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22. Replicating studies of genetic modifiers in spinocerebellar ataxia type 3: can homogeneous cohorts aid? Raposo M; Ramos A; Bettencourt C; Lima M Brain; 2015 Dec; 138(Pt 12):e398. PubMed ID: 26173860 [No Abstract] [Full Text] [Related]
23. Reply: Replicating studies of genetic modifiers in spinocerebellar ataxia type 3: can homogeneous cohorts aid? Tezenas du Montcel S Brain; 2015 Dec; 138(Pt 12):e399. PubMed ID: 26173862 [No Abstract] [Full Text] [Related]
24. Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype. Bauer P; Laccone F; Rolfs A; Wüllner U; Bösch S; Peters H; Liebscher S; Scheible M; Epplen JT; Weber BH; Holinski-Feder E; Weirich-Schwaiger H; Morris-Rosendahl DJ; Andrich J; Riess O J Med Genet; 2004 Mar; 41(3):230-2. PubMed ID: 14985389 [No Abstract] [Full Text] [Related]
25. 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. PubMed ID: 12112122 [No Abstract] [Full Text] [Related]
26. [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; 126(3-4):77-82. PubMed ID: 9863360 [TBL] [Abstract][Full Text] [Related]
27. Late onset Huntington's disease with 29 CAG repeat expansion. Garcia-Ruiz PJ; Garcia-Caldentey J; Feliz C; del Val J; Herranz A; Martínez-Castrillo JC J Neurol Sci; 2016 Apr; 363():114-5. PubMed ID: 27000233 [No Abstract] [Full Text] [Related]
28. Reply to: "Reply to Late onset Huntington's disease with 29 CAG repeat expansion" JNS-D-16-00732. Garcia-Ruiz PJ; Garcia-Caldentey J; Herranz A; Del Val J; Feliz C; Martínez-Castrillo JC J Neurol Sci; 2016 Oct; 369():390. PubMed ID: 27431298 [No Abstract] [Full Text] [Related]
29. Non-choreic movement disorders as initial manifestations of Huntington's disease. Becker N; Munhoz RP; Raskin S; Werneck LC; Teive HA Arq Neuropsiquiatr; 2007 Jun; 65(2B):402-5. PubMed ID: 17665004 [TBL] [Abstract][Full Text] [Related]
30. Reply: Late onset Huntington's disease with 29 CAG repeat expansion. Oosterloo M; Van Belzen MJ; Bijlsma EK; Roos RA J Neurol Sci; 2016 Sep; 368():343. PubMed ID: 27538661 [No Abstract] [Full Text] [Related]
31. Pearls & Oy-sters: Family history of Huntington disease disguised a case of dentatorubral-pallidoluysian atrophy. Tunc S; Tadic V; Zühlke C; Hellenbroich Y; Brüggemann N Neurology; 2018 Jan; 90(3):142-143. PubMed ID: 29335306 [No Abstract] [Full Text] [Related]
32. Spinocerebellar ataxia type-7: Report of a family in Northwest Nigeria. Alkali NH; Bwala SA; Alimi SA; Oyakhire SI Ann Afr Med; 2016; 15(2):87-90. PubMed ID: 27044733 [TBL] [Abstract][Full Text] [Related]
33. Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings. Trott A; Jardim LB; Ludwig HT; Saute JA; Artigalás O; Kieling C; Wanderley HY; Rieder CR; Monte TL; Socal M; Alonso I; Ferro A; Carvalho T; do Céu Moreira M; Mendonça P; Ferreirinha F; Silveira I; Sequeiros J; Giugliani R; Saraiva-Pereira ML Clin Genet; 2006 Aug; 70(2):173-6. PubMed ID: 16879203 [No Abstract] [Full Text] [Related]
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