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Archives Francaises De Pediatrie|December 1, 1992
[Enzymatic and molecular studies in a case of hepato-erythropoietic porphyria. Homozygote form of type familial cutaneous porphyria]H de Verneuil, F Moreau-Gaudry, S Laradi, et al.
Clinical Endocrinology|June 26, 1998
Corticotroph axis sensitivity after exercise in endurance-trained athletesM Duclos, J B Corcuff, L Arsac, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Identification of two new mutations in congenital erythropoietic porphyriaM Bensidhoum, C Ged, I Hombrados, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 2, 2003
Lentivirus-mediated gene transfer of uroporphyrinogen III synthase fully corrects the porphyric phenotype in human cellsF Géronimi, E Richard, I Lamrissi-Garcia, et al.
Cancer Gene Therapy|January 23, 1999
Retroviral vector-mediated transfer of the interferon-alpha gene in chronic myeloid leukemia cellsS Salesse, F Moreau-Gaudry, V Pigeonnier-Lagarde, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 29, 2001
Correction of deficient CD34+ cells from peripheral blood after mobilization in a patient with congenital erythropoietic porphyriaF Mazurier, F Géronimi, I Lamrissi-Garcia, et al.
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