236 related articles for article (PubMed ID: 9932964)
1. Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease.
Nance MA; Mathias-Hagen V; Breningstall G; Wick MJ; McGlennen RC
Neurology; 1999 Jan; 52(2):392-4. PubMed ID: 9932964
[TBL] [Abstract][Full Text] [Related]
2. A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington's Disease Symptoms.
Chheda P; Chanekar M; Salunkhe Y; Dama T; Pais A; Pande S; Bendre R; Shah N
Mol Diagn Ther; 2018 Jun; 22(3):353-359. PubMed ID: 29619771
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 7484060
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 9184242
[TBL] [Abstract][Full Text] [Related]
5. Huntington Disease: Molecular Diagnostics Approach.
Bastepe M; Xin W
Curr Protoc Hum Genet; 2015 Oct; 87():9.26.1-9.26.23. PubMed ID: 26439718
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. XL PCR for the detection of large trinucleotide expansions in juvenile Huntington's disease.
Milunsky JM; Maher TA; Loose BA; Darras BT; Ito M
Clin Genet; 2003 Jul; 64(1):70-3. PubMed ID: 12791042
[TBL] [Abstract][Full Text] [Related]
8. Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease.
Masuda N; Goto J; Murayama N; Watanabe M; Kondo I; Kanazawa I
J Med Genet; 1995 Sep; 32(9):701-5. PubMed ID: 8544189
[TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 8528671
[TBL] [Abstract][Full Text] [Related]
10. Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis.
Fusilli C; Migliore S; Mazza T; Consoli F; De Luca A; Barbagallo G; Ciammola A; Gatto EM; Cesarini M; Etcheverry JL; Parisi V; Al-Oraimi M; Al-Harrasi S; Al-Salmi Q; Marano M; Vonsattel JG; Sabatini U; Landwehrmeyer GB; Squitieri F
Lancet Neurol; 2018 Nov; 17(11):986-993. PubMed ID: 30243861
[TBL] [Abstract][Full Text] [Related]
11. [Molecular genetics of Huntington's disease].
Goto J; Masuda N; Watanabe M; Kanazawa I
Rinsho Shinkeigaku; 1995 Dec; 35(12):1529-31. PubMed ID: 8752453
[TBL] [Abstract][Full Text] [Related]
12. Intergeneration CAG expansion and contraction in a Chinese HD family.
Tang Y; Wang Y; Yang P; Liu Y; Wang B; Podolsky R; McIndoe R; Wang CY
Am J Med Genet B Neuropsychiatr Genet; 2006 Apr; 141B(3):242-4. PubMed ID: 16526033
[TBL] [Abstract][Full Text] [Related]
13. Juvenile onset Huntington disease resulting from a very large maternal expansion.
Nahhas FA; Garbern J; Krajewski KM; Roa BB; Feldman GL
Am J Med Genet A; 2005 Sep; 137A(3):328-31. PubMed ID: 16096998
[TBL] [Abstract][Full Text] [Related]
14. Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.
Agostinho Lde A; Rocha CF; Medina-Acosta E; Barboza HN; da Silva AF; Pereira SP; da Silva Idos S; Paradela ER; Figueiredo AL; Nogueira Ede M; Alvarenga RM; Hernan Cabello P; dos Santos SR; Paiva CL
J Hum Genet; 2012 Dec; 57(12):796-803. PubMed ID: 23051704
[TBL] [Abstract][Full Text] [Related]
15. The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease.
Klempíř J; Zidovská J; Stochl J; Ing VK; Uhrová T; Roth J
Mov Disord; 2011 Jan; 26(1):125-9. PubMed ID: 21322024
[TBL] [Abstract][Full Text] [Related]
16. Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.
De Rooij KE; De Koning Gans PA; Skraastad MI; Belfroid RD; Vegter-Van Der Vlis M; Roos RA; Bakker E; Van Ommen GJ; Den Dunnen JT; Losekoot M
J Med Genet; 1993 Dec; 30(12):996-1002. PubMed ID: 8133511
[TBL] [Abstract][Full Text] [Related]
17. Increased Steady-State Mutant Huntingtin mRNA in Huntington's Disease Brain.
Liu W; Chaurette J; Pfister EL; Kennington LA; Chase KO; Bullock J; Vonsattel JP; Faull RL; Macdonald D; DiFiglia M; Zamore PD; Aronin N
J Huntingtons Dis; 2013; 2(4):491-500. PubMed ID: 25062733
[TBL] [Abstract][Full Text] [Related]
18. Enhanced Detection and Sizing of the HTT CAG Repeat Expansion in Huntington Disease Using an Improved Triplet-Primed PCR Assay.
Zhao M; Lee CG; Law HY; Chong SS
Neurodegener Dis; 2016; 16(5-6):348-51. PubMed ID: 27207688
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 8558157
[TBL] [Abstract][Full Text] [Related]
20. Exploring the correlates of intermediate CAG repeats in Huntington disease.
Ha AD; Jankovic J
Postgrad Med; 2011 Sep; 123(5):116-21. PubMed ID: 21904093
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]