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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.
Annales De Dermatologie Et De Venereologie|October 12, 2010
[Congenital erythropoeietic porphyria treated by haematopoietic stem cell allograft]I Lebreuilly-Sohyer, A Morice, A Acher, et al.
Annales De Dermatologie Et De Venereologie|September 25, 1998
[Allogeneic bone marrow transplantation in congenital erythropoietic porphyria. Gunther's disease]C Lagarde, D Hamel-Teillac, Y De Prost, et al.
American Journal of Human Genetics|April 1, 1996
Uroporphyrinogen decarboxylase: complete human gene sequence and molecular study of three families with hepatoerythropoietic porphyriaM J Moran-Jimenez, C Ged, M Romana, 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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