Porphyria cutanea tarda during maintenance haemodialysis.

作者: J Garcia Parrilla , R Ortega , M L Pena , J L Rodicio , R E de Salamanca

DOI: 10.1136/BMJ.280.6228.1358

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参考文章(4)
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Maureen B. Poh-Fitzpatrick, Neil Bellet, Vincent A. DeLeo, Marc E. Grossman, David R. Bickers, Porphyria Cutanea Tarda in Two Patients Treated with Hemodialysis for Chronic Renal Failure The New England Journal of Medicine. ,vol. 299, pp. 292- 294 ,(1978) , 10.1056/NEJM197808102990607
J P Kushner, A J Barbuto, G R Lee, An inherited enzymatic defect in porphyria cutanea tarda: decreased uroporphyrinogen decarboxylase activity. Journal of Clinical Investigation. ,vol. 58, pp. 1089- 1097 ,(1976) , 10.1172/JCI108560
H. de Verneuil, G. Aitken, Y. Nordmann, Familial and sporadic porphyria cutanea: two different diseases. Human Genetics. ,vol. 44, pp. 145- 151 ,(1978) , 10.1007/BF00295407