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J-GLOBAL ID:201902262314016533   Reference number:19A1814936

Aceruloplasminemia: A Severe Neurodegenerative Disorder Deserving an Early Diagnosis

アセロplasmin血症: 早期診断を受けた重度神経変性疾患【JST・京大機械翻訳】
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Material:
Volume: 13  Page: 325  Publication year: 2019 
JST Material Number: U7087A  ISSN: 1662-453X  Document type: Article
Article type: 文献レビュー  Country of issue: Switzerland (CHE)  Language: ENGLISH (EN)
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Aceruloplasminemia (ACP) is a ...
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Basic neurology  ,  Nervous system diseases 
Reference (63):
  • Aschemeyer S., Qiao B., Stefanova D., Valore E. V., Sek A. C., Ruwe T. A., et al (2018). Structure-function analysis of ferroportin defines the binding site and an alternative mechanism of action of hepcidin. Blood 131 899-910. doi: 10.1182/blood-2017-05-786590
  • Badat M., Kaya B., Telfer P. (2015). Combination-therapy with concurrent deferoxamine and deferiprone is effective in treating resistant cardiac iron-loading in aceruloplasminaemia. Br. J. Haematol. 171 430-432. doi: 10.1111/bjh.13401
  • Bento I., Peixoto C., Zaitsev V. N., Lindley P. F. (2007). Ceruloplasmin revisited: structural and functional roles of various metal cation-binding sites. Acta Crystallogr. D Biol. Crystallogr. 63 240-248. doi: 10.1107/s090744490604947x
  • Breuer W., Hershko C., Cabantchik Z. I. (2000). The importance of non-transferrin bound iron in disorders of iron metabolism. Transfus. Sci. 23 185-192. doi: 10.1016/s0955-3886(00)00087-4
  • Brissot P., Bernard D. G., Brissot E., Loréal O., Troadec M. B. (2018). Rare anemias due to genetic iron metabolism defects. Mutat. Res. 777 52-63. doi: 10.1016/j.mrrev.2018.06.003
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