Format
Items per page
Sort by

Send to:

Choose Destination

Results: 20

Related Articles by Review for PubMed (Select 23254636)

1.

C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing.

Le Ber I, Camuzat A, Guillot-Noel L, Hannequin D, Lacomblez L, Golfier V, Puel M, Martinaud O, Deramecourt V, Rivaud-Pechoux S, Millecamps S, Vercelletto M, Couratier P, Sellal F, Pasquier F, Salachas F, Thomas-Antérion C, Didic M, Pariente J, Seilhean D, Ruberg M, Wargon I, Blanc F, Camu W, Michel BF, Berger E, Sauvée M, Thauvin-Robinet C, Mondon K, Tournier-Lasserve E, Goizet C, Fleury M, Viennet G, Verpillat P, Meininger V, Duyckaerts C, Dubois B, Brice A.

J Alzheimers Dis. 2013;34(2):485-99. doi: 10.3233/JAD-121456.

PMID:
23254636
2.

How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?

van Blitterswijk M, DeJesus-Hernandez M, Rademakers R.

Curr Opin Neurol. 2012 Dec;25(6):689-700. doi: 10.1097/WCO.0b013e32835a3efb. Review.

3.

The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype.

Cooper-Knock J, Shaw PJ, Kirby J.

Acta Neuropathol. 2014 Mar;127(3):333-45. doi: 10.1007/s00401-014-1251-9. Epub 2014 Feb 4. Review.

4.

C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis.

Rohrer JD, Isaacs AM, Mizielinska S, Mead S, Lashley T, Wray S, Sidle K, Fratta P, Orrell RW, Hardy J, Holton J, Revesz T, Rossor MN, Warren JD.

Lancet Neurol. 2015 Mar;14(3):291-301. doi: 10.1016/S1474-4422(14)70233-9. Epub 2015 Jan 29. Review. Erratum in: Lancet Neurol. 2015 Apr;14(4):350.

PMID:
25638642
5.

Frontotemporal lobar degeneration: epidemiology, pathology, diagnosis and management.

Seltman RE, Matthews BR.

CNS Drugs. 2012 Oct 1;26(10):841-70. doi: 10.2165/11640070-000000000-00000. Review.

PMID:
22950490
6.

Tale of two diseases: amyotrophic lateral sclerosis and frontotemporal dementia.

Verma A.

Neurol India. 2014 Jul-Aug;62(4):347-51. doi: 10.4103/0028-3886.141174. Review.

7.

Genetics of frontotemporal lobar degeneration: an up-date and diagnosis algorithm.

Le Ber I.

Rev Neurol (Paris). 2013 Oct;169(10):811-9. doi: 10.1016/j.neurol.2013.07.014. Epub 2013 Sep 4. Review.

PMID:
24011980
8.

C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia.

Cruts M, Engelborghs S, van der Zee J, Van Broeckhoven C.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
2015 Jan 8.

9.

Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion.

Fong JC, Karydas AM, Goldman JS.

Alzheimers Res Ther. 2012 Jul 19;4(4):27. doi: 10.1186/alzrt130. eCollection 2012. Review.

10.

C9ORF72 mutations in neurodegenerative diseases.

Liu Y, Yu JT, Zong Y, Zhou J, Tan L.

Mol Neurobiol. 2014 Feb;49(1):386-98. doi: 10.1007/s12035-013-8528-1. Epub 2013 Aug 10. Review.

PMID:
23934648
11.

[Genetic coherence between hereditary amyotrophic lateral sclerosis and frontotemporal dementia].

Gjerde KV, Tysnes OB.

Tidsskr Nor Laegeforen. 2014 Feb 11;134(3):302-6. doi: 10.4045/tidsskr.13.0049. Review. Norwegian.

12.

The clinical and pathological phenotypes of frontotemporal dementia with C9ORF72 mutations.

Liu Y, Yu JT, Sun FR, Ou JR, Qu SB, Tan L.

J Neurol Sci. 2013 Dec 15;335(1-2):26-35. doi: 10.1016/j.jns.2013.09.013. Epub 2013 Sep 17. Review.

PMID:
24090760
13.

C9orf72; abnormal RNA expression is the key.

Heutink P, Jansen IE, Lynes EM.

Exp Neurol. 2014 Dec;262 Pt B:102-10. doi: 10.1016/j.expneurol.2014.05.020. Epub 2014 May 27. Review.

PMID:
24873727
14.

Frontotemporal dementia.

Perry DC, Miller BL.

Semin Neurol. 2013 Sep;33(4):336-41. doi: 10.1055/s-0033-1359316. Epub 2013 Nov 14. Review.

PMID:
24234354
15.

Biomarker development for C9orf72 repeat expansion in ALS.

Mendez EF, Sattler R.

Brain Res. 2015 May 14;1607:26-35. doi: 10.1016/j.brainres.2014.09.041. Epub 2014 Sep 27. Review.

PMID:
25261695
16.

GRN-Related Frontotemporal Dementia .

Hsiung GYR, Feldman HH.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
2007 Sep 7 [updated 2013 Mar 14].

17.

Frontotemporal dementia: a bridge between dementia and neuromuscular disease.

Ng AS, Rademakers R, Miller BL.

Ann N Y Acad Sci. 2015 Mar;1338:71-93. doi: 10.1111/nyas.12638. Epub 2014 Dec 30. Review.

PMID:
25557955
18.

Presymptomatic studies in genetic frontotemporal dementia.

Rohrer JD, Warren JD, Fox NC, Rossor MN.

Rev Neurol (Paris). 2013 Oct;169(10):820-4. doi: 10.1016/j.neurol.2013.07.010. Epub 2013 Sep 4. Review.

19.

Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not.

Hardy J, Rogaeva E.

Exp Neurol. 2014 Dec;262 Pt B:75-83. doi: 10.1016/j.expneurol.2013.11.006. Epub 2013 Nov 15. Review.

PMID:
24246281
20.

Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD).

Lattante S, Ciura S, Rouleau GA, Kabashi E.

Trends Genet. 2015 May;31(5):263-273. doi: 10.1016/j.tig.2015.03.005. Epub 2015 Apr 10. Review.

PMID:
25869998
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk