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Results: 17

Cited In for PubMed (Select 12476321)

1.

Recent insights into the involvement of progranulin in frontotemporal dementia.

Sun L, Eriksen JL.

Curr Neuropharmacol. 2011 Dec;9(4):632-42. doi: 10.2174/157015911798376361.

2.

Genetics of frontotemporal lobar degeneration.

Galimberti D, Scarpini E.

Front Neurol. 2012 Apr 10;3:52. doi: 10.3389/fneur.2012.00052. eCollection 2012.

3.

Genetics and biology of Alzheimer's disease and frontotemporal lobar degeneration.

Galimberti D, Scarpini E.

Int J Clin Exp Med. 2010 May 15;3(2):129-43.

4.

Update on recent molecular and genetic advances in frontotemporal lobar degeneration.

Bigio EH.

J Neuropathol Exp Neurol. 2008 Jul;67(7):635-48. doi: 10.1097/NEN.0b013e31817d751c. Review.

5.

Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene.

Rohrer JD, Warren JD, Omar R, Mead S, Beck J, Revesz T, Holton J, Stevens JM, Al-Sarraj S, Pickering-Brown SM, Hardy J, Fox NC, Collinge J, Warrington EK, Rossor MN.

Arch Neurol. 2008 Apr;65(4):506-13. doi: 10.1001/archneur.65.4.506.

6.

Refining frontotemporal dementia with parkinsonism linked to chromosome 17: introducing FTDP-17 (MAPT) and FTDP-17 (PGRN).

Boeve BF, Hutton M.

Arch Neurol. 2008 Apr;65(4):460-4. doi: 10.1001/archneur.65.4.460. Review.

7.

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.

Beck J, Rohrer JD, Campbell T, Isaacs A, Morrison KE, Goodall EF, Warrington EK, Stevens J, Revesz T, Holton J, Al-Sarraj S, King A, Scahill R, Warren JD, Fox NC, Rossor MN, Collinge J, Mead S.

Brain. 2008 Mar;131(Pt 3):706-20. doi: 10.1093/brain/awm320. Epub 2008 Jan 29.

8.

The two faces of protein misfolding: gain- and loss-of-function in neurodegenerative diseases.

Winklhofer KF, Tatzelt J, Haass C.

EMBO J. 2008 Jan 23;27(2):336-49. doi: 10.1038/sj.emboj.7601930. Review.

9.

Prominent phenotypic variability associated with mutations in Progranulin.

Kelley BJ, Haidar W, Boeve BF, Baker M, Graff-Radford NR, Krefft T, Frank AR, Jack CR Jr, Shiung M, Knopman DS, Josephs KA, Parashos SA, Rademakers R, Hutton M, Pickering-Brown S, Adamson J, Kuntz KM, Dickson DW, Parisi JE, Smith GE, Ivnik RJ, Petersen RC.

Neurobiol Aging. 2009 May;30(5):739-51. Epub 2007 Oct 18.

10.

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype.

Mackenzie IR, Baborie A, Pickering-Brown S, Du Plessis D, Jaros E, Perry RH, Neary D, Snowden JS, Mann DM.

Acta Neuropathol. 2006 Nov;112(5):539-49. Epub 2006 Sep 26.

11.

Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies.

Sampathu DM, Neumann M, Kwong LK, Chou TT, Micsenyi M, Truax A, Bruce J, Grossman M, Trojanowski JQ, Lee VM.

Am J Pathol. 2006 Oct;169(4):1343-52.

12.

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin.

Mukherjee O, Pastor P, Cairns NJ, Chakraverty S, Kauwe JS, Shears S, Behrens MI, Budde J, Hinrichs AL, Norton J, Levitch D, Taylor-Reinwald L, Gitcho M, Tu PH, Tenenholz Grinberg L, Liscic RM, Armendariz J, Morris JC, Goate AM.

Ann Neurol. 2006 Sep;60(3):314-22.

13.

Characteristics of frontotemporal dementia patients with a Progranulin mutation.

Huey ED, Grafman J, Wassermann EM, Pietrini P, Tierney MC, Ghetti B, Spina S, Baker M, Hutton M, Elder JW, Berger SL, Heflin KA, Hardy J, Momeni P.

Ann Neurol. 2006 Sep;60(3):374-80.

14.

Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease.

Mackenzie IR, Butland SL, Devon RS, Dwosh E, Feldman H, Lindholm C, Neal SJ, Ouellette BF, Leavitt BR.

BMC Neurol. 2006 Aug 31;6:32.

15.

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).

Wszolek ZK, Tsuboi Y, Ghetti B, Pickering-Brown S, Baba Y, Cheshire WP.

Orphanet J Rare Dis. 2006 Aug 9;1:30. Review.

16.

Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample.

Rademakers R, Cruts M, Sleegers K, Dermaut B, Theuns J, Aulchenko Y, Weckx S, De Pooter T, Van den Broeck M, Corsmit E, De Rijk P, Del-Favero J, van Swieten J, van Duijn CM, Van Broeckhoven C.

Am J Hum Genet. 2005 Oct;77(4):643-52. Epub 2005 Aug 30.

17.

Evidence for defective retinoid transport and function in late onset Alzheimer's disease.

Goodman AB, Pardee AB.

Proc Natl Acad Sci U S A. 2003 Mar 4;100(5):2901-5. Epub 2003 Feb 25. Review.

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