Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy
Reference12 articles.
1. Phang JM, Yeh GC, Scriver CR. Disorders of proline and hydroxiproline metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic and molecular bases of inherited disease. New york: Mcgraw Hill; 1995. p. 1125–46.
2. Lopes I, Marques L, Neves E, Silva A, Taveira M, Pena R, et al. Prolidase deficiency with hyperimmunoglobulin E: a case report. Pediatr Allergy Immunol. 2002;13:140–2.
3. Fukumura A, Asaka T, Kasakura H, Doshita T, Chen W, Yokoji H, et al. Prolidase deficiency with various clinical conditions including hyper-IgE and multiple lung bulla formation. Nippon Naika Gakkai Zasshi. 2009;98:150–2.
4. Hershkovitz T, Hassoun G, Indelman M, Shlush LI, Bergman R, Pollack S, et al. A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndrome. Clin Exp Dermatol. 2006;31:435–40.
5. Butbul Aviel Y, Mandel H, Avitan Hersh E, Bergman R, Adiv O, Luder A, et al. Prolidase deficiency associated with systemic lupus erythematosus (SLE): single site experience and literature review. Pediatr Rheumatol Online J. 2012;10:18.
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献