285 related articles for article (PubMed ID: 7648240)
1. Autosomal recessive erythropoietic protoporphyria: a syndrome of severe photosensitivity and liver failure.
Sarkany RP; Cox TM
QJM; 1995 Aug; 88(8):541-9. PubMed ID: 7648240
[TBL] [Abstract][Full Text] [Related]
2. Recessive inheritance of erythropoietic protoporphyria with liver failure.
Sarkany RP; Alexander GJ; Cox TM
Lancet; 1994 Jun; 343(8910):1394-6. PubMed ID: 7910885
[TBL] [Abstract][Full Text] [Related]
3. Hypermethylation of the wild-type ferrochelatase allele is closely associated with severe liver complication in a family with erythropoietic protoporphyria.
Onaga Y; Ido A; Uto H; Hasuike S; Kusumoto K; Moriuchi A; Numata M; Nagata K; Hori T; Hayashi K; Tsubouchi H
Biochem Biophys Res Commun; 2004 Sep; 321(4):851-8. PubMed ID: 15358105
[TBL] [Abstract][Full Text] [Related]
4. Ferrochelatase gene mutations in erythropoietic protoporphyria: focus on liver disease.
Chen FP; Risheg H; Liu Y; Bloomer J
Cell Mol Biol (Noisy-le-grand); 2002 Feb; 48(1):83-9. PubMed ID: 11929052
[TBL] [Abstract][Full Text] [Related]
5. Haplotype analysis of families with erythropoietic protoporphyria and novel mutations of the ferrochelatase gene.
Wang X; Yang L; Kurtz L; Lichtin A; DeLeo VA; Bloomer J; Poh-Fitzpatrick MB
J Invest Dermatol; 1999 Jul; 113(1):87-92. PubMed ID: 10417624
[TBL] [Abstract][Full Text] [Related]
6. [Homozygote erythropoietic protoporphyria associated with porokeratosis].
Philippot V; Bérard F; Perrot H
Ann Dermatol Venereol; 1996; 123(6-7):382-6. PubMed ID: 8959061
[TBL] [Abstract][Full Text] [Related]
7. Clinical implications of the molecular biology of erythropoietic protoporphyria.
Todd DJ
J Eur Acad Dermatol Venereol; 1998 Nov; 11(3):207-13. PubMed ID: 9883431
[TBL] [Abstract][Full Text] [Related]
8. Protoporphyria.
Cox TM; Alexander GJ; Sarkany RP
Semin Liver Dis; 1998; 18(1):85-93. PubMed ID: 9516682
[TBL] [Abstract][Full Text] [Related]
9. [Often unrecognized: erythropoietic protoporphyria].
Minder EI; Schneider-Yin X
Schweiz Med Wochenschr; 1993 Feb; 123(6):229-33. PubMed ID: 8434252
[TBL] [Abstract][Full Text] [Related]
10. Recessive inheritance of erythropoietic protoporphyria with liver failure.
Goerz G; Bolsen K; Bunselmeyer S; Schürer NY
Lancet; 1994 Jul; 344(8918):337. PubMed ID: 7914283
[No Abstract] [Full Text] [Related]
11. An exon 10 deletion in the mouse ferrochelatase gene has a dominant-negative effect and causes mild protoporphyria.
Magness ST; Maeda N; Brenner DA
Blood; 2002 Aug; 100(4):1470-7. PubMed ID: 12149233
[TBL] [Abstract][Full Text] [Related]
12. Recessive inheritance of erythropoietic protoporphyria with liver failure.
Schneider-Yin X; Taketani S; Schäfer B; Minder EI
Lancet; 1994 Jul; 344(8918):337. PubMed ID: 7914284
[No Abstract] [Full Text] [Related]
13. Ferrochelatase activities in patients with erythropoietic protoporphyria and their families.
Goerz G; Bunselmeyer S; Bolsen K; Schürer NY
Br J Dermatol; 1996 May; 134(5):880-5. PubMed ID: 8736329
[TBL] [Abstract][Full Text] [Related]
14. Liver failure in erythropoietic protoporphyria.
Sarkany RP; Cox TM
J Am Acad Dermatol; 1996 Mar; 34(3):540-1. PubMed ID: 8609281
[No Abstract] [Full Text] [Related]
15. Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease.
Tutois S; Montagutelli X; Da Silva V; Jouault H; Rouyer-Fessard P; Leroy-Viard K; Guénet JL; Nordmann Y; Beuzard Y; Deybach JC
J Clin Invest; 1991 Nov; 88(5):1730-6. PubMed ID: 1939658
[TBL] [Abstract][Full Text] [Related]
16. Erythropoietic protoporphyria: identification of novel mutations in the ferrochelatase gene and comparison of biochemical markers versus molecular analysis as diagnostic strategies.
Frank J; Nelson J; Wang X; Yang L; Ahmad W; Lam H; Jugert FK; Kalka K; Poh-Fitzpatrick MB; Goerz G; Merk HF; Christiano AM
J Investig Med; 1999 Jul; 47(6):278-84. PubMed ID: 10431482
[TBL] [Abstract][Full Text] [Related]
17. Systematic analysis of molecular defects in the ferrochelatase gene from patients with erythropoietic protoporphyria.
Rüfenacht UB; Gouya L; Schneider-Yin X; Puy H; Schäfer BW; Aquaron R; Nordmann Y; Minder EI; Deybach JC
Am J Hum Genet; 1998 Jun; 62(6):1341-52. PubMed ID: 9585598
[TBL] [Abstract][Full Text] [Related]
18. Long-term cure of the photosensitivity of murine erythropoietic protoporphyria by preselective gene therapy.
Pawliuk R; Bachelot T; Wise RJ; Mathews-Roth MM; Leboulch P
Nat Med; 1999 Jul; 5(7):768-73. PubMed ID: 10395321
[TBL] [Abstract][Full Text] [Related]
19. Molecular genetics of erythropoietic protoporphyria.
Todd DJ
Photodermatol Photoimmunol Photomed; 1998 Apr; 14(2):70-3. PubMed ID: 9638728
[TBL] [Abstract][Full Text] [Related]
20. Human erythropoietic protoporphyria: identification of a mutation at the splice donor site of intron 7 causing exon 7 skipping of the ferrochelatase gene.
Nakahashi Y; Miyazaki H; Kadota Y; Naitoh Y; Inoue K; Yamamoto M; Hayashi N; Taketani S
Hum Mol Genet; 1993 Jul; 2(7):1069-70. PubMed ID: 8364548
[No Abstract] [Full Text] [Related]
[Next] [New Search]
