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Results: 1 to 20 of 45

1.

Primary progressive aphasia: A dementia of the language network.

Mesulam M.

Dement Neuropsychol. 2013 Jan 1;7(1):2-9.

PMID:
24707349
[PubMed]
Free PMC Article
2.

Frontotemporal lobar degeneration: current perspectives.

Riedl L, Mackenzie IR, Förstl H, Kurz A, Diehl-Schmid J.

Neuropsychiatr Dis Treat. 2014 Feb 13;10:297-310. doi: 10.2147/NDT.S38706. eCollection 2014. Review.

PMID:
24600223
[PubMed]
Free PMC Article
3.

Biology and genetics of prions causing neurodegeneration.

Prusiner SB.

Annu Rev Genet. 2013;47:601-23. doi: 10.1146/annurev-genet-110711-155524. Review.

PMID:
24274755
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

The epidemiology of frontotemporal dementia.

Onyike CU, Diehl-Schmid J.

Int Rev Psychiatry. 2013 Apr;25(2):130-7. doi: 10.3109/09540261.2013.776523. Review.

PMID:
23611343
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Progranulin mutations as risk factors for Alzheimer disease.

Perry DC, Lehmann M, Yokoyama JS, Karydas A, Lee JJ, Coppola G, Grinberg LT, Geschwind D, Seeley WW, Miller BL, Rosen H, Rabinovici G.

JAMA Neurol. 2013 Jun;70(6):774-8. doi: 10.1001/2013.jamaneurol.393. Review.

PMID:
23609919
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

C9orf72 hexanucleotide repeat expansions in clinical Alzheimer disease.

Harms M, Benitez BA, Cairns N, Cooper B, Cooper P, Mayo K, Carrell D, Faber K, Williamson J, Bird T, Diaz-Arrastia R, Foroud TM, Boeve BF, Graff-Radford NR, Mayeux R, Chakraverty S, Goate AM, Cruchaga C; NIA-LOAD/NCRAD Family Study Consortium.

JAMA Neurol. 2013 Jun;70(6):736-41. doi: 10.1001/2013.jamaneurol.537.

PMID:
23588422
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Circulating progranulin as a biomarker for neurodegenerative diseases.

Ghidoni R, Paterlini A, Benussi L.

Am J Neurodegener Dis. 2012;1(2):180-90. Epub 2012 Aug 2.

PMID:
23383391
[PubMed]
Free PMC Article
8.

C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo Clinic.

Wojtas A, Heggeli KA, Finch N, Baker M, Dejesus-Hernandez M, Younkin SG, Dickson DW, Graff-Radford NR, Rademakers R.

Am J Neurodegener Dis. 2012;1(1):107-18. Epub 2012 May 16.

PMID:
23383383
[PubMed]
Free PMC Article
9.

Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysis.

Dobson-Stone C, Luty AA, Thompson EM, Blumbergs P, Brooks WS, Short CL, Field CD, Panegyres PK, Hecker J, Solski JA, Blair IP, Fullerton JM, Halliday GM, Schofield PR, Kwok JB.

Acta Neuropathol. 2013 Apr;125(4):523-33. doi: 10.1007/s00401-013-1078-9. Epub 2013 Jan 22.

PMID:
23338750
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Mechanisms of granulin deficiency: lessons from cellular and animal models.

Kleinberger G, Capell A, Haass C, Van Broeckhoven C.

Mol Neurobiol. 2013 Feb;47(1):337-60. doi: 10.1007/s12035-012-8380-8. Epub 2012 Dec 13. Review.

PMID:
23239020
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Tau pathology in frontotemporal lobar degeneration with C9ORF72 hexanucleotide repeat expansion.

Bieniek KF, Murray ME, Rutherford NJ, Castanedes-Casey M, DeJesus-Hernandez M, Liesinger AM, Baker MC, Boylan KB, Rademakers R, Dickson DW.

Acta Neuropathol. 2013 Feb;125(2):289-302. doi: 10.1007/s00401-012-1048-7. Epub 2012 Sep 28.

PMID:
23053135
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Neuropsychiatric features of C9orf72-associated behavioral variant frontotemporal dementia and frontotemporal dementia with motor neuron disease.

Takada LT, Sha SJ.

Alzheimers Res Ther. 2012 Oct 3;4(5):38. doi: 10.1186/alzrt141. eCollection 2012. Review.

PMID:
23034079
[PubMed]
Free PMC Article
13.

The genetics and neuropathology of frontotemporal lobar degeneration.

Sieben A, Van Langenhove T, Engelborghs S, Martin JJ, Boon P, Cras P, De Deyn PP, Santens P, Van Broeckhoven C, Cruts M.

Acta Neuropathol. 2012 Sep;124(3):353-72. doi: 10.1007/s00401-012-1029-x. Epub 2012 Aug 14. Review.

PMID:
22890575
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Progranulin: a proteolytically processed protein at the crossroads of inflammation and neurodegeneration.

Cenik B, Sephton CF, Kutluk Cenik B, Herz J, Yu G.

J Biol Chem. 2012 Sep 21;287(39):32298-306. Epub 2012 Aug 2. Review.

PMID:
22859297
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

The non-fluent/agrammatic variant of primary progressive aphasia.

Grossman M.

Lancet Neurol. 2012 Jun;11(6):545-55. doi: 10.1016/S1474-4422(12)70099-6. Epub 2012 May 16. Review.

PMID:
22608668
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage.

Smith KR, Damiano J, Franceschetti S, Carpenter S, Canafoglia L, Morbin M, Rossi G, Pareyson D, Mole SE, Staropoli JF, Sims KB, Lewis J, Lin WL, Dickson DW, Dahl HH, Bahlo M, Berkovic SF.

Am J Hum Genet. 2012 Jun 8;90(6):1102-7. doi: 10.1016/j.ajhg.2012.04.021. Epub 2012 May 17.

PMID:
22608501
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features.

Mahoney CJ, Beck J, Rohrer JD, Lashley T, Mok K, Shakespeare T, Yeatman T, Warrington EK, Schott JM, Fox NC, Rossor MN, Hardy J, Collinge J, Revesz T, Mead S, Warren JD.

Brain. 2012 Mar;135(Pt 3):736-50. doi: 10.1093/brain/awr361.

PMID:
22366791
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families.

Cruchaga C, Haller G, Chakraverty S, Mayo K, Vallania FL, Mitra RD, Faber K, Williamson J, Bird T, Diaz-Arrastia R, Foroud TM, Boeve BF, Graff-Radford NR, St Jean P, Lawson M, Ehm MG, Mayeux R, Goate AM; NIA-LOAD/NCRAD Family Study Consortium.

PLoS One. 2012;7(2):e31039. doi: 10.1371/journal.pone.0031039. Epub 2012 Feb 1. Erratum in: PLoS One. 2012;7(5): doi/10.1371/annotation/c92e16da-7733-421d-b063-1db19488daa6. Haller, Gabe [added]..

PMID:
22312439
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72.

Murray ME, DeJesus-Hernandez M, Rutherford NJ, Baker M, Duara R, Graff-Radford NR, Wszolek ZK, Ferman TJ, Josephs KA, Boylan KB, Rademakers R, Dickson DW.

Acta Neuropathol. 2011 Dec;122(6):673-90. doi: 10.1007/s00401-011-0907-y. Epub 2011 Nov 15.

PMID:
22083254
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations.

Kocerha J, Kouri N, Baker M, Finch N, DeJesus-Hernandez M, Gonzalez J, Chidamparam K, Josephs KA, Boeve BF, Graff-Radford NR, Crook J, Dickson DW, Rademakers R.

BMC Genomics. 2011 Oct 27;12:527. doi: 10.1186/1471-2164-12-527.

PMID:
22032330
[PubMed - indexed for MEDLINE]
Free PMC Article

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