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Volumn 80, Issue 17, 2013, Pages 1544-1545

Lysosomal enzyme defects and Parkinson disease

Author keywords

[No Author keywords available]

Indexed keywords

LEVODOPA; LYSOSOME ENZYME; SPHINGOMYELIN PHOSPHODIESTERASE; SPHINGOMYELIN PHOSPHODIESTERASE 1, HUMAN;

EID: 84878901392     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e31828f1958     Document Type: Editorial
Times cited : (3)

References (6)
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    • 33750017421 scopus 로고    scopus 로고
    • The discovery of dopamine deficiency in the parkinsonian brain
    • Hornykiewicz O. The discovery of dopamine deficiency in the parkinsonian brain. J Neural Transm Suppl 2006;70:9-15.
    • (2006) J Neural Transm Suppl , vol.70 , pp. 9-15
    • Hornykiewicz, O.1
  • 2
    • 41549114279 scopus 로고    scopus 로고
    • The role of autophagylysosome pathway in neurodegeneration associated with Parkinson's disease
    • Pan T, Kondo S, Le W, Jankovic J. The role of autophagylysosome pathway in neurodegeneration associated with Parkinson's disease. Brain 2008;131:1969-1978.
    • (2008) Brain , vol.131 , pp. 1969-1978
    • Pan, T.1    Kondo, S.2    Le, W.3    Jankovic, J.4
  • 3
    • 84865860748 scopus 로고    scopus 로고
    • Protein degradation pathways in Parkinson's disease: Curse or blessing
    • Ebrahimi-Fakhari D, Wahlster L, McLean PJ. Protein degradation pathways in Parkinson's disease: curse or blessing. Acta Neuropathol 2012;124:153-172.
    • (2012) Acta Neuropathol , vol.124 , pp. 153-172
    • Ebrahimi-Fakhari, D.1    Wahlster, L.2    McLean, P.J.3
  • 4
    • 7444237665 scopus 로고    scopus 로고
    • Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews
    • Aharon-Peretz J, Rosenbaum H, Gershoni-Baruch R Z Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews. N Engl J Med 2004;351:1972-1977.
    • (2004) N Engl J Med , vol.351 , pp. 1972-1977
    • Aharon-Peretz, J.1    Rosenbaum, H.2    Gershoni-Baruch, R.Z.3
  • 5
    • 46049112735 scopus 로고    scopus 로고
    • Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset
    • Gan-Or Z, Giladi N, Rozovski U, et al. Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset. Neurology 2008;70:2277-2283.
    • (2008) Neurology , vol.70 , pp. 2277-2283
    • Gan-Or, Z.1    Giladi, N.2    Rozovski, U.3
  • 6
    • 84878911804 scopus 로고    scopus 로고
    • The p. L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease
    • Gan-Or Z, Ozelius LJ, Bar-Shira A, et al. The p. L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease. Neurology 2013;80:1606-1610.
    • (2013) Neurology , vol.80 , pp. 1606-1610
    • Gan-Or, Z.1    Ozelius, L.J.2    Bar-Shira, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.