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The British Journal of Dermatology|July 1, 1984
Recovery from porphyria cutanea tarda with no specific therapy other than avoidance of hepatic toxinsG C Topi, A Amantea, D GrisoThe New Microbiologica|November 13, 1998
Hepatitis C virus in patients with porphyria cutanea tarda: relationship to HCV-genotypesD Rivanera, D Lilli, D Griso, et al.Archives of Dermatological Research|January 1, 1992
Incidence of hereditary porphyria cutanea tarda (PCT) in a sample of the Italian populationL D'Alessandro, D Griso, G Biolcati, et al.Dermatologica|January 1, 1989
Familial porphyria cutanea tarda with normal erythrocytic urodecarboxylase: an exception to the rule?L D'Alessandro Gandolfo, D Griso, A Macri, et al.Dermatologica|January 1, 1983
Acquired cutaneous toxoplasmosisG Topi, L D'Alessandro Gandolfo, B Giacalone, et al.Cellular and Molecular Biology (Noisy-Le-Grand, France)|February 1, 1997
Iron and porphyria cutanea tardaL D'Alessandro Gandolfo, D Griso, A Macrì, et al.Journal of Neurology|January 1, 1984
Hereditary coproporphyria: unusual nervous system involvement in two casesC Casali, M Lo Monaco, L D'Alessandro, et al.The British Journal of Dermatology|May 1, 1981
Porphyria cutanea tarda in a haemodialysed patientG C Topi, G L Alessandro, G C Cancarini, et al.Human Mutation|May 2, 2000
Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria: report of four novel mutationsF Martinez di Montemuros, E Di Pierro, S Fargion, et al.Hepato-Gastroenterology|February 1, 1986
Porphyrins in Rotor's syndrome: a study on an Italian familyG L Rapaccini, G C Topi, M Anti, et al.Pageof 2