BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 30231129)

  • 1. 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]  

  • 2. 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]  

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

  • 4. [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]  

  • 5. 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]  

  • 6. The clinical diagnosis of autosomal dominant spinocerebellar ataxias.
    Klockgether T
    Cerebellum; 2008; 7(2):101-5. PubMed ID: 18418679
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mini-review: spinocerebellar ataxias: an update of SCA genes.
    Trott A; Houenou LJ
    Recent Pat DNA Gene Seq; 2012 Aug; 6(2):115-21. PubMed ID: 22670601
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic Distribution of Five Spinocerebellar Ataxia Microsatellite Loci in Mexican Native American Populations and Its Impact on Contemporary Mestizo Populations.
    Gómez R; Tapia-Guerrero YS; Cisneros B; Orozco L; Cerecedo-Zapata C; Mendoza-Caamal E; Leyva-Gómez G; Leyva-García N; Velázquez-Pérez L; Magaña JJ
    Genes (Basel); 2022 Jan; 13(1):. PubMed ID: 35052497
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CAG repeat mosaicism is gene specific in spinocerebellar ataxias.
    Kacher R; Lejeune FX; David I; Boluda S; Coarelli G; Leclere-Turbant S; Heinzmann A; Marelli C; Charles P; Goizet C; Kabir N; Hilab R; Jornea L; Six J; Dommergues M; Fauret AL; Brice A; Humbert S; Durr A
    Am J Hum Genet; 2024 May; 111(5):913-926. PubMed ID: 38626762
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. HD and SCA1: Tales from two 30-year journeys since gene discovery.
    Thompson LM; Orr HT
    Neuron; 2023 Nov; 111(22):3517-3530. PubMed ID: 37863037
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The spinocerebellar ataxias: order emerges from chaos.
    Margolis RL
    Curr Neurol Neurosci Rep; 2002 Sep; 2(5):447-56. PubMed ID: 12169226
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in southern India.
    Krishna N; Mohan S; Yashavantha BS; Rammurthy A; Kiran Kumar HB; Mittal U; Tyagi S; Mukerji M; Jain S; Pal PK; Purushottam M
    Indian J Med Res; 2007 Nov; 126(5):465-70. PubMed ID: 18160752
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fluorescent multiplex PCR--fast method for autosomal dominant spinocerebellar ataxias screening.
    Bauer PO; Kotliarova SE; Matoska V; Musova Z; Hedvicakova P; Boday A; Tomek A; Nukina N; Goetz P
    Genetika; 2005 Jun; 41(6):830-7. PubMed ID: 16080609
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic Modeling of the Neurodegenerative Disease Spinocerebellar Ataxia Type 1 in Zebrafish.
    Elsaey MA; Namikawa K; Köster RW
    Int J Mol Sci; 2021 Jul; 22(14):. PubMed ID: 34298970
    [TBL] [Abstract][Full Text] [Related]  

  • 16. (CAG)
    Wang P; Chen Z; Peng Y; Cao L; Li X; Wang C; Yang H; Peng H; Shi Y; Zhou X; Li T; Feng L; Wu C; Qiu R; Xia K; Tang B; Jiang H
    Eur J Neurol; 2019 Aug; 26(8):1130-1136. PubMed ID: 30891880
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Spinocerebellar ataxia: eight cases from one pedigree].
    Tian S; Zhao Q; Yang X; An R; Xu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):726-7. PubMed ID: 27577232
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Spinocerebellar ataxia 7 (SCA7).
    Lebre AS; Brice A
    Cytogenet Genome Res; 2003; 100(1-4):154-63. PubMed ID: 14526176
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.