Authors:
Luzi, P
Rafi, MA
Zaka, M
Curtis, M
Vanier, MT
Wenger, DA
Citation: P. Luzi et al., Generation of a mouse with low galactocerebrosidase activity by gene targeting: A new model of globoid cell leukodystrophy (Krabbe disease), MOL GEN MET, 73(3), 2001, pp. 211-223
Authors:
Luddi, A
Volterrani, M
Strazza, M
Smorlesi, A
Rafi, MA
Datto, J
Wenger, DA
Costantino-Ceccarini, E
Citation: A. Luddi et al., Retrovirus-mediated gene transfer and galactocerebrosidase uptake into twitcher glial cells results in appropriate localization and phenotype correction, NEUROBIOL D, 8(4), 2001, pp. 600-610
Authors:
De Stefano, N
Dotti, MT
Mortilla, M
Pappagallo, E
Luzi, P
Rafi, MA
Formichi, P
Inzitari, D
Wenger, DA
Federico, A
Citation: N. De Stefano et al., Evidence of diffuse brain pathology and unspecific genetic characterization in a patient with an atypical form of adult-onset Krabbe disease, J NEUROL, 247(3), 2000, pp. 226-228
Authors:
Costantino-Ceccarini, E
Luddi, A
Volterrani, M
Strazza, M
Rafi, MA
Wenger, DA
Citation: E. Costantino-ceccarini et al., Transduction of cultured oligodendrocytes from normal and twitcher mice bya retroviral vector containing human galactocerebrosidase (GALC) cDNA, NEUROCHEM R, 24(2), 1999, pp. 287-293
Authors:
Millat, G
Marcais, C
Rafi, MA
Yamamoto, T
Morris, JA
Pentchev, PG
Ohno, K
Wenger, DA
Vanier, MT
Citation: G. Millat et al., Niemann-Pick C1 disease: The I1061T substitutions a frequent mutant allelein patients of Western European descent and correlates with a classic juvenile phenotype, AM J HU GEN, 65(5), 1999, pp. 1321-1329