BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

278 related articles for article (PubMed ID: 23828538)

  • 1. 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]  

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

  • 3. 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]  

  • 4. Other autosomal recessive and childhood ataxias.
    De Michele G; Filla A
    Handb Clin Neurol; 2012; 103():343-57. PubMed ID: 21827899
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes.
    Filla A; De Michele G; Cavalcanti F; Perretti A; Santoro L; Barbieri F; D'Arienzo G; Campanella G
    J Neurol Neurosurg Psychiatry; 1990 Aug; 53(8):667-70. PubMed ID: 2213043
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.
    El Euch-Fayache G; Lalani I; Amouri R; Turki I; Ouahchi K; Hung WY; Belal S; Siddique T; Hentati F
    Arch Neurol; 2003 Jul; 60(7):982-8. PubMed ID: 12873855
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia.
    Harding AE
    J Neurol Neurosurg Psychiatry; 1981 Jun; 44(6):503-8. PubMed ID: 7276963
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Clinico-genetic study of type I spinocerebelllar ataxia].
    Svetel M; Culjković B; Sternić N; Dragasević B; Stojković I; Romac S; Kostić VS
    Srp Arh Celok Lek; 1999; 127(5-6):157-62. PubMed ID: 10500422
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [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]  

  • 12. Early-onset cerebellar ataxia with retained tendon reflexes.
    Ozeren A; Araç N; Ulkü A
    Acta Neurol Scand; 1989 Dec; 80(6):593-7. PubMed ID: 2618587
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature.
    Bhidayasiri R; Perlman SL; Pulst SM; Geschwind DH
    Arch Neurol; 2005 Dec; 62(12):1865-9. PubMed ID: 16344344
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Achalasia of the cardia associated with hereditary cerebellar ataxia.
    Murphy MS; Gardner-Medwin D; Eastham EJ
    Am J Gastroenterol; 1989 Oct; 84(10):1329-30. PubMed ID: 2801688
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diagnosis and management of early- and late-onset cerebellar ataxia.
    Brusse E; Maat-Kievit JA; van Swieten JC
    Clin Genet; 2007 Jan; 71(1):12-24. PubMed ID: 17204042
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.
    Berciano J; García A; Infante J
    Handb Clin Neurol; 2013; 115():907-32. PubMed ID: 23931821
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset].
    Iwabuchi K; Kogure T; Oda T; Kato Y; Ohtani K; Endo K; Kosaka K; Amano N; Yagishita S
    No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation study.
    Renaud M; Anheim M; Kamsteeg EJ; Mallaret M; Mochel F; Vermeer S; Drouot N; Pouget J; Redin C; Salort-Campana E; Kremer HP; Verschuuren-Bemelmans CC; Muller J; Scheffer H; Durr A; Tranchant C; Koenig M
    JAMA Neurol; 2014 Oct; 71(10):1305-10. PubMed ID: 25089919
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.
    Mrissa N; Belal S; Hamida CB; Amouri R; Turki I; Mrissa R; Hamida MB; Hentati F
    Neurology; 2000 Apr; 54(7):1408-14. PubMed ID: 10751248
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reduced life expectancy in 40 cases of early onset cerebellar ataxia with retained tendon reflexes: a population-based study.
    Chiò A; Orsi L; Mortara P; Schiffer D
    Acta Neurol Scand; 1993 Nov; 88(5):358-62. PubMed ID: 8296536
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.