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5. Is There Convincing Evidence that Intermediate Repeats in the HTT Gene Cause Huntington's Disease? Oosterloo M; Van Belzen MJ; Bijlsma EK; Roos RA J Huntingtons Dis; 2015; 4(2):141-8. PubMed ID: 26397895 [TBL] [Abstract][Full Text] [Related]
6. Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India. Pramanik S; Basu P; Gangopadhaya PK; Sinha KK; Jha DK; Sinha S; Das SK; Maity BK; Mukherjee SC; Roychoudhuri S; Majumder PP; Bhattacharyya NP Eur J Hum Genet; 2000 Sep; 8(9):678-82. PubMed ID: 10980573 [TBL] [Abstract][Full Text] [Related]
8. Parent-of-origin differences of mutant HTT CAG repeat instability in Huntington's disease. Aziz NA; van Belzen MJ; Coops ID; Belfroid RD; Roos RA Eur J Med Genet; 2011; 54(4):e413-8. PubMed ID: 21540131 [TBL] [Abstract][Full Text] [Related]
9. Clinical and genetic characteristics in patients with Huntington's disease from China. Yang J; Chen K; Wei Q; Chen Y; Cao B; Burgunder JM; Shang HF Neurol Res; 2016 Oct; 38(10):916-20. PubMed ID: 27483361 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Genetic features of Huntington disease in Cuban population: implications for phenotype, epidemiology and predictive testing. Vázquez-Mojena Y; Laguna-Salvia L; Laffita-Mesa JM; González-Zaldívar Y; Almaguer-Mederos LE; Rodríguez-Labrada R; Almaguer-Gotay D; Zayas-Feria P; Velázquez-Pérez L J Neurol Sci; 2013 Dec; 335(1-2):101-4. PubMed ID: 24054538 [TBL] [Abstract][Full Text] [Related]
12. [From gene to disease; HD gene and Huntington disease]. Maat-Kievit JA; Losekoot M; Roos RA Ned Tijdschr Geneeskd; 2001 Nov; 145(44):2120-3. PubMed ID: 11723754 [TBL] [Abstract][Full Text] [Related]
13. Clinical and Molecular Features of Late Onset Huntington Disease in a Peruvian Cohort. Cornejo-Olivas MR; Inca-Martinez MA; Espinoza-Huertas K; Veliz-Otani D; Velit-Salazar MR; Marca V; Ortega O; Cornejo-Herrera IF; Lindo-Samanamud S; Mora-Alferez P; Mazzetti P J Huntingtons Dis; 2015; 4(1):99-105. PubMed ID: 26333261 [TBL] [Abstract][Full Text] [Related]
14. HD CAGnome: a search tool for huntingtin CAG repeat length-correlated genes. Galkina EI; Shin A; Coser KR; Shioda T; Kohane IS; Seong IS; Wheeler VC; Gusella JF; Macdonald ME; Lee JM PLoS One; 2014; 9(4):e95556. PubMed ID: 24751919 [TBL] [Abstract][Full Text] [Related]
15. The neurology and natural history of patients with indeterminate CAG repeat length mutations of the Huntington disease gene. Panegyres PK; Goh JG J Neurol Sci; 2011 Feb; 301(1-2):14-20. PubMed ID: 21147489 [TBL] [Abstract][Full Text] [Related]
16. Weight loss in Huntington disease increases with higher CAG repeat number. Aziz NA; van der Burg JM; Landwehrmeyer GB; Brundin P; Stijnen T; ; Roos RA Neurology; 2008 Nov; 71(19):1506-13. PubMed ID: 18981372 [TBL] [Abstract][Full Text] [Related]
17. [Study of the association of genotype and phenotype features of the pathogenesis of Huntington's chorea]. Hryshchenko NV; Kucherenko AM; Patskun EI; Livshyts' LA Tsitol Genet; 2009; 43(3):42-7. PubMed ID: 19938636 [TBL] [Abstract][Full Text] [Related]
18. The clinical and genetic features of Huntington disease. Sturrock A; Leavitt BR J Geriatr Psychiatry Neurol; 2010 Dec; 23(4):243-59. PubMed ID: 20923757 [TBL] [Abstract][Full Text] [Related]
19. The Danish HD Registry-a nationwide family registry of HD families in Denmark. Gilling M; Budtz-Jørgensen E; Boonen SE; Lildballe D; Bojesen A; Hertz JM; Sørensen SA Clin Genet; 2017 Sep; 92(3):338-341. PubMed ID: 28155235 [TBL] [Abstract][Full Text] [Related]
20. Clinical and genetic characteristics in patients with Huntington's Disease from Argentina. Gatto E; Parisi V; Persi G; Converso DP; Etcheverry JL; Varela V; Lopez A; Alba L; Fretchel G Parkinsonism Relat Disord; 2012 Feb; 18(2):166-9. PubMed ID: 21962718 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]