메뉴 건너뛰기




Volumn 26, Issue 3, 2011, Pages 565-566

Atypical juvenile parkinsonism in a consanguineous SPG15 family

Author keywords

[No Author keywords available]

Indexed keywords

2BETA CARBOMETOXY 3BETA (4 IODOPHENYL)N(3 FLUOROPROPYL)NORTROPANE I 123; LEVODOPA; RADIOPHARMACEUTICAL AGENT; UNCLASSIFIED DRUG; 2 CARBOMETHOXY 8 (3 FLUOROPROPYL) 3 (4 IODOPHENYL)TROPANE; 2-CARBOMETHOXY-8-(3-FLUOROPROPYL)-3-(4-IODOPHENYL)TROPANE; CARRIER PROTEIN; DIAGNOSTIC AGENT; FLUORINE; SPASTIZIN PROTEIN, HUMAN; TROPANE DERIVATIVE;

EID: 79953284488     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.23472     Document Type: Letter
Times cited : (26)

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. Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. Am J Hum Genet 2008; 82: 992-1002.
    • (2008) Am J Hum Genet , vol.82 , pp. 992-1002
    • Hanein, S.1    Martin, E.2    Boukhris, A.3
  • 3
    • 24744447964 scopus 로고    scopus 로고
    • Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset
    • Brockmann K, Simpson MA, Faber A, Bonnemann C, Crosby AH, Gartner J. Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset. Neuropediatrics 2005; 36: 274-278.
    • (2005) Neuropediatrics , vol.36 , pp. 274-278
    • Brockmann, K.1    Simpson, M.A.2    Faber, A.3    Bonnemann, C.4    Crosby, A.H.5    Gartner, J.6
  • 4
    • 72449147350 scopus 로고    scopus 로고
    • Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia
    • Schule R, Schlipf N, Synofzik M, et al. Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia. J Neurol Neurosurg Psychiatry 2009; 80: 1402-1404.
    • (2009) J Neurol Neurosurg Psychiatry , vol.80 , pp. 1402-1404
    • Schule, R.1    Schlipf, N.2    Synofzik, M.3
  • 5
    • 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. SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum. Neurology 2009; 73: 1111-1119.
    • (2009) Neurology , vol.73 , pp. 1111-1119
    • Goizet, C.1    Boukhris, A.2    Maltete, D.3
  • 6
    • 62149140219 scopus 로고    scopus 로고
    • SPG11 spastic paraplegia. A new cause of juvenile parkinsonism
    • Anheim M, Lagier-Tourenne C, Stevanin G, et al. SPG11 spastic paraplegia. A new cause of juvenile parkinsonism. J Neurol 2009; 256: 104-108.
    • (2009) J Neurol , vol.256 , pp. 104-108
    • Anheim, M.1    Lagier-Tourenne, C.2    Stevanin, G.3
  • 7
    • 40849083525 scopus 로고    scopus 로고
    • Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity
    • Boukhris A, Stevanin G, Feki I, et al. Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity. Arch Neurol 2008; 65: 393-402.
    • (2008) Arch Neurol , vol.65 , pp. 393-402
    • Boukhris, A.1    Stevanin, G.2    Feki, I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.