Childhood porphyriasAHMED, Iftikhar.Mayo Clinic proceedings. 2002, Vol 77, Num 8, pp 825-836, issn 0025-6196Article

Development of porphyria cutanea tarda in a hemodialysis patient after reactivation of hepatitis C virus infectionALBALATE, Marta; FARINAS, M. Carmen; GOMEZ OCTAVIO, Juan et al.Nephron. 2001, Vol 88, Num 2, pp 170-173, issn 0028-2766Article

Lipid and DNA oxidative damage in experimentally induced hepatic porphyria in C57BL/10ScSn miceHORVATH, M. E; FAUX, S. P; BLAZOVICS, A et al.Zeitschrift für Gastroenterologie. 2001, Vol 39, Num 6, pp 452-458, issn 0044-2771, 4 p.Article

Prediction of hyperbilirubinaemia in the healthy term newbornCARBONELL, X; BOTET, F; FIGUERAS, J et al.Acta paediatrica (Oslo). 2001, Vol 90, Num 2, pp 166-170, issn 0803-5253Article

Treatment of porphyria cutanea tarda with phlebotomy in a patient on peritoneal dialysisKELLY, Maureen A; O'ROURKE, Katherine D.Journal of the American Academy of Dermatology. 2001, Vol 44, Num 2, pp 336-338, issn 0190-9622, 2Article

Uroporphyria in Hfe mutant mice given 5-aminolevulinate : A new model of Fe-mediated porphyria cutanea tardaSINCLAIR, Peter R; GORMAN, Nadia; WALTON, Heidi S et al.Hepatology (Baltimore, Md.). 2001, Vol 33, Num 2, pp 406-412, issn 0270-9139Article

New missense mutation in the human ferrochelatase gene in a family with erythropoietic protoporphyria: Functional studies and correlation of genotype and phenotypeRÜFENACHT, Urszula B; GREGOR, Anita; GOUYA, Laurent et al.Clinical chemistry (Baltimore, Md.). 2001, Vol 47, Num 6, pp 1112-1113, issn 0009-9147Article

HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda : a prospective study of 36 cases from southern FranceDEREURE, O; AGUILAR-MARTINEZ, P; BESSIS, D et al.British journal of dermatology (1951). 2001, Vol 144, Num 3, pp 533-539, issn 0007-0963Conference Paper

Porphyria cutanea tardaBLEASEL, Narelle R; VARIGOS, George A.Australasian journal of dermatology. 2000, Vol 41, Num 4, pp 197-208, issn 0004-8380Article

Disorders of phosphate metabolismDIMEGLIO, Linda A; WHITE, Kenneth E; ECONS, Michael J et al.Endocrinology and metabolism clinics of North America. 2000, Vol 29, Num 3, pp vii-viii, issn 0889-8529, 21 p.Article

BASES MOLECULAIRES DE LA PROTOPORPHYRIE ERYTHROPOÏÉTIQUE HUMAINE = MOLECULAR BASIS OF ERYTRHOPOIETIC PROTOPORPHYRIAGouya, Laurent; Deybach, Jean-Charles.2000, 159 p.Thesis

The W198X and R173W mutations in the porphobilinogen deaminase gene in acute intermittent porphyria have higher clinical penetrance than R167W. A population-based studyANDERSSON, C; FLODERUS, Y; WIKBERG, A et al.Scandinavian journal of clinical & laboratory investigation. 2000, Vol 60, Num 7, pp 643-648, issn 0036-5513Article

Activity and immunohistochemical localization of porphobilinogen deaminase in rat tissuesJØRGENSEN, P. E; ERLANDSEN, E. J; POULSEN, S. S et al.Scandinavian journal of clinical & laboratory investigation. 2000, Vol 60, Num 7, pp 635-641, issn 0036-5513Article

Gilbert syndrome : analysis of the promoter region of the uridine diphosphate-glucuronosyltransferase 1 gene in the Greek populationKAVAZARAKIS, Emmanuel; TSEZOU, Aspasia; TZETIS, Maria et al.European journal of pediatrics. 2000, Vol 159, Num 11, pp 873-874, issn 0340-6199Article

Iron overload in porphyria cutanea tardaBYGUM, A; BRANDRUP, F.British journal of dermatology (1951). 2000, Vol 143, Num 5, issn 0007-0963, p. 1116Article

Lipoprotein abnormalities in patients with asymptomatic acute porphyriaFERNANDEZ-MIRANDA, C; DE LA CALLE, M; LARUMBE, S et al.Clinica chimica acta. 2000, Vol 294, Num 1-2, pp 37-43, issn 0009-8981Article

Management of porphyria cutanea tarda in the setting of chronic renal failure : A case report and reviewSHIEH, S; COHEN, J. L; LIM, H. W et al.Journal of the American Academy of Dermatology. 2000, Vol 42, Num 4, pp 645-652, issn 0190-9622Article

Molecular aspects of the inherited porphyriasSASSA, S; KAPPAS, A.Journal of internal medicine. 2000, Vol 247, Num 2, pp 169-178, issn 0954-6820Article

Porphyria cutanea tarda : Fallbericht und Differentialdiagnosen = Porphyria cutanea tardaOELZNER, S; GEBHARDT, M; ELSNER, P et al.Aktuelle Dermatologie. 1999, Vol 25, Num 5, pp 148-151, issn 0340-2541Article

Determination of hepatic iron concentration in fresh and paraffin-embedded tissueBEILBY, J. P; PRINS, A. W; SWANSON, N. R et al.Clinical chemistry (Baltimore, Md.). 1999, Vol 45, Num 4, pp 573-574, issn 0009-9147Article

Congenital erythropoietic porphyria affecting two brothersSAVAL, A. H; TIRADO, A. M.British journal of dermatology (1951). 1999, Vol 141, Num 3, pp 547-550, issn 0007-0963Article

Premenstrual attacks of acute intermittent porphyria : hormonal and metabolic aspects : a case reportDE BLOCK, C. E. M; DE LEEUW, I. H; VAN GAAL, L. F et al.European journal of endocrinology. 1999, Vol 141, Num 1, pp 50-54, issn 0804-4643Article

Studies on coproporphyrin isomers in urine and feces in the porphyriasKÜHNEL, A; GROSS, U; JACOB, K et al.Clinica chimica acta. 1999, Vol 282, Num 1-2, pp 45-58, issn 0009-8981Article

The porphyriasNORDMANN, Y; PUY, H; DEYBACH, J.-C et al.Journal of hepatology. Supplement. 1999, Vol 30, Num 1, pp 12-16, issn 0169-5185Conference Paper

Acute intermittent porphyria with central pontine myelinolysis and cortical laminar necrosisSUSA, S; DAIMON, M; MORITA, Y et al.Neuroradiology (Berlin. Print). 1999, Vol 41, Num 11, pp 835-839, issn 0028-3940Article