BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

603 related articles for article (PubMed ID: 30284037)

  • 1. Spinocerebellar ataxia: an update.
    Sullivan R; Yau WY; O'Connor E; Houlden H
    J Neurol; 2019 Feb; 266(2):533-544. PubMed ID: 30284037
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical Characteristics and Possible Drug Targets in Autosomal Dominant Spinocerebellar Ataxias.
    Szpisjak L; Zadori D; Klivenyi P; Vecsei L
    CNS Neurol Disord Drug Targets; 2019; 18(4):279-293. PubMed ID: 30864514
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Genetics, Mechanisms, and Therapeutic Progress in Polyglutamine Spinocerebellar Ataxias.
    Buijsen RAM; Toonen LJA; Gardiner SL; van Roon-Mom WMC
    Neurotherapeutics; 2019 Apr; 16(2):263-286. PubMed ID: 30607747
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical neurogenetics: autosomal dominant spinocerebellar ataxia.
    Shakkottai VG; Fogel BL
    Neurol Clin; 2013 Nov; 31(4):987-1007. PubMed ID: 24176420
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal-dominant cerebellar ataxias.
    Mundwiler A; Shakkottai VG
    Handb Clin Neurol; 2018; 147():173-185. PubMed ID: 29325610
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Diagnosis of Spinocerebellar Ataxias Caused by Trinucleotide Repeat Expansions.
    Martindale JE
    Curr Protoc Hum Genet; 2017 Jan; 92():9.30.1-9.30.22. PubMed ID: 28075481
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Twenty-five years since the identification of the first SCA gene: history, clinical features and perspectives for SCA1.
    Martins Junior CR; Borba FC; Martinez ARM; Rezende TJR; Cendes IL; Pedroso JL; Barsottini OGP; França Júnior MC
    Arq Neuropsiquiatr; 2018 Aug; 76(8):555-562. PubMed ID: 30231129
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The ever expanding spinocerebellar ataxias. Editorial.
    Matilla-Dueñas A
    Cerebellum; 2012 Dec; 11(4):821-7. PubMed ID: 22447528
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spinocerebellar ataxia: relationship between phenotype and genotype - a review.
    Sun YM; Lu C; Wu ZY
    Clin Genet; 2016 Oct; 90(4):305-14. PubMed ID: 27220866
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spinocerebellar ataxias (SCAs) caused by common mutations.
    Müller U
    Neurogenetics; 2021 Oct; 22(4):235-250. PubMed ID: 34401960
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Recent advances in understanding dominant spinocerebellar ataxias from clinical and genetic points of view.
    Coarelli G; Brice A; Durr A
    F1000Res; 2018; 7():. PubMed ID: 30473770
    [No Abstract]   [Full Text] [Related]  

  • 14. Widespread alternative splicing dysregulation occurs presymptomatically in CAG expansion spinocerebellar ataxias.
    Shorrock HK; Lennon CD; Aliyeva A; Davey EE; DeMeo CC; Pritchard CE; Planco L; Velez JM; Mascorro-Huamancaja A; Shin DS; Cleary JD; Berglund JA
    Brain; 2024 Feb; 147(2):486-504. PubMed ID: 37776516
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch families.
    Sinke RJ; Ippel EF; Diepstraten CM; Beemer FA; Wokke JH; van Hilten BJ; Knoers NV; van Amstel HK; Kremer HP
    Arch Neurol; 2001 Nov; 58(11):1839-44. PubMed ID: 11708993
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spinocerebellar ataxia type 6.
    Solodkin A; Gomez CM
    Handb Clin Neurol; 2012; 103():461-73. PubMed ID: 21827907
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Molecular genetic diagnosis and clinical analysis of spinocerebellar ataxia type 7].
    Xie QY; Liang XL; Li XH; Feng YQ
    Di Yi Jun Yi Da Xue Xue Bao; 2004 Jan; 24(1):62-5. PubMed ID: 14724100
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The molecular mechanisms of spinocerebellar ataxias for DNA repeat expansion in disease.
    Kumar M; Tyagi N; Faruq M
    Emerg Top Life Sci; 2023 Dec; 7(3):289-312. PubMed ID: 37668011
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
    Silveira I; Miranda C; Guimarães L; Moreira MC; Alonso I; Mendonça P; Ferro A; Pinto-Basto J; Coelho J; Ferreirinha F; Poirier J; Parreira E; Vale J; Januário C; Barbot C; Tuna A; Barros J; Koide R; Tsuji S; Holmes SE; Margolis RL; Jardim L; Pandolfo M; Coutinho P; Sequeiros J
    Arch Neurol; 2002 Apr; 59(4):623-9. PubMed ID: 11939898
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Spinocerebellar ataxia.
    Klockgether T; Mariotti C; Paulson HL
    Nat Rev Dis Primers; 2019 Apr; 5(1):24. PubMed ID: 30975995
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 31.