BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1430 related articles for article (PubMed ID: 17112370)

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

  • 2. [Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology].
    Espinós-Armero C; González-Cabo P; Palau-Martínez F
    Rev Neurol; 2005 Oct 1-15; 41(7):409-22. PubMed ID: 16193447
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Autosomal recessive cerebellar ataxias].
    Tranchant C; Anheim M
    Presse Med; 2009 Dec; 38(12):1852-9. PubMed ID: 19442480
    [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. [Autosomal recessive cerebellar ataxias].
    Anheim M
    Rev Neurol (Paris); 2011 May; 167(5):372-84. PubMed ID: 21087783
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
    Hamza W; Ali Pacha L; Hamadouche T; Muller J; Drouot N; Ferrat F; Makri S; Chaouch M; Tazir M; Koenig M; Benhassine T
    BMC Med Genet; 2015 Jun; 16():36. PubMed ID: 26068213
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management.
    Anheim M; Fleury M; Monga B; Laugel V; Chaigne D; Rodier G; Ginglinger E; Boulay C; Courtois S; Drouot N; Fritsch M; Delaunoy JP; Stoppa-Lyonnet D; Tranchant C; Koenig M
    Neurogenetics; 2010 Feb; 11(1):1-12. PubMed ID: 19440741
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Therapeutic developments in chronic ataxias].
    Buompadre MC
    Medicina (B Aires); 2013; 73 Suppl 1():49-54. PubMed ID: 24072051
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical features and molecular genetics of autosomal recessive cerebellar ataxias.
    Fogel BL; Perlman S
    Lancet Neurol; 2007 Mar; 6(3):245-57. PubMed ID: 17303531
    [TBL] [Abstract][Full Text] [Related]  

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

  • 11. [Recent advance in genetic study of hereditary autosomal recessive cerebellar ataxia].
    Guan WJ; Wang JL; Tang BS
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):673-6. PubMed ID: 23225047
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical spectrum of early onset cerebellar ataxia with retained tendon reflexes: an autosomal recessive ataxia not to be missed.
    Pedroso JL; Braga-Neto P; Ricarte IF; Albuquerque MV; Barsottini OG
    Arq Neuropsiquiatr; 2013 Jun; 71(6):345-8. PubMed ID: 23828538
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Clinical details and genetics of recessive ataxias].
    Zühlke C; Kreuz F; Bürk K
    Nervenarzt; 2011 Apr; 82(4):447-8, 450-8. PubMed ID: 20640395
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.
    Bouhlal Y; Zouari M; Kefi M; Ben Hamida C; Hentati F; Amouri R
    J Neurogenet; 2008; 22(2):139-48. PubMed ID: 18569450
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.
    Le Ber I; Moreira MC; Rivaud-Péchoux S; Chamayou C; Ochsner F; Kuntzer T; Tardieu M; Saïd G; Habert MO; Demarquay G; Tannier C; Beis JM; Brice A; Koenig M; Dürr A
    Brain; 2003 Dec; 126(Pt 12):2761-72. PubMed ID: 14506070
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Peripheral neuropathies associated with hereditary cerebellar ataxias].
    Anheim M; Tranchant C
    Rev Neurol (Paris); 2011 Jan; 167(1):72-6. PubMed ID: 21195440
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Recessive hereditary ataxia with early onset. Clinical study of 27 cases].
    Serlenga L; Trizio M; Pozio G; Oteri G; Caldarazzo M
    Riv Neurol; 1987; 57(5):285-9. PubMed ID: 3445070
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
    Ben Hamida M; Attia-Romdhane N; Triki CH; Oueslati S; Hentati F
    Rev Neurol (Paris); 1991; 147(12):798-808. PubMed ID: 1780608
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Early onset hereditary spinocerebellar ataxia: an autosomal recessive disorder distinct from Friedreich's ataxia.
    Kumar D; Blank CE
    Indian Pediatr; 1989 Oct; 26(10):1014-9. PubMed ID: 2630444
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Distinct phenotypes within autosomal recessive ataxias not linked to already known loci.
    Bouhlal Y; El-Euch-Fayeche G; Amouri R; Hentati F
    Acta Myol; 2005 Oct; 24(2):155-61. PubMed ID: 16550933
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 72.