Citation: L. Poenaru, From gene transfer to gene therapy in lysosomal storage diseases affectingthe central nervous system, ANN MED, 33(1), 2001, pp. 28-36
Authors:
Laforet, P
Eymard, B
Fardeau, M
Caillaud, C
Nicolino, M
Poenaru, L
Citation: P. Laforet et al., Juvenile and adult-onset acid maltase deficiency in France: Genotype-phenotype correlation - Reply, NEUROLOGY, 57(10), 2001, pp. 1938-1938
Authors:
Laforet, P
Nicolino, M
Eymard, B
Puech, JP
Caillaud, C
Poenaru, L
Fardeau, M
Citation: P. Laforet et al., Juvenile and adult-onset acid maltase deficiency in France - Genotype-phenotype correlation, NEUROLOGY, 55(8), 2000, pp. 1122-1128
Authors:
Diaz, GA
Gelb, BD
Risch, N
Nygaard, TG
Frisch, A
Cohen, IJ
Miranda, CS
Amaral, O
Maire, I
Poenaru, L
Caillaud, C
Weizberg, M
Mistry, P
Desnick, RJ
Citation: Ga. Diaz et al., Gaucher disease: The origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations, AM J HU GEN, 66(6), 2000, pp. 1821-1832
Authors:
Guidotti, JE
Mignon, A
Haase, G
Caillaud, C
McDonell, N
Kahn, A
Poenaru, L
Citation: Je. Guidotti et al., Adenoviral gene therapy of the Tay-Sachs disease in hexosaminidase A-deficient knock-out mice, HUM MOL GEN, 8(5), 1999, pp. 831-838
Citation: Dp. Germain et L. Poenaru, Fabry disease: Identification of novel alpha-galactosidase a mutations andmolecular carrier detection by use of fluorescent chemical cleavage of mismatches, BIOC BIOP R, 257(3), 1999, pp. 708-713