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 *

184 related articles for article (PubMed ID: 11030803)

  • 1. Extrapyramidal motor signs in degenerative ataxias.
    Schöls L; Peters S; Szymanski S; Krüger R; Lange S; Hardt C; Riess O; Przuntek H
    Arch Neurol; 2000 Oct; 57(10):1495-500. PubMed ID: 11030803
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Profile of extrapyramidal manifestations in 85 patients with spinocerebellar ataxia type 1, 2 and 3.
    Jhunjhunwala K; Netravathi M; Purushottam M; Jain S; Pal PK
    J Clin Neurosci; 2014 Jun; 21(6):1002-6. PubMed ID: 24602359
    [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. No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra.
    Schöls L; Reimold M; Seidel K; Globas C; Brockmann K; Hauser TK; Auburger G; Bürk K; den Dunnen W; Reischl G; Korf HW; Brunt ER; Rüb U
    Brain; 2015 Nov; 138(Pt 11):3316-26. PubMed ID: 26362908
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The parkinsonian phenotype of spinocerebellar ataxia type 2.
    Lu CS; Wu Chou YH; Kuo PC; Chang HC; Weng YH
    Arch Neurol; 2004 Jan; 61(1):35-8. PubMed ID: 14732617
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spinocerebellar ataxia type 2 with Levodopa-responsive parkinsonism culminating in motor neuron disease.
    Infante J; Berciano J; Volpini V; Corral J; Polo JM; Pascual J; Combarros O
    Mov Disord; 2004 Jul; 19(7):848-852. PubMed ID: 15254952
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6).
    Khan NL; Giunti P; Sweeney MG; Scherfler C; Brien MO; Piccini P; Wood NW; Lees AJ
    Mov Disord; 2005 Sep; 20(9):1115-9. PubMed ID: 15954136
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical Parkinsonism.
    Tan EK; Tong J; Pavanni R; Wong MC; Zhao Y
    Mov Disord; 2007 Oct; 22(13):1971-4. PubMed ID: 17712857
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].
    Rakowicz M; Zdzienicka E; Poniatowska R; Waliniowska E; Sułek A; Jakubowska T; Niedzielska K; Rola R; Wierzbicka A; Hoffman-Zacharska D; Głazowski C; Jakubczyk T; Niewiadomska M; Zaremba J
    Neurol Neurochir Pol; 2005; 39(4):263-275. PubMed ID: 16096942
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.
    Globas C; du Montcel ST; Baliko L; Boesch S; Depondt C; DiDonato S; Durr A; Filla A; Klockgether T; Mariotti C; Melegh B; Rakowicz M; Ribai P; Rola R; Schmitz-Hubsch T; Szymanski S; Timmann D; Van de Warrenburg BP; Bauer P; Schols L
    Mov Disord; 2008 Nov; 23(15):2232-8. PubMed ID: 18759344
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).
    Furtado S; Payami H; Lockhart PJ; Hanson M; Nutt JG; Singleton AA; Singleton A; Bower J; Utti RJ; Bird TD; de la Fuente-Fernandez R; Tsuboi Y; Klimek ML; Suchowersky O; Hardy J; Calne DB; Wszolek ZK; Farrer M; Gwinn-Hardy K; Stoessl AJ
    Mov Disord; 2004 Jun; 19(6):622-9. PubMed ID: 15197699
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Parkinsonism in spinocerebellar ataxia.
    Park H; Kim HJ; Jeon BS
    Biomed Res Int; 2015; 2015():125273. PubMed ID: 25866756
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dystonia and ataxia progression in spinocerebellar ataxias.
    Kuo PH; Gan SR; Wang J; Lo RY; Figueroa KP; Tomishon D; Pulst SM; Perlman S; Wilmot G; Gomez CM; Schmahmann JD; Paulson H; Shakkottai VG; Ying SH; Zesiewicz T; Bushara K; Geschwind MD; Xia G; Subramony SH; Ashizawa T; Kuo SH
    Parkinsonism Relat Disord; 2017 Dec; 45():75-80. PubMed ID: 29089256
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work.
    Gebus O; Montaut S; Monga B; Wirth T; Cheraud C; Alves Do Rego C; Zinchenko I; Carré G; Hamdaoui M; Hautecloque G; Nguyen-Them L; Lannes B; Chanson JB; Lagha-Boukbiza O; Fleury MC; Devys D; Nicolas G; Rudolf G; Bereau M; Mallaret M; Renaud M; Acquaviva C; Koenig M; Koob M; Kremer S; Namer IJ; Cazeneuve C; Echaniz-Laguna A; Tranchant C; Anheim M
    J Neurol; 2017 Jun; 264(6):1118-1126. PubMed ID: 28478596
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Non-ataxic manifestations of Spinocerebellar ataxia-2, their determinants and predictors.
    Stezin A; Venkatesh SD; Thennarasu K; Purushottam M; Jain S; Yadav R; Pal PK
    J Neurol Sci; 2018 Nov; 394():14-18. PubMed ID: 30196130
    [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. Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6.
    Linnemann C; Tezenas du Montcel S; Rakowicz M; Schmitz-Hübsch T; Szymanski S; Berciano J; van de Warrenburg BP; Pedersen K; Depondt C; Rola R; Klockgether T; García A; Mutlu G; Schöls L
    Cerebellum; 2016 Apr; 15(2):165-73. PubMed ID: 26054379
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Three spinocerebellar ataxia type 2 siblings with ataxia, parkinsonism, and motor neuronopathy.
    Nishikawa N; Nagai M; Tsujii T; Tanabe N; Takashima H; Nomoto M
    Intern Med; 2011; 50(13):1429-32. PubMed ID: 21720065
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2.
    Wang C; Xu Y; Feng X; Ma J; Xie S; Zhang Y; Tang BS; Chan P
    Neurobiol Aging; 2015 Jan; 36(1):545.e1-7. PubMed ID: 25189117
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.