ACNP - Italian Periodicals Catalogue

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Results: 1-9 |

Results: 9

From gene transfer to gene therapy in lysosomal storage diseases affectingthe central nervous system

Authors: Poenaru, L

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

LAMP-2 deficiency causes vacuolar myopathy

Authors: Caillaud, C Poenaru, L

Citation: C. Caillaud et L. Poenaru, LAMP-2 deficiency causes vacuolar myopathy, M S-MED SCI, 17(1), 2001, pp. 94-95

Juvenile and adult-onset acid maltase deficiency in France: Genotype-phenotype correlation - Reply

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

Approach to gene therapy of glycogenosis type II (Pompe disease)

Authors: Poenaru, L

Citation: L. Poenaru, Approach to gene therapy of glycogenosis type II (Pompe disease), MOL GEN MET, 70(3), 2000, pp. 163-169

Gene therapy in lysosomal diseases

Authors: Caillaud, C Poenaru, L

Citation: C. Caillaud et L. Poenaru, Gene therapy in lysosomal diseases, BIOMED PHAR, 54(10), 2000, pp. 505-512

Juvenile and adult-onset acid maltase deficiency in France - Genotype-phenotype correlation

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

Gaucher disease: The origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations

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

Adenoviral gene therapy of the Tay-Sachs disease in hexosaminidase A-deficient knock-out mice

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

Fabry disease: Identification of novel alpha-galactosidase a mutations andmolecular carrier detection by use of fluorescent chemical cleavage of mismatches

Authors: Germain, DP Poenaru, L

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

Risultati: 1-9 |