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Results: 1-8 |
Results: 8

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: Wenger, DA Rafi, MA Luzi, P Datto, J Costantino-Ceccarini, E
Citation: Da. Wenger et al., Krabbe disease: Genetic aspects and progress toward therapy, MOL GEN MET, 70(1), 2000, pp. 1-9

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: Wenger, DA Victoria, T Rafi, MA Luzi, P Vanier, MT Vite, C Patterson, DF Haskins, MH
Citation: Da. Wenger et al., Globoid cell leukodystrophy in cairn and West Highland white terriers, J HEREDITY, 90(1), 1999, pp. 138-142

Authors: Jardim, LB Giugliani, R Pires, RF Haussen, S Burin, MG Rafi, MA Wenger, DA
Citation: Lb. Jardim et al., Protracted course of Krabbe disease in an adult patient bearing a novel mutation, ARCH NEUROL, 56(8), 1999, pp. 1014-1017

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
Risultati: 1-8 |