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Journal Abstract Search

130 related items for PubMed ID: 9254866

  • 1. Evidence of a third locus in X-linked recessive spastic paraplegia.
    Steinmüller R, Lantigua-Cruz A, Garcia-Garcia R, Kostrzewa M, Steinberger D, Müller U.
    Hum Genet; 1997 Aug; 100(2):287-9. PubMed ID: 9254866
    [Abstract] [Full Text] [Related]

  • 2. X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus.
    Bonneau D, Rozet JM, Bulteau C, Berthier M, Mettey R, Gil R, Munnich A, Le Merrer M.
    J Med Genet; 1993 May; 30(5):381-4. PubMed ID: 8320699
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  • 3. Molecular genetics of familial spastic paraplegia: a multitude of responsible genes.
    Kobayashi H, Garcia CA, Alfonso G, Marks HG, Hoffman EP.
    J Neurol Sci; 1996 May; 137(2):131-8. PubMed ID: 8782167
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  • 4. X-linked spastic paraplegia.
    Ulkü A, Karasoy H, Karatepe A, Gökçay F.
    Acta Neurol Scand; 1991 Jun; 83(6):403-6. PubMed ID: 1887764
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  • 5. X-linked spastic paraplegia: evidence for homogeneity with a variable phenotype.
    Goldblatt J, Ballo R, Sachs B, Moosa A.
    Clin Genet; 1989 Feb; 35(2):116-20. PubMed ID: 2470540
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  • 6. The spectrum of "complicated spastic paraplegia, MASA syndrome and X-linked hydrocephalus". Contribution of DNA linkage analysis in genetic counseling of individual families.
    Schrander-Stumpel C, Meyer H, Merckx D, Jones M, Israel J, Sommer A, Stevens C, Tinschert S, Wilson G, Willems P.
    Genet Couns; 1994 Feb; 5(1):1-10. PubMed ID: 8031529
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  • 7. Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2.
    Tamagaki A, Shima M, Tomita R, Okumura M, Shibata M, Morichika S, Kurahashi H, Giddings JC, Yoshioka A, Yokobayashi Y.
    Am J Med Genet; 2000 Sep 04; 94(1):5-8. PubMed ID: 10982474
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  • 8. Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.
    Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T.
    Hum Mol Genet; 1994 Aug 04; 3(8):1263-7. PubMed ID: 7987300
    [Abstract] [Full Text] [Related]

  • 9. Novel syndromic form of X-linked complicated spastic paraplegia.
    Claes S, Devriendt K, Van Goethem G, Roelen L, Meireleire J, Raeymaekers P, Cassiman JJ, Fryns JP.
    Am J Med Genet; 2000 Sep 04; 94(1):1-4. PubMed ID: 10982473
    [Abstract] [Full Text] [Related]

  • 10. Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description.
    Klebe S, Durr A, Bouslam N, Grid D, Paternotte C, Depienne C, Hanein S, Bouhouche A, Elleuch N, Azzedine H, Poea-Guyon S, Forlani S, Denis E, Charon C, Hazan J, Brice A, Stevanin G.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Oct 05; 144B(7):854-61. PubMed ID: 17503452
    [Abstract] [Full Text] [Related]

  • 11. Recent advances in hereditary spastic paraplegia.
    Tallaksen CM, Dürr A, Brice A.
    Curr Opin Neurol; 2001 Aug 05; 14(4):457-63. PubMed ID: 11470961
    [Abstract] [Full Text] [Related]

  • 12. Further evidence for a fourth gene causing X-linked pure spastic paraplegia.
    Starling A, Rocco P, Cambi F, Hobson GM, Passos Bueno MR, Zatz M.
    Am J Med Genet; 2002 Aug 01; 111(2):152-6. PubMed ID: 12210342
    [Abstract] [Full Text] [Related]

  • 13. Male neonatal death and progressive weakness and immune deficiency in females: an unknown X linked condition.
    Woods G, Black G, Norbury G.
    J Med Genet; 1995 Mar 01; 32(3):191-6. PubMed ID: 7783167
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  • 16. Screening of patients with hereditary spastic paraparesis and Addison's disease for adrenoleukodystrophy/adrenomyeloneuropathy.
    Holmberg BH, Hägg E, Duchek M, Hagenfeldt L.
    Acta Neurol Scand; 1992 Feb 01; 85(2):147-9. PubMed ID: 1574990
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  • 17. Spastic paraplegia, optic atrophy, microcephaly with normal intelligence, and XY sex reversal: a new autosomal recessive syndrome?
    Teebi AS, Miller S, Ostrer H, Eydoux P, Colomb-Brockmann C, Oudjhane K, Watters G.
    J Med Genet; 1998 Sep 01; 35(9):759-62. PubMed ID: 9733035
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  • 19. Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methods.
    Kobayashi H, Matise TC, Perlin MW, Marks HG, Hoffman EP.
    Hum Genet; 1995 May 01; 95(5):483-90. PubMed ID: 7759066
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