134 related articles for article (PubMed ID: 866144)
1. [Demonstration of hereditary enzyme defect in coproporphyria].
Grandchamp B; Phung N; Grelier M; de Verneuil H; Noiré J; Ohnet JP; Nordmann Y
Nouv Presse Med; 1977 Apr; 6(18):1537-9. PubMed ID: 866144
[TBL] [Abstract][Full Text] [Related]
2. Decreased lymphocyte coproporphyrinogen III oxidase activity in hereditary coproporphyria.
Grandchamp B; Nordmann Y
Biochem Biophys Res Commun; 1977 Feb; 74(3):1089-95. PubMed ID: 843348
[No Abstract] [Full Text] [Related]
3. Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
Gross U; Puy H; Kühnel A; Meissauer U; Deybach JC; Jacob K; Martasek P; Nordmann Y; Doss MO
Cell Mol Biol (Noisy-le-grand); 2002 Feb; 48(1):49-55. PubMed ID: 11929047
[TBL] [Abstract][Full Text] [Related]
4. Coproporphyrinogen-oxidase deficiency in hereditary coproporphyria.
Nordmann Y; Grandchamp B; Phung N; de Verneuil H; Grelier M; Neiré J
Lancet; 1977 Jan; 1(8003):140. PubMed ID: 64669
[No Abstract] [Full Text] [Related]
5. The primary enzyme defect in hereditary coproporphyria.
Elder GH; Evans JO; Thomas N
Lancet; 1976 Dec; 2(7997):1217-9. PubMed ID: 63041
[TBL] [Abstract][Full Text] [Related]
6. Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney.
Doss M; von Tiepermann R; Pflüger KH
J Neurol; 1981; 226(1):25-33. PubMed ID: 6181213
[No Abstract] [Full Text] [Related]
7. [Hereditary coproporphyria in 2 Dutch families].
te Velde K; Noordhoek KH
Ned Tijdschr Geneeskd; 1984 May; 128(19):892-5. PubMed ID: 6728057
[No Abstract] [Full Text] [Related]
8. [A family study of the initial Dutch patients with porphyria].
te Velde K; Noordhoek KH; Wilson JH; de Roody FW
Ned Tijdschr Geneeskd; 1989 Dec; 133(51):2547-52. PubMed ID: 2601755
[TBL] [Abstract][Full Text] [Related]
9. Deficiency of hepatic coproporphyrinogen oxidase in hereditary coproporphyria.
Hawk JL; Magnus IA; Parkes A; Elder GH; Doyle M
J R Soc Med; 1978 Oct; 71(10):775-7. PubMed ID: 712737
[No Abstract] [Full Text] [Related]
10. Harderoporphyria: a variant hereditary coproporphyria.
Nordmann Y; Grandchamp B; de Verneuil H; Phung L; Cartigny B; Fontaine G
J Clin Invest; 1983 Sep; 72(3):1139-49. PubMed ID: 6886003
[TBL] [Abstract][Full Text] [Related]
11. Hereditary coproporphyria: demonstration of a genetic defect in coproporphyrinogen metabolism.
Nordmann Y; Grandchamp B
Monogr Hum Genet; 1978; 10():217-22. PubMed ID: 723897
[No Abstract] [Full Text] [Related]
12. [Hereditary coproporphyria. A familial study].
Rocchi E; Pietrangelo A; Gibertini P; Cassanelli M; Trenti T; Borghi A; Silingardi M; Jensen J; Ventura E
Recenti Prog Med; 1984 Feb; 75(2):123-31. PubMed ID: 6729195
[No Abstract] [Full Text] [Related]
13. Acquired immunodeficiency syndrome in a patient affected by hereditary coproporphyria: safety of zidovudine treatment.
Herrero C; Bassas S; Azon A; Mascaro JM; Miro J
Arch Dermatol; 1990 Jan; 126(1):122-3. PubMed ID: 2297248
[No Abstract] [Full Text] [Related]
14. Molecular characterization of porphyrias in Italy: a diagnostic flow-chart.
Martinez di Montemuros F; Di Pierro E; Patti E; Tavazzi D; Danielli MG; Biolcati G; Rocchi E; Cappellini MD
Cell Mol Biol (Noisy-le-grand); 2002 Dec; 48(8):867-76. PubMed ID: 12699245
[TBL] [Abstract][Full Text] [Related]
15. Studies in porphyria IX: Detection of the gene defect of erythropoietic protoporphyria in mitogen-stimulated human lymphocytes.
Sassa S; Zalar GL; Poh-Fitzpatrick MB; Kappas A
Trans Assoc Am Physicians; 1979; 92():268-76. PubMed ID: 549253
[TBL] [Abstract][Full Text] [Related]
16. Hereditary coproporphyria. Demonstration of the abnormalities in haem biosynthesis in peripheral blood.
Brodie MJ; Thompson GG; Moore MR; Beattie AD; Goldberg A
Q J Med; 1977 Apr; 46(182):229-41. PubMed ID: 866576
[TBL] [Abstract][Full Text] [Related]
17. [Hereditary coproporphyria: 1st proven homozygous case].
Nordmann Y; Grandchamp B; Phung N; de Verneuil H; Grelier M; Noire J; Gajdos A; Lamotte-Barillon S; Guérin JM; Barrier J; Weil J; Deleche H
Nouv Presse Med; 1978 Mar; 7(10):847-8. PubMed ID: 643550
[No Abstract] [Full Text] [Related]
18. [Clinical heterogeneity of hereditary coproporphyria: diagnostic usefulness of biochemical studies. Study of a familial case].
Savi M; David S; Dall'Aglio P
Pathologica; 1983; 75 Suppl():134-7. PubMed ID: 6680417
[No Abstract] [Full Text] [Related]
19. The enzymatic defect in variegate prophyria. Studies with human cultured skin fibroblasts.
Brenner DA; Bloomer JR
N Engl J Med; 1980 Apr; 302(14):765-9. PubMed ID: 7354807
[TBL] [Abstract][Full Text] [Related]
20. Hereditary coproporphyria in Germany: clinical-biochemical studies in 53 patients.
Kühnel A; Gross U; Doss MO
Clin Biochem; 2000 Aug; 33(6):465-73. PubMed ID: 11074238
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
