F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II.

Por Scaioli, V, Pareyson, D, Avanzini, G, Sghirlanzoni, A
Publicado em 1992

Acute treatment of myasthenia gravis with intranasal neostigmine: clinical and electromyographic evaluation.

Por Ricciardi, R, Rossi, B, Nicora, M, Sghirlanzoni, A, Muratorio, A
Publicado em 1991

Specific involvement of peripheral T lymphocytes against acetylcholine receptors in myasthenia gravis.

Por Conti-Tronconi, B M, Scotti, A, Sghirlanzoni, A, Clementi, F
Publicado em 1983

Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families.

Por Bellone, E, Mandich, P, Mancardi, G L, Schenone, A, Uccelli, A, Abbruzzese, M, Sghirlanzoni, A, Pareyson, D, Ajmar, F
Publicado em 1992

A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies.

Por Lorenzetti, D, Pareyson, D, Sghirlanzoni, A, Roa, B B, Abbas, N E, Pandolfo, M, Di Donato, S, Lupski, J R
Publicado em 1995