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 *

278 related articles for article (PubMed ID: 28432641)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Late onset ataxia phenotype in dentatorubro-pallidoluysian atrophy (DRPLA).
    Yabe I; Sasaki H; Kikuchi S; Nonaka M; Moriwaka F; Tashiro K
    J Neurol; 2002 Apr; 249(4):432-6. PubMed ID: 11967648
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. 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]  

  • 8. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
    Pujana MA; Corral J; Gratacòs M; Combarros O; Berciano J; Genís D; Banchs I; Estivill X; Volpini V
    Hum Genet; 1999 Jun; 104(6):516-22. PubMed ID: 10453742
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.
    Silveira I; Coutinho P; Maciel P; Gaspar C; Hayes S; Dias A; Guimarães J; Loureiro L; Sequeiros J; Rouleau GA
    Am J Med Genet; 1998 Mar; 81(2):134-8. PubMed ID: 9613852
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
    Silveira I; Miranda C; Guimarães L; Moreira MC; Alonso I; Mendonça P; Ferro A; Pinto-Basto J; Coelho J; Ferreirinha F; Poirier J; Parreira E; Vale J; Januário C; Barbot C; Tuna A; Barros J; Koide R; Tsuji S; Holmes SE; Margolis RL; Jardim L; Pandolfo M; Coutinho P; Sequeiros J
    Arch Neurol; 2002 Apr; 59(4):623-9. PubMed ID: 11939898
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients.
    Lopes-Cendes I; Teive HG; Calcagnotto ME; Da Costa JC; Cardoso F; Viana E; Maciel JA; Radvany J; Arruda WO; Trevisol-Bittencourt PC; Rosa Neto P; Silveira I; Steiner CE; Pinto Júnior W; Santos AS; Correa Neto Y; Werneck LC; Araújo AQ; Carakushansky G; Mello LR; Jardim LB; Rouleau GA
    Arq Neuropsiquiatr; 1997 Sep; 55(3B):519-29. PubMed ID: 9629399
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
    Tang B; Xia J; Wang D; Tang X; Shen L; Liu C; Dai H; Yan X; Pan Q; Xiao J; Zhang B; Ou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India.
    Basu P; Chattopadhyay B; Gangopadhaya PK; Mukherjee SC; Sinha KK; Das SK; Roychoudhury S; Majumder PP; Bhattacharyya NP
    Hum Genet; 2000 Jun; 106(6):597-604. PubMed ID: 10942107
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study.
    Choubtum L; Witoonpanich P; Hanchaiphiboolkul S; Bhidayasiri R; Jitkritsadakul O; Pongpakdee S; Wetchaphanphesat S; Boonkongchuen P; Pulkes T
    BMC Neurol; 2015 Sep; 15():166. PubMed ID: 26374734
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease.
    Wu YR; Lin HY; Chen CM; Gwinn-Hardy K; Ro LS; Wang YC; Li SH; Hwang JC; Fang K; Hsieh-Li HM; Li ML; Tung LC; Su MT; Lu KT; Lee-Chen GJ
    Clin Genet; 2004 Mar; 65(3):209-14. PubMed ID: 14756671
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. Frequency of spinocerebellar ataxia mutations in the Kinki district of Japan.
    Matsumura R; Futamura N; Ando N; Ueno S
    Acta Neurol Scand; 2003 Jan; 107(1):38-41. PubMed ID: 12542511
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.