BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

309 related articles for article (PubMed ID: 8320699)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 111(2):152-6. PubMed ID: 12210342
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 94(1):1-4. PubMed ID: 10982473
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.
    Hazan J; Fontaine B; Bruyn RP; Lamy C; van Deutekom JC; Rime CS; Dürr A; Melki J; Lyon-Caen O; Agid Y
    Hum Mol Genet; 1994 Sep; 3(9):1569-73. PubMed ID: 7833913
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).
    Bouslam N; Benomar A; Azzedine H; Bouhouche A; Namekawa M; Klebe S; Charon C; Durr A; Ruberg M; Brice A; Yahyaoui M; Stevanin G
    Ann Neurol; 2005 Apr; 57(4):567-71. PubMed ID: 15786464
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus.
    Saugier-Veber P; Munnich A; Bonneau D; Rozet JM; Le Merrer M; Gil R; Boespflug-Tanguy O
    Nat Genet; 1994 Mar; 6(3):257-62. PubMed ID: 8012387
    [TBL] [Abstract][Full Text] [Related]  

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

  • 14. A new phenotype linked to SPG27 and refinement of the critical region on chromosome.
    Ribai P; Stevanin G; Bouslam N; Pontier B; Nelson I; Fontaine B; Dussert C; Charon C; Durr A; Brice A
    J Neurol; 2006 Jun; 253(6):714-9. PubMed ID: 16511635
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical observations in autosomal recessive spastic paraplegia in childhood and further evidence for genetic heterogeneity.
    Topaloğlu H; Pinarli G; Erdem H; Gücüyener K; Karaduman A; Topçu M; Akarsu AN; Ozgüç M
    Neuropediatrics; 1998 Aug; 29(4):189-94. PubMed ID: 9762694
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 5(1):1-10. PubMed ID: 8031529
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegia.
    Warner TT; Patel H; Proukakis C; Reed JA; McKie L; Wills A; Patton MA; Crosby AH
    J Neurol; 2004 Sep; 251(9):1068-74. PubMed ID: 15372247
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1.
    Orlacchio A; Kawarai T; Gaudiello F; St George-Hyslop PH; Floris R; Bernardi G
    Ann Neurol; 2005 Sep; 58(3):423-9. PubMed ID: 16130112
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 3(8):1263-7. PubMed ID: 7987300
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees.
    De Jonghe P; Krols L; Michalik A; Hazan J; Smeyers G; Löfgren A; Weissenbach J; Martin JJ; Van Broeckhoven C
    Eur J Hum Genet; 1996; 4(5):260-6. PubMed ID: 8946171
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.