Davide Pareyson
Department of Neurology
Istituto Nazionale Neurologico "C.Besta
" Via Celoria 11
20133 Milan
Italy
Name/email consistency: high
- Diagnosis of hereditary neuropathies in adult patients. Pareyson, D. J. Neurol. (2003)
- Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins?. Pareyson, D., Testa, D., Morbin, M., Erbetta, A., Ciano, C., Lauria, G., Milani, M., Taroni, F. Neurology (2003)
- Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation. Pareyson, D., Taroni, F., Botti, S., Morbin, M., Baratta, S., Lauria, G., Ciano, C., Sghirlanzoni, A. Neurology (2000)
- Charcot-marie-tooth disease and related neuropathies: molecular basis for distinction and diagnosis. Pareyson, D. Muscle. Nerve (1999)
- Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease. Pareyson, D., Menichella, D., Botti, S., Sghirlanzoni, A., Fallica, E., Mora, M., Ciano, C., Shy, M.E., Taroni, F. Ann. N. Y. Acad. Sci. (1999)









