• 815 Citations
  • 13 h-Index
20052019
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Fingerprint Dive into the research topics where Maria Margherita Mancardi is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 40 Similar Profiles
Epilepsy Medicine & Life Sciences
Brain Diseases Medicine & Life Sciences
Seizures Medicine & Life Sciences
Myoclonic Epilepsy Medicine & Life Sciences
Electroencephalography Medicine & Life Sciences
Mutation Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences
Partial Epilepsy Medicine & Life Sciences

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Research Output 2005 2019

  • 815 Citations
  • 13 h-Index
  • 76 Article
  • 1 Comment/debate

Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2

De Mori, R., Severino, M., Mancardi, M. M., Anello, D., Tardivo, S., Biagini, T., Capra, V., Casella, A., Cereda, C., Copeland, B. R., Gagliardi, S., Gamucci, A., Ginevrino, M., Illi, B., Lorefice, E., Musaev, D., Stanley, V., Micalizzi, A., Gleeson, J. G., Mazza, T. & 2 others, Rossi, A. & Valente, E. M., Aug 14 2019, In : Brain : a journal of neurology.

Research output: Contribution to journalArticle

Globus Pallidus
Homeobox Genes
Putamen
Basal Ganglia
Mutation

Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2

De Mori, R., Severino, M., Mancardi, M. M., Anello, D., Tardivo, S., Biagini, T., Capra, V., Casella, A., Cereda, C., Copeland, B. R., Gagliardi, S., Gamucci, A., Ginevrino, M., Illi, B., Lorefice, E., Musaev, D., Stanley, V., Micalizzi, A., Gleeson, J. G., Mazza, T. & 2 others, Rossi, A. & Valente, E. M., 2019, In : Brain : a journal of neurology. 142, 10, p. 2965-2978 14 p.

Research output: Contribution to journalArticle

Encephalitis
Aspartic Acid
Autoimmune Diseases of the Nervous System
Pediatrics
Immunotherapy

EA-DIVA score (Enhanced Adult DIVA score): A new scale to predict difficult preoperative venous cannulation in adult surgical patients

Civetta, G., Cortesi, S., Mancardi, M., De Pirro, A., Vischio, M., Mazzocchi, M., Scudeller, L., Bottazzi, A., Iotti, G. A. & Palo, A., 2019, In : Journal of Vascular Access. 20, 3, p. 281-289 9 p.

Research output: Contribution to journalArticle

Catheterization
Validation Studies
Risk Management
ROC Curve
Area Under Curve

Epileptic Encephalopathy, Myoclonus-Dystonia, and Premature Pubarche in Siblings with a Novel C-Terminal Truncating Mutation in ATRX Gene

Giacomini, T., Vari, M. S., Janis, S., Prato, G., Pisciotta, L., Rocchi, A., Michelucci, A., Di Rocco, M., Gandullia, P., Mattioli, G., Sacco, O., Morana, G. & Mancardi, M. M., Oct 1 2019, In : Neuropediatrics. 50, 5, p. 327-331 5 p.

Research output: Contribution to journalArticle

Brain Diseases
Siblings
Mutation
Genes
Movement Disorders