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Journal Abstract Search

209 related items for PubMed ID: 7987300

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

  • 3. 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 Sep; 48(3):169-78. PubMed ID: 9618065
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  • 4. 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; 5(1):49-54. PubMed ID: 14658060
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  • 6. Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15.
    Martínez Murillo F, Kobayashi H, Pegoraro E, Galluzzi G, Creel G, Mariani C, Farina E, Ricci E, Alfonso G, Pauli RM, Hoffman EP.
    Neurology; 1999 Jul 13; 53(1):50-6. PubMed ID: 10408536
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  • 7. Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 families.
    Coutinho P, Barros J, Zemmouri R, Guimarães J, Alves C, Chorão R, Lourenço E, Ribeiro P, Loureiro JL, Santos JV, Hamri A, Paternotte C, Hazan J, Silva MC, Prud'homme JF, Grid D.
    Arch Neurol; 1999 Aug 13; 56(8):943-9. PubMed ID: 10448799
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  • 8. 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 13; 137(2):131-8. PubMed ID: 8782167
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  • 9. 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 13; 56(1):188-92. PubMed ID: 7825577
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  • 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 13; 57(4):567-71. PubMed ID: 15786464
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  • 12. 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 13; 3(2):91-7. PubMed ID: 11354831
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  • 13. 'Complicated' autosomal dominant familial spastic paraplegia is genetically distinct from 'pure' forms.
    Meierkord H, Nürnberg P, Mainz A, Marczinek K, Mrug M, Hampe J.
    Arch Neurol; 1997 Apr 13; 54(4):379-84. PubMed ID: 9109738
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  • 14. 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 13; 19(11):1435-8. PubMed ID: 8874401
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  • 15. 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 13; 35(2):89-93. PubMed ID: 9507385
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  • 16. A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia.
    Wilkinson PA, Crosby AH, Turner C, Patel H, Wood NW, Schapira AH, Warner TT.
    Neurology; 2003 Jul 22; 61(2):235-8. PubMed ID: 12874406
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  • 17. Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.
    Gispert S, Santos N, Damen R, Voit T, Schulz J, Klockgether T, Orozco G, Kreuz F, Weissenbach J, Auburger G.
    Am J Hum Genet; 1995 Jan 22; 56(1):183-7. PubMed ID: 7825576
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  • 18. A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28.
    Vazza G, Zortea M, Boaretto F, Micaglio GF, Sartori V, Mostacciuolo ML.
    Am J Hum Genet; 2000 Aug 22; 67(2):504-9. PubMed ID: 10877981
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  • 19. A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1.
    Meijer IA, Cossette P, Roussel J, Benard M, Toupin S, Rouleau GA.
    Ann Neurol; 2004 Oct 22; 56(4):579-82. PubMed ID: 15455396
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  • 20. 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 14; 60(4):307-11. PubMed ID: 7485266
    [Abstract] [Full Text] [Related]

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