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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

161 related items for 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
    [Abstract] [Full Text] [Related]

  • 2. Dominantly inherited congenital cerebellar ataxia with atrophy of the vermis.
    Tomiwa K, Baraitser M, Wilson J.
    Pediatr Neurol; 1987 Apr; 3(6):360-2. PubMed ID: 3334022
    [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
    [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
    [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 Aug; 9(1):43-53. PubMed ID: 7246619
    [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
    [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
    [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
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No 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 08; 71(2):134-8. PubMed ID: 9217210
    [Abstract] [Full Text] [Related]

  • 11. Autosomal recessive cerebellar ataxias.
    Palau F, Espinós C.
    Orphanet J Rare Dis; 2006 Nov 17; 1():47. PubMed ID: 17112370
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No 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 15; 101(2):135-41. PubMed ID: 11391656
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No 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 15; 50(2):250-3. PubMed ID: 11506409
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No 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 15; 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 15; 45(8):747-51. PubMed ID: 6813427
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.