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

156 related items for PubMed ID: 3479019

  • 1. Etiological heterogeneity in X-linked spastic paraplegia.
    Keppen LD, Leppert MF, O'Connell P, Nakamura Y, Stauffer D, Lathrop M, Lalouel JM, White R.
    Am J Hum Genet; 1987 Nov; 41(5):933-43. PubMed ID: 3479019
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia.
    Cambi F, Tang XM, Cordray P, Fain PR, Keppen LD, Barker DF.
    Neurology; 1996 Apr; 46(4):1112-7. PubMed ID: 8780101
    [Abstract] [Full Text] [Related]

  • 5. A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3.
    De Michele G, De Fusco M, Cavalcanti F, Filla A, Marconi R, Volpe G, Monticelli A, Ballabio A, Casari G, Cocozza S.
    Am J Hum Genet; 1998 Jul; 63(1):135-9. PubMed ID: 9634528
    [Abstract] [Full Text] [Related]

  • 6. Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.
    Fink JK, Heiman-Patterson T, Bird T, Cambi F, Dubé MP, Figlewicz DA, Fink JK, Haines JL, Heiman-Patterson T, Hentati A, Pericak-Vance MA, Raskind W, Rouleau GA, Siddique T.
    Neurology; 1996 Jun; 46(6):1507-14. PubMed ID: 8649538
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. X-linked spastic paraplegia.
    Ulkü A, Karasoy H, Karatepe A, Gökçay F.
    Acta Neurol Scand; 1991 Jun; 83(6):403-6. PubMed ID: 1887764
    [Abstract] [Full Text] [Related]

  • 9. Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q.
    Hedera P, DiMauro S, Bonilla E, Wald J, Eldevik OP, Fink JK.
    Neurology; 1999 Jul 13; 53(1):44-50. PubMed ID: 10408535
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.
    Reid E, Dearlove AM, Whiteford ML, Rhodes M, Rubinsztein DC.
    Neurology; 1999 Nov 10; 53(8):1844-9. PubMed ID: 10563637
    [Abstract] [Full Text] [Related]

  • 12. Locus-phenotype correlations in autosomal dominant pure hereditary spastic paraplegia. A clinical and molecular genetic study of 28 United Kingdom families.
    Reid E, Grayson C, Rogers MT, Rubinsztein DC.
    Brain; 1999 Sep 10; 122 ( Pt 9)():1741-55. PubMed ID: 10468513
    [Abstract] [Full Text] [Related]

  • 13. X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg.
    Zatz M, Penha-Serrano C, Otto PA.
    J Med Genet; 1976 Jun 10; 13(3):217-22. PubMed ID: 1084423
    [Abstract] [Full Text] [Related]

  • 14. Hereditary spastic paraplegia: LOD-score considerations for confirmation of linkage in a heterogeneous trait.
    Dubé MP, Mlodzienski MA, Kibar Z, Farlow MR, Ebers G, Harper P, Kolodny EH, Rouleau GA, Figlewicz DA.
    Am J Hum Genet; 1997 Mar 10; 60(3):625-9. PubMed ID: 9042923
    [Abstract] [Full Text] [Related]

  • 15. Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.
    Hentati A, Pericak-Vance MA, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist MH, Hung WY, Boustany RM, Bohlega S.
    Hum Mol Genet; 1994 Oct 10; 3(10):1867-71. PubMed ID: 7849714
    [Abstract] [Full Text] [Related]

  • 16. Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus.
    Muglia M, Criscuolo C, Magariello A, De Michele G, Scarano V, D'Adamo P, Ambrosio G, Gabriele AL, Patitucci A, Mazzei R, Conforti FL, Sprovieri T, Morgante L, Epifanio A, La Spina P, Valentino P, Gasparini P, Filla A, Quattrone A.
    Neurogenetics; 2004 Feb 10; 5(1):49-54. PubMed ID: 14658060
    [Abstract] [Full Text] [Related]

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

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. X-linked hydrocephalus: clinical heterogeneity at a single gene locus.
    Serville F, Lyonnet S, Pelet A, Reynaud M, Louail C, Munnich A, Le Merrer M.
    Eur J Pediatr; 1992 Jul 10; 151(7):515-8. PubMed ID: 1396913
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.