These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1446 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 73.