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Items: 1 to 20 of 187

1.

Huntington's disease phenocopy syndromes.

Wild EJ, Tabrizi SJ.

Curr Opin Neurol. 2007 Dec;20(6):681-7. Review.

PMID:
17992089
2.

The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test.

Schneider SA, Walker RH, Bhatia KP.

Nat Clin Pract Neurol. 2007 Sep;3(9):517-25. Review.

PMID:
17805246
3.

Huntington's disease phenocopies are clinically and genetically heterogeneous.

Wild EJ, Mudanohwo EE, Sweeney MG, Schneider SA, Beck J, Bhatia KP, Rossor MN, Davis MB, Tabrizi SJ.

Mov Disord. 2008 Apr 15;23(5):716-20. doi: 10.1002/mds.21915.

PMID:
18181206
4.

Huntington's disease and Huntington's disease-like syndromes: an overview.

Gövert F, Schneider SA.

Curr Opin Neurol. 2013 Aug;26(4):420-7. doi: 10.1097/WCO.0b013e3283632d90. Review.

PMID:
23812307
5.

The differential diagnosis of chorea.

Wild EJ, Tabrizi SJ.

Pract Neurol. 2007 Nov;7(6):360-73. Review.

PMID:
18024776
6.

Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype.

Rodrigues GR, Walker RH, Bader B, Danek A, Brice A, Cazeneuve C, Russaouen O, Lopes-Cendes I, Marques Jr W, Tumas V.

Arq Neuropsiquiatr. 2011 Jun;69(3):419-23.

7.

Differential diagnosis of Huntington's disease: what the clinician should know.

Cardoso F.

Neurodegener Dis Manag. 2014;4(1):67-72. doi: 10.2217/nmt.13.78.

PMID:
24640980
8.

Huntington's disease look-alikes.

Schneider SA, Bhatia KP.

Handb Clin Neurol. 2011;100:101-12. doi: 10.1016/B978-0-444-52014-2.00005-7. Review.

PMID:
21496572
9.

Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion.

Koutsis G, Karadima G, Pandraud A, Sweeney MG, Paudel R, Houlden H, Wood NW, Panas M.

J Neurol. 2012 Sep;259(9):1874-8.

PMID:
22297462
10.

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.

Stevanin G, Fujigasaki H, Lebre AS, Camuzat A, Jeannequin C, Dode C, Takahashi J, San C, Bellance R, Brice A, Durr A.

Brain. 2003 Jul;126(Pt 7):1599-603. Epub 2003 May 6.

PMID:
12805114
11.

Neuropathological diagnosis and CAG repeat expansion in Huntington's disease.

Xuereb JH, MacMillan JC, Snell R, Davies P, Harper PS.

J Neurol Neurosurg Psychiatry. 1996 Jan;60(1):78-81.

12.

Phenotypic homogeneity of the Huntington disease-like presentation in a SCA17 family.

Schneider SA, van de Warrenburg BP, Hughes TD, Davis M, Sweeney M, Wood N, Quinn NP, Bhatia KP.

Neurology. 2006 Nov 14;67(9):1701-3.

PMID:
17101913
13.

Huntington disease and Huntington disease-like in a case series from Brazil.

Castilhos RM, Souza AF, Furtado GV, Gheno TC, Silva AL, Vargas FR, Lima MA, Barsottini O, Pedroso JL, Godeiro C Jr, Salarini D, Pereira ET, Lin K, Toralles MB, Saute JA, Rieder CR, Quintas M, Sequeiros J, Alonso I, Saraiva-Pereira ML, Jardim LB.

Clin Genet. 2014 Oct;86(4):373-7. doi: 10.1111/cge.12283. Epub 2013 Oct 17.

PMID:
24102565
14.

Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

MacMillan JC, Davies P, Harper PS.

J Neurol Neurosurg Psychiatry. 1995 Apr;58(4):496-8.

15.

Huntington disease phenocopy is a familial prion disease.

Moore RC, Xiang F, Monaghan J, Han D, Zhang Z, Edström L, Anvret M, Prusiner SB.

Am J Hum Genet. 2001 Dec;69(6):1385-8. Epub 2001 Oct 9.

16.

[Importance of the number of trinucleotide repeat expansions in the clinical manifestations of Huntington's chorea].

Vojvodić N, Culjković B, Romac S, Stojković O, Sternić N, Sokić D, Kostić VS.

Srp Arh Celok Lek. 1998 Mar-Apr;126(3-4):77-82. Serbian.

PMID:
9863360
17.

Should spinocerebellar ataxias be included in the differential diagnosis for Huntington's diseases-like syndromes?

Pedroso JL, de Freitas ME, Albuquerque MV, Saraiva-Pereira ML, Jardim LB, Barsottini OG.

J Neurol Sci. 2014 Dec 15;347(1-2):356-8. doi: 10.1016/j.jns.2014.09.050. Epub 2014 Oct 8.

PMID:
25456461
18.

[Diagnostic DNA testing for Huntington disease].

Helle JR, Braathen GJ, Skodje T, Berg K.

Tidsskr Nor Laegeforen. 2000 Aug 30;120(20):2408-10. Norwegian.

19.

Huntington's disease-like and ataxia syndromes: identification of a family with a de novo SCA17/TBP mutation.

Bech S, Petersen T, Nørremølle A, Gjedde A, Ehlers L, Eiberg H, Hjermind LE, Hasholt L, Lundorf E, Nielsen JE.

Parkinsonism Relat Disord. 2010 Jan;16(1):12-5. doi: 10.1016/j.parkreldis.2009.06.006.

PMID:
19595623
20.

Late onset levodopa responsive Huntington's disease with minimal chorea masquerading as Parkinson plus syndrome.

Reuter I, Hu MT, Andrews TC, Brooks DJ, Clough C, Chaudhuri KR.

J Neurol Neurosurg Psychiatry. 2000 Feb;68(2):238-41.

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