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J-GLOBAL ID:201802231989364989   Reference number:18A0226856

新生児マススクリーニングで診断されたシトルリン血症I型の3例

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Material:
Volume: 27  Issue:Page: 283-287  Publication year: Dec. 01, 2017 
JST Material Number: L3053A  ISSN: 0917-3803  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Diagnostics of congenital diseases, deformities.  ,  Diagnostics of metabolic diseases,nutritional diseases.  ,  Blood tests(=hematologic tests) 
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Reference (11):
  • Yorifuji T, Kawai M, Muroi J, et al.: Unexpectedly high prevalence of the mild form of propionic acidemia in Japan: presence of a common mutation and possible clinical implications. Hum Genet 111: 161-165, 2002
  • Quinonez SC, Thoene JG: Citrullinemia Type. In: Adam MP, Ardinger HH, Pagon RA, et.al, editors. GeneReviews® [Internet]. Seattle (WA) : University of Washington, Seattle, 2004 Jul 7 [updated 2016 Sep 1].
  • 坂本 修:シトルリン血症I型,タンデムマス・スクリーニング ガイドブック(山口清次 編集):診断と治療社,東京,2013,p74-75
  • Go H, Imamura T, Hashimoto K, Ogasawara K, Sakamoto O, Takubo N, Momoi N. et al.: Successful prospective management of neonatal citrullinemia. J Pediatr Endocrinol Metab. 25: 371-373, 2012
  • Karall D, Haberlandt E, Albrecht U, Rostasy K, Häberle J, Scholl-Bürgi S, et al.: Unrecognized citrullinemia mimicking encephalitis in a 14-year-old boy: unexpected result through the use of a standardized lumbar puncture protocol. Neuropediatrics. 43: 59-63, 2012
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