BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 64669)

  • 1. 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]  

  • 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. [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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphisms.
    Martasek P; Nordmann Y; Grandchamp B
    Hum Mol Genet; 1994 Mar; 3(3):477-80. PubMed ID: 8012360
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria.
    Grandchamp B; Lamoril J; Puy H
    J Bioenerg Biomembr; 1995 Apr; 27(2):215-9. PubMed ID: 7592568
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. [Hydroa vacciniforme type eruption disclosing hereditary coproporphyria].
    Jeanmougin M; Pedreiro J; Manciet JR; Moulin JP; Civatte J
    Ann Dermatol Venereol; 1988; 115(11):1236-8. PubMed ID: 3239925
    [No Abstract]   [Full Text] [Related]  

  • 16. Hereditary coproporphyria and epilepsy.
    Houston AB; Brodie MJ; Moore MR; Thompson GG; Stephenson JB
    Arch Dis Child; 1977 Aug; 52(8):646-50. PubMed ID: 921312
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Progress in dermatology: new biochemical aspects].
    Goerz G; Merk H
    Fortschr Med; 1982 Aug; 100(31-32):1467-71. PubMed ID: 6290359
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization and expression of cDNA encoding coproporphyrinogen oxidase from a patient with hereditary coproporphyria.
    Fujita H; Kondo M; Taketani S; Nomura N; Furuyama K; Akagi R; Nagai T; Terajima M; Galbraith RA; Sassa S
    Hum Mol Genet; 1994 Oct; 3(10):1807-10. PubMed ID: 7849704
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Compound heterozygous hereditary coproporphyria with fluorescing teeth.
    Doss MO; Gross U; Lamoril J; Kranl C; Jacob K; Doss M; da Silva V; Freesemann AG; Deybach JC; Sepp N; Nordmann Y
    Ann Clin Biochem; 1999 Sep; 36 ( Pt 5)():680-2. PubMed ID: 10505225
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.