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Results:
1-10
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Results: 10
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
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:
Caillaud, C
Poenaru, L
Citation: C. Caillaud et L. Poenaru, Gene therapy in lysosomal diseases, BIOMED PHAR, 54(10), 2000, pp. 505-512
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
Authors:
Caillaud, C
Py, G
Eydoux, N
Legros, P
Prefaut, C
Mercier, J
Citation: C. Caillaud et al., Antioxidants and mitochondrial respiration in lung, diaphragm, and locomotor muscles: Effect of exercise, FREE RAD B, 26(9-10), 1999, pp. 1292-1299
Authors:
Mucci, P
Anselme-Poujol, F
Caillaud, C
Couret, I
Rossi, M
Prefaut, C
Citation: P. Mucci et al., Basophil releasability in young highly trained and older athletes, MED SCI SPT, 31(4), 1999, pp. 507-513
Authors:
Megarbane, A
Khalil, G
Waked, N
Rotig, A
Caillaud, C
Loiselet, J
Citation: A. Megarbane et al., Two sibs with myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders, AM J MED G, 87(4), 1999, pp. 289-293
Authors:
Megarbane, A
Choueiri, R
Bleik, J
Mezzina, M
Caillaud, C
Citation: A. Megarbane et al., Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?, J MED GENET, 36(8), 1999, pp. 637-640
Risultati:
1-10
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