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Items: 1 to 20 of 26

1.

Uroporphyrinogen decarboxylase structural mutant (Gly281----Glu) in a case of porphyria.

de Verneuil H, Grandchamp B, Beaumont C, Picat C, Nordmann Y.

Science. 1986 Nov 7;234(4777):732-4.

PMID:
3775362
2.

Uroporphyrinogen decarboxylase.

Elder GH, Roberts AG.

J Bioenerg Biomembr. 1995 Apr;27(2):207-14. Review.

PMID:
7592567
3.

Enzymes of the heme biosynthesis pathway: recent advances in molecular genetics.

Grandchamp B, Nordmann Y.

Semin Hematol. 1988 Oct;25(4):303-11. Review. No abstract available.

PMID:
3064311
4.

[Porphyria cutanea tarda (PCT)].

Goerz G, Merk H.

Z Hautkr. 1985 Jan;60(1-2):137-46. Review. German.

PMID:
3885597
5.

[Porphyria cutanea tarda is the most common type of porphyria. Medical control is a team work].

Harper P, Thunell S, Hultcrantz R, Ros AM, Wennersten G.

Lakartidningen. 1998 Jul 8;95(28-29):3195-9. Review. Swedish.

PMID:
9700265
6.

[Enzyme deficiency of erythrocytes in human porphyria].

Doss MO.

Gematol Transfuziol. 1992 Nov-Dec;37(11-12):10-5. Review. Russian.

PMID:
1295774
7.

New aspects of porphyrias.

Mascaro JM, Lecha M, Herrero C, Muniesa AM.

Curr Probl Dermatol. 1985;13:11-32. Review. No abstract available.

PMID:
3882335
8.

[Polymerase chain reaction with subsequent direct gene sequence analysis. A possibility for molecular analysis in dermatology].

Volkenandt M, Scharffetter K, Plewig G, Goerz G.

Hautarzt. 1991 Nov;42(11):700-3. Review. German.

PMID:
1769833
9.

Hepatoerythropoietic porphyria: relationship with familial porphyria cutanea tarda.

Castaño Suárez E, Zamarro Sanz O, Guerra Tapia A, Enríquez de Salamanca R.

Dermatology. 1996;193(4):332-5. Review.

PMID:
8993961
10.

Enzyme defects in hereditary porphyria.

Civin WH, Epstein E.

Ann Clin Lab Sci. 1980 Sep-Oct;10(5):395-401. Review.

PMID:
6999973
11.

Porphyria cutanea tarda: pathogenesis in relation to therapy.

Elder GH.

Curr Probl Dermatol. 1991;20:91-6. Review. No abstract available.

PMID:
1935223
12.

Porphyria cutanea tarda.

Pimstone NR.

Semin Liver Dis. 1982 May;2(2):132-42. Review. No abstract available.

PMID:
6753163
13.

Hepatic porphyrias in children.

Elder GH.

J Inherit Metab Dis. 1997 Jun;20(2):237-46. Review.

PMID:
9211196
14.

Porphyria cutanea tarda, or the uroporphyrinogen decarboxylase deficiency diseases.

Sweeney GD.

Clin Biochem. 1986 Feb;19(1):3-15. Review.

PMID:
3513989
15.

Recent advances in the identification of enzyme deficiencies in the porphyrias.

Elder GH.

Br J Dermatol. 1983 Jun;108(6):729-34. Review. No abstract available.

PMID:
6344903
16.

Hematologic and hepatic manifestations of the cutaneous porphyrias.

Pimstone NR.

Clin Dermatol. 1985 Apr-Jun;3(2):83-102. Review.

PMID:
3916835
17.

Haem biosynthesis and human porphyria cutanea tarda: effects of alcohol intake.

Mukerji SK.

Indian J Exp Biol. 2000 Jul;38(7):635-42. Review.

PMID:
11215304
18.

Update on enzyme and molecular defects in porphyria.

Elder GH.

Photodermatol Photoimmunol Photomed. 1998 Apr;14(2):66-9. Review.

PMID:
9638727
19.

Molecular genetics of porphyrias.

Nordmann Y, de Verneuil H, Deybach JC, Delfau MH, Grandchamp B.

Ann Med. 1990 Dec;22(6):387-91. Review. No abstract available.

PMID:
2076270
20.

[The enzymopathic nature of porphyria].

Gajdos A.

Nouv Presse Med. 1976 May 29;5(22):1417-22. Review. French. No abstract available.

PMID:
778793

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