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Research Output

2017

A novel NDRG1 mutation in a non-Romani patient with CMT4D/HMSN-Lom

Piscosquito, G., Magri, S., Saveri, P., Milani, M., Ciano, C., Farina, L., Taroni, F. & Pareyson, D., Mar 1 2017, In : Journal of the Peripheral Nervous System. 22, 1, p. 47-50 4 p.

Research output: Contribution to journalArticle

Paclitaxel-releasing mesenchymal stromal cells inhibit in vitro proliferation of human mesothelioma cells

Petrella, F., Coccè, V., Masia, C., Milani, M., Salè, E. O., Alessandri, G., Parati, E., Sisto, F., Pentimalli, F., Brini, A. T., Pessina, A. & Spaggiari, L., 2017, In : Biomedicine and Pharmacotherapy. 87, p. 755-758 4 p.

Research output: Contribution to journalArticle

2015
2014

Clinical, electrophysiological and pathological findings in a patient with Charcot-Marie-Tooth disease 4D caused by the NDRG1 Lom mutation

Luigetti, M., Taroni, F., Milani, M., Del Grande, A., Romano, A., Bisogni, G., Conte, A., Contaldo, I., Mercuri, E. & Sabatelli, M., Oct 15 2014, In : Journal of the Neurological Sciences. 345, 1, p. 271-273 3 p.

Research output: Contribution to journalArticle

Double-trouble in pediatric neurology: Myotonia congenita combined with charcot-marie-tooth disease type 1a

Ardissone, A., Brugnoni, R., Gandioli, C., Milani, M., Ciano, C., Uziel, G. & Moroni, I., 2014, In : Muscle and Nerve. 50, 1, p. 145-147 3 p.

Research output: Contribution to journalArticle

2012

Myelin protein zero Arg36Gly mutation with very late onset and rapidly progressive painful neuropathy

Dacci, P., Taroni, F., Bella, E. D., Milani, M., Pareyson, D., Morbin, M. & Lauria, G., Dec 2012, In : Journal of the Peripheral Nervous System. 17, 4, p. 422-425 4 p.

Research output: Contribution to journalArticle

2011

Co-occurrence of amyotrophic lateral sclerosis and Charcot-Marie-Tooth disease type 2A in a patient with a novel mutation in the mitofusin-2 gene

Marchesi, C., Ciano, C., Salsano, E., Nanetti, L., Milani, M., Gellera, C., Taroni, F., Fabrizi, G. M., Uncini, A. & Pareyson, D., Feb 2011, In : Neuromuscular Disorders. 21, 2, p. 129-131 3 p.

Research output: Contribution to journalArticle

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

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., Jul 12 2011, In : Neurology. 77, 2, p. 168-173 6 p.

Research output: Contribution to journalArticle

2010

Four novel cases of periaxin-related neuropathy and review of the literature

Marchesi, C., Milani, M., Morbin, M., Cesani, M., Lauria, G., Scaioli, V., Piccolo, G., Fabrizi, G. M., Cavallaro, T., Taroni, F. & Pareyson, D., Nov 16 2010, In : Neurology. 75, 20, p. 1830-1838 9 p.

Research output: Contribution to journalArticle

2009

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

Muglia, M., Vazza, G., Patitucci, A., Milani, M., Pareyson, D., Taroni, F., Quattrone, A. & Mostacciuolo, M. L., Jan 23 2009, In : BMJ Case Reports.

Research output: Contribution to journalArticle

Novel mutations in the GDAP1 gene in patients affected with early-onset axonal Charcot-Marie-Tooth type 4A

Moroni, I., Morbin, M., Milani, M., Ciano, C., Bugiani, M., Pagliano, E., Cavallaro, T., Pareyson, D. & Taroni, F., Jul 2009, In : Neuromuscular Disorders. 19, 7, p. 476-480 5 p.

Research output: Contribution to journalArticle

2007

A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy [5]

Muglia, M., Vazza, G., Patitucci, A., Milani, M., Pareyson, D., Taroni, F., Quattrone, A. & Mostacciuolo, M. L., Nov 2007, In : Journal of Neurology, Neurosurgery and Psychiatry. 78, 11, p. 1286-1287 2 p.

Research output: Contribution to journalArticle

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., May 27 2003, In : Neurology. 60, 10, p. 1721-1722 2 p.

Research output: Contribution to journalArticle

2001

Charcot-marie-tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families

Mostacciuolo, M. L., Righetti, E., Zortea, M., Bosello, V., Schiavon, F., Vallo, L., Merlini, L., Siciliano, G., Fabrizi, G. M., Rizzuto, N., Milani, M., Baratta, S. & Taroni, F., 2001, In : Human Mutation. 18, 1, p. 32-41 10 p.

Research output: Contribution to journalArticle