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Original Article

Porphyrin Distribution and Porphyrin Excretion in Human Congenital Erythropoietic Porphyria

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Pages 323-332 | Received 11 Feb 1974, Accepted 08 Mar 1974, Published online: 28 Aug 2009

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Read on this site (3)

Leif Eriksen. (1980) Urinary excretion of position isomers type III in normal man and a series of different types of porphyrias. Scandinavian Journal of Clinical and Laboratory Investigation 40:1, pages 85-88.
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Leif Eriksen & Per O. Thune. (1978) Urinary excretion of porphyrins in two cases of porphyria cutanea tarda during a period of various treatments. Scandinavian Journal of Clinical and Laboratory Investigation 38:3, pages 273-277.
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Leif Eriksen & Nora Eriksen. (1977) Urinary excretion of position isomers of penta-and hexa-carboxylated porphyrins belonging to the isomer III series in a case of congenital erythropoietic porphyrin. Scandinavian Journal of Clinical and Laboratory Investigation 37:4, pages 357-361.
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Articles from other publishers (16)

Clemens Fritsch, Klaus Bolsen, Thomas Ruzicka & Günter Goerz. (1997) Congenital erythropoietic porphyria. Journal of the American Academy of Dermatology 36:4, pages 594-610.
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L. Verstraeten, N. Van Regemorter, A. Pardou, H. de Verneuil, V. Da Silva, F. Rodesch, D. Vermeylen, C. Donner, J. C. Noël, Y. Nordmann & A. Hassoun. (1993) Biochemical Diagnosis of a Fatal Case of Günther’s Disease in a Newborn with Hydrops Foetalis. Clinical Chemistry and Laboratory Medicine 31:3.
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J A Miller & G M Levene. (2016) Congenital Erythropoietic Porphyria and Congenital Adrenal Hyperplasia with Evidence for Hepatic Δ-5α-Reductase Deficiency. Journal of the Royal Society of Medicine 82:2, pages 107-108.
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M. B. Poh-Fitzpatrick, M. Lecha Carralero, M. O. Doss, D. R. Bickers, C. Herrero, J. M. Mascaró, G. H. Elder, S. Sassa, H. Fujita, A. Toback, L. Harber, A. Kappas, H. W. Lim, A. M. Muniesa, H. Lloveras, S. Piomelli, C. Seaman & L. M. Skolnick. 1988. Dermatology in Five Continents. Dermatology in Five Continents 846 879 .
Arnold C. Toback, Shigeru Sassa, Maureen B. Poh-Fitzpatrick, Jay Schechter, Edith Zaider, Leonard C. Harber & Attallah Kappas. (1987) Hepatoerythropoietic Porphyria: Clinical, Biochemical, and Enzymatic Studies in a Three-Generation Family Lineage. New England Journal of Medicine 316:11, pages 645-650.
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Michael R. Moore, Kenneth E. L. McColl, Claude Rimington & Abraham GoldbergMichael R. Moore, Kenneth E. L. Mccoll, Claude Rimington & Abraham Goldberg. 1987. Disorders of Porphyrin Metabolism. Disorders of Porphyrin Metabolism 291 361 .
Neville R. Pimstone. (1985) Hematologic and hepatic manifestations of the cutaneous porphyrias. Clinics in Dermatology 3:2, pages 83-102.
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Maureen B. Poh-Fitzpatrick. (1985) Porphyrin-sensitized cutaneous photosensitivity. Clinics in Dermatology 3:2, pages 41-82.
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G.H. Elder, S.G. Smith, C. Herrero, J.M. Mascaro, M. Lecha, A.M. Muniesa, D.B. Czarnecki, J. Brenan, V. Poulos & R.E. De Salamanca. (1981) HEPATOERYTHROPOIETIC PORPHYRIA: A NEW UROPORPHYRINOGEN DECARBOXYLASE DEFECT OR HOMOZYGOUS PORPHYRIA CUTANEA TARDA?. The Lancet 317:8226, pages 916-919.
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Shigeru Sassa & Attallah Kappas. 1981. Advances in Human Genetics 11. Advances in Human Genetics 11 121 231 .
H. IPPEN & T. FUCHS. (1980) Congenital Porphyria. Clinics in Haematology 9:2, pages 323-344.
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IAN A. MAGNUS. (1980) Cutaneous Porphyria. Clinics in Haematology 9:2, pages 273-302.
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LENNOX EALES. 1979. The Porphyrins. The Porphyrins 663 804 .
A Gregor, E Kostrzewska, H Prokurat, Z Pucek & E Torbicka. (1977) Increased protoporphyrin in erythrocytes in a child with acute intermittent porphyria.. Archives of Disease in Childhood 52:12, pages 947-950.
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Ken Miyagi, Z. J. Petryka, Irene Bossenmaier, Ruth Cardinal & C. J. Watson. (2006) The activities of uroporphyrinogen synthetase and cosynthetase in congenital erythropoietic porphyria (cep). American Journal of Hematology 1:1, pages 3-21.
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J.PINOL AGUADE, C. HERRERO, J. ALMEIDA, S.G. SMITH & R.V. BELCHER. (1975) Thin layer chromatography and counter-current analysis in porphyrias. British Journal of Dermatology 93:3, pages 277-289.
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