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Volumn 63, Issue 5, 2004, Pages 922-924

Infantile neuroaxonal dystrophy and pantothenate kinase-associated neurodegeneration: Locus heterogeneity

Author keywords

[No Author keywords available]

Indexed keywords

PANTOTHENATE KINASE;

EID: 4644349437     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000137046.28085.B2     Document Type: Article
Times cited : (17)

References (10)
  • 1
    • 0007950753 scopus 로고
    • Eine unbekannte form von infantiler lipoid-speicher-krankheit des gehirns
    • Turin: Rosenberg and Sellier
    • Seitelberger F. Eine unbekannte Form von infantiler Lipoid-Speicher- Krankheit des Gehirns. In: Proceedings of the 1st International Congress of Neuropathology (Vol. 3). Turin: Rosenberg and Sellier, 1952;323-333.
    • (1952) Proceedings of the 1st International Congress of Neuropathology , vol.3 , pp. 323-333
    • Seitelberger, F.1
  • 4
    • 0032935631 scopus 로고    scopus 로고
    • Infantile neuroaxonal dystrophy: Neuroradiological studies in 11 patients
    • Farina L, Nardocci N, Bruzzone MG, et al. Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patients. Neuroradiology 1999;41:376-380.
    • (1999) Neuroradiology , vol.41 , pp. 376-380
    • Farina, L.1    Nardocci, N.2    Bruzzone, M.G.3
  • 5
    • 0033594368 scopus 로고    scopus 로고
    • Infantile neuroaxonal dystrophy: Clinical spectrum and diagnostic criteria
    • Nardocci N, Zorzi G, Farina L, et al. Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria. Neurology 1999;52:1472-1478.
    • (1999) Neurology , vol.52 , pp. 1472-1478
    • Nardocci, N.1    Zorzi, G.2    Farina, L.3
  • 6
    • 0014402373 scopus 로고
    • Infantile neuroaxonal dystrophy. Early form with preferential cerebellar involvement
    • Jellinger K, Seitelberger F, Rosenkranz W. [Infantile neuroaxonal dystrophy. Early form with preferential cerebellar involvement.] Acta Neuropathol 1968;10:123-131.
    • (1968) Acta Neuropathol , vol.10 , pp. 123-131
    • Jellinger, K.1    Seitelberger, F.2    Rosenkranz, W.3
  • 8
    • 0029589683 scopus 로고
    • Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy
    • Malandrini A, Cavallaro T, Fabrizi GM, et al. Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Virchows Arch 1995;427:415-421.
    • (1995) Virchows Arch , vol.427 , pp. 415-421
    • Malandrini, A.1    Cavallaro, T.2    Fabrizi, G.M.3
  • 9
    • 9144256038 scopus 로고    scopus 로고
    • Clinical and molecular findings in patients with giant axonal neuropathy (GAN)
    • Bruno C, Bertini E, Federico A, et al. Clinical and molecular findings in patients with giant axonal neuropathy (GAN). Neurology 2004;62:13-16.
    • (2004) Neurology , vol.62 , pp. 13-16
    • Bruno, C.1    Bertini, E.2    Federico, A.3
  • 10
    • 0037413484 scopus 로고    scopus 로고
    • Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome
    • Hayflick SJ, Westaway SK, Levinson B, et al. Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome. N Engl J Med 2003;348:33-40.
    • (2003) N Engl J Med , vol.348 , pp. 33-40
    • Hayflick, S.J.1    Westaway, S.K.2    Levinson, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.