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Journal of Neurology
Volumn 261, Issue 2, 2014, Pages 435-437
SPG15: A cause of juvenile atypical levodopa responsive parkinsonism
Author keywords

[No Author keywords available]
Indexed keywords

CERULOPLASMIN; IOFLUPANE I 123; LEVODOPA;
EID: 84899124201     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-013-7216-4     Document Type: Letter
Times cited : (23)
References (7)
  • 1
    • 41549153666 scopus 로고    scopus 로고
    • Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome
    • Hanein S, Martin E, Boukhris A et al (2008) Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. Am J Hum Genet 82:992-1002
    • (2008) Am J Hum Genet , vol.82 , pp. 992-1002
    • Hanein, S.1    Martin, E.2    Boukhris, A.3
  • 2
    • 79953284488 scopus 로고    scopus 로고
    • Atypical juvenile parkinsonism in a consanguineous SPG15 family
    • Schicks J, Synofzik M, Pétursson H et al (2011) Atypical juvenile parkinsonism in a consanguineous SPG15 family. Mov Disord 26:564-566
    • (2011) Mov Disord , vol.26 , pp. 564-566
    • Schicks, J.1    Synofzik, M.2    Pétursson, H.3
  • 3
    • 70349753265 scopus 로고    scopus 로고
    • SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum
    • Goizet C, Boukhris A, Maltete D et al (2009) SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum. Neurology 73:1111-1119
    • (2009) Neurology , vol.73 , pp. 1111-1119
    • Goizet, C.1    Boukhris, A.2    Maltete, D.3
  • 4
    • 77953512439 scopus 로고    scopus 로고
    • Early-onset L-dopa responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations
    • Paisán-Ruiz C, Guevara R, Federoff M et al (2010) Early-onset L-dopa responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations. Mov Disord 25:1791-1800
    • (2010) Mov Disord , vol.25 , pp. 1791-1800
    • Paisán-Ruiz, C.1    Guevara, R.2    Federoff, M.3
  • 5
    • 62149140219 scopus 로고    scopus 로고
    • SPG11 spastic paraplegia. A new cause of juvenile parkinsonism
    • Anheim M, Lagier-Tourenne C, Stevanin G et al (2009) SPG11 spastic paraplegia. A new cause of juvenile parkinsonism. J Neurol 256:104-108
    • (2009) J Neurol , vol.256 , pp. 104-108
    • Anheim, M.1    Lagier-Tourenne, C.2    Stevanin, G.3
  • 6
    • 79953285214 scopus 로고    scopus 로고
    • Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism
    • Guidubaldi A, Piano C, Santorelli FM et al (2011) Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism. Mov Disord 26:553-556
    • (2011) Mov Disord , vol.26 , pp. 553-556
    • Guidubaldi, A.1    Piano, C.2    Santorelli, F.M.3
  • 7
    • 84864808982 scopus 로고    scopus 로고
    • Spatacsin and spastizin act in the same pathway required for proper spinal motor neuron axon outgrowth in zebrafish
    • Martin E, Yanicostas C, Rastetter A et al (2012) Spatacsin and spastizin act in the same pathway required for proper spinal motor neuron axon outgrowth in zebrafish. Neurobiol Dis 48:299-308
    • (2012) Neurobiol Dis , vol.48 , pp. 299-308
    • Martin, E.1    Yanicostas, C.2    Rastetter, A.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.