These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

231 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]
    of 12.