Zobrazeno 1 - 5
of 5
pro vyhledávání: '"L. N. Phung"'
Autor:
Hervé Puy, Jean Charles Deybach, L. N. Phung, V. Da Silva, Sylvie Simonin, Yves Nordmann, C. Bonaiti, A. M. Robreau
Publikováno v:
Journal of Internal Medicine. 242:213-217
Nordmann Y, Puy H, Da Silva V, Simonin S, Robreau AM, Bonaiti C, Phung LN, Deybach JC (Centre Francais des Porphyries, Hopital Louis Mourier, Colombes Cedex, France, and the Institut Gustave Roussy, Cedex, France). Acute intermittent porphyria: preva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::772afb51064ea3cea5a35957a574ebfb
https://doi.org/10.1046/j.1365-2796.1997.00189.x
https://doi.org/10.1046/j.1365-2796.1997.00189.x
Publikováno v:
Journal of inherited metabolic disease. 13(5)
We present data on one patient with an inheritance pattern for two porphyrias. From her mother she inherited the trait of hereditary coproporphyria; from both parents she inherited the trait of congenital erythropoietic porphyria (Gunther disease). E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea7ca41acb09f38f08b5a6bd5c17002d
https://pubmed.ncbi.nlm.nih.gov/2246853
https://pubmed.ncbi.nlm.nih.gov/2246853
Autor:
Jean Charles Deybach, L. N. Phung, V. Da Silva, Yves Nordmann, L. D’Alessandro Gandolfo, A. Macri, G. C. Topi, D. Griso, G. Biolcati
Publikováno v:
British Journal of Dermatology. 124:211-211
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56fc54728683f3e8161de5bd0015003e
https://doi.org/10.1111/j.1365-2133.1991.tb00441.x
https://doi.org/10.1111/j.1365-2133.1991.tb00441.x
Publikováno v:
Presse medicale (Paris, France : 1983). 16(2)
Hepatic porphyrias (acute intermittent porphyria, coproporphyria, porphyria variegata and porphyria cutanea) are inherited diseases affecting porphyrin-heme metabolism in the liver. A situation analogous to the latent stage of human hepatic porphyria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c41f021cbab25b952fd65cb19ce994a0
https://pubmed.ncbi.nlm.nih.gov/2949310
https://pubmed.ncbi.nlm.nih.gov/2949310
Publikováno v:
Gastroenterology. 92(6)
This study was designed to test the hypothesis that a hemochromatosis allele is implicated in the expression of porphyria cutanea tarda. HLA phenotypes were determined in 69 porphyria cutanea tarda patients, 42 of which had the sporadic type (normal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::99fdb0c6382fdc9770177d492cbd5395
https://pubmed.ncbi.nlm.nih.gov/3569756
https://pubmed.ncbi.nlm.nih.gov/3569756