Journal Article

The genetic basis of porphyria cutanea tarda

R. Enriquez de Salamanca, A. Olmos, M. L. Peña, L. Berges and J. Perpiñá

Archives of Dermatological Research, 1984, Volume 277, Number 1, Pages 8-12

• Download PDF (427.4 KB)

Journal Article

Hereditary uroporphyrinogen-decarboxylase deficiency predisposing porphyria cutanea tarda (chronic hepatic porphyria) in females after oral contraceptive medication

F. Sixel-Dietrich and M. Doss

Archives of Dermatological Research, 1985, Volume 278, Number 1, Pages 13-16

• Download PDF (409.2 KB)

Journal Article

Hepatic acetylator phenotype in porphyria cutanea tarda

J. M. Ladero, R. Enriquez Salamanca and S. Chinarro

Archives of Dermatological Research, 1981, Volume 270, Number 2, Pages 171-173

• Download PDF (131.4 KB)

Journal Article

Incidence of hereditary porphyria cutanea tarda (PCT) in a sample of the Italian population

L. D'Alessandro, D. Griso, G. Biolcati, A. Macri and G. C. Topi

Archives of Dermatological Research, 1992, Volume 284, Number 4, Pages 212-214

• Download PDF (314.6 KB)

Journal Article

Hereditäre und nicht-hereditäre Form der chronischen hepatischen Porphyrie: Unterschiedliches Verhalten der Uroporphyrinogen-Decarboxylase in Leber und Erythrozyten

M. Doss, R. v. Tiepermann, D. Look, H. Henning and J. Nikolowski, et al.

Journal of Molecular Medicine, 1980, Volume 58, Number 24, Pages 1347-1356

• Download PDF (1.3 MB)

Journal Article

HLA and porphyria cutanea tarda

L. Llorente, R. Enríquez, F. Campillo and M. L. Peña

Archives of Dermatological Research, 1980, Volume 269, Number 2, Pages 209-210

• Download PDF (70.6 KB)

Journal Article

The effects of ethanol, estrogen, and hexachlorobenzene on the activities of hepatic δ-aminolevulinate synthetase, δ-aminolevulinate dehydratase, and uroporphyrinogen decarboxylase in male rats

Masao Kondo and Yoshitaka Shimizu

Archives of Toxicology, 1986, Volume 59, Number 3, Pages 141-145

• Download PDF (580.3 KB)

Journal Article

Porphyria Cutanea Tarda: Multiplicity of Risk Factors Including HFE Mutations, Hepatitis C, and Inherited Uroporphyrinogen Decarboxylase Deficiency

Norman G. Egger, Douglas E. Goeger, Deborah A. Payne, Emil P. Miskovsky and Steven A. Weinman, et al.

Digestive Diseases and Sciences, 2002, Volume 47, Number 2, Pages 419-426

• Download PDF (74.4 KB)

Journal Article

Characterization of a new mutation (R292G) and a deletion at the human uroporphyrinogen decarboxylase locus in two patients with hepatoerythropoietic porphyria

Hubert Verneuil1, Francine Bourgeois, Felix Rooij, Peter D. Siersema and J. H. P. Wilson, et al.

Human Genetics, 1992, Volume 89, Number 5, Pages 548-552

• Download PDF (672.1 KB)