247 related articles for article (PubMed ID: 11914418)
1. CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients.
Stevanin G; Camuzat A; Holmes SE; Julien C; Sahloul R; Dodé C; Hahn-Barma V; Ross CA; Margolis RL; Durr A; Brice A
Neurology; 2002 Mar; 58(6):965-7. PubMed ID: 11914418
[TBL] [Abstract][Full Text] [Related]
2. Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.
Stevanin G; Fujigasaki H; Lebre AS; Camuzat A; Jeannequin C; Dode C; Takahashi J; San C; Bellance R; Brice A; Durr A
Brain; 2003 Jul; 126(Pt 7):1599-603. PubMed ID: 12805114
[TBL] [Abstract][Full Text] [Related]
3. Huntington's Disease-like 2 (HDL2) in North America and Japan.
Margolis RL; Holmes SE; Rosenblatt A; Gourley L; O'Hearn E; Ross CA; Seltzer WK; Walker RH; Ashizawa T; Rasmussen A; Hayden M; Almqvist EW; Harris J; Fahn S; MacDonald ME; Mysore J; Shimohata T; Tsuji S; Potter N; Nakaso K; Adachi Y; Nakashima K; Bird T; Krause A; Greenstein P
Ann Neurol; 2004 Nov; 56(5):670-4. PubMed ID: 15468075
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. Huntington's disease-like 2 in Brazil--report of 4 patients.
Rodrigues GG; Walker RH; Brice A; Cazeneuve C; Russaouen O; Teive HA; Munhoz RP; Becker N; Raskin S; Werneck LC; Junior WM; Tumas V
Mov Disord; 2008 Nov; 23(15):2244-7. PubMed ID: 18816802
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene.
Sułek-Piatkowska A; Krysa W; Zdzienicka E; Szirkowiec W; Hoffman-Zacharska D; Rajkiewicz M; Fidziańska E; Kowalska G; Zaremba J
Neurol Neurochir Pol; 2008; 42(3):203-9. PubMed ID: 18651325
[TBL] [Abstract][Full Text] [Related]
8. Huntington's disease like-2: review and update.
Margolis RL; Rudnicki DD; Holmes SE
Acta Neurol Taiwan; 2005 Mar; 14(1):1-8. PubMed ID: 15835282
[TBL] [Abstract][Full Text] [Related]
9. Huntington's disease as caused by 34 CAG repeats.
Andrich J; Arning L; Wieczorek S; Kraus PH; Gold R; Saft C
Mov Disord; 2008 Apr; 23(6):879-81. PubMed ID: 18307262
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Null alleles at the Huntington disease locus: implications for diagnostics and CAG repeat instability.
Williams LC; Hegde MR; Nagappan R; Faull RL; Giles J; Winship I; Snow K; Love DR
Genet Test; 2000; 4(1):55-60. PubMed ID: 10794362
[TBL] [Abstract][Full Text] [Related]
12. Age-, tissue- and length-dependent bidirectional somatic CAG•CTG repeat instability in an allelic series of R6/2 Huntington disease mice.
Larson E; Fyfe I; Morton AJ; Monckton DG
Neurobiol Dis; 2015 Apr; 76():98-111. PubMed ID: 25662336
[TBL] [Abstract][Full Text] [Related]
13. Autopsy-proven Huntington's disease with 29 trinucleotide repeats.
Kenney C; Powell S; Jankovic J
Mov Disord; 2007 Jan; 22(1):127-30. PubMed ID: 17115386
[TBL] [Abstract][Full Text] [Related]
14. Huntington disease-like 2: the first patient with apparent European ancestry.
Santos C; Wanderley H; Vedolin L; Pena SD; Jardim L; Sequeiros J
Clin Genet; 2008 May; 73(5):480-5. PubMed ID: 18341606
[TBL] [Abstract][Full Text] [Related]
15. Investigations of Huntington's Disease and Huntington's Disease-Like Syndromes in Indian Choreatic Patients.
Kaur J; Parveen S; Shamim U; Sharma P; Suroliya V; Sonkar AK; Ahmad I; Garg J; Anand KS; Laskar S; Chowdhury D; Kushwaha S; Goyal V; Srivastava AK; Singh G; Faruq M
J Huntingtons Dis; 2020; 9(3):283-289. PubMed ID: 32675418
[TBL] [Abstract][Full Text] [Related]
16. Huntington's disease-like and ataxia syndromes: identification of a family with a de novo SCA17/TBP mutation.
Bech S; Petersen T; Nørremølle A; Gjedde A; Ehlers L; Eiberg H; Hjermind LE; Hasholt L; Lundorf E; Nielsen JE
Parkinsonism Relat Disord; 2010 Jan; 16(1):12-5. PubMed ID: 19595623
[TBL] [Abstract][Full Text] [Related]
17. Absence of unidentified CAG repeat expansion in patients with Huntington's disease-like phenotype.
Vuillaume I; Meynieu P; Schraen-Maschke S; Destée A; Sablonnière B
J Neurol Neurosurg Psychiatry; 2000 May; 68(5):672-5. PubMed ID: 10766906
[TBL] [Abstract][Full Text] [Related]
18. Novel BAC Mouse Model of Huntington's Disease with 225 CAG Repeats Exhibits an Early Widespread and Stable Degenerative Phenotype.
Wegrzynowicz M; Bichell TJ; Soares BD; Loth MK; McGlothan JS; Mori S; Alikhan FS; Hua K; Coughlin JM; Holt HK; Jetter CS; Pomper MG; Osmand AP; Guilarte TR; Bowman AB
J Huntingtons Dis; 2015; 4(1):17-36. PubMed ID: 26333255
[TBL] [Abstract][Full Text] [Related]
19. 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 Dec; 50(6):373-80. PubMed ID: 11761463
[TBL] [Abstract][Full Text] [Related]
20. Clinical and genetic characteristics of Mexican Huntington's disease patients.
Alonso ME; Ochoa A; Boll MC; Sosa AL; Yescas P; López M; Macias R; Familiar I; Rasmussen A
Mov Disord; 2009 Oct; 24(13):2012-5. PubMed ID: 19672992
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
