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Items: 1 to 20 of 105

1.

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
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.

[Differential diagnosis of chorea].

Shimohata T, Nishizawa M.

Brain Nerve. 2009 Aug;61(8):963-71. Review. Japanese.

PMID:
19697886
4.

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
5.

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
6.

Huntington's disease phenocopy syndromes.

Wild EJ, Tabrizi SJ.

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

PMID:
17992089
7.

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
8.

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
9.

Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene.

Sułek-Piatkowska A, Krysa W, Zdzienicka E, Szirkowiec W, Hoffman-Zacharska D, Rajkiewicz M, Fidziańska E, Kowalska G, Zaremba J.

Neurol Neurochir Pol. 2008 May-Jun;42(3):203-9.

PMID:
18651325
10.
11.

Patients with features similar to Huntington's disease, without CAG expansion in huntingtin.

Rosenblatt A, Ranen NG, Rubinsztein DC, Stine OC, Margolis RL, Wagster MV, Becher MW, Rosser AE, Leggo J, Hodges JR, ffrench-Constant CK, Sherr M, Franz ML, Abbott MH, Ross CA.

Neurology. 1998 Jul;51(1):215-20.

PMID:
9674805
12.

[From gene to disease; HD gene and Huntington disease].

Maat-Kievit JA, Losekoot M, Roos RA.

Ned Tijdschr Geneeskd. 2001 Nov 3;145(44):2120-3. Review. Dutch.

PMID:
11723754
13.

Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype.

Krause A, Mitchell C, Essop F, Tager S, Temlett J, Stevanin G, Ross C, Rudnicki D, Margolis R.

Am J Med Genet B Neuropsychiatr Genet. 2015 Oct;168(7):573-85. doi: 10.1002/ajmg.b.32332. Epub 2015 Jun 16.

14.

Towards a transgenic model of Huntington's disease in a non-human primate.

Yang SH, Cheng PH, Banta H, Piotrowska-Nitsche K, Yang JJ, Cheng EC, Snyder B, Larkin K, Liu J, Orkin J, Fang ZH, Smith Y, Bachevalier J, Zola SM, Li SH, Li XJ, Chan AW.

Nature. 2008 Jun 12;453(7197):921-4. doi: 10.1038/nature06975. Epub 2008 May 18.

15.

Huntington's disease: genetic heterogeneity in black African patients.

Magazi DS, Krause A, Bonev V, Moagi M, Iqbal Z, Dludla M, van der Meyden CH.

S Afr Med J. 2008 Mar;98(3):200-3.

PMID:
18350222
16.

Normal CAG repeats in the Huntington gene in a family with benign familial chorea.

Meszaros K, Brücke T, Fuchs K, Gerhard E, Sieghart W, vanDer Meer CH, Aschauer HN.

Psychiatr Genet. 1996 Summer;6(2):91-4.

PMID:
8840396
17.

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
18.

Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype.

Costa Mdo C, Teixeira-Castro A, Constante M, Magalhães M, Magalhães P, Cerqueira J, Vale J, Passão V, Barbosa C, Robalo C, Coutinho P, Barros J, Santos MM, Sequeiros J, Maciel P.

J Hum Genet. 2006;51(8):645-51. Epub 2006 Jul 21.

19.

Genetically confirmed Huntington's disease masquerading as motor neuron disease.

Kanai K, Kuwabara S, Sawai S, Nakata M, Misawa S, Isose S, Hirano S, Kawaguchi N, Katayama K, Hattori T.

Mov Disord. 2008 Apr 15;23(5):748-51. doi: 10.1002/mds.21937.

PMID:
18186118
20.

Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteins.

Huang CC, Faber PW, Persichetti F, Mittal V, Vonsattel JP, MacDonald ME, Gusella JF.

Somat Cell Mol Genet. 1998 Jul;24(4):217-33.

PMID:
10410676

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