BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

324 related articles for article (PubMed ID: 27044733)

  • 1. Spinocerebellar ataxia type-7: Report of a family in Northwest Nigeria.
    Alkali NH; Bwala SA; Alimi SA; Oyakhire SI
    Ann Afr Med; 2016; 15(2):87-90. PubMed ID: 27044733
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Lethal form of spinocerebellar ataxia type 7 with early onset in childhood.
    Gousse G; Patural H; Touraine R; Chabrier S; Rolland E; Antoine JC; Perrin L
    Arch Pediatr; 2018 Jan; 25(1):42-44. PubMed ID: 29248324
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population.
    Faruq M; Srivastava AK; Singh S; Gupta R; Dada T; Garg A; Behari M; Mukerji M
    Indian J Med Res; 2015 Feb; 141(2):187-98. PubMed ID: 25900954
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family (case report).
    Bouzid FZ; Mansouri M; Abdelaziz C; Louhab N; Bernard S; Strubi-Vuillaume I; Dafir K; Aboussair N
    Pan Afr Med J; 2021; 38():162. PubMed ID: 33995769
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Trinucleotide expansions in the SCA7 gene in a large family with spinocerebellar ataxia and craniocervical dystonia.
    Lin Y; Zheng JY; Jin YH; Xie YC; Jin ZB
    Neurosci Lett; 2008 Mar; 434(2):230-3. PubMed ID: 18325672
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family.
    Martin J; Van Regemorter N; Del-Favero J; Löfgren A; Van Broeckhoven C
    J Neurol Sci; 1999 Sep; 168(1):37-46. PubMed ID: 10500272
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evidence for a common founder effect amongst South African and Zambian individuals with Spinocerebellar ataxia type 7.
    Smith DC; Atadzhanov M; Mwaba M; Greenberg LJ
    J Neurol Sci; 2015 Jul; 354(1-2):75-8. PubMed ID: 26003224
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular Mechanisms and Therapeutic Strategies in Spinocerebellar Ataxia Type 7.
    Karam A; Trottier Y
    Adv Exp Med Biol; 2018; 1049():197-218. PubMed ID: 29427104
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spinocerebellar ataxia type 7: report of a new Italian family.
    Italiano D; Tarantino P; De Marco EV; Calabrò RS; Bramanti P; Quattrone A; Annesi G
    Intern Med; 2012; 51(20):2953-5. PubMed ID: 23064575
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Somatic instability of expanded CAG repeats of ATXN7 in Japanese patients with spinocerebellar ataxia type 7.
    Katagiri S; Hayashi T; Takeuchi T; Yamada H; Gekka T; Kawabe K; Kurita A; Tsuneoka H
    Doc Ophthalmol; 2015 Jun; 130(3):189-95. PubMed ID: 25643591
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Voice Alterations in Patients With Spinocerebellar Ataxia Type 7 (SCA7): Clinical-Genetic Correlations.
    Gómez-Coello A; Valadez-Jiménez VM; Cisneros B; Carrillo-Mora P; Parra-Cárdenas M; Hernández-Hernández O; Magaña JJ
    J Voice; 2017 Jan; 31(1):123.e1-123.e5. PubMed ID: 26992556
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Typical anticipation in type 7 spinocerebellar ataxia].
    Jäger M; von Rosen F; Fesl G; Gasser T
    Nervenarzt; 2000 Oct; 71(10):835-8. PubMed ID: 11082815
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].
    Yin XZ; Zhang BR; Wu DW; Tian J; Zhang H
    Yi Chuan; 2007 Jun; 29(6):688-92. PubMed ID: 17650485
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Primary degeneration of oculomotor, motor, and somatosensory systems and auditory and visual pathways in spinocerebellar ataxia type 7: A clinicopathological study in a Japanese autopsy case.
    Ouchi H; Ishiguro H; Shibano K; Hara K; Sugawara M; Enomoto K; Miyata H
    Neuropathology; 2023 Apr; 43(2):164-175. PubMed ID: 36168676
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spinocerebellar ataxia type 7.
    Martin JJ
    Handb Clin Neurol; 2012; 103():475-91. PubMed ID: 21827908
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular Targets and Therapeutic Strategies in Spinocerebellar Ataxia Type 7.
    Niewiadomska-Cimicka A; Trottier Y
    Neurotherapeutics; 2019 Oct; 16(4):1074-1096. PubMed ID: 31432449
    [TBL] [Abstract][Full Text] [Related]  

  • 19. AAV-Mediated CAG-Targeting Selectively Reduces Polyglutamine-Expanded Protein and Attenuates Disease Phenotypes in a Spinocerebellar Ataxia Mouse Model.
    Niewiadomska-Cimicka A; Fievet L; Surdyka M; Jesion E; Keime C; Singer E; Eisenmann A; Kalinowska-Poska Z; Nguyen HHP; Fiszer A; Figiel M; Trottier Y
    Int J Mol Sci; 2024 Apr; 25(8):. PubMed ID: 38673939
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region.
    Hellenbroich Y; Bubel S; Pawlack H; Opitz S; Vieregge P; Schwinger E; Zühlke C
    J Neurol; 2003 Jun; 250(6):668-71. PubMed ID: 12796826
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.