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Volumn 25, Issue 14, 2010, Pages 2470-2472

Dramatic response of facial stereotype/tic to tetrabenazine in the first reported cases of neuroferritinopathy in the United States

Author keywords

[No Author keywords available]

Indexed keywords

ESCITALOPRAM; FERRITIN; TETRABENAZINE;

EID: 77958538143     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.23299     Document Type: Letter
Times cited : (25)

References (6)
  • 1
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    • Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease
    • Curtis AR, Fey C, Morris CM, et al. Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. Nat Genet 2001; 28: 350-354.
    • (2001) Nat Genet , vol.28 , pp. 350-354
    • Curtis, A.R.1    Fey, C.2    Morris, C.M.3
  • 2
    • 67649414590 scopus 로고    scopus 로고
    • Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
    • e109.
    • Devos D, Tchofo PJ, Vuillaume I, et al. Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation. Brain 2009; 132: 1-3, e109.
    • (2009) Brain , vol.132 , pp. 1-3
    • Devos, D.1    Tchofo, P.J.2    Vuillaume, I.3
  • 3
    • 42049109697 scopus 로고    scopus 로고
    • Neuroferritinopathy in a Japanese family with a duplication in the ferritin light chain gene
    • Ohta E, Nagasaka T, Shindo K, et al. Neuroferritinopathy in a Japanese family with a duplication in the ferritin light chain gene. Neurology 2008; 70 (Part 2): 1493-1494.
    • (2008) Neurology , vol.70 , Issue.PART 2 , pp. 1493-1494
    • Ohta, E.1    Nagasaka, T.2    Shindo, K.3
  • 4
    • 23844553465 scopus 로고    scopus 로고
    • Neuroferritinopathy: missense mutation in FTL causing early-onset bilateral pallidal involvement
    • Maciel P, Cruz VT, Constante M, et al. Neuroferritinopathy: missense mutation in FTL causing early-onset bilateral pallidal involvement. Neurology 2005; 65: 603-605.
    • (2005) Neurology , vol.65 , pp. 603-605
    • Maciel, P.1    Cruz, V.T.2    Constante, M.3
  • 5
    • 14544294357 scopus 로고    scopus 로고
    • Neuroferritinopathy: a neurodegenerative disorder associated with L-ferritin mutation
    • Levi S, Cozzi A, Arosio P. Neuroferritinopathy: a neurodegenerative disorder associated with L-ferritin mutation. Best Pract Res Clin Haematol 2005; 18: 265-276.
    • (2005) Best Pract Res Clin Haematol , vol.18 , pp. 265-276
    • Levi, S.1    Cozzi, A.2    Arosio, P.3
  • 6
    • 16844363930 scopus 로고    scopus 로고
    • Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights
    • Mancuso M, Davidzon G, Kurlan RM, et al. Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights. J Neuropathol Exp Neurol 2005; 64: 280-294.
    • (2005) J Neuropathol Exp Neurol , vol.64 , pp. 280-294
    • Mancuso, M.1    Davidzon, G.2    Kurlan, R.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.