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

Propriospinal myoclonus with life threatening tonic spasms as paraneoplastic presentation of breast cancer

Por Salsano, E, Ciano, C, Romano, S, Cornelio, F, Di Donato, S, Pareyson, D
Publicado em 2006

Vitamin C and Charcot–Marie–Tooth 1A: Pharmacokinetic considerations

Por Visioli, F., Reilly, M.M., Rimoldi, M., Solari, A., Pareyson, D.
Publicado em 2013

A novel founder mutation in the MFN2 gene associated with variable Charcot–Marie–Tooth type 2 phenotype in two families from Southern Italy

Por Muglia, M, Vazza, G, Patitucci, A, Milani, M, Pareyson, D, Taroni, F, Quattrone, A, Mostacciuolo, M L
Publicado em 2007

Postural stabilization and balance assessment in Charcot–Marie–Tooth 1A subjects

Por Lencioni, T., Rabuffetti, M., Piscosquito, G., Pareyson, D., Aiello, A., Di Sipio, E., Padua, L., Stra, F., Ferrarin, M.
Publicado em 2014

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

Reliability of instrumented movement analysis as outcome measure in Charcot–Marie–Tooth disease: Results from a multitask locomotor protocol

Por Ferrarin, M., Bovi, G., Rabuffetti, M., Mazzoleni, P., Montesano, A., Moroni, I., Pagliano, E., Marchi, A., Marchesi, C., Beghi, E., Pareyson, D.
Publicado em 2011

Gait pattern classification in children with Charcot–Marie–Tooth disease type 1A

Por Ferrarin, M., Bovi, G., Rabuffetti, M., Mazzoleni, P., Montesano, A., Pagliano, E., Marchi, A., Magro, A., Marchesi, C., Pareyson, D., Moroni, I.
Publicado em 2011

NERVE CONDUCTION VELOCITY IN CMT1A: WHAT ELSE CAN WE TELL

Por Manganelli, F, Pisciotta, C, Reilly, MM, Tozza, S, Schenone, A, Fabrizi, GM, Cavallaro, T, Vita, G, Padua, L, Gemignani, F, Laura, M, Hughes, RAC, Solari, A, Pareyson, D, Santoro, L
Publicado no Eur J Neurol (2016)

Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations

Por Polke, J.M., Laurá, M., Pareyson, D., Taroni, F., Milani, M., Bergamin, G., Gibbons, V.S., Houlden, H., Chamley, S.C., Blake, J., DeVile, C., Sandford, R., Sweeney, M.G., Davis, M.B., Reilly, M.M.
Publicado em 2011

Phenotypic variability of childhood Charcot-Marie-Tooth disease

Por Cornett, KMD, Menezes, MP, Bray, P, Halaki, M, Shy, R, Yum, SW, Estilow, T, Moroni, I, Foscan, M, Pagliano, E, Pareyson, D, Laura, M, Bandhari, T, Muntoni, F, Reilly, MM, Finkel, RS, Sowden, J, Eichinger, K, Herrmann, DN, Shy, ME, Burns, J
Publicado no JAMA Neurol (2016)

CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis

Por Fridman, V, Bundy, B, Reilly, M M, Pareyson, D, Bacon, C, Burns, J, Day, J, Feely, S, Finkel, R S, Grider, T, Kirk, C A, Herrmann, D N, Laurá, M, Li, J, Lloyd, T, Sumner, C J, Muntoni, F, Piscosquito, G, Ramchandren, S, Shy, R, Siskind, C E, Yum, S W, Moroni, I, Pagliano, E, Zuchner, S, Scherer, S S, Shy, M E
Publicado no J Neurol Neurosurg Psychiatry (2015)