These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

367 related articles for article (PubMed ID: 29891056)

  • 1. Spinocerebellar ataxias.
    Soong BW; Morrison PJ
    Handb Clin Neurol; 2018; 155():143-174. PubMed ID: 29891056
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Machado-Joseph disease and other rare spinocerebellar ataxias.
    Matilla-Dueñas A
    Adv Exp Med Biol; 2012; 724():172-88. PubMed ID: 22411243
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SCA-LSVD: a repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.
    Faruq M; Scaria V; Singh I; Tyagi S; Srivastava AK; Mukerji M
    Hum Mutat; 2009 Jul; 30(7):1037-42. PubMed ID: 19370769
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spinocerebellar ataxia: relationship between phenotype and genotype - a review.
    Sun YM; Lu C; Wu ZY
    Clin Genet; 2016 Oct; 90(4):305-14. PubMed ID: 27220866
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Autosomal dominant spinocerebellar ataxias: an Asian perspective.
    Tan EK
    Can J Neurol Sci; 2003 Nov; 30(4):361-7. PubMed ID: 14672269
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary ataxias.
    Evidente VG; Gwinn-Hardy KA; Caviness JN; Gilman S
    Mayo Clin Proc; 2000 May; 75(5):475-90. PubMed ID: 10807077
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. The wide spectrum of spinocerebellar ataxias (SCAs).
    Manto MU
    Cerebellum; 2005; 4(1):2-6. PubMed ID: 15895552
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The spinocerebellar ataxias: order emerges from chaos.
    Margolis RL
    Curr Neurol Neurosci Rep; 2002 Sep; 2(5):447-56. PubMed ID: 12169226
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The hereditary spinocerebellar ataxias in Japan.
    Sasaki H; Yabe I; Tashiro K
    Cytogenet Genome Res; 2003; 100(1-4):198-205. PubMed ID: 14526181
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spinocerebellar ataxias type 8, 12, and 17 and dentatorubro-pallidoluysian atrophy in Czech ataxic patients.
    Musova Z; Sedlacek Z; Mazanec R; Klempir J; Roth J; Plevova P; Vyhnalek M; Kopeckova M; Apltova L; Krepelova A; Zumrova A
    Cerebellum; 2013 Apr; 12(2):155-61. PubMed ID: 22872568
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DRPLA: An unusual disease or an underestimated cause of ataxia in Brazil?
    Pinto WBVR; Salomão RPA; Bergamasco NC; da Cunha Ribas G; da Graça FF; Lopes-Cendes I; Bonadia L; de Souza PVS; Bulle Oliveira AS; Saraiva-Pereira ML; Jardim LB; Tumas V; Junior WM; França MC; Pedroso JL; Barsottini OGP; Teive HAG
    Parkinsonism Relat Disord; 2021 Nov; 92():67-71. PubMed ID: 34700111
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prevalence of dentatorubral-pallidoluysian atrophy in a large series of white patients with cerebellar ataxia.
    Le Ber I; Camuzat A; Castelnovo G; Azulay JP; Genton P; Gastaut JL; Broglin D; Labauge P; Brice A; Durr A
    Arch Neurol; 2003 Aug; 60(8):1097-9. PubMed ID: 12925365
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated population.
    Juvonen V; Hietala M; Kairisto V; Savontaus ML
    Acta Neurol Scand; 2005 Mar; 111(3):154-62. PubMed ID: 15691283
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1.
    Hashida H; Goto J; Kurisaki H; Mizusawa H; Kanazawa I
    Ann Neurol; 1997 Apr; 41(4):505-11. PubMed ID: 9124808
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [Clinical features of autosomal dominant spinocerebellar ataxias genetically unclassified into any known triplet-repeat diseases].
    Aoki K; Kawata A; Suda M; Hirai S
    Rinsho Shinkeigaku; 2001 Jan; 41(1):18-23. PubMed ID: 11433762
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dilemma of multiple system atrophy and spinocerebellar ataxias.
    Li M; Ma Q; Zhao X; Wang C; Wu H; Li J; Yang W
    J Neurol; 2018 Dec; 265(12):2764-2772. PubMed ID: 29700645
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Incidence of genetic subgroups of hereditary spinocerebellar ataxia in Fukushima Prefecture.
    Kumagai Y; Sugiura Y; Shimoji S; Kumagai T; Tochikubo S; Yamamoto T
    Tohoku J Exp Med; 2001 Oct; 195(2):85-91. PubMed ID: 11846212
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.