I, Bagnoli S, Sorbi S, Gearing M, Glass J, Beach TG, Black SE, Masellis M, Rogaeva E, Vonsattel JP, Honig LS, Kofler J, Bruni AC, Snowden J, Mann D, Pickering-Brown S, Diehl-Schmid J, Winkelmann J, Galimberti D, Graff C, Öijerstedt L, Troakes C, Al-Sarraj S, Cruchaga C, Cairns NJ, Rohrer JD, Halliday GM, Kwok JB, van Swieten JC, White CL, Ghetti B, Murell JR, Mackenzie IRA, Hsiung GR, Borroni B, Rossi G, Tagliavini F, Wszolek ZK, Petersen RC, Bigio EH, Grossman M, Van Deerlin VM, Seeley WW, Miller BL, Graff-Radford NR, Boeve BF, Dickson DW, Biernacka JM, Rademakers R.
    Lancet Neurol; 2018 Jun; 17(6):548-558. PubMed ID: 29724592
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  • 6. Glucose metabolism alterations in patients with bipolar disorder.
    Rosso G, Cattaneo A, Zanardini R, Gennarelli M, Maina G, Bocchio-Chiavetto L.
    J Affect Disord; 2015 Sep 15; 184():293-8. PubMed ID: 26120808
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  • 8. 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 15; 6(9):1782-1796. PubMed ID: 31448566
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  • 9. Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration.
    Chen-Plotkin AS, Martinez-Lage M, Sleiman PM, Hu W, Greene R, Wood EM, Bing S, Grossman M, Schellenberg GD, Hatanpaa KJ, Weiner MF, White CL, Brooks WS, Halliday GM, Kril JJ, Gearing M, Beach TG, Graff-Radford NR, Dickson DW, Rademakers R, Boeve BF, Pickering-Brown SM, Snowden J, van Swieten JC, Heutink P, Seelaar H, Murrell JR, Ghetti B, Spina S, Grafman J, Kaye JA, Woltjer RL, Mesulam M, Bigio E, Lladó A, Miller BL, Alzualde A, Moreno F, Rohrer JD, Mackenzie IR, Feldman HH, Hamilton RL, Cruts M, Engelborghs S, De Deyn PP, Van Broeckhoven C, Bird TD, Cairns NJ, Goate A, Frosch MP, Riederer PF, Bogdanovic N, Lee VM, Trojanowski JQ, Van Deerlin VM.
    Arch Neurol; 2011 Apr 15; 68(4):488-97. PubMed ID: 21482928
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  • 10. 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 Apr 15; 49(6):557-564. PubMed ID: 33486486
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  • 13. Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family.
    Sieben A, Van Mossevelde S, Wauters E, Engelborghs S, van der Zee J, Van Langenhove T, Santens P, Praet M, Boon P, Miatton M, Van Hoecke S, Vandenbulcke M, Vandenberghe R, Cras P, Cruts M, De Deyn PP, Van Broeckhoven C, Martin JJ.
    Alzheimers Res Ther; 2018 Jan 22; 10(1):7. PubMed ID: 29370838
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  • 14. Plasma Small Extracellular Vesicles with Complement Alterations in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration.
    Bellini S, Saraceno C, Benussi L, Squitti R, Cimini S, Ricci M, Canafoglia L, Coppola C, Puoti G, Ferrari C, Longobardi A, Nicsanu R, Lombardi M, D'Arrigo G, Verderio C, Binetti G, Rossi G, Ghidoni R.
    Cells; 2022 Jan 30; 11(3):. PubMed ID: 35159297
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  • 17. Promoter DNA methylation regulates progranulin expression and is altered in FTLD.
    Banzhaf-Strathmann J, Claus R, Mücke O, Rentzsch K, van der Zee J, Engelborghs S, De Deyn PP, Cruts M, van Broeckhoven C, Plass C, Edbauer D.
    Acta Neuropathol Commun; 2013 May 13; 1():16. PubMed ID: 24252647
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  • 18. 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 May 13; 55(3):1167-1174. PubMed ID: 27767988
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  • 19. 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 13; 54(7):1066-71. PubMed ID: 23687363
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  • 20. Secretory leukocyte protease inhibitor protein regulates the penetrance of frontotemporal lobar degeneration in progranulin mutation carriers.
    Ghidoni R, Flocco R, Paterlini A, Glionna M, Caruana L, Tonoli E, Binetti G, Benussi L.
    J Alzheimers Dis; 2014 Jul 13; 38(3):533-9. PubMed ID: 24018267
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