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J-GLOBAL ID:200902256523771953   Reference number:09A0099068

高IgE血症,多発性肺嚢胞など多彩な所見を呈したプロリダーゼ欠損症の1例

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Material:
Volume: 98  Issue:Page: 150-152  Publication year: Jan. 10, 2009 
JST Material Number: F0916A  ISSN: 0021-5384  CODEN: NNGAA  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Immunologic diseases,allergic diseases in general.  ,  Clinical hematology in general 
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Reference (9):
  • HECHTMAN, P. Prolidase deficiency. The Metabolic & Molecular Bases of Inherited Disease. 2001, 1839-1856
  • LUDER, AS. Chronic lung disease and cystic fibrosis phenotype in prolidase deficiency : a newly recognized association. J Pediatr. 2007, 150, 656-658
  • SEKIYA, M. An autopsy case of prolidase deficiency. Virchows Arch A Pathol Anat Histopathol. 1985, 406, 125-131
  • LOPES, I. Prolidase deficiency with hyperimmunoglobulin E : a case report. Pediatr Allergy Immunol. 2002, 13, 140-142
  • WANG, H. A nonsense mutation of PEPD in four Amish children with prolidase deficiency. Am J Med Genet A. 2006, 140, 580-585
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