125 related articles for article (PubMed ID: 7917128)
1. Paternal line of transmission in chorea of Huntington with very early onset.
Navarrete C; Martinez I; Salamanca F
Genet Couns; 1994; 5(2):175-8. PubMed ID: 7917128
[TBL] [Abstract][Full Text] [Related]
2. Psychiatric and cognitive difficulties as indicators of juvenile huntington disease onset in 29 patients.
Ribaï P; Nguyen K; Hahn-Barma V; Gourfinkel-An I; Vidailhet M; Legout A; Dodé C; Brice A; Dürr A
Arch Neurol; 2007 Jun; 64(6):813-9. PubMed ID: 17562929
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Analysis of trinucleotide repeat expansion as a new mechanism of mutation in Huntington's chorea: theoretical and applied aspects].
Illarioshkin SN; Ivanova-Smolenskaia IA; Markova ED; Nikol'skaia NN; Chabrashvili TZ; Insarova NG
Genetika; 1996 Jan; 32(1):103-9. PubMed ID: 8647411
[TBL] [Abstract][Full Text] [Related]
5. Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.
Telenius H; Kremer B; Goldberg YP; Theilmann J; Andrew SE; Zeisler J; Adam S; Greenberg C; Ives EJ; Clarke LA
Nat Genet; 1994 Apr; 6(4):409-14. PubMed ID: 8054984
[TBL] [Abstract][Full Text] [Related]
6. [Chorea with prominent spasticity associated with an expansion of the CAG trinucleotide repeat in the IT15 gene: a case report].
Akanuma J; Saito N; Aoki M; Abe K; Yamamoto T
Rinsho Shinkeigaku; 1995 Nov; 35(11):1253-5. PubMed ID: 8720339
[TBL] [Abstract][Full Text] [Related]
7. Trinucleotide repeat length instability and age of onset in Huntington's disease.
Duyao M; Ambrose C; Myers R; Novelletto A; Persichetti F; Frontali M; Folstein S; Ross C; Franz M; Abbott M
Nat Genet; 1993 Aug; 4(4):387-92. PubMed ID: 8401587
[TBL] [Abstract][Full Text] [Related]
8. [Huntington's chorea: clinical aspects, genetics and current diagnosis].
Spiegel R
Ther Umsch; 1995 Dec; 52(12):814-20. PubMed ID: 8539653
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease.
Andrew SE; Goldberg YP; Kremer B; Telenius H; Theilmann J; Adam S; Starr E; Squitieri F; Lin B; Kalchman MA
Nat Genet; 1993 Aug; 4(4):398-403. PubMed ID: 8401589
[TBL] [Abstract][Full Text] [Related]
11. [Huntington chorea: clniical and molecular analysis in Asturian patients].
Hernando I; Alvarez V; García Martínez A; Salas Puig J; Fernández Uría D; Martínez C; Vidal Sánchez JA; Lahoz C; Coto E
Neurologia; 1999 Jan; 14(1):11-5. PubMed ID: 10079686
[TBL] [Abstract][Full Text] [Related]
12. [A case of adult-onset Huntington disease presenting with spasticity and cerebellar ataxia, mimicking spinocerebellar degeneration].
Kageyama Y; Yamamoto S; Ueno M; Ichikawa K
Rinsho Shinkeigaku; 2003; 43(1-2):16-9. PubMed ID: 12820545
[TBL] [Abstract][Full Text] [Related]
13. Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease.
Snell RG; MacMillan JC; Cheadle JP; Fenton I; Lazarou LP; Davies P; MacDonald ME; Gusella JF; Harper PS; Shaw DJ
Nat Genet; 1993 Aug; 4(4):393-7. PubMed ID: 8401588
[TBL] [Abstract][Full Text] [Related]
14. [Presymptomatic diagnosis in Huntington chorea families using the gene amplification technique].
Lucotte G; Berriche S; Petit MC; Burckel A; Turpin JC
Rev Neurol (Paris); 1991; 147(8-9):602-4. PubMed ID: 1835796
[TBL] [Abstract][Full Text] [Related]
15. Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.
Goldberg YP; Kremer B; Andrew SE; Theilmann J; Graham RK; Squitieri F; Telenius H; Adam S; Sajoo A; Starr E
Nat Genet; 1993 Oct; 5(2):174-9. PubMed ID: 8252043
[TBL] [Abstract][Full Text] [Related]
16. Predictive testing for Huntington disease: interpretation and significance of intermediate alleles.
Semaka A; Creighton S; Warby S; Hayden MR
Clin Genet; 2006 Oct; 70(4):283-94. PubMed ID: 16965319
[TBL] [Abstract][Full Text] [Related]
17. De novo expansion of a (CAG)n repeat in sporadic Huntington's disease.
Myers RH; MacDonald ME; Koroshetz WJ; Duyao MP; Ambrose CM; Taylor SA; Barnes G; Srinidhi J; Lin CS; Whaley WL
Nat Genet; 1993 Oct; 5(2):168-73. PubMed ID: 8252042
[TBL] [Abstract][Full Text] [Related]
18. Trinucleotide repeat length and rate of progression of Huntington's disease.
Illarioshkin SN; Igarashi S; Onodera O; Markova ED; Nikolskaya NN; Tanaka H; Chabrashwili TZ; Insarova NG; Endo K; Ivanova-Smolenskaya IA
Ann Neurol; 1994 Oct; 36(4):630-5. PubMed ID: 7944295
[TBL] [Abstract][Full Text] [Related]
19. Juvenile Huntington disease.
Geevasinga N; Richards FH; Jones KJ; Ryan MM
J Paediatr Child Health; 2006 Sep; 42(9):552-4. PubMed ID: 16925544
[TBL] [Abstract][Full Text] [Related]
20. [Huntington chorea in childhood].
Dralle D; Schock G; Neuhäuser G
Klin Padiatr; 1985; 197(2):90-3. PubMed ID: 3157827
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
