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 *

319 related articles for article (PubMed ID: 19953482)

  • 41. Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes.
    Aydin G; Dekomien G; Hoffjan S; Gerding WM; Epplen JT; Arning L
    BMC Neurol; 2018 Jan; 18(1):3. PubMed ID: 29316893
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals.
    Freund AA; Scola RH; Teive HA; Arndt RC; da Costa-Ribeiro MC; Alle LF; Werneck LC
    Arq Neuropsiquiatr; 2009 Dec; 67(4):1124-32. PubMed ID: 20069235
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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]  

  • 44. [Identification of ATXN3 intermedial allele associated with a disease phenotype in an SCA3 Han Chinese family].
    Yu J; Ma JH; Zhang XN; Lei J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):190-3. PubMed ID: 20376803
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Molecular spectrum, family screening and genetic counselling of Spinocerebellar Ataxia (SCA) cases in an Indian scenario.
    Vishwakarma P; Agarwal S; Dean DD; Muthuswamy S; Mandal K
    J Neurogenet; 2021; 35(4):370-380. PubMed ID: 34159894
    [TBL] [Abstract][Full Text] [Related]  

  • 46. APOE ε2 allele may decrease the age at onset in patients with spinocerebellar ataxia type 3 or Machado-Joseph disease from the Chinese Han population.
    Peng H; Wang C; Chen Z; Sun Z; Jiao B; Li K; Huang F; Hou X; Wang J; Shen L; Xia K; Tang B; Jiang H
    Neurobiol Aging; 2014 Sep; 35(9):2179.e15-8. PubMed ID: 24746364
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Molecular analysis of CAG repeats at five different spinocerebellar ataxia loci: correlation and alternative explanations for disease pathogenesis.
    Alluri RV; Komandur S; Wagheray A; Chaudhuri JR; Sitajayalakshmi ; Meena AK; Jabeen A; Chawda K; Subhash K; Krishnaveni A; Hasan Q
    Mol Cells; 2007 Dec; 24(3):338-42. PubMed ID: 18182848
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Trinucleotide expansions in the SCA7 gene in a large family with spinocerebellar ataxia and craniocervical dystonia.
    Lin Y; Zheng JY; Jin YH; Xie YC; Jin ZB
    Neurosci Lett; 2008 Mar; 434(2):230-3. PubMed ID: 18325672
    [TBL] [Abstract][Full Text] [Related]  

  • 49. High prevalence of spinocerebellar ataxia type 1 (SCA1) in an isolated region of Japan.
    Onodera Y; Aoki M; Tsuda T; Kato H; Nagata T; Kameya T; Abe K; Itoyama Y
    J Neurol Sci; 2000 Sep; 178(2):153-8. PubMed ID: 11018707
    [TBL] [Abstract][Full Text] [Related]  

  • 50. The shortest expanded allele of the MJD1 gene in a Chinese MJD kindred with autonomic dysfunction.
    Gu W; Ma H; Wang K; Jin M; Zhou Y; Liu X; Wang G; Shen Y
    Eur Neurol; 2004; 52(2):107-11. PubMed ID: 15316156
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings.
    Wang JL; Xiao B; Cui XX; Guo JF; Lei LF; Song XW; Shen L; Jiang H; Yan XX; Pan Q; Long ZG; Xia K; Tang BS
    Mov Disord; 2009 Oct; 24(13):2007-11. PubMed ID: 19672991
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Molecular and clinical study of spinocerebellar ataxia type 7 in Chinese kindreds.
    Gu W; Wang Y; Liu X; Zhou B; Zhou Y; Wang G
    Arch Neurol; 2000 Oct; 57(10):1513-8. PubMed ID: 11030806
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.
    Sinha KK; Worth PF; Jha DK; Sinha S; Stinton VJ; Davis MB; Wood NW; Sweeney MG; Bhatia KP
    J Neurol Neurosurg Psychiatry; 2004 Mar; 75(3):448-52. PubMed ID: 14966163
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxia.
    Ranum LP; Lundgren JK; Schut LJ; Ahrens MJ; Perlman S; Aita J; Bird TD; Gomez C; Orr HT
    Am J Hum Genet; 1995 Sep; 57(3):603-8. PubMed ID: 7668288
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Diagnosis of five spinocerebellar ataxia disorders by multiplex amplification and capillary electrophoresis.
    Dorschner MO; Barden D; Stephens K
    J Mol Diagn; 2002 May; 4(2):108-13. PubMed ID: 11986402
    [TBL] [Abstract][Full Text] [Related]  

  • 57. No association of the SCA1 (CAG)31 allele with Huntington's disease, myotonic dystrophy type 1 and spinocerebellar ataxia type 3.
    Hellenbroich Y; Kaulich M; Opitz S; Schwinger E; Zühlke C
    Psychiatr Genet; 2004 Jun; 14(2):61-3. PubMed ID: 15167689
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?
    Savić D; Topisirović I; Keckarević M; Keckarević D; Major T; Culjković B; Stojković O; Rakocević-Stojanović V; Mladenović J; Todorović S; Apostolski S; Romac S
    Psychiatr Genet; 2001 Dec; 11(4):201-5. PubMed ID: 11807410
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Molecular and prenatal diagnosis of a pedigree with spinocerebellar ataxia].
    Cao DH; Ren MH; Liu XL; Jin CL; Meng ZY; Qiu GB
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Jun; 27(3):320-3. PubMed ID: 20533274
    [TBL] [Abstract][Full Text] [Related]  

  • 60. High frequency of Machado-Joseph disease identified in southeastern Chinese kindreds with spinocerebellar ataxia.
    Gan SR; Shi SS; Wu JJ; Wang N; Zhao GX; Weng ST; Murong SX; Lu CZ; Wu ZY
    BMC Med Genet; 2010 Mar; 11():47. PubMed ID: 20334689
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.