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Fingerprint Dive into the research topics where Davide Pareyson is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 23 Similar Profiles
Charcot-Marie-Tooth Disease Medicine & Life Sciences
Mutation Medicine & Life Sciences
Tooth Medicine & Life Sciences
Genes Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Peripheral Nervous System Diseases Medicine & Life Sciences
Atrophic Muscular Disorders Medicine & Life Sciences
Outcome Assessment (Health Care) Medicine & Life Sciences

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Research Output 1988 2019

A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs)

Pareyson, D., Stojkovic, T., Reilly, M. M., Leonard-Louis, S., Laurà, M., Blake, J., Parman, Y., Battaloglu, E., Tazir, M., Bellatache, M., Bonello-Palot, N., Lévy, N., Sacconi, S., Guimarães-Costa, R., Attarian, S., Latour, P., Solé, G., Megarbane, A., Horvath, R., Ricci, G. & 22 others, Choi, B. O., Schenone, A., Gemelli, C., Geroldi, A., Sabatelli, M., Luigetti, M., Santoro, L., Manganelli, F., Quattrone, A., Valentino, P., Murakami, T., Scherer, S. S., Dankwa, L., Shy, M. E., Bacon, C. J., Herrmann, D. N., Zambon, A., Tramacere, I., Pisciotta, C., Magri, S., Previtali, S. C. & Bolino, A., Jul 1 2019, In : Annals of Neurology. 86, 1, p. 55-67 13 p.

Research output: Contribution to journalArticle

Multicenter Studies
Retrospective Studies
Mutation
Proteins
Neural Conduction

Are novel outcome measures for Charcot–Marie–Tooth disease sensitive to change? The 6-minute walk test and StepWatch™ Activity Monitor in a 12-month longitudinal study

Pazzaglia, C., Padua, L., Pareyson, D., Schenone, A., Aiello, A., Fabrizi, G. M., Cavallaro, T., Santoro, L., Manganelli, F., Coraci, D., Gemignani, F., Vitetta, F., Quattrone, A., Mazzeo, A., Russo, M., Vita, G. & Group, F. T. CMT-TRIAAL., 2019, In : Neuromuscular Disorders.

Research output: Contribution to journalArticle

Expanding the spectrum of genes responsible for hereditary motor neuropathies

Previtali, S. C., Zhao, E., Lazarevic, D., Pipitone, G. B., Fabrizi, G. M., Manganelli, F., Mazzeo, A., Pareyson, D., Schenone, A., Taroni, F., Vita, G., Bellone, E., Ferrarini, M., Garibaldi, M., Magri, S., Padua, L., Pennisi, E., Pisciotta, C., Riva, N., Scaioli, V. & 11 others, Scarlato, M., Tozza, S., Geroldi, A., Jordanova, A., Ferrari, M., Molineris, I., Reilly, M. M., Comi, G., Carrera, P., Devoto, M. & Bolino, A., Jan 1 2019, In : Journal of Neurology, Neurosurgery and Psychiatry.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Genes
Exome
Phenotype
Neuromuscular Diseases

Instrumented balance and gait assessment in patients with charcot-marie-tooth peripheral neuropathy

Picardi, M., Caronni, A., Tropea, P., Montesano, M., Pisciotta, C., Pareyson, D. & Corbo, M., Jan 1 2019, Biosystems and Biorobotics. Springer International Publishing, p. 410-414 5 p. (Biosystems and Biorobotics; vol. 21).

Research output: Chapter in Book/Report/Conference proceedingChapter

Patient rehabilitation
Sensors

Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotype

Callegari, I., Gemelli, C., Geroldi, A., Veneri, F., Mandich, P., D’Antonio, M., Pareyson, D., Shy, M. E., Schenone, A., Prada, V. & Grandis, M., Jan 1 2019, In : Journal of Neurology.

Research output: Contribution to journalArticle

Myelin P0 Protein
Neural Conduction
Phenotype
Mutation
Genes