BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

385 related articles for article (PubMed ID: 37000369)

  • 1. A Review of Ocular Movement Abnormalities in Hereditary Cerebellar Ataxias.
    Salari M; Etemadifar M; Rashedi R; Mardani S
    Cerebellum; 2024 Apr; 23(2):702-721. PubMed ID: 37000369
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare forms of autosomal recessive neurodegenerative ataxia.
    Koenig M
    Semin Pediatr Neurol; 2003 Sep; 10(3):183-92. PubMed ID: 14653406
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Eye movement changes in autosomal dominant spinocerebellar ataxias.
    Rosini F; Pretegiani E; Battisti C; Dotti MT; Federico A; Rufa A
    Neurol Sci; 2020 Jul; 41(7):1719-1734. PubMed ID: 32130555
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
    Wolf NI; Koenig M
    Handb Clin Neurol; 2013; 113():1869-78. PubMed ID: 23622410
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spinocerebellar ataxia type 11 (SCA11): An update.
    Gong Z; Lei L
    Eur J Neurosci; 2023 Jul; 58(2):2623-2640. PubMed ID: 37329117
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal recessive cerebellar ataxias: the current state of affairs.
    Vermeer S; van de Warrenburg BP; Willemsen MA; Cluitmans M; Scheffer H; Kremer BP; Knoers NV
    J Med Genet; 2011 Oct; 48(10):651-9. PubMed ID: 21856962
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spinocerebellar ataxia type 23 (SCA23): a review.
    Wu F; Wang X; Li X; Teng H; Tian T; Bai J
    J Neurol; 2021 Dec; 268(12):4630-4645. PubMed ID: 33175256
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spinocerebellar ataxia 27B (SCA27B), a frequent late-onset cerebellar ataxia.
    Clément G; Puisieux S; Pellerin D; Brais B; Bonnet C; Renaud M
    Rev Neurol (Paris); 2024 May; 180(5):410-416. PubMed ID: 38609751
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: a novel entity?
    Wictorin K; Brådvik B; Nilsson K; Soller M; van Westen D; Bynke G; Bauer P; Schöls L; Puschmann A
    Parkinsonism Relat Disord; 2014 Jul; 20(7):748-54. PubMed ID: 24787759
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical, genetic and neuropathological characterization of spinocerebellar ataxia type 37.
    Corral-Juan M; Serrano-Munuera C; Rábano A; Cota-González D; Segarra-Roca A; Ispierto L; Cano-Orgaz AT; Adarmes AD; Méndez-Del-Barrio C; Jesús S; Mir P; Volpini V; Alvarez-Ramo R; Sánchez I; Matilla-Dueñas A
    Brain; 2018 Jul; 141(7):1981-1997. PubMed ID: 29939198
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal recessive cerebellar ataxias.
    Palau F; Espinós C
    Orphanet J Rare Dis; 2006 Nov; 1():47. PubMed ID: 17112370
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force.
    Beaudin M; Matilla-Dueñas A; Soong BW; Pedroso JL; Barsottini OG; Mitoma H; Tsuji S; Schmahmann JD; Manto M; Rouleau GA; Klein C; Dupre N
    Cerebellum; 2019 Dec; 18(6):1098-1125. PubMed ID: 31267374
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics.
    Whaley NR; Fujioka S; Wszolek ZK
    Orphanet J Rare Dis; 2011 May; 6():33. PubMed ID: 21619691
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of novel senataxin mutations in Chinese patients with autosomal recessive cerebellar ataxias by targeted next-generation sequencing.
    Lu C; Zheng YC; Dong Y; Li HF
    BMC Neurol; 2016 Sep; 16(1):179. PubMed ID: 27644330
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary ataxias: overview.
    Jayadev S; Bird TD
    Genet Med; 2013 Sep; 15(9):673-83. PubMed ID: 23538602
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New autosomal recessive cerebellar ataxias with oculomotor apraxia.
    Le Ber I; Brice A; Dürr A
    Curr Neurol Neurosci Rep; 2005 Sep; 5(5):411-7. PubMed ID: 16131425
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Chronic ataxia in childhood].
    Erazo Torricelli R
    Medicina (B Aires); 2013; 73 Suppl 1():38-48. PubMed ID: 24072050
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular Characterization of Portuguese Patients with Hereditary Cerebellar Ataxia.
    Santos M; Damásio J; Carmona S; Neto JL; Dehghani N; Guedes LC; Barbot C; Barros J; Brás J; Sequeiros J; Guerreiro R
    Cells; 2022 Mar; 11(6):. PubMed ID: 35326432
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ocular motor characteristics of different subtypes of spinocerebellar ataxia: distinguishing features.
    Kim JS; Kim JS; Youn J; Seo DW; Jeong Y; Kang JH; Park JH; Cho JW
    Mov Disord; 2013 Aug; 28(9):1271-7. PubMed ID: 23609488
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cerebellar ataxias: an update.
    Manto M; Gandini J; Feil K; Strupp M
    Curr Opin Neurol; 2020 Feb; 33(1):150-160. PubMed ID: 31789706
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.