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 *

125 related articles for article (PubMed ID: 17920187)

  • 1. White matter hyperintense lesions in genetically proven spinocerebellar ataxia 8.
    Kumar N; Miller GM
    Clin Neurol Neurosurg; 2008 Jan; 110(1):65-8. PubMed ID: 17920187
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spinocerebellar ataxia type 2 (SCA2) with white matter involvement.
    Armstrong J; Bonaventura I; Rojo A; González G; Corral J; Nadal N; Volpini V; Ferrer I
    Neurosci Lett; 2005 Jun; 381(3):247-51. PubMed ID: 15896478
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Patterns of fractional anisotropy changes in white matter of cerebellar peduncles distinguish spinocerebellar ataxia-1 from multiple system atrophy and other ataxia syndromes.
    Prakash N; Hageman N; Hua X; Toga AW; Perlman SL; Salamon N
    Neuroimage; 2009 Aug; 47 Suppl 2():T72-81. PubMed ID: 19446636
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Type 8 spinocerebellar ataxia. A report of a family].
    Sempere AP; Millán JM; Royo-Vilanova C; Medrano V
    Rev Neurol; 2001 Jul 16-31; 33(2):150-2. PubMed ID: 11562876
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Case of spinocerebellar ataxia type 1 showing high intensity lesions in the frontal white matter on T2-weighted magnetic resonance images.
    Nakayama T; Nakayama K; Takahashi Y; Ohkubo K; Tobe H; Soma M; Ozawa Y; Kanmatsuse K; Nakamura M; Hironaga T; Makizumi Y; Nagura H
    Med Sci Monit; 2001; 7(2):299-303. PubMed ID: 11257739
    [TBL] [Abstract][Full Text] [Related]  

  • 6. ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias.
    Della Nave R; Foresti S; Tessa C; Moretti M; Ginestroni A; Gavazzi C; Guerrini L; Salvi F; Piacentini S; Mascalchi M
    Neuroimage; 2004 Jun; 22(2):698-705. PubMed ID: 15193598
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cranial magnetic resonance imaging in genetically proven myotonic dystrophy type 1 and 2.
    Kornblum C; Reul J; Kress W; Grothe C; Amanatidis N; Klockgether T; Schröder R
    J Neurol; 2004 Jun; 251(6):710-4. PubMed ID: 15311347
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17).
    Lasek K; Lencer R; Gaser C; Hagenah J; Walter U; Wolters A; Kock N; Steinlechner S; Nagel M; Zühlke C; Nitschke MF; Brockmann K; Klein C; Rolfs A; Binkofski F
    Brain; 2006 Sep; 129(Pt 9):2341-52. PubMed ID: 16760196
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.
    Gupta A; Jankovic J
    Parkinsonism Relat Disord; 2009 Nov; 15(9):621-6. PubMed ID: 19559641
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.
    Reetz K; Costa AS; Mirzazade S; Lehmann A; Juzek A; Rakowicz M; Boguslawska R; Schöls L; Linnemann C; Mariotti C; Grisoli M; Dürr A; van de Warrenburg BP; Timmann D; Pandolfo M; Bauer P; Jacobi H; Hauser TK; Klockgether T; Schulz JB;
    Brain; 2013 Mar; 136(Pt 3):905-17. PubMed ID: 23423669
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [A familial case of spinocerebellar ataxia type 8 (SCA 8)--its clinical findings and an issue about the genetic basis].
    Hokezu Y; Takiyama Y; Sakoe K; Nagamatsu K
    Rinsho Shinkeigaku; 2000 Nov; 40(11):1116-21. PubMed ID: 11332193
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sporadic SCA8 mutation resembling corticobasal degeneration.
    Baba Y; Uitti RJ; Farrer MJ; Wszolek ZK
    Parkinsonism Relat Disord; 2005 May; 11(3):147-50. PubMed ID: 15823478
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Brain structural damage in spinocerebellar ataxia type 2. A voxel-based morphometry study.
    Della Nave R; Ginestroni A; Tessa C; Cosottini M; Giannelli M; Salvatore E; Sartucci F; De Michele G; Dotti MT; Piacentini S; Mascalchi M
    Mov Disord; 2008 Apr; 23(6):899-903. PubMed ID: 18311829
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinicopathologic investigation of a family with expanded SCA8 CTA/CTG repeats.
    Ito H; Kawakami H; Wate R; Matsumoto S; Imai T; Hirano A; Kusaka H
    Neurology; 2006 Oct; 67(8):1479-81. PubMed ID: 17060579
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.
    Schulz JB; Borkert J; Wolf S; Schmitz-Hübsch T; Rakowicz M; Mariotti C; Schöls L; Timmann D; van de Warrenburg B; Dürr A; Pandolfo M; Kang JS; Mandly AG; Nägele T; Grisoli M; Boguslawska R; Bauer P; Klockgether T; Hauser TK
    Neuroimage; 2010 Jan; 49(1):158-68. PubMed ID: 19631275
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dissociation of grey and white matter reduction in spinocerebellar ataxia type 3 and 6: a voxel-based morphometry study.
    Lukas C; Schöls L; Bellenberg B; Rüb U; Przuntek H; Schmid G; Köster O; Suchan B
    Neurosci Lett; 2006 Nov; 408(3):230-5. PubMed ID: 17005321
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spinocerebellar ataxia type 8 in Scotland: frequency, neurological, neuropsychological and neuropsychiatric findings.
    Torrens L; Burns E; Stone J; Graham C; Wright H; Summers D; Sellar R; Porteous M; Warner J; Zeman A
    Acta Neurol Scand; 2008 Jan; 117(1):41-8. PubMed ID: 18095954
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23.
    Gribaa M; Salih M; Anheim M; Lagier-Tourenne C; H'mida D; Drouot N; Mohamed A; Elmalik S; Kabiraj M; Al-Rayess M; Almubarak M; Bétard C; Goebel H; Koenig M
    Brain; 2007 Jul; 130(Pt 7):1921-8. PubMed ID: 17470496
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of SCA8 and SCA12 loci in 134 Italian ataxic patients negative for SCA1-3, 6 and 7 CAG expansions.
    Brusco A; Cagnoli C; Franco A; Dragone E; Nardacchione A; Grosso E; Mortara P; Mutani R; Migone N; Orsi L
    J Neurol; 2002 Jul; 249(7):923-9. PubMed ID: 12140678
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pattern and significance of white matter abnormalities in myotonic dystrophy type 1: an MRI study.
    Di Costanzo A; Di Salle F; Santoro L; Tessitore A; Bonavita V; Tedeschi G
    J Neurol; 2002 Sep; 249(9):1175-82. PubMed ID: 12242535
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.