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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 3587641)

  • 1. The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigree.
    Boustany RM; Fleischnick E; Alper CA; Marazita ML; Spence MA; Martin JB; Kolodny EH
    Neurology; 1987 Jun; 37(6):910-5. PubMed ID: 3587641
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Extensive genetic heterogeneity in the "pure" form of autosomal dominant familial spastic paraplegia (Strümpell's disease).
    Kobayashi H; Garcia CA; Tay PN; Hoffman EP
    Muscle Nerve; 1996 Nov; 19(11):1435-8. PubMed ID: 8874401
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 3(10):1867-71. PubMed ID: 7849714
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 122 ( Pt 9)():1741-55. PubMed ID: 10468513
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia.
    Speer MC; Kingston HM; Boustany RM; Gaskell PC; Robinson LC; Lennon F; Wolpert CM; Yamaoka LH; Kahler SG; Hogan EL
    Am J Med Genet; 1995 Aug; 60(4):307-11. PubMed ID: 7485266
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Autosomal dominant, familial spastic paraplegia, type I: clinical and genetic analysis of a large North American family.
    Fink JK; Sharp GB; Lange BM; Wu CB; Haley T; Otterud B; Peacock M; Leppert M
    Neurology; 1995 Feb; 45(2):325-31. PubMed ID: 7854534
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Linkage studies of X-linked recessive spastic paraplegia using DNA probes.
    Kenwrick S; Ionasescu V; Ionasescu G; Searby C; King A; Dubowitz M; Davies KE
    Hum Genet; 1986 Jul; 73(3):264-6. PubMed ID: 3460961
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21.
    Nance MA; Raabe WA; Midani H; Kolodny EH; David WS; Megna L; Pericak-Vance MA; Haines JL
    Hum Hered; 1998; 48(3):169-78. PubMed ID: 9618065
    [TBL] [Abstract][Full Text] [Related]  

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

  • 13. 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]  

  • 14. Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia.
    Fontaine B; Rime CS; Hazan J; Dürr A; Stevanin G; Penet C; Reboul J; Agid Y; Lyon-Caen O; Baumann N
    Neuromuscul Disord; 1995 Jan; 5(1):11-7. PubMed ID: 7719135
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family.
    Bürger J; Metzke H; Paternotte C; Schilling F; Hazan J; Reis A
    Hum Genet; 1996 Sep; 98(3):371-5. PubMed ID: 8707310
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity.
    Reid E; Dearlove AM; Rhodes M; Rubinsztein DC
    Am J Hum Genet; 1999 Sep; 65(3):757-63. PubMed ID: 10441583
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recessively inherited 'pure' spastic paraplegia: case study.
    de Coo IF; Gabreëls FJ; Renier WO; Colon EJ; ter Haar BG
    Clin Neurol Neurosurg; 1982; 84(4):247-53. PubMed ID: 6301736
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13.
    Reid E; Dearlove AM; Osborn O; Rogers MT; Rubinsztein DC
    Am J Hum Genet; 2000 Feb; 66(2):728-32. PubMed ID: 10677333
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.
    Scott WK; Gaskell PC; Lennon F; Wolpert CM; Menold MM; Aylsworth AS; Warner C; Farrell CD; Boustany RM; Albright SG; Boyd E; Kingston HM; Cumming WJ; Vance JM; Pericak-Vance MA
    Neurogenetics; 1997 Sep; 1(2):95-102. PubMed ID: 10732810
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q.
    Hazan J; Lamy C; Melki J; Munnich A; de Recondo J; Weissenbach J
    Nat Genet; 1993 Oct; 5(2):163-7. PubMed ID: 8252041
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.