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Movement Disorders
Volumn 28, Issue 10, 2013, Pages 1462-1463
Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutation
Author keywords

[No Author keywords available]
Indexed keywords

BACLOFEN; BOTULINUM TOXIN; CARBIDOPA PLUS LEVODOPA;
EID: 84884715844     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.25410     Document Type: Letter
Times cited : (11)
References (7)
  • 1
    • 84855962257 scopus 로고    scopus 로고
    • Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations
    • Schneider SA, Hardy J, Bhatia KP. Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations. Mov Disord 2012;27:42-53.
    • (2012) Mov Disord , vol.27 , pp. 42-53
    • Schneider, S.A.1    Hardy, J.2    Bhatia, K.P.3
  • 2
    • 62149099955 scopus 로고    scopus 로고
    • Clinical and genetic delineation of neurodegeneration with brain iron accumulation
    • Gregory A, Polster BJ, Hayflick SJ. Clinical and genetic delineation of neurodegeneration with brain iron accumulation. J Med Genet 2009;46:73-80.
    • (2009) J Med Genet , vol.46 , pp. 73-80
    • Gregory, A.1    Polster, B.J.2    Hayflick, S.J.3
  • 3
    • 79961146091 scopus 로고    scopus 로고
    • Genetics of neurodegeneration with brain iron accumulation
    • Gregory A, Hayflick SJ. Genetics of neurodegeneration with brain iron accumulation. Curr Neurol Neurosci Rep 2011;11:254-261.
    • (2011) Curr Neurol Neurosci Rep , vol.11 , pp. 254-261
    • Gregory, A.1    Hayflick, S.J.2
  • 4
    • 80053916609 scopus 로고    scopus 로고
    • Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation
    • Hartig MB, Iuso A, Haack T, et al. Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation. Am J Hum Genet 2011;89:543-550.
    • (2011) Am J Hum Genet , vol.89 , pp. 543-550
    • Hartig, M.B.1    Iuso, A.2    Haack, T.3
  • 5
    • 84873649203 scopus 로고    scopus 로고
    • Hogarth P, Gregory A, Sanford L, et al. New NBIA subtype: genetic, clinical, pathologic, and radiographic features of MPAN
    • Hogarth P, Gregory A, Sanford L, et al. New NBIA subtype: genetic, clinical, pathologic, and radiographic features of MPAN. Neurology 2013:80:268-275.
    • (2013) Neurology , vol.80 , pp. 268-275
  • 6
    • 84868206031 scopus 로고    scopus 로고
    • C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis
    • Deschauer M, Gaul C, Behrmann C, Prokisch H, Zierz S, Haack TB. C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis. J Neurol 2012;259:2434-2439.
    • (2012) J Neurol , vol.259 , pp. 2434-2439
    • Deschauer, M.1    Gaul, C.2    Behrmann, C.3    Prokisch, H.4    Zierz, S.5    Haack, T.B.6
  • 7
    • 80355138252 scopus 로고    scopus 로고
    • Hayflick SJ, Hogarth P. As iron goes, so goes disease?
    • Hayflick SJ, Hogarth P. As iron goes, so goes disease? Haematologica 2011;96:1571-1572.
    • (2011) Haematologica , vol.96 , pp. 1571-1572

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.