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Items: 1 to 20 of 108

1.

CHMP2B mutations are rare in French families with frontotemporal lobar degeneration.

Ghanim M, Guillot-Noel L, Pasquier F, Jornea L, Deramecourt V, Dubois B, Le Ber I, Brice A; French Research Network on FTD and FTD/MND.

J Neurol. 2010 Dec;257(12):2032-6. doi: 10.1007/s00415-010-5655-8. Epub 2010 Jul 14.

PMID:
20625756
2.

CHMP2B mutations are not a common cause of frontotemporal lobar degeneration.

Cannon A, Baker M, Boeve B, Josephs K, Knopman D, Petersen R, Parisi J, Dickison D, Adamson J, Snowden J, Neary D, Mann D, Hutton M, Pickering-Brown SM.

Neurosci Lett. 2006 May 1;398(1-2):83-4. Epub 2006 Jan 23.

PMID:
16431024
3.

Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients.

Kaivorinne AL, Krüger J, Udd B, Majamaa K, Remes AM.

Eur J Neurol. 2010 Nov;17(11):1393-5. doi: 10.1111/j.1468-1331.2010.03028.x.

PMID:
20412296
4.

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro.

van der Zee J, Urwin H, Engelborghs S, Bruyland M, Vandenberghe R, Dermaut B, De Pooter T, Peeters K, Santens P, De Deyn PP, Fisher EM, Collinge J, Isaacs AM, Van Broeckhoven C.

Hum Mol Genet. 2008 Jan 15;17(2):313-22. Epub 2007 Oct 22.

5.

Genetic contribution of FUS to frontotemporal lobar degeneration.

Van Langenhove T, van der Zee J, Sleegers K, Engelborghs S, Vandenberghe R, Gijselinck I, Van den Broeck M, Mattheijssens M, Peeters K, De Deyn PP, Cruts M, Van Broeckhoven C.

Neurology. 2010 Feb 2;74(5):366-71. doi: 10.1212/WNL.0b013e3181ccc732.

PMID:
20124201
6.

FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis.

Broustal O, Camuzat A, Guillot-Noël L, Guy N, Millecamps S, Deffond D, Lacomblez L, Golfier V, Hannequin D, Salachas F, Camu W, Didic M, Dubois B, Meininger V, Le Ber I, Brice A; French clinical and genetic research network on FTD/FTD-MND.

J Alzheimers Dis. 2010;22(3):765-9.

PMID:
21158017
7.

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;32(1):13-6. doi: 10.1007/s10571-011-9741-y. Epub 2011 Jul 29.

PMID:
21800185
8.

Brain perfusion patterns in familial frontotemporal lobar degeneration.

Seelaar H, Papma JM, Garraux G, de Koning I, Reijs AE, Valkema R, Rozemuller AJ, Salmon E, van Swieten JC.

Neurology. 2011 Jul 26;77(4):384-92. doi: 10.1212/WNL.0b013e3182270456. Epub 2011 Jul 13.

PMID:
21753175
9.

No association of chromatin-modifying protein 2B with sporadic frontotemporal dementia.

Schumacher A, Friedrich P, Diehl-Schmid J, Ibach B, Eisele T, Laws SM, Förstl H, Kurz A, Riemenschneider M.

Neurobiol Aging. 2007 Nov;28(11):1789-90. Epub 2006 Sep 18.

PMID:
16979267
10.

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

Gijselinck I, Engelborghs S, Maes G, Cuijt I, Peeters K, Mattheijssens M, Joris G, Cras P, Martin JJ, De Deyn PP, Kumar-Singh S, Van Broeckhoven C, Cruts M.

Arch Neurol. 2010 May;67(5):606-16. doi: 10.1001/archneurol.2010.82.

PMID:
20457961
11.

Frontotemporal dementia caused by CHMP2B mutations.

Isaacs AM, Johannsen P, Holm I, Nielsen JE; FReJA consortium.

Curr Alzheimer Res. 2011 May;8(3):246-51. Review.

12.

Screening UBQLN-2 in French frontotemporal lobar degeneration and frontotemporal lobar degeneration-amyotrophic lateral sclerosis patients.

Lattante S, Le Ber I, Camuzat A, Pariente J, Brice A, Kabashi E; French Research Network on FTD and FTD-ALS.

Neurobiol Aging. 2013 Aug;34(8):2078.e5-6. doi: 10.1016/j.neurobiolaging.2013.03.002. Epub 2013 Apr 10.

PMID:
23582661
13.

Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS).

Cox LE, Ferraiuolo L, Goodall EF, Heath PR, Higginbottom A, Mortiboys H, Hollinger HC, Hartley JA, Brockington A, Burness CE, Morrison KE, Wharton SB, Grierson AJ, Ince PG, Kirby J, Shaw PJ.

PLoS One. 2010 Mar 24;5(3):e9872. doi: 10.1371/journal.pone.0009872.

14.

Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His.

van der Zee J, Pirici D, Van Langenhove T, Engelborghs S, Vandenberghe R, Hoffmann M, Pusswald G, Van den Broeck M, Peeters K, Mattheijssens M, Martin JJ, De Deyn PP, Cruts M, Haubenberger D, Kumar-Singh S, Zimprich A, Van Broeckhoven C.

Neurology. 2009 Aug 25;73(8):626-32. doi: 10.1212/WNL.0b013e3181b389d9.

PMID:
19704082
15.

Absence of TARDBP gene mutations in an italian series of patients with frontotemporal lobar degeneration.

Gallone S, Giordana MT, Scarpini E, Rainero I, Rubino E, Fenoglio P, Galimberti D, Grifoni S, Venturelli E, Acutis PL, Peletto S, Maniaci MG, Ferrero P, Zotta M, Pinessi L.

Dement Geriatr Cogn Disord. 2009;28(3):239-43. doi: 10.1159/000241876. Epub 2009 Sep 25.

PMID:
19786775
16.

CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia.

Rizzu P, van Mil SE, Anar B, Rosso SM, Donker Kaat L, Heutink P, van Swieten JC.

Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):944-6.

PMID:
16941655
17.

Genetic causes of frontotemporal degeneration.

See TM, LaMarre AK, Lee SE, Miller BL.

J Geriatr Psychiatry Neurol. 2010 Dec;23(4):260-8. doi: 10.1177/0891988710383574. Epub 2010 Oct 11. Review.

PMID:
20938042
18.

Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration.

Krüger J, Kaivorinne AL, Udd B, Majamaa K, Remes AM.

Eur J Neurol. 2009 Jan;16(1):27-30. doi: 10.1111/j.1468-1331.2008.02272.x. Epub 2008 Nov 25.

PMID:
19049508
19.

Establishing short-term prognosis in Frontotemporal Lobar Degeneration spectrum: role of genetic background and clinical phenotype.

Borroni B, Grassi M, Agosti C, Premi E, Archetti S, Alberici A, Bellelli G, Caimi L, Di Luca M, Padovani A.

Neurobiol Aging. 2010 Feb;31(2):270-9. doi: 10.1016/j.neurobiolaging.2008.04.004. Epub .

PMID:
18495299
20.

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration.

Benajiba L, Le Ber I, Camuzat A, Lacoste M, Thomas-Anterion C, Couratier P, Legallic S, Salachas F, Hannequin D, Decousus M, Lacomblez L, Guedj E, Golfier V, Camu W, Dubois B, Campion D, Meininger V, Brice A; French Clinical and Genetic Research Network on Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration with Motoneuron Disease.

Ann Neurol. 2009 Apr;65(4):470-3. doi: 10.1002/ana.21612.

PMID:
19350673
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