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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1995
[Congenital erythropoietic porphyria. Apropos of a fatal case in the neonatal period due to acute hemolysis with hepatic failure]H de Verneuil, F Moreau-Gaudry, C Ged, et al.
Journal of Inherited Metabolic Disease|June 1, 1997
Gene transfer of the uroporphyrinogen III synthase cDNA into haematopoietic progenitor cells in view of a future gene therapy in congenital erythropoietic porphyriaF Mazurier, F Moreau-Gaudry, S Salesse, et al.
Prenatal Diagnosis|January 1, 1996
Prenatal diagnosis in congenital erythropoietic porphyria by metabolic measurement and DNA mutation analysisC Ged, F Moreau-Gaudry, L Taine, et al.
The British Journal of Dermatology|May 23, 2012
Usefulness of a global clinical ichthyosis vulgaris scoring system for predicting common FLG null mutations in an adult caucasian populationK Ezzedine, C Droitcourt, C Ged, et al.
Dermatology (Basel, Switzerland)|June 25, 2011
A prospective study of filaggrin null mutations in keratoconus patients with or without atopic disordersC Droitcourt, D Touboul, C Ged, et al.
Archives Francaises De Pediatrie|August 1, 1985
[Pharmacokinetics of prednisone after oral administration in children with renal grafts. Changes induced by phenobarbital and renal insufficiency]F Perignon, M A Pecquinot, C Ged, et al.
Human Mutation|September 8, 1999
Screening for mutations in the uroporphyrinogen decarboxylase gene using denaturing gradient gel electrophoresis. Identification and characterization of six novel mutations associated with familial PCTL Christiansen, C Ged, I Hombrados, et al.
British Journal of Clinical Pharmacology|October 1, 1989
The increase in urinary excretion of 6 beta-hydroxycortisol as a marker of human hepatic cytochrome P450IIIA inductionC Ged, J M Rouillon, L Pichard, et al.
Journal of Nephrology|April 3, 2001
Impact of high-flux/high-efficiency dialysis on folate and homocysteine metabolismC Lasseur, F Parrot, Y Delmas, et al.
Human Gene Therapy|January 1, 1995
Correction of the enzyme defect in cultured congenital erythropoietic porphyria disease cells by retrovirus-mediated gene transferF Moreau-Gaudry, C Ged, C Barbot, et al.
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