Valerio Conti

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 4

Top Topics

Subarachnoid Hemorrhage

Newly Diagnosed

Mitochondrial Dna

Top Venues

Journal of personalized medicine

Nature reviews. Neurology

European journal of human genetics : EJHG

Neurology. Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Anna Maria Costa, Tommaso Lo Barco, Elisabetta Spezia, Valerio Conti, Laura Roli, Lorenza Marini, Sara Minghetti, Elisa Caramaschi, Laura Pietrangelo, Luca Pecoraro, Fabio D'Achille, Paola Accorsi, Tommaso Trenti, Federico Melani, Carla Marini, Renzo Guerrini, Francesca Darra, Patrizia Bergonzini, Giuseppe Biagini
Prospective Evaluation of Ghrelin and Des-Acyl Ghrelin Plasma Levels in Children with Newly Diagnosed Epilepsy: Evidence for Reduced Ghrelin-to-Des-Acyl Ghrelin Ratio in Generalized Epilepsies. Journal of personalized medicine 12 (4) (2022)
Renske Oegema, Tahsin Stefan Barakat, Martina Wilke, Katrien Stouffs, Dina Amrom, Eleonora Aronica, Nadia Bahi-Buisson, Valerio Conti, Andrew E Fry, Tobias Geis, David Gomez Andres, Elena Parrini, Ivana Pogledic, Edith Said, Doriette Soler, Luis M Valor, Maha Saad Zaki, Ghayda M Mirzaa, William B Dobyns, Orly Reiner, Renzo Guerrini, Daniela T Pilz, Ute Hehr, Richard J Leventer, Anna C Jansen, Grazia M S Mancini, Nataliya Di Donato
International consensus recommendations on the diagnostic work-up for malformations of cortical development. Nature reviews. Neurology 16 (11) (2020)
Renzo Guerrini, Mara Cavallin, Tommaso Pippucci, Anna Rosati, Francesca Bisulli, Paola Dimartino, Carmen Barba, Rita Garbelli, Anna Maria Buccoliero, Laura Tassi, Valerio Conti
Is Focal Cortical Dysplasia/Epilepsy Caused by Somatic MTOR Mutations Always a Unilateral Disorder? Neurology. Genetics 7 (1) (2020)
Elena Cellini, Annalisa Vetro, Valerio Conti, Carla Marini, Viola Doccini, Claudia Clementella, Elena Parrini, Sabrina Rita Giglio, Matteo Della Monica, Marco Fichera, Sebastiano Antonino Musumeci, Renzo Guerrini
Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity. European journal of human genetics : EJHG 27 (6) (2019)