BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

388 related articles for article (PubMed ID: 9577387)

  • 1. 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]  

  • 2. 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]  

  • 3. Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3.
    Klockgether T; Skalej M; Wedekind D; Luft AR; Welte D; Schulz JB; Abele M; Bürk K; Laccone F; Brice A; Dichgans J
    Brain; 1998 Sep; 121 ( Pt 9)():1687-93. PubMed ID: 9762957
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Clinico-genetic study of type I spinocerebelllar ataxia].
    Svetel M; Culjković B; Sternić N; Dragasević B; Stojković I; Romac S; Kostić VS
    Srp Arh Celok Lek; 1999; 127(5-6):157-62. PubMed ID: 10500422
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.
    Bürk K; Abele M; Fetter M; Dichgans J; Skalej M; Laccone F; Didierjean O; Brice A; Klockgether T
    Brain; 1996 Oct; 119 ( Pt 5)():1497-505. PubMed ID: 8931575
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6.
    Watanabe H; Tanaka F; Matsumoto M; Doyu M; Ando T; Mitsuma T; Sobue G
    Clin Genet; 1998 Jan; 53(1):13-9. PubMed ID: 9550356
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.
    Schöls L; Gispert S; Vorgerd M; Menezes Vieira-Saecker AM; Blanke P; Auburger G; Amoiridis G; Meves S; Epplen JT; Przuntek H; Pulst SM; Riess O
    Arch Neurol; 1997 Sep; 54(9):1073-80. PubMed ID: 9311350
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Identification of five spinocerebellar ataxia type 2 pedigrees in patients with autosomal dominant cerebellar ataxia in Taiwan.
    Hsieh M; Li SY; Tsai CJ; Chen YY; Liu CS; Chang CY; Ro LS; Chen DF; Chen SS; Li C
    Acta Neurol Scand; 1999 Sep; 100(3):189-94. PubMed ID: 10478584
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics.
    Whaley NR; Fujioka S; Wszolek ZK
    Orphanet J Rare Dis; 2011 May; 6():33. PubMed ID: 21619691
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Uncloned expanded CAG/CTG repeat sequences in autosomal dominant cerebellar ataxia (ADCA) detected by the repeat expansion detection (RED) method.
    Pujana MA; Volpini V; Gratacós M; Corral J; Banchs I; Sánchez A; Genís D; Cervera C; Estivill X
    J Med Genet; 1998 Feb; 35(2):99-102. PubMed ID: 9507387
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Primary degenerative cerebellar ataxias in ethnic Bengalees in West Bengal: some observations.
    Chakravarty A; Mukherjee SC
    Neurol India; 2003 Jun; 51(2):227-34. PubMed ID: 14571010
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Early onset cerebellar ataxia with retained tendon reflexes. Clinical, electrophysiological and MRI observations in comparison with Friedreich's ataxia.
    Klockgether T; Petersen D; Grodd W; Dichgans J
    Brain; 1991 Aug; 114 ( Pt 4)():1559-73. PubMed ID: 1884166
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3.
    Bürk K; Fetter M; Abele M; Laccone F; Brice A; Dichgans J; Klockgether T
    J Neurol; 1999 Sep; 246(9):789-97. PubMed ID: 10525976
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cerebral blood flow in spinocerebellar degenerations: a single photon emission tomography study in 28 patients.
    De Michele G; Mainenti PP; Soricelli A; Di Salle F; Salvatore E; Longobardi MR; Postiglione A; Salvatore M; Filla A
    J Neurol; 1998 Sep; 245(9):603-8. PubMed ID: 9758299
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
    Schöls L; Amoiridis G; Büttner T; Przuntek H; Epplen JT; Riess O
    Ann Neurol; 1997 Dec; 42(6):924-32. PubMed ID: 9403486
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.