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J-GLOBAL ID：201502209538369264   Reference number：15A0954956

脳卒中の臨床病態-最近の話題 遺伝性脳卒中

Author (1)：
YAGITA YOSHIKI

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(川崎医大 脳卒中医学)

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Material：
脳21  (Brain 21)

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Volume： 18  Issue： 3  Page： 147-151  Publication year： Jul. 20, 2015 
JST Material Number： L3821A  ISSN： 1344-0128  Document type： Article
Article type： 解説  Country of issue： Japan (JPN)  Language： JAPANESE (JA)
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*cerebral apoplexy

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Clinical medicine on cardiovascular system in general 
(GJ01030V)

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Reference (28)：
  • Desnick RJ, et al : a-Galactosidase A deficiency: Fabry disease. In: Scriver CR et al. (eds), The Metabolic and Molecular Bases of Inherited Disease. 8th ed. Mc-Graw-Hill, New York, 2001; 3733-3774.
  • Lidove O, et al : Aseptic meningitis and ischaemic stroke in Fabry disease. Int J Clin Pract 63 : 1663-1667, 2009.
  • Inoue T, et al : Newborn screening for Fabry disease in Japan: prevalence and genotypes of Fabry disease in a pilot study. J Hum Genet 58 : 548-552, 2013.
  • Rolfs A, et al : Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study. Lancet 366: 1794-1796, 2005.
  • Banikazemi M, et al : Fabry Disease Clinical Trial Study Group. Agalsidase-beta therapy for advanced Fabry disease: a randomized trial. Ann Intern Med 146 : 77-86, 2007.
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Terms in the title (3)：
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脳卒中

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, 
話題

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, 
遺伝

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