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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
Outcome Assessment (Health Care) Medicine & Life Sciences
Peripheral Nervous System Diseases Medicine & Life Sciences
Atrophic Muscular Disorders 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
Longitudinal Studies
Outcome Assessment (Health Care)
Multicenter Studies
Quality of Life
Pharmacology

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

Leukoencephalopathy With Predominant Infratentorial Involvement Caused by a Novel ABCD1 Mutation: Does the Spinocerebellar Variant of Adrenoleukodystrophy Exist?

Benzoni, C., Farina, L., Pensato, V., Marotta, G., Kuqo, A., Mauro, E., Pareyson, D. & Salsano, E., Nov 1 2019, In : The neurologist. 24, 6, p. 194-197 4 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Leukoencephalopathies
Mutation
Brain Stem
Phenotype