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Volumn 50, Issue 3, 2001, Pages 283-285

Parkin and Parkinson's: More than homonymy?

Author keywords

[No Author keywords available]

Indexed keywords

LEVODOPA; PARKIN; PROTEIN; UNCLASSIFIED DRUG;

EID: 0034846242     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.1143     Document Type: Editorial
Times cited : (4)

References (27)
  • 3
    • 0033849550 scopus 로고    scopus 로고
    • Autosomal recessive early-onset parkinsonism with diurnal fluctuation: Clinicopathologic characteristics and molecular genetic identification
    • (2000) Brain Dev , Issue.SUPPL. 1 , pp. 87-91
    • Yamamura, Y.1    Hattori, N.2    Matsumine, H.3
  • 8
    • 18244412384 scopus 로고    scopus 로고
    • Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the Parkin gene in affected individuals
    • (1998) Ann Neurol , vol.44 , pp. 935-941
    • Hattori, N.1    Kitada, T.2    Matsumine, H.3
  • 10
    • 0032564235 scopus 로고    scopus 로고
    • Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism
    • The European Consortium on Genetic Susceptibility in Parkinson's Disease and The French Parkinson's Disease Genetics Study Group
    • (1998) Lancet , vol.352 , pp. 1355-1356
    • Lücking, C.B.1    Abbas, N.2    Dürr, A.3
  • 11
    • 0345490853 scopus 로고    scopus 로고
    • A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe
    • The French Parkinson's Disease Genetics Study Group and The European Consortium on Genetic Susceptibility in Parkinson's Disease
    • (1999) Hum Mol Genet , vol.8 , pp. 567-574
    • Abbas, N.1    Lücking, C.B.2    Ricard, S.3
  • 18
    • 0033868381 scopus 로고    scopus 로고
    • Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism
    • (2000) Ann Neurol , vol.48 , pp. 245-250
    • Maruyama, M.1    Ikeuchi, T.2    Saito, M.3
  • 21
    • 0035096967 scopus 로고    scopus 로고
    • Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene
    • (2001) Ann Neurol , vol.49 , pp. 367-376
    • Hilker, R.1    Klein, C.2    Ghaemi, M.3
  • 24
    • 0025326719 scopus 로고
    • Ubiquitin carboxy-terminal hydrolase (PGP 9.5) is selectively present in ubiquitinated inclusion bodies characteristic of human neurodegenerative diseases
    • (1990) J Pathol , vol.161 , pp. 153-160
    • Lowe, J.1    McDermott, H.2    Landon, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.