207 related articles for article (PubMed ID: 9491297)
1. Genetic screening for Huntington's disease in Chinese patients with involuntary movements.
Shan DE; Soong BW; Yeh SI; Cheng CH; Wu ZA
Clin Neurol Neurosurg; 1997 Dec; 99(4):244-7. PubMed ID: 9491297
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea.
MacMillan JC; Morrison PJ; Nevin NC; Shaw DJ; Harper PS; Quarrell OW; Snell RG
J Med Genet; 1993 Dec; 30(12):1012-3. PubMed ID: 8133497
[TBL] [Abstract][Full Text] [Related]
4. Risk Assessment for Huntington's Disease for (Future) Offspring Requires Offering Preconceptional CAG Analysis to Both Partners.
Tibben A; Dondorp WJ; de Wert GM; de Die-Smulders CE; Losekoot M; Bijlsma EK
J Huntingtons Dis; 2019; 8(1):71-78. PubMed ID: 30689590
[TBL] [Abstract][Full Text] [Related]
5. Usefulness of molecular testing in Huntington's disease.
Wang V; Yeh TP; Chen CM; Yan SH; Soong BW
Zhonghua Yi Xue Za Zhi (Taipei); 1999 Sep; 62(9):586-90. PubMed ID: 10502848
[TBL] [Abstract][Full Text] [Related]
6. Analysis of the (CAG)n repeat at the IT15 locus in a population from Calabria (southern Italy).
Leone O; Muglia M; Gabriele AL; Annesi G; Conforti FL; Imbrogno E; Imbrogno L; Brancati C
Hum Biol; 1997 Oct; 69(5):653-62. PubMed ID: 9299885
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Huntington disease and Huntington disease-like in a case series from Brazil.
Castilhos RM; Souza AF; Furtado GV; Gheno TC; Silva AL; Vargas FR; Lima MA; Barsottini O; Pedroso JL; Godeiro C; Salarini D; Pereira ET; Lin K; Toralles MB; Saute JA; Rieder CR; Quintas M; Sequeiros J; Alonso I; Saraiva-Pereira ML; Jardim LB
Clin Genet; 2014 Oct; 86(4):373-7. PubMed ID: 24102565
[TBL] [Abstract][Full Text] [Related]
9. Diagnosis of "sporadic" Huntington's disease.
Dürr A; Dodé C; Hahn V; Pêcheux C; Pillon B; Feingold J; Kaplan JC; Agid Y; Brice A
J Neurol Sci; 1995 Mar; 129(1):51-5. PubMed ID: 7751845
[TBL] [Abstract][Full Text] [Related]
10. [Molecular diagnosis of Huntington's disease: an analysis of two large families].
Zeng Y; Chen M; Mao Y
Zhonghua Yi Xue Za Zhi; 1995 Nov; 75(11):689-93, 711-2. PubMed ID: 8697093
[TBL] [Abstract][Full Text] [Related]
11. Family history in juvenile Huntington disease: do the signs point to "yes" or "very doubtful"?
Lehman RK; Nance M
Neurology; 2013 Mar; 80(11):976-7. PubMed ID: 23390171
[TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of the IT15 gene in patients with apparently 'sporadic' Huntington's disease.
Mandich P; Di Maria E; Bellone E; Ajmar F; Abbruzzese G
Eur Neurol; 1996; 36(6):348-52. PubMed ID: 8954302
[TBL] [Abstract][Full Text] [Related]
13. [Huntington chorea. Molecular genetic principles, mutation detection and predictive diagnosis].
Zühlke C; Thies U
Nervenarzt; 1996 Jan; 67(1):25-35. PubMed ID: 8676985
[TBL] [Abstract][Full Text] [Related]
14. Epidemiological and genetic studies of Huntington's disease in the San-in area of Japan.
Nakashima K; Watanabe Y; Kusumi M; Nanba E; Maeoka Y; Nakagawa M; Igo M; Irie H; Ishino H; Fujimoto A; Goto J; Takahashi K
Neuroepidemiology; 1996; 15(3):126-31. PubMed ID: 8700304
[TBL] [Abstract][Full Text] [Related]
15. Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis.
Jih KY; Lai KL; Lin KP; Liao YC; Lee YC
J Chin Med Assoc; 2023 Jan; 86(1):47-51. PubMed ID: 36599142
[TBL] [Abstract][Full Text] [Related]
16. Hereditary chorea - what else to consider when the Huntington's disease genetics test is negative?
Malek N; Newman EJ
Acta Neurol Scand; 2017 Jan; 135(1):25-33. PubMed ID: 27150574
[TBL] [Abstract][Full Text] [Related]
17. Molecular analysis of the Huntington's disease gene in New Zealand.
Whitefield JE; Williams L; Snow K; Dixon J; Winship I; Stapleton PM; Faull RM; Love DR
N Z Med J; 1996 Feb; 109(1015):27-30. PubMed ID: 8606810
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A reproducible assay of polymerase chain reaction to detect trinucleotide repeat expansion of Huntington's disease and senile chorea.
Watanabe M; Abe K; Aoki M; Kameya T; Itoyama Y; Shoji M; Ikeda M; Iizuka T; Hirai S
Neurol Res; 1996 Feb; 18(1):16-8. PubMed ID: 8714530
[TBL] [Abstract][Full Text] [Related]
20. Trinucleotide repeat analysis of Huntington's disease gene in Singapore.
Law HY; Ng IS; Yoon CS; Zhao Y; Wong MC
Ann Acad Med Singap; 2001 Mar; 30(2):122-7. PubMed ID: 11379408
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
