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Results: 1 to 20 of 128

Similar articles for PubMed (Select 20183548)

1.

Of brain and bone: the unusual case of Dr. A.

Narvid J, Gorno-Tempini ML, Slavotinek A, Dearmond SJ, Cha YH, Miller BL, Rankin K.

Neurocase. 2009 Jun;15(3):190-205. doi: 10.1080/13554790802632967.

2.

Right anterior temporal lobe dysfunction underlies theory of mind impairments in semantic dementia.

Irish M, Hodges JR, Piguet O.

Brain. 2014 Apr;137(Pt 4):1241-53. doi: 10.1093/brain/awu003. Epub 2014 Feb 12.

3.

[Frontal dementia or dementia praecox? A case report of a psychotic disorder with a severe decline].

Vanderzeypen F, Bier JC, Genevrois C, Mendlewicz J, Lotstra F.

Encephale. 2003 Mar-Apr;29(2):172-80. French.

PMID:
14567169
4.

Clinical characterization of bvFTD due to FUS neuropathology.

Lee SE, Seeley WW, Poorzand P, Rademakers R, Karydas A, Stanley CM, Miller BL, Rankin KP.

Neurocase. 2012;18(4):305-17. doi: 10.1080/13554794.2011.604637. Epub 2011 Nov 7.

5.

My belief or yours? Differential theory of mind deficits in frontotemporal dementia and Alzheimer's disease.

Le Bouc R, Lenfant P, Delbeuck X, Ravasi L, Lebert F, Semah F, Pasquier F.

Brain. 2012 Oct;135(Pt 10):3026-38. doi: 10.1093/brain/aws237.

6.

Mentalising music in frontotemporal dementia.

Downey LE, Blezat A, Nicholas J, Omar R, Golden HL, Mahoney CJ, Crutch SJ, Warren JD.

Cortex. 2013 Jul-Aug;49(7):1844-55. doi: 10.1016/j.cortex.2012.09.011. Epub 2012 Oct 5.

7.

Distinct anatomical subtypes of the behavioural variant of frontotemporal dementia: a cluster analysis study.

Whitwell JL, Przybelski SA, Weigand SD, Ivnik RJ, Vemuri P, Gunter JL, Senjem ML, Shiung MM, Boeve BF, Knopman DS, Parisi JE, Dickson DW, Petersen RC, Jack CR Jr, Josephs KA.

Brain. 2009 Nov;132(Pt 11):2932-46. doi: 10.1093/brain/awp232. Epub 2009 Sep 17.

8.

[Frontotemporal dementia: a review].

Chauvire V, Even C, Thuile J, Rouillon F, Guelfi JD.

Encephale. 2007 Dec;33(6):933-40. doi: 10.1016/j.encep.2006.12.001. Epub 2007 Sep 6. Review. French.

PMID:
18789785
9.

Disturbance of emotion processing in frontotemporal dementia: a synthesis of cognitive and neuroimaging findings.

Kumfor F, Piguet O.

Neuropsychol Rev. 2012 Sep;22(3):280-97. doi: 10.1007/s11065-012-9201-6. Epub 2012 May 11. Review.

PMID:
22577002
10.

Grey and white matter changes across the amyotrophic lateral sclerosis-frontotemporal dementia continuum.

Lillo P, Mioshi E, Burrell JR, Kiernan MC, Hodges JR, Hornberger M.

PLoS One. 2012;7(8):e43993. doi: 10.1371/journal.pone.0043993. Epub 2012 Aug 29.

11.

Cognitive and behavioral profile in a case of right anterior temporal lobe neurodegeneration.

Gorno-Tempini ML, Rankin KP, Woolley JD, Rosen HJ, Phengrasamy L, Miller BL.

Cortex. 2004 Sep-Dec;40(4-5):631-44.

PMID:
15505973
12.

A novel EXT1 gene mutation causing hereditary multiple exostoses in a Chinese pedigree.

Li Y, Wang J, Li H, Wang J, Wang X, Fu Q.

Pathology. 2010 Jan;42(1):91-3. doi: 10.3109/00313020903434694. No abstract available.

PMID:
20025490
13.

[Hereditary multiple exostoses. Molecular genetic analysis of the EXT1 gene in an unusual family].

Heinritz W, Pretzsch M, Koall S, Matzen PF, Froster UG.

Orthopade. 2005 May;34(5):470-6. German.

PMID:
15739063
14.

Facial emotion recognition and cerebral white matter lesions in myotonic dystrophy type 1.

Kobayakawa M, Tsuruya N, Takeda A, Suzuki A, Kawamura M.

J Neurol Sci. 2010 Mar 15;290(1-2):48-51. doi: 10.1016/j.jns.2009.11.011. Epub 2009 Dec 16.

PMID:
20006353
15.

Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.

Vanita V, Sperling K, Sandhu HS, Sandhu PS, Singh JR.

Genet Test Mol Biomarkers. 2009 Feb;13(1):43-9. doi: 10.1089/gtmb.2008.0055.

PMID:
19309273
16.

[A new EXT2 mutation in a Chinese family with hereditary multiple exostoses].

Zhao WQ, Song SJ, Wei Q, Qiao J.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Jun;26(3):241-4. doi: 10.3760/cma.j.issn.1003-9406.2009.03.001. Chinese.

PMID:
19504431
17.

Three novel EXT1 and EXT2 gene mutations in Taiwanese patients with multiple exostoses.

Chen WC, Chi CH, Chuang CC, Jou IM.

J Formos Med Assoc. 2006 May;105(5):434-7.

PMID:
16638657
18.

A splice mutation and mRNA decay of EXT2 provoke hereditary multiple exostoses.

Tian C, Yan R, Wen S, Li X, Li T, Cai Z, Li X, Du H, Chen H.

PLoS One. 2014 Apr 11;9(4):e94848. doi: 10.1371/journal.pone.0094848. eCollection 2014.

19.

Extensive left temporal pole damage does not impact on theory of mind abilities.

Michel C, Dricot L, Lhommel R, Grandin C, Ivanoiu A, Pillon A, Samson D.

J Cogn Neurosci. 2013 Dec;25(12):2025-46. doi: 10.1162/jocn_a_00488. Epub 2013 Sep 18.

PMID:
24047381
20.

Atrophy patterns in histologic vs clinical groupings of frontotemporal lobar degeneration.

Pereira JM, Williams GB, Acosta-Cabronero J, Pengas G, Spillantini MG, Xuereb JH, Hodges JR, Nestor PJ.

Neurology. 2009 May 12;72(19):1653-60. doi: 10.1212/WNL.0b013e3181a55fa2.

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