Ged C - Search Results

1

Metabolic correction of congenital erythropoietic porphyria by retrovirus-mediated gene transfer into Epstein-Barr virus-transformed B-cell lines.

Moreau-Gaudry F, Mazurier F, Bensidhoum M, Ged C, de Verneuil H. Moreau-Gaudry F, et al. Among authors: ged c. Blood. 1995 Mar 15;85(6):1449-53. Blood. 1995. PMID: 7888667 Free article.

2

[Congenital erythropoietic porphyria. Apropos of a fatal case in the neonatal period due to acute hemolysis with hepatic failure].

de Verneuil H, Moreau-Gaudry F, Ged C, Bensidhoum M, Hombrados I, Tricoire J, Rolland M. de Verneuil H, et al. Among authors: ged c. Arch Pediatr. 1995 Aug;2(8):755-61. doi: 10.1016/0929-693x(96)81246-2. Arch Pediatr. 1995. PMID: 7550841 French.

3

Identification of two new mutations in congenital erythropoietic porphyria.

Bensidhoum M, Ged C, Hombrados I, Moreau-Gaudry F, Hift RS, Meissner P, Sturrock ED, de Verneuil H. Bensidhoum M, et al. Among authors: ged c. Eur J Hum Genet. 1995;3(2):102-7. doi: 10.1159/000472283. Eur J Hum Genet. 1995. PMID: 7552139

4

Is genotyping useful for the screening of medium-chain acyl-CoA dehydrogenase deficiency in France?

Ged C, el Sebai H, de Verneuil H, Parrot-Rouleau F. Ged C, et al. J Inherit Metab Dis. 1995;18(2):253-6. doi: 10.1007/BF00711781. J Inherit Metab Dis. 1995. PMID: 7564261 No abstract available.

5

Porphyrias: animal models and prospects for cellular and gene therapy.

de Verneuil H, Ged C, Boulechfar S, Moreau-Gaudry F. de Verneuil H, et al. Among authors: ged c. J Bioenerg Biomembr. 1995 Apr;27(2):239-48. doi: 10.1007/BF02110039. J Bioenerg Biomembr. 1995. PMID: 7592571 Review.

6

Correction of the enzyme defect in cultured congenital erythropoietic porphyria disease cells by retrovirus-mediated gene transfer.

Moreau-Gaudry F, Ged C, Barbot C, Mazurier F, Boiron JM, Bensidhoum M, Reiffers J, de Verneuil H. Moreau-Gaudry F, et al. Among authors: ged c. Hum Gene Ther. 1995 Jan;6(1):13-20. doi: 10.1089/hum.1995.6.1-13. Hum Gene Ther. 1995. PMID: 7703283

7

The cDNA sequence of mouse uroporphyrinogen III synthase and assignment to mouse chromosome 7.

Bensidhoum M, Ged CM, Poirier C, Guénet JL, de Verneuil H. Bensidhoum M, et al. Among authors: ged cm. Mamm Genome. 1994 Nov;5(11):728-30. doi: 10.1007/BF00426082. Mamm Genome. 1994. PMID: 7873885 No abstract available.

8

Uroporphyrinogen decarboxylase: complete human gene sequence and molecular study of three families with hepatoerythropoietic porphyria.

Moran-Jimenez MJ, Ged C, Romana M, Enriquez De Salamanca R, Taïeb A, Topi G, D'Alessandro L, de Verneuil H. Moran-Jimenez MJ, et al. Among authors: ged c. Am J Hum Genet. 1996 Apr;58(4):712-21. Am J Hum Genet. 1996. PMID: 8644733 Free PMC article.

9

A novel point mutation in congenital erythropoietic porphyria in two members of Japanese family.

Tanigawa K, Bensidhoum M, Takamura N, Namba H, Yamashita S, de Verneuil H, Ged C. Tanigawa K, et al. Among authors: ged c. Hum Genet. 1996 May;97(5):557-60. doi: 10.1007/BF02281859. Hum Genet. 1996. PMID: 8655129

10

Correction of congenital erythropoietic porphyria by bone marrow transplantation.

Thomas C, Ged C, Nordmann Y, de Verneuil H, Pellier I, Fischer A, Blanche S. Thomas C, et al. Among authors: ged c. J Pediatr. 1996 Sep;129(3):453-6. doi: 10.1016/s0022-3476(96)70082-3. J Pediatr. 1996. PMID: 8804339

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