231 related articles for article (PubMed ID: 21755114)
1. Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype.
Rodrigues GR; Walker RH; Bader B; Danek A; Brice A; Cazeneuve C; Russaouen O; Lopes-Cendes I; Marques W; Tumas V
Arq Neuropsiquiatr; 2011 Jun; 69(3):419-23. PubMed ID: 21755114
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Huntington's disease like phenotype: new data from Brazil and what we know between heaven and earth.
Teive HA
Arq Neuropsiquiatr; 2011 Jun; 69(3):417-8. PubMed ID: 21755113
[No Abstract] [Full Text] [Related]
4. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J
Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
[TBL] [Abstract][Full Text] [Related]
5. [Differential diagnosis of chorea].
Shimohata T; Nishizawa M
Brain Nerve; 2009 Aug; 61(8):963-71. PubMed ID: 19697886
[TBL] [Abstract][Full Text] [Related]
6. Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion.
Koutsis G; Karadima G; Pandraud A; Sweeney MG; Paudel R; Houlden H; Wood NW; Panas M
J Neurol; 2012 Sep; 259(9):1874-8. PubMed ID: 22297462
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Autophagy and Polyglutamine Disease.
Ren H; Hao Z; Wang G
Adv Exp Med Biol; 2020; 1207():149-161. PubMed ID: 32671744
[TBL] [Abstract][Full Text] [Related]
10. [Gene diagnosis of patients with chorea].
Shimohata T; Onodera O; Honma Y; Hirota K; Nunomura Y; Kimura T; Kawachi I; Sanpei K; Nishizawa M; Tsuji S
Rinsho Shinkeigaku; 2004 Mar; 44(3):149-53. PubMed ID: 15233265
[TBL] [Abstract][Full Text] [Related]
11. Should spinocerebellar ataxias be included in the differential diagnosis for Huntington's diseases-like syndromes?
Pedroso JL; de Freitas ME; Albuquerque MV; Saraiva-Pereira ML; Jardim LB; Barsottini OG
J Neurol Sci; 2014 Dec; 347(1-2):356-8. PubMed ID: 25456461
[TBL] [Abstract][Full Text] [Related]
12. The first identified French family with dentatorubral-pallidoluysian atrophy.
Destée A; Delalande I; Vuillaume I; Schraen-Maschke S; Defebvre L; Sablonnière B
Mov Disord; 2000 Sep; 15(5):996-9. PubMed ID: 11009212
[TBL] [Abstract][Full Text] [Related]
13. Dentatorubro-Pallidoluysian Atrophy (DRPLA) among 700 Families with Ataxia in Brazil.
Braga-Neto P; Pedroso JL; Furtado GV; Gheno TC; Saraiva-Pereira ML; Jardim LB; Barsottini OGP;
Cerebellum; 2017 Aug; 16(4):812-816. PubMed ID: 28432641
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population].
Wang JL; Wu YQ; Lei LF; Shen L; Jiang H; Zhou YF; Yi JP; Zhou J; Yan XX; Pan Q; Xia K; Tang BS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):501-5. PubMed ID: 20931525
[TBL] [Abstract][Full Text] [Related]
16. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Brusco A; Gellera C; Cagnoli C; Saluto A; Castucci A; Michielotto C; Fetoni V; Mariotti C; Migone N; Di Donato S; Taroni F
Arch Neurol; 2004 May; 61(5):727-33. PubMed ID: 15148151
[TBL] [Abstract][Full Text] [Related]
17. Huntington's disease-like disorders in Latin America and the Caribbean.
Walker RH; Gatto EM; Bustamante ML; Bernal-Pacheco O; Cardoso F; Castilhos RM; Chana-Cuevas P; Cornejo-Olivas M; Estrada-Bellmann I; Jardim LB; López-Castellanos R; López-Contreras R; Maia DP; Mazzetti P; Miranda M; Rodríguez-Violante M; Teive H; Tumas V
Parkinsonism Relat Disord; 2018 Aug; 53():10-20. PubMed ID: 29853295
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Spinocerebellar ataxia type 17 in Indian patients: two rare cases of homozygous expansions.
Hire RR; Katrak SM; Vaidya S; Radhakrishnan K; Seshadri M
Clin Genet; 2011 Nov; 80(5):472-7. PubMed ID: 21108634
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
