BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 20818609)

  • 1. Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients.
    Teive HA; Munhoz RP; Raskin S; Arruda WO; de Paola L; Werneck LC; Ashizawa T
    Mov Disord; 2010 Dec; 25(16):2875-8. PubMed ID: 20818609
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical phenotype of Brazilian families with spinocerebellar ataxia 10.
    Teive HA; Roa BB; Raskin S; Fang P; Arruda WO; Neto YC; Gao R; Werneck LC; Ashizawa T
    Neurology; 2004 Oct; 63(8):1509-12. PubMed ID: 15505178
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and Genetic Evaluation of Spinocerebellar Ataxia Type 10 in 16 Brazilian Families.
    Domingues BMD; Nascimento FA; Meira AT; Moro A; Raskin S; Ashizawa T; Teive HAG
    Cerebellum; 2019 Oct; 18(5):849-854. PubMed ID: 31377949
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease.
    Leonardi L; Marcotulli C; McFarland KN; Tessa A; DiFabio R; Santorelli FM; Pierelli F; Ashizawa T; Casali C
    J Neurol; 2014 Sep; 261(9):1691-4. PubMed ID: 24935856
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10.
    Raskin S; Ashizawa T; Teive HA; Arruda WO; Fang P; Gao R; White MC; Werneck LC; Roa B
    Arch Neurol; 2007 Apr; 64(4):591-4. PubMed ID: 17420323
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Spinocerebellar ataxia type 10 - A review.
    Teive HA; Munhoz RP; Arruda WO; Raskin S; Werneck LC; Ashizawa T
    Parkinsonism Relat Disord; 2011 Nov; 17(9):655-61. PubMed ID: 21531163
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures.
    McFarland KN; Liu J; Landrian I; Zeng D; Raskin S; Moscovich M; Gatto EM; Ochoa A; Teive HA; Rasmussen A; Ashizawa T
    Neurogenetics; 2014 Mar; 15(1):59-64. PubMed ID: 24318420
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inheritance patterns of ATCCT repeat interruptions in spinocerebellar ataxia type 10 (SCA10) expansions.
    Landrian I; McFarland KN; Liu J; Mulligan CJ; Rasmussen A; Ashizawa T
    PLoS One; 2017; 12(4):e0175958. PubMed ID: 28423040
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?
    Matsuura T; Fang P; Pearson CE; Jayakar P; Ashizawa T; Roa BB; Nelson DL
    Am J Hum Genet; 2006 Jan; 78(1):125-9. PubMed ID: 16385455
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10).
    Almeida T; Alonso I; Martins S; Ramos EM; Azevedo L; Ohno K; Amorim A; Saraiva-Pereira ML; Jardim LB; Matsuura T; Sequeiros J; Silveira I
    PLoS One; 2009; 4(2):e4553. PubMed ID: 19234597
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.
    Bampi GB; Bisso-Machado R; Hünemeier T; Gheno TC; Furtado GV; Veliz-Otani D; Cornejo-Olivas M; Mazzeti P; Bortolini MC; Jardim LB; Saraiva-Pereira ML;
    Neuromolecular Med; 2017 Dec; 19(4):501-509. PubMed ID: 28905220
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry.
    Bushara K; Bower M; Liu J; McFarland KN; Landrian I; Hutter D; Teive HA; Rasmussen A; Mulligan CJ; Ashizawa T
    PLoS One; 2013; 8(11):e81342. PubMed ID: 24278426
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
    Matsuura T; Yamagata T; Burgess DL; Rasmussen A; Grewal RP; Watase K; Khajavi M; McCall AE; Davis CF; Zu L; Achari M; Pulst SM; Alonso E; Noebels JL; Nelson DL; Zoghbi HY; Ashizawa T
    Nat Genet; 2000 Oct; 26(2):191-4. PubMed ID: 11017075
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SMRT Sequencing of Long Tandem Nucleotide Repeats in SCA10 Reveals Unique Insight of Repeat Expansion Structure.
    McFarland KN; Liu J; Landrian I; Godiska R; Shanker S; Yu F; Farmerie WG; Ashizawa T
    PLoS One; 2015; 10(8):e0135906. PubMed ID: 26295943
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients.
    Sułek-Piatkowska A; Zdzienicka E; Raczyńska-Rakowicz M; Krysa W; Rajkiewicz M; Szirkowiec W; Zaremba J
    Neurol Neurochir Pol; 2010; 44(3):238-45. PubMed ID: 20625959
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ataxin-10, the spinocerebellar ataxia type 10 neurodegenerative disorder protein, is essential for survival of cerebellar neurons.
    März P; Probst A; Lang S; Schwager M; Rose-John S; Otten U; Ozbek S
    J Biol Chem; 2004 Aug; 279(34):35542-50. PubMed ID: 15201271
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10.
    Wakamiya M; Matsuura T; Liu Y; Schuster GC; Gao R; Xu W; Sarkar PS; Lin X; Ashizawa T
    Neurology; 2006 Aug; 67(4):607-13. PubMed ID: 16924013
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability.
    McFarland KN; Liu J; Landrian I; Gao R; Sarkar PS; Raskin S; Moscovich M; Gatto EM; Teive HA; Ochoa A; Rasmussen A; Ashizawa T
    Eur J Hum Genet; 2013 Nov; 21(11):1272-6. PubMed ID: 23443018
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.