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Hallervorder-Spatz病3例

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出处 《河北医药》 CAS 2010年第9期1179-1180,共2页 Hebei Medical Journal
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  • 1鲁晓燕,陈巨坤,王鲁宁,桂秋萍.Shy-Drager综合征与纹状体黑质变性MRI-病理对照研究[J].中华放射学杂志,1997,31(2):111-111. 被引量:16
  • 2Zhou B, Westaway SK, Levinson B, et al. A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome.Nat Genet,2001,28:345- 349.
  • 3Hayflick SJ, Westaway SK, Levinson B, et al. Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome. N Engl J Med,2003,348 : 33 -40.
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  • 7Thomas M, Hayflick SJ, Jankovic J. Clinical heterogeneity of neurodegeneration with brain iron accumulation ( Hallervorden-Spatz syndrome ) and pankothenate kinase-associated neurodegeneration. Mov Disord ,2004,19:36-42.
  • 8Johnson MA, Kuo YM, Westaway SK, et al. Mitochondrial localization of human PANK2 and hypotheses of secondary iron accumulation in pantothenate kinase-associated neurodegeneration.Ann N Y Acad Sci,2004,1012:282-298.
  • 9Yoon SJ, Koh YH, Floyd RA, et al. Copper, zinc superoxide dismutase enhances DNA damage and mutagenicity induced by cysteine/iron. Mutat Res,2000, 448:97-104.
  • 10卢文甫,王鲁宁,贾建军,汤洪川,陈彤.哈勒沃登-施帕茨病的诊断[J].中华神经科杂志,2000,33(3):165-167. 被引量:9

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