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Volumn 121, Issue 4, 2011, Pages 224-227

Young-onset Parkinsonism in a Hong Kong Chinese man with adult-onset Hallervorden-Spatz syndrome

Author keywords

Hallervorden Spatz disease; Hong Kong Chinese; PANK2; pantothenate kinase 2; young onset parkinsonism

Indexed keywords

PANTOTHENATE KINASE 2;

EID: 79951926412     PISSN: 00207454     EISSN: 15635279     Source Type: Journal    
DOI: 10.3109/00207454.2010.542843     Document Type: Article
Times cited : (18)

References (18)
  • 1
    • 77955005938 scopus 로고    scopus 로고
    • Indian-subcontinent NBIA: Unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms
    • Aggarwal, A., Schneider, S. A., Houlden, H., Silverdale, M., Paudel, R., Paisan-Ruiz, C., et al. (2010). Indian-subcontinent NBIA: Unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms. Movement Disorders, 25(10), 1424-1431.
    • (2010) Movement Disorders , vol.25 , Issue.10 , pp. 1424-1431
    • Aggarwal, A.1    Schneider, S.A.2    Houlden, H.3    Silverdale, M.4    Paudel, R.5    Paisan-Ruiz, C.6
  • 2
    • 23644462058 scopus 로고    scopus 로고
    • The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome
    • DOI 10.1055/s-2005-865714
    • Baumeister, F. A., Auer, D. P., et al. (2005). The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome. Neuropediatrics, 36(3), 221-222. (Pubitemid 41117122)
    • (2005) Neuropediatrics , vol.36 , Issue.3 , pp. 221-222
    • Baumeister, F.A.M.1    Auer, D.P.2    Hortnagel, K.3    Freisinger, P.4    Meitinger, T.5
  • 3
    • 62149099955 scopus 로고    scopus 로고
    • Clinical and genetic delineation of neurodegeneration with brain iron accumulation
    • Gregory, A., Polster, B. J., & Hayflick, S. J. (2009). Clinical and genetic delineation of neurodegeneration with brain iron accumulation. Journal of Medical Genetics, 46(2), 73-80.
    • (2009) Journal of Medical Genetics , vol.46 , Issue.2 , pp. 73-80
    • Gregory, A.1    Polster, B.J.2    Hayflick, S.J.3
  • 4
    • 51849174137 scopus 로고
    • Eigenartige Erkrankun im extrapyramidalen System mit besonderer Beteiligung des Globus pallidus und der Substantia nigra
    • Hallervorden, J., & Spatz, H. (1922). Eigenartige Erkrankun im extrapyramidalen System mit besonderer Beteiligung des Globus pallidus und der Substantia nigra. Journal of Neurology & Psychiatry, 79, 254-302.
    • (1922) Journal of Neurology & Psychiatry , vol.79 , pp. 254-302
    • Hallervorden, J.1    Spatz, H.2
  • 7
    • 0026410630 scopus 로고
    • Pattern recognition in magnetic resonance imaging of white matter disorders in children and young adults
    • Van der Knaap, M. S., Valk, J., de Neeling, N., & Nauta, J. J. (1991). Pattern recognition in magnetic resonance imaging of white matter disorders in children and young adults. Neuroradiology, 33(6), 478-493.
    • (1991) Neuroradiology , vol.33 , Issue.6 , pp. 478-493
    • Van Der Knaap, M.S.1    Valk, J.2    De Neeling, N.3    Nauta, J.J.4
  • 8
    • 28344455574 scopus 로고    scopus 로고
    • A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: Evidence for a founder effect
    • DOI 10.1007/s10048-005-0018-9
    • Rump, P., Lemmink, H. H., Verschuuren-Bemelmans, C. C., Grootscholten, P. M., Fock, J. M., Hayflick, S. J., et al. (2005). A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: Evidence for a founder effect. Neurogenetics, 6(4), 201-207. (Pubitemid 41720892)
    • (2005) Neurogenetics , vol.6 , Issue.4 , pp. 201-207
    • Rump, P.1    Lemmink, H.H.2    Verschuuren-Bemelmans, C.C.3    Grootscholten, P.M.4    Fock, J.M.5    Hayflick, S.J.6    Westaway, S.K.7    Vos, Y.J.8    Van, E.A.J.9
  • 11
    • 79951899462 scopus 로고    scopus 로고
    • A novel PANK2 mutation in a patient with atypical pantothenate-kinase- associated neurodegeneration presenting with adult-onset parkinsonism
    • Seo, J. H., Song, S. K., & Lee, P. H. (2009). A novel PANK2 mutation in a patient with atypical pantothenate-kinase-associated neurodegeneration presenting with adult-onset parkinsonism. The Journal of Clinical Neurology, 5(4), 192-194.
    • (2009) The Journal of Clinical Neurology , vol.5 , Issue.4 , pp. 192-194
    • Seo, J.H.1    Song, S.K.2    Lee, P.H.3
  • 12
    • 84871455380 scopus 로고    scopus 로고
    • Clinical manifestations and detection of pantothenate kinase 2 gene mutation in a patient with Hallervorden-Spatz syndrome
    • Song, X. W., Wang, Y. L., Shi, Y. W., Deng, W. Y., Chen, S. Q., Lin, H., et al. (2009). Clinical manifestations and detection of pantothenate kinase 2 gene mutation in a patient with Hallervorden-Spatz syndrome. Zhonghua Yi Xue Za Zhi, 89(47), 3320-3323.
    • (2009) Zhonghua Yi Xue Za Zhi , vol.89 , Issue.47 , pp. 3320-3323
    • Song, X.W.1    Wang, Y.L.2    Shi, Y.W.3    Deng, W.Y.4    Chen, S.Q.5    Lin, H.6
  • 13
    • 0026317374 scopus 로고
    • Hallervorden-Spatz syndrome and brain iron metabolism
    • Swaiman, K. F. (1991). Hallervorden-Spatz syndrome and brain iron metabolism. Archives of Neurology, 48(12), 1285-1293.
    • (1991) Archives of Neurology , vol.48 , Issue.12 , pp. 1285-1293
    • Swaiman, K.F.1
  • 14
    • 0034838767 scopus 로고    scopus 로고
    • Hallervorden-Spatz syndrome
    • Swaiman, K. F. (2001). Hallervorden-Spatz syndrome. Pediatric Neurology, 25(2), 102-108.
    • (2001) Pediatric Neurology , vol.25 , Issue.2 , pp. 102-108
    • Swaiman, K.F.1
  • 15
    • 33644946103 scopus 로고    scopus 로고
    • Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern
    • Valentino, P., Annesi, G., Ciro Candiano, I. C., Annesi, F., Civitelli, D., Tarantino, P., et al. (2006). Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern. Movement Disorders, 21(2), 252-254.
    • (2006) Movement Disorders , vol.21 , Issue.2 , pp. 252-254
    • Valentino, P.1    Annesi, G.2    Ciro Candiano, I.C.3    Annesi, F.4    Civitelli, D.5    Tarantino, P.6
  • 17
    • 24144493669 scopus 로고    scopus 로고
    • Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration
    • DOI 10.1002/mds.20408
    • Zhang, Y. H., Tang, B. S., Zhao, A. L., Xia, K., Long, Z. G., Guo, J. F., et al. (2005). Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration. Movement Disorders, 20(7), 819-821. (Pubitemid 41227148)
    • (2005) Movement Disorders , vol.20 , Issue.7 , pp. 819-821
    • Zhang, Y.-H.1    Tang, B.-S.2    Zhao, A.-L.3    Xia, K.4    Long, Z.-G.5    Guo, J.-F.6    Westaway, S.K.7    Hayflick, S.J.8
  • 18
    • 0034935036 scopus 로고    scopus 로고
    • A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome
    • DOI 10.1038/ng572
    • Zhou, B., Westaway, S. K., Levinson, B., Johnson, M. A., Gitschier, J., & Hayflick, S. J. (2001). A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome. Nature Genetics, 28(4), 345-349. (Pubitemid 32702423)
    • (2001) Nature Genetics , vol.28 , Issue.4 , pp. 345-349
    • Zhou, B.1    Westaway, S.K.2    Levinson, B.3    Johnson, M.A.4    Gitschier, J.5    Hayflick, S.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.