84 related articles for article (PubMed ID: 11071143)
1. Huntington disease in children: genotype-phenotype correlation.
Rasmussen A; Macias R; Yescas P; Ochoa A; Davila G; Alonso E
Neuropediatrics; 2000 Aug; 31(4):190-4. PubMed ID: 11071143
[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. 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]
5. A South African mixed ancestry family with Huntington disease-like 2: clinical and genetic features.
Bardien S; Abrahams F; Soodyall H; van der Merwe L; Greenberg J; Brink T; Carr J
Mov Disord; 2007 Oct; 22(14):2083-9. PubMed ID: 17708569
[TBL] [Abstract][Full Text] [Related]
6. Inherited CAG.CTG allele length is a major modifier of somatic mutation length variability in Huntington disease.
Veitch NJ; Ennis M; McAbney JP; ; Shelbourne PF; Monckton DG
DNA Repair (Amst); 2007 Jun; 6(6):789-96. PubMed ID: 17293170
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Case of maternally transmitted juvenile Huntington's disease with a very large trinucleotide repeat.
Papapetropoulos S; Lopez-Alberola R; Baumbach L; Russell A; Gonzalez MA; Bowen BC; Singer C
Mov Disord; 2005 Oct; 20(10):1380-3. PubMed ID: 16007623
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide scan for CAG/CTG repeat expansions in Pimas with early onset of type 2 diabetes mellitus.
Wolford JK; Bogardus C; Prochazka M
Mol Genet Metab; 1999 Jan; 66(1):62-7. PubMed ID: 9973549
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice.
Costa MC; Magalhães P; Ferreirinha F; Guimarães L; Januário C; Gaspar I; Loureiro L; Vale J; Garrett C; Regateiro F; Magalhães M; Sousa A; Maciel P; Sequeiros J
Eur J Hum Genet; 2003 Nov; 11(11):872-8. PubMed ID: 14571273
[TBL] [Abstract][Full Text] [Related]
14. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset.
Wexler NS; Lorimer J; Porter J; Gomez F; Moskowitz C; Shackell E; Marder K; Penchaszadeh G; Roberts SA; Gayán J; Brocklebank D; Cherny SS; Cardon LR; Gray J; Dlouhy SR; Wiktorski S; Hodes ME; Conneally PM; Penney JB; Gusella J; Cha JH; Irizarry M; Rosas D; Hersch S; Hollingsworth Z; MacDonald M; Young AB; Andresen JM; Housman DE; De Young MM; Bonilla E; Stillings T; Negrette A; Snodgrass SR; Martinez-Jaurrieta MD; Ramos-Arroyo MA; Bickham J; Ramos JS; Marshall F; Shoulson I; Rey GJ; Feigin A; Arnheim N; Acevedo-Cruz A; Acosta L; Alvir J; Fischbeck K; Thompson LM; Young A; Dure L; O'Brien CJ; Paulsen J; Brickman A; Krch D; Peery S; Hogarth P; Higgins DS; Landwehrmeyer B;
Proc Natl Acad Sci U S A; 2004 Mar; 101(10):3498-503. PubMed ID: 14993615
[TBL] [Abstract][Full Text] [Related]
15. [Clinical and genetic study of juvenile form of Huntington's disease].
Zdzienicka E; Rakowicz M; Mierzewska H; Hoffman-Zacharska D; Jakubowska T; Poniatowska R; Sułek A; Waliniowska E; Zalewska U; Kulczycki J; Zaremba J
Neurol Neurochir Pol; 2002; 36(2):245-58. PubMed ID: 12046502
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. [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]
18. [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]
19. 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]
20. Case of the month: August 1997--a 13 year old girl with progressive movement disorder.
Hofgärtner WT; La Spada AR; Tait JF
Brain Pathol; 1998 Jan; 8(1):237-8. PubMed ID: 9458182
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
