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Items: 1 to 20 of 430

1.

CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients.

Stevanin G, Camuzat A, Holmes SE, Julien C, Sahloul R, Dodé C, Hahn-Barma V, Ross CA, Margolis RL, Durr A, Brice A.

Neurology. 2002 Mar 26;58(6):965-7.

PMID:
11914418
2.

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.

3.

Huntington's Disease-like 2 (HDL2) in North America and Japan.

Margolis RL, Holmes SE, Rosenblatt A, Gourley L, O'Hearn E, Ross CA, Seltzer WK, Walker RH, Ashizawa T, Rasmussen A, Hayden M, Almqvist EW, Harris J, Fahn S, MacDonald ME, Mysore J, Shimohata T, Tsuji S, Potter N, Nakaso K, Adachi Y, Nakashima K, Bird T, Krause A, Greenstein P.

Ann Neurol. 2004 Nov;56(5):670-4. Erratum in: Ann Neurol. 2004 Dec;56(6):911.

PMID:
15468075
4.

Huntington's disease-like 2 in Brazil--report of 4 patients.

Rodrigues GG, Walker RH, Brice A, Cazeneuve C, Russaouen O, Teive HA, Munhoz RP, Becker N, Raskin S, Werneck LC, Junior WM, Tumas V.

Mov Disord. 2008 Nov 15;23(15):2244-7. doi: 10.1002/mds.22223.

PMID:
18816802
5.

[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
6.

Huntington disease-like 2: the first patient with apparent European ancestry.

Santos C, Wanderley H, Vedolin L, Pena SD, Jardim L, Sequeiros J.

Clin Genet. 2008 May;73(5):480-5. doi: 10.1111/j.1399-0004.2008.00981.x. Epub 2008 Mar 12.

PMID:
18341606
7.

Expansion of a (CAG)n repeat region in a sporadic case of HD.

Bozza A, Malagù S, Calzolari E, Novelletto A, Pavoni M, del Senno L.

Acta Neurol Scand. 1995 Aug;92(2):132-4.

PMID:
7484060
8.

Absence of unidentified CAG repeat expansion in patients with Huntington's disease-like phenotype.

Vuillaume I, Meynieu P, Schraen-Maschke S, Destée A, Sablonnière B.

J Neurol Neurosurg Psychiatry. 2000 May;68(5):672-5.

9.

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
10.

Huntington's disease as caused by 34 CAG repeats.

Andrich J, Arning L, Wieczorek S, Kraus PH, Gold R, Saft C.

Mov Disord. 2008 Apr 30;23(6):879-81. doi: 10.1002/mds.21958.

PMID:
18307262
11.

A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion.

Margolis RL, O'Hearn E, Rosenblatt A, Willour V, Holmes SE, Franz ML, Callahan C, Hwang HS, Troncoso JC, Ross CA.

Ann Neurol. 2001 Dec;50(6):373-80.

PMID:
11761463
12.

Clinical and genetic characteristics of Mexican Huntington's disease patients.

Alonso ME, Ochoa A, Boll MC, Sosa AL, Yescas P, López M, Macias R, Familiar I, Rasmussen A.

Mov Disord. 2009 Oct 15;24(13):2012-5. doi: 10.1002/mds.22737.

PMID:
19672992
13.

Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype.

Bauer I, Gencik M, Laccone F, Peters H, Weber BH, Feder EH, Weirich H, Morris-Rosendahl DJ, Rolfs A, Gencikova A, Bauer P, Wenning GK, Epplen JT, Holmes SE, Margolis RL, Ross CA, Riess O.

Ann Neurol. 2002 May;51(5):662. No abstract available.

PMID:
12112122
14.

Linkage disequilibrium between the expanded (CAG)n repeat and an allele of the adjacent (CCG)n repeat in Huntington's disease patients of Greek origin.

Yapijakis C, Vassilopoulos D, Tzagournisakis M, Maris T, Fesdjian C, Papageorgiou C, Plaitakis A.

Eur J Hum Genet. 1995;3(4):228-34.

PMID:
8528671
15.

A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion.

Margolis RL, O'Hearn E, Rosenblatt A, Willour V, Holmes SE, Franz ML, Callahan C, Hwang HS, Troncoso JC, Ross CA.

Ann Neurol. 2001 Sep;50(3):373-80. Corrected and republished in: Ann Neurol. 2001 Dec;50(6):373-80.

PMID:
11558794
16.

Analysis of the (CAG)n repeat causing Huntington's disease in a Mexican population.

Alonso ME, Yescas P, Cisneros B, Martínez C, Silva G, Ochoa A, Montañez C.

Clin Genet. 1997 Apr;51(4):225-30.

PMID:
9184242
17.

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.

18.

A South African mixed ancestry family with Huntington disease-like 2: clinical and genetic features.

Bardien S, Abrahams F, Soodyall H, van der Merwe L, Greenberg J, Brink T, Carr J.

Mov Disord. 2007 Oct 31;22(14):2083-9.

PMID:
17708569
19.

Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains.

Persichetti F, Srinidhi J, Kanaley L, Ge P, Myers RH, D'Arrigo K, Barnes GT, MacDonald ME, Vonsattel JP, Gusella JF, et al.

Neurobiol Dis. 1994 Dec;1(3):159-66.

PMID:
9173995
20.

Polymorphism of HD and UCHL-1 genes in Huntington's disease.

Xu EH, Tang Y, Li D, Jia JP.

J Clin Neurosci. 2009 Nov;16(11):1473-7. doi: 10.1016/j.jocn.2009.03.027. Epub 2009 Aug 14.

PMID:
19683447
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