236 related articles for article (PubMed ID: 11929047)
1. 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]
2. [Coexistence of hereditary coproporphyria and porphyria cutanea tarda: a new form of dual porphyria].
Doss MO; Gross U; Puy H; Doss M; Kühnel A; Jacob K; Deybach JC; Nordmann Y
Med Klin (Munich); 2002 Jan; 97(1):1-5. PubMed ID: 11831056
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update.
Rosipal R; Lamoril J; Puy H; Da Silva V; Gouya L; De Rooij FW; Te Velde K; Nordmann Y; Martàsek P; Deybach JC
Hum Mutat; 1999; 13(1):44-53. PubMed ID: 9888388
[TBL] [Abstract][Full Text] [Related]
5. Molecular defects of the coproporphyrinogen oxidase gene in hereditary coproporphyria.
Sassa S; Kondo M; Taketani S; Nomura N; Furuyama K; Akagi R; Nagai T; Terajima M; Galbraith RA; Fujita H
Cell Mol Biol (Noisy-le-grand); 1997 Feb; 43(1):59-66. PubMed ID: 9074789
[TBL] [Abstract][Full Text] [Related]
6. Hereditary coproporphyria: exon screening by heteroduplex analysis detects three novel mutations in the coproporphyrinogen oxidase gene.
Schreiber WE; Zhang X; Senz J; Jamani A
Hum Mutat; 1997; 10(3):196-200. PubMed ID: 9298818
[TBL] [Abstract][Full Text] [Related]
7. Hormonal oral contraceptives, urinary porphyrin excretion and porphyrias.
Gross U; Honcamp M; Daume E; Frank M; Düsterberg B; Doss MO
Horm Metab Res; 1995 Aug; 27(8):379-83. PubMed ID: 7590628
[TBL] [Abstract][Full Text] [Related]
8. A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family.
Susa S; Daimon M; Yamamori I; Kondo M; Yamatani K; Sasaki H; Kato T
J Hum Genet; 1998; 43(3):182-4. PubMed ID: 9747031
[TBL] [Abstract][Full Text] [Related]
9. Biochemical and genetic characterization of four cases of hereditary coproporphyria in Spain.
To-Figueras J; Badenas C; Enríquez MT; Segura S; Alvarez C; Milà M; Lecha M; Herrero C
Mol Genet Metab; 2005 Jun; 85(2):160-3. PubMed ID: 15896662
[TBL] [Abstract][Full Text] [Related]
10. Identification of a novel mutation of the CPO gene in a Japanese hereditary coproporphyria family.
Susa S; Daimon M; Kondo H; Kondo M; Yamatani K; Sasaki H
Am J Med Genet; 1998 Nov; 80(3):204-6. PubMed ID: 9843038
[TBL] [Abstract][Full Text] [Related]
11. A molecular, enzymatic and clinical study in a family with hereditary coproporphyria.
Gross U; Puy H; Meissauer U; Lamoril J; Deybach JC; Doss M; Nordmann Y; Doss MO
J Inherit Metab Dis; 2002 Aug; 25(4):279-86. PubMed ID: 12227458
[TBL] [Abstract][Full Text] [Related]
12. Co-existence of hereditary coproporphyria and porphyria cutanea tarda: The importance of genetic testing.
Rudd A; Grant J; Varigos G; Morgan V; Winship I
Australas J Dermatol; 2013 May; 54(2):e50-2. PubMed ID: 23582006
[TBL] [Abstract][Full Text] [Related]
13. Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria.
Schmitt C; Gouya L; Malonova E; Lamoril J; Camadro JM; Flamme M; Rose C; Lyoumi S; Da Silva V; Boileau C; Grandchamp B; Beaumont C; Deybach JC; Puy H
Hum Mol Genet; 2005 Oct; 14(20):3089-98. PubMed ID: 16159891
[TBL] [Abstract][Full Text] [Related]
14. Dual porphyria of coexisting variegata and cutanea tarda.
Sieg I; Bhutani LK; Doss MO
Eur J Clin Chem Clin Biochem; 1995 Jul; 33(7):405-10. PubMed ID: 7548446
[TBL] [Abstract][Full Text] [Related]
15. [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]
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. Coexistence of hereditary coproporphyria with acute intermittent porphyria.
Gregor A; Kostrzewska E; Tarczynska-Nosal S; Stachurska H
Ann Med; 1994 Apr; 26(2):125-7. PubMed ID: 8024730
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria.
Wiman A; Floderus Y; Harper P
J Hum Genet; 2002; 47(8):407-12. PubMed ID: 12181641
[TBL] [Abstract][Full Text] [Related]
20. A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria.
Lamoril J; Martasek P; Deybach JC; Da Silva V; Grandchamp B; Nordmann Y
Hum Mol Genet; 1995 Feb; 4(2):275-8. PubMed ID: 7757079
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]