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 *

294 related articles for article (PubMed ID: 11030410)

  • 1. Genetic background of apparently idiopathic sporadic cerebellar ataxia.
    Schöls L; Szymanski S; Peters S; Przuntek H; Epplen JT; Hardt C; Riess O
    Hum Genet; 2000 Aug; 107(2):132-7. PubMed ID: 11030410
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 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. 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]  

  • 5. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.
    Tsai HF; Liu CS; Leu TM; Wen FC; Lin SJ; Liu CC; Yang DK; Li C; Hsieh M
    Acta Neurol Scand; 2004 May; 109(5):355-60. PubMed ID: 15080863
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.
    Geschwind DH; Perlman S; Figueroa CP; Treiman LJ; Pulst SM
    Am J Hum Genet; 1997 Apr; 60(4):842-50. PubMed ID: 9106530
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
    Schöls L; Krüger R; Amoiridis G; Przuntek H; Epplen JT; Riess O
    J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):67-73. PubMed ID: 9436730
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.
    Leggo J; Dalton A; Morrison PJ; Dodge A; Connarty M; Kotze MJ; Rubinsztein DC
    J Med Genet; 1997 Dec; 34(12):982-5. PubMed ID: 9429138
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. Friedreich's ataxia. Revision of the phenotype according to molecular genetics.
    Schöls L; Amoiridis G; Przuntek H; Frank G; Epplen JT; Epplen C
    Brain; 1997 Dec; 120 ( Pt 12)():2131-40. PubMed ID: 9448568
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families.
    Moseley ML; Benzow KA; Schut LJ; Bird TD; Gomez CM; Barkhaus PE; Blindauer KA; Labuda M; Pandolfo M; Koob MD; Ranum LP
    Neurology; 1998 Dec; 51(6):1666-71. PubMed ID: 9855520
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes].
    Chen P; Ma M; Shang H; Su D; Zhang S; Yang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):626-33. PubMed ID: 19953483
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The natural history of degenerative ataxia: a retrospective study in 466 patients.
    Klockgether T; Lüdtke R; Kramer B; Abele M; Bürk K; Schöls L; Riess O; Laccone F; Boesch S; Lopes-Cendes I; Brice A; Inzelberg R; Zilber N; Dichgans J
    Brain; 1998 Apr; 121 ( Pt 4)():589-600. PubMed ID: 9577387
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.
    Giunti P; Sabbadini G; Sweeney MG; Davis MB; Veneziano L; Mantuano E; Federico A; Plasmati R; Frontali M; Wood NW
    Brain; 1998 Mar; 121 ( Pt 3)():459-67. PubMed ID: 9549522
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients.
    Maruyama H; Izumi Y; Morino H; Oda M; Toji H; Nakamura S; Kawakami H
    Am J Med Genet; 2002 Jul; 114(5):578-83. PubMed ID: 12116198
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].
    Yin XZ; Zhang BR; Wu DW; Tian J; Zhang H
    Yi Chuan; 2007 Jun; 29(6):688-92. PubMed ID: 17650485
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CAG repeat expansions in patients with sporadic cerebellar ataxia.
    Futamura N; Matsumura R; Fujimoto Y; Horikawa H; Suzumura A; Takayanagi T
    Acta Neurol Scand; 1998 Jul; 98(1):55-9. PubMed ID: 9696528
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype and phenotype analysis of Friedreich's ataxia compound heterozygous patients.
    De Castro M; García-Planells J; Monrós E; Cañizares J; Vázquez-Manrique R; Vílchez JJ; Urtasun M; Lucas M; Navarro G; Izquierdo G; Moltó MD; Palau F
    Hum Genet; 2000 Jan; 106(1):86-92. PubMed ID: 10982187
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.
    Kim JY; Park SS; Joo SI; Kim JM; Jeon BS
    Mol Cells; 2001 Dec; 12(3):336-41. PubMed ID: 11804332
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].
    Tang B; Wang D; Xia J
    Zhonghua Yi Xue Za Zhi; 1997 Nov; 77(11):819-22. PubMed ID: 9772474
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.