234 related articles for article (PubMed ID: 21755114)
21. 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. PubMed ID: 26079385
[TBL] [Abstract][Full Text] [Related]
22. Polyglutamine (PolyQ) diseases: genetics to treatments.
Fan HC; Ho LI; Chi CS; Chen SJ; Peng GS; Chan TM; Lin SZ; Harn HJ
Cell Transplant; 2014; 23(4-5):441-58. PubMed ID: 24816443
[TBL] [Abstract][Full Text] [Related]
23. 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; 23(5):716-20. PubMed ID: 18181206
[TBL] [Abstract][Full Text] [Related]
24. Chinese patients with Huntington's disease initially presenting with spinocerebellar ataxia.
Dong Y; Sun YM; Liu ZJ; Ni W; Shi SS; Wu ZY
Clin Genet; 2013 Apr; 83(4):380-3. PubMed ID: 22775398
[TBL] [Abstract][Full Text] [Related]
25. 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. PubMed ID: 17805246
[TBL] [Abstract][Full Text] [Related]
26. 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. PubMed ID: 12805114
[TBL] [Abstract][Full Text] [Related]
27. 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. PubMed ID: 11558794
[TBL] [Abstract][Full Text] [Related]
28. Huntington's Disease: Relationship Between Phenotype and Genotype.
Sun YM; Zhang YB; Wu ZY
Mol Neurobiol; 2017 Jan; 54(1):342-348. PubMed ID: 26742514
[TBL] [Abstract][Full Text] [Related]
29. 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. PubMed ID: 11761463
[TBL] [Abstract][Full Text] [Related]
30. Emerging differences between Huntington's disease-like 2 and Huntington's disease: A comparison using MRI brain volumetry.
Anderson DG; Haagensen M; Ferreira-Correia A; Pierson R; Carr J; Krause A; Margolis RL
Neuroimage Clin; 2019; 21():101666. PubMed ID: 30682531
[TBL] [Abstract][Full Text] [Related]
31. 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. PubMed ID: 19595623
[TBL] [Abstract][Full Text] [Related]
32. Targeting several CAG expansion diseases by a single antisense oligonucleotide.
Evers MM; Pepers BA; van Deutekom JC; Mulders SA; den Dunnen JT; Aartsma-Rus A; van Ommen GJ; van Roon-Mom WM
PLoS One; 2011; 6(9):e24308. PubMed ID: 21909428
[TBL] [Abstract][Full Text] [Related]
33. Huntington's disease masquerading as spinocerebellar ataxia.
Rodríguez-Quiroga SA; Gonzalez-Morón D; Garretto N; Kauffman MA
BMJ Case Rep; 2013 Jul; 2013():. PubMed ID: 23853009
[TBL] [Abstract][Full Text] [Related]
34. Patterns of CAG repeat instability in the central nervous system and periphery in Huntington's disease and in spinocerebellar ataxia type 1.
Mouro Pinto R; Arning L; Giordano JV; Razghandi P; Andrew MA; Gillis T; Correia K; Mysore JS; Grote Urtubey DM; Parwez CR; von Hein SM; Clark HB; Nguyen HP; Förster E; Beller A; Jayadaev S; Keene CD; Bird TD; Lucente D; Vonsattel JP; Orr H; Saft C; Petrasch-Parwez E; Wheeler VC
Hum Mol Genet; 2020 Aug; 29(15):2551-2567. PubMed ID: 32761094
[TBL] [Abstract][Full Text] [Related]
35. Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia.
Cellini E; Forleo P; Nacmias B; Tedde A; Bagnoli S; Piacentini S; Sorbi S
Ann Neurol; 2004 Jul; 56(1):163; author reply 163-4. PubMed ID: 15236416
[No Abstract] [Full Text] [Related]
36. Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach.
Mariani LL; Tesson C; Charles P; Cazeneuve C; Hahn V; Youssov K; Freeman L; Grabli D; Roze E; Noël S; Peuvion JN; Bachoud-Levi AC; Brice A; Stevanin G; Durr A
JAMA Neurol; 2016 Sep; 73(9):1105-14. PubMed ID: 27400454
[TBL] [Abstract][Full Text] [Related]
37. Differential diagnosis of Huntington's disease: what the clinician should know.
Cardoso F
Neurodegener Dis Manag; 2014; 4(1):67-72. PubMed ID: 24640980
[TBL] [Abstract][Full Text] [Related]
38. HD and SCA1: Tales from two 30-year journeys since gene discovery.
Thompson LM; Orr HT
Neuron; 2023 Nov; 111(22):3517-3530. PubMed ID: 37863037
[TBL] [Abstract][Full Text] [Related]
39. Huntington's disease and Huntington's disease-like syndromes: an overview.
Gövert F; Schneider SA
Curr Opin Neurol; 2013 Aug; 26(4):420-7. PubMed ID: 23812307
[TBL] [Abstract][Full Text] [Related]
40. Absence of Acanthocytosis in Huntington's Disease-like 2: A Prospective Comparison with Huntington's Disease.
Anderson DG; Carmona S; Naidoo K; Coetzer TL; Carr J; Rudnicki DD; Walker RH; Margolis RL; Krause A
Tremor Other Hyperkinet Mov (N Y); 2017; 7():512. PubMed ID: 29226019
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
