Veggiotti Pierangelo

Full professor
SSD
MED/39 - CHILD NEUROPSYCHIATRY
Competition sector
06/G1 - PAEDIATRICS AND CHILD NEUROPSYCHIATRY

Contacts

Workplace

Via Castelvetro, 32 - Ospedale dei Bambini Vittore Buzzi - Pad. A
20154 MILANO (MI)

University email address
Teaching - Programme courses

Postgraduate programmes

A.Y. 2019/2020
Postgraduate Schools - Medicine, Healthcare, Dental Medicine
A.Y. 2018/2019
Postgraduate Schools - Medicine, Healthcare, Dental Medicine
Research

Publications

Publications
  • Italian cohort of Lafora disease : clinical features, disease evolution, and genotype-phenotype correlations / A. Riva, A. Orsini, M. Scala, V. Taramasso, L. Canafoglia, G. d'Orsi, M.T. Di Claudio, C. Avolio, A. D'Aniello, M. Elia, S. Franceschetti, G. Di Gennaro, F. Bisulli, P. Tinuper, M. Tappatà, A. Romeo, E. Freri, C. Marini, C. Costa, V. Sofia, E. Ferlazzo, A. Magaudda, P. Veggiotti, E. Gennaro, A. Pistorio, C. Minetti, A. Bianchi, S. Striano, R. Michelucci, F. Zara, B.A. Minassian, P. Striano. - In: JOURNAL OF THE NEUROLOGICAL SCIENCES. - ISSN 0022-510X. - 424(2021 May 15), pp. 117409.1-117409.7.
  • CDKL5 deficiency disorder in males : Five new variants and review of the literature / B. Siri, C. Varesio, E. Freri, F. Darra, S. Gana, D. Mei, F. Porta, E. Fontana, G. Galati, R. Solazzi, M. Niceta, P. Veggiotti, E. Alfei. - In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. - ISSN 1532-2130. - 33(2021 Apr 30), pp. 9-20.
  • Case Report: Novel Compound Heterozygous RNASEH2B Mutations Cause Aicardi–Goutières Syndrome / J. Garau, S. Masnada, F. Dragoni, D. Sproviero, F. Fogolari, S. Gagliardi, G. Izzo, C. Varesio, S. Orcesi, P. Veggiotti, G.V. Zuccotti, O. Pansarasa, D. Tonduti, C. Cereda. - In: FRONTIERS IN IMMUNOLOGY. - ISSN 1664-3224. - 12(2021 Apr 26). [Epub ahead of print]
  • PRKRA-Related Disorders: Bilateral Striatal Degeneration in Addition to DYT16 Spectrum / S. Masnada, D. Martinelli, M. Correa-Vela, E. Agolini, H. Baide-Mairena, A. Marcé-Grau, C. Parazzini, P. Veggiotti, B. Perez-Duenas, D. Tonduti. - In: MOVEMENT DISORDERS. - ISSN 0885-3185. - (2021). [Epub ahead of print]
  • Spinal cord involvement and paroxysmal events in “Infantile Onset Transient Hypomyelination” due to TMEM63A mutation / D. Tonduti, E. Mura, S. Masnada, E. Bertini, C. Aiello, D. Zini, L. Parmeggiani, G. Cantalupo, G. Talenti, P. Veggiotti, L. Spaccini, M. Iascone, C. Parazzini. - In: JOURNAL OF HUMAN GENETICS. - ISSN 1434-5161. - (2021). [Epub ahead of print]