BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 4003033)

  • 1. Autosomal recessive non-progressive ataxia with an early childhood debut.
    Kvistad PH; Dahl A; Skre H
    Acta Neurol Scand; 1985 Apr; 71(4):295-302. PubMed ID: 4003033
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dominantly inherited congenital cerebellar ataxia with atrophy of the vermis.
    Tomiwa K; Baraitser M; Wilson J
    Pediatr Neurol; 1987; 3(6):360-2. PubMed ID: 3334022
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.
    Pascual-Castroviejo I; Gutierrez M; Morales C; Gonzalez-Mediero I; Martínez-Bermejo A; Pascual-Pascual SI
    Neuropediatrics; 1994 Aug; 25(4):183-90. PubMed ID: 7824090
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal recessive late onset multisystem disorder with cerebellar cortical atrophy at necropsy: report of a family.
    Harding AE; Diengdoh JV; Lees AJ
    J Neurol Neurosurg Psychiatry; 1984 Aug; 47(8):853-6. PubMed ID: 6470726
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Nonprogressive cerebellar disorder with mental retardation and autosomal recessive inheritance in Hutterites.
    Schurig V; Orman AV; Bowen P
    Am J Med Genet; 1981; 9(1):43-53. PubMed ID: 7246619
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Non-progressive congenital ataxia with cerebellar hypoplasia in three families.
    Yapici Z; Eraksoy M
    Acta Paediatr; 2005 Feb; 94(2):248-53. PubMed ID: 15981765
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families.
    Gücüyener K; Ozgül K; Paternotte C; Erdem H; Prud'homme JF; Ozgüç M; Topaloğlu H
    Neuropediatrics; 2001 Jun; 32(3):142-6. PubMed ID: 11521210
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.
    Harding AE
    Brain; 1982 Mar; 105(Pt 1):1-28. PubMed ID: 7066668
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Unique cerebellar-cerebral form of autosomal recessive ataxia.
    Matsubara E; Nagata T; Kageyama Y; Shiote M; Namba R; Nagano I; Shoji M; Abe K
    Tohoku J Exp Med; 2005 Sep; 207(1):81-5. PubMed ID: 16082159
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gillespie syndrome: a report of two further cases.
    Nelson J; Flaherty M; Grattan-Smith P
    Am J Med Genet; 1997 Aug; 71(2):134-8. PubMed ID: 9217210
    [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. Autosomal recessive spino-olivo-cerebellar degeneration without ataxia.
    Staal A; Stefanko SZ; Jennekens FG; Vries-Bos LH; van Gijn J
    J Neurol Neurosurg Psychiatry; 1983 Jul; 46(7):648-52. PubMed ID: 6886703
    [TBL] [Abstract][Full Text] [Related]  

  • 13. New autosomal recessive cerebellar ataxia disorder in a large inbred Lebanese family.
    Mégarbané A; Delague V; Ruchoux MM; Rizkallah E; Maurage CA; Viollet L; Rouaix-Emery N; Urtizberea A
    Am J Med Genet; 2001 Jun; 101(2):135-41. PubMed ID: 11391656
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism.
    Neuhäuser G; Opitz JM
    Clin Genet; 1975; 7(5):426-34. PubMed ID: 1149314
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Nonprogressive autosomal recessive ataxia maps to chromosome 9q34-9qter in a large consanguineous Lebanese family.
    Delague V; Bareil C; Bouvagnet P; Salem N; Chouery E; Loiselet J; Mégarbané A; Claustres M
    Ann Neurol; 2001 Aug; 50(2):250-3. PubMed ID: 11506409
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.
    Thiffault I; Rioux MF; Tetreault M; Jarry J; Loiselle L; Poirier J; Gros-Louis F; Mathieu J; Vanasse M; Rouleau GA; Bouchard JP; Lesage J; Brais B
    Brain; 2006 Sep; 129(Pt 9):2332-40. PubMed ID: 16672289
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel locus for autosomal recessive spastic ataxia on chromosome 17p.
    Bouslam N; Bouhouche A; Benomar A; Hanein S; Klebe S; Azzedine H; Di Giandomenico S; Boland-Augé A; Santorelli FM; Durr A; Brice A; Yahyaoui M; Stevanin G
    Hum Genet; 2007 May; 121(3-4):413-20. PubMed ID: 17273843
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Late onset autosomal dominant cerebellar ataxia. A family description and linkage analysis with the HLA system.
    Arruda WO; Petzl-Erler ML; Cardoso MA; Lehner T; Ott J
    Arq Neuropsiquiatr; 1991 Sep; 49(3):285-91. PubMed ID: 1807228
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel sacsin mutation in a Japanese woman showing clinical uniformity of autosomal recessive spastic ataxia of Charlevoix-Saguenay.
    Okawa S; Sugawara M; Watanabe S; Imota T; Toyoshima I
    J Neurol Neurosurg Psychiatry; 2006 Feb; 77(2):280-2. PubMed ID: 16421146
    [No Abstract]   [Full Text] [Related]  

  • 20. Familial cerebellar ataxia and hypogonadotropic hypogonadism: evidence for hypothalamic LHRH deficiency.
    Berciano J; Amado JA; Freijanes J; Rebollo M; Vaquero A
    J Neurol Neurosurg Psychiatry; 1982 Aug; 45(8):747-51. PubMed ID: 6813427
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.