BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

234 related articles for article (PubMed ID: 9436729)

  • 1. Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study.
    Nielsen JE; Krabbe K; Jennum P; Koefoed P; Jensen LN; Fenger K; Eiberg H; Hasholt L; Werdelin L; Sørensen SA
    J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):61-6. PubMed ID: 9436729
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 53(1):44-50. PubMed ID: 10408535
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Autosomal dominant spastic paraplegia linked to chromosome 2p: clinical and genetic studies of a large Japanese pedigree.
    Matsuura T; Sasaki H; Wakisaka A; Hamada T; Moriwaka F; Tashiro K
    J Neurol Sci; 1997 Oct; 151(1):65-70. PubMed ID: 9335012
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.
    Fink JK; Wu CT; Jones SM; Sharp GB; Lange BM; Lesicki A; Reinglass T; Varvil T; Otterud B; Leppert M
    Am J Hum Genet; 1995 Jan; 56(1):188-92. PubMed ID: 7825577
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2-q24.3.
    Huang S; Zhuyu ; Li H; Labu ; Baizhu ; Lo WH; Fischer C; Vogel F
    Hum Genet; 1997 Oct; 100(5-6):620-3. PubMed ID: 9341882
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p.
    Byrne PC; Mc Monagle P; Webb S; Fitzgerald B; Parfrey NA; Hutchinson M
    Neurology; 2000 Apr; 54(7):1510-7. PubMed ID: 10751268
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
    Ashley-Koch A; Bonner ER; Gaskell PC; West SG; Tim R; Wolpert CM; Jones R; Farrell CD; Nance M; Svenson IK; Marchuk DA; Boustany RM; Vance JM; Scott WK; Pericak-Vance MA
    Neurogenetics; 2001 Mar; 3(2):91-7. PubMed ID: 11354831
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.
    Nielsen JE; Koefoed P; Abell K; Hasholt L; Eiberg H; Fenger K; Niebuhr E; Sørensen SA
    Hum Mol Genet; 1997 Oct; 6(11):1811-6. PubMed ID: 9302257
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and genetic study of SPG6 mutation in a Chinese family with hereditary spastic paraplegia.
    Liu SG; Zhao JJ; Zhuang MY; Li FF; Zhang QJ; Huang SZ; Che FY; Lu DG; Liu SE; Teng JJ; Ma X
    J Neurol Sci; 2008 Mar; 266(1-2):109-14. PubMed ID: 17928003
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Urodynamic evaluation of patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.
    Jensen LN; Gerstenberg T; Kallestrup EB; Koefoed P; Nordling J; Nielsen JE
    J Neurol Neurosurg Psychiatry; 1998 Nov; 65(5):693-6. PubMed ID: 9810939
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation.
    Del-Favero J; Goossens D; De Jonghe P; Benson K; Michalik A; Van den Bossche D; Horwitz M; Van Broeckhoven C
    Hum Genet; 1999 Sep; 105(3):217-25. PubMed ID: 10987648
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Increased intracortical facilitation in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p.
    Nielsen JE; Jennum P; Fenger K; Sørensen SA; Fuglsang-Frederiksen A
    Eur J Neurol; 2001 Jul; 8(4):335-9. PubMed ID: 11422430
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial spastic paraplegia: evidence for a fourth locus.
    Bruyn RP; van Veen MM; Kremer H; Scheltens PH; Padberg GW
    Clin Neurol Neurosurg; 1997 May; 99(2):87-90. PubMed ID: 9213050
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.
    Heinzlef O; Paternotte C; Mahieux F; Prud'homme JF; Dien J; Madigand M; Pouget J; Weissenbach J; Roullet E; Hazan J
    J Med Genet; 1998 Feb; 35(2):89-93. PubMed ID: 9507385
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.