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Volumn 22, Issue 8, 2007, Pages 1202-1203

Dopa-responsive dystonia (Segawa disease)-like disease accompanied by mental retardation: A case report [1]

Author keywords

[No Author keywords available]

Indexed keywords

LEVODOPA;

EID: 34447550361     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.21517     Document Type: Letter
Times cited : (6)

References (6)
  • 1
    • 0027354028 scopus 로고
    • CSF biopterin levels and clinical features of patients with juvenile Parkinsonism
    • Narabayashi H, Nagatsu T, Yanagisawa N, Mizuno Y, editors, New York: Raven;
    • Furukawa Y, Nishi K, Kondo T, Mizuno Y, Narabayashi H. CSF biopterin levels and clinical features of patients with juvenile Parkinsonism. In: Narabayashi H, Nagatsu T, Yanagisawa N, Mizuno Y, editors. Advances in neurology. New York: Raven; 1993. p 562-567.
    • (1993) Advances in neurology , pp. 562-567
    • Furukawa, Y.1    Nishi, K.2    Kondo, T.3    Mizuno, Y.4    Narabayashi, H.5
  • 2
    • 0023775566 scopus 로고
    • Dopa-responsive dystonia
    • Fahn S, Marden CD, Calne DB, editors, New York: Raven;
    • Nygaard TG, Marsden CD, Duvosin RC. Dopa-responsive dystonia. In: Fahn S, Marden CD, Calne DB, editors. Advances in neurology. New York: Raven; 1988. p 377-384.
    • (1988) Advances in neurology , pp. 377-384
    • Nygaard, T.G.1    Marsden, C.D.2    Duvosin, R.C.3
  • 3
    • 0042868558 scopus 로고    scopus 로고
    • Autosomal dominant guanosine triphosphate cyclohydrolase I deficiency
    • Segawa M, Nomura Y, Nishiyama N. Autosomal dominant guanosine triphosphate cyclohydrolase I deficiency. Ann Neurol 2003;54:S32-S45.
    • (2003) Ann Neurol , vol.54
    • Segawa, M.1    Nomura, Y.2    Nishiyama, N.3
  • 4
    • 0028151448 scopus 로고
    • Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene
    • Ichinose H, Ohye T, Takahashi E, et al. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene. Nat Genet 1994;8:236-242.
    • (1994) Nat Genet , vol.8 , pp. 236-242
    • Ichinose, H.1    Ohye, T.2    Takahashi, E.3
  • 5
    • 0033846461 scopus 로고    scopus 로고
    • Molecular mechanisms of hereditary progressive dystonia with marked diurnal fluctuation, Segawa's disease
    • Ichinose H, Inagaki H, Suzuki T, Ohye T, Nagatsu T. Molecular mechanisms of hereditary progressive dystonia with marked diurnal fluctuation, Segawa's disease. Brain Dev 2000;22:S107-S110.
    • (2000) Brain Dev , vol.22
    • Ichinose, H.1    Inagaki, H.2    Suzuki, T.3    Ohye, T.4    Nagatsu, T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.