Familial idiopathic basal ganglia calcification: a challenging clinical-pathological correlation.
作者信息
Wider Christian, Dickson Dennis W, Schweitzer Katherine J, Broderick Daniel F, Wszolek Zbigniew K
出版信息
J Neurol. 2009 May;256(5):839-42. doi: 10.1007/s00415-009-5025-6. Epub 2009 Mar 1.
Abstract
摘要
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本文引用的文献
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Autosomal dominant dystonia-plus with cerebral calcifications.伴有脑钙化的常染色体显性肌张力障碍叠加综合征
Neurology. 2006 Aug 22;67(4):620-5. doi: 10.1212/01.wnl.0000230141.40784.09.
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Severe vascular disturbance in a case of familial brain calcinosis.家族性脑钙化症一例中的严重血管紊乱。
Acta Neuropathol. 2005 Jun;109(6):643-53. doi: 10.1007/s00401-005-1007-7. Epub 2005 Jun 4.
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Heredofamilial brain calcinosis syndrome.遗传性家族性脑钙化综合征
Mayo Clin Proc. 2005 May;80(5):641-51. doi: 10.4065/80.5.641.
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Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease).家族性特发性基底节钙化（法尔病）中的遗传异质性。
Neurology. 2004 Dec 14;63(11):2165-7. doi: 10.1212/01.wnl.0000145601.88274.88.
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Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look-alike?伴有基底节钙化的皮质基底节变性综合征：法尔病会是类似皮质基底节变性的疾病吗？
Mov Disord. 2002 May;17(3):563-7. doi: 10.1002/mds.10122.
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Parkinsonism associated with autosomal dominant bilateral striopallidodentate calcinosis.
Parkinsonism Relat Disord. 2001 Oct;7(4):289-295. doi: 10.1016/s1353-8020(00)00036-5.
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Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease).14号染色体长臂上特发性基底节钙化（法尔病）相关基因座的鉴定。
Am J Hum Genet. 1999 Sep;65(3):764-72. doi: 10.1086/302558.
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