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Davide Pareyson

Department of Neurology

Istituto Nazionale Neurologico "C.Besta

" Via Celoria 11

20133 Milan

Italy

[email]@tin.it

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Neurology, Istituto Nazionale Neurologico "C.Besta, " Via Celoria 11, 20133 Milan, Italy. 1999 - 2003
  • Division of Neurology, Carlo Besta National Neurological Institute, Milan, Italy. 2003
  • Istituto Nazionale Neurologico C. Besta, Milan, Italy. 1999

References

  1. Diagnosis of hereditary neuropathies in adult patients. Pareyson, D. J. Neurol. (2003) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
  4. Charcot-marie-tooth disease and related neuropathies: molecular basis for distinction and diagnosis. Pareyson, D. Muscle. Nerve (1999) [Pubmed]
  5. 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) [Pubmed]
 
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