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 *

182 related articles for article (PubMed ID: 31323545)

  • 1. Spinocerebellar ataxias in Southern Brazil: Genotypic and phenotypic evaluation of 213 families.
    Nascimento FA; Rodrigues VOR; Pelloso FC; Camargo CHF; Moro A; Raskin S; Ashizawa T; Teive HAG
    Clin Neurol Neurosurg; 2019 Sep; 184():105427. PubMed ID: 31323545
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Central auditory processing in patients with spinocerebellar ataxia.
    Zeigelboim BS; de Carvalho HA; Teive HA; Liberalesso PB; Jurkiewicz AL; da Silva Abdulmassih EM; Marques JM; Cordeiro ML
    Hear Res; 2015 Sep; 327():235-44. PubMed ID: 26183435
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.
    Vale J; Bugalho P; Silveira I; Sequeiros J; Guimarães J; Coutinho P
    Eur J Neurol; 2010 Jan; 17(1):124-8. PubMed ID: 19659750
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutational screening of 320 Brazilian patients with autosomal dominant spinocerebellar ataxia.
    Cintra VP; Lourenço CM; Marques SE; de Oliveira LM; Tumas V; Marques W
    J Neurol Sci; 2014 Dec; 347(1-2):375-9. PubMed ID: 25466696
    [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. Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
    Soong B W; Lu Y C; Choo K B; Lee H Y
    Arch Neurol; 2001 Jul; 58(7):1105-9. PubMed ID: 11448300
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
    Jiang H; Tang BS; Xu B; Zhao GH; Shen L; Tang JG; Li QH; Xia K
    Chin Med J (Engl); 2005 May; 118(10):837-43. PubMed ID: 15989765
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Founder Effects of Spinocerebellar Ataxias in the American Continents and the Caribbean.
    Rodríguez-Labrada R; Martins AC; Magaña JJ; Vazquez-Mojena Y; Medrano-Montero J; Fernandez-Ruíz J; Cisneros B; Teive H; McFarland KN; Saraiva-Pereira ML; Cerecedo-Zapata CM; Gomez CM; Ashizawa T; Velázquez-Pérez L; Jardim LB;
    Cerebellum; 2020 Jun; 19(3):446-458. PubMed ID: 32086717
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6].
    Jiang H; Tang B; Xu B; Zhao GH; Shen L; Tang JG; Li QH; Xia K
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):1-4. PubMed ID: 15696468
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Upward Gaze Palsy: a Valuable Sign to Distinguish Spinocerebellar Ataxias.
    Franklin GL; Meira AT; Camargo CHF; Nascimento FA; Teive HAG
    Cerebellum; 2020 Oct; 19(5):685-690. PubMed ID: 32557336
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.
    Jiang H; Tang B; Xia K; Zhou Y; Xu B; Zhao G; Li H; Shen L; Pan Q; Cai F
    J Neurol Sci; 2005 Sep; 236(1-2):25-9. PubMed ID: 15979648
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.
    de Castilhos RM; Furtado GV; Gheno TC; Schaeffer P; Russo A; Barsottini O; Pedroso JL; Salarini DZ; Vargas FR; de Lima MA; Godeiro C; Santana-da-Silva LC; Toralles MB; Santos S; van der Linden H; Wanderley HY; de Medeiros PF; Pereira ET; Ribeiro E; Saraiva-Pereira ML; Jardim LB;
    Cerebellum; 2014 Feb; 13(1):17-28. PubMed ID: 23943520
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Spinocerebellar ataxia in a cohort of patients from Rio de Janeiro.
    Alvarenga MP; Siciliani LC; Carvalho RS; Ganimi MC; Penna PS
    Neurol Sci; 2022 Aug; 43(8):4997-5005. PubMed ID: 35469073
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent.
    Paradisi I; Ikonomu V; Arias S
    J Hum Genet; 2016 Mar; 61(3):215-22. PubMed ID: 26538302
    [TBL] [Abstract][Full Text] [Related]  

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

  • 18. Comparing loss of balance and functional capacity among patients with SCA2, SCA3 and SCA10.
    Zonta MB; Teive HAG; Camargo CHF; Meira AT; Lopes Neto FDN; Tensini FS; Braga CB; Ashizawa T; Munhoz RP
    Clin Neurol Neurosurg; 2022 Mar; 214():107150. PubMed ID: 35123369
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia.
    Koutsis G; Pemble S; Sweeney MG; Paudel R; Wood NW; Panas M; Kladi A; Houlden H
    J Neurol Sci; 2012 Jul; 318(1-2):178-80. PubMed ID: 22520093
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.