Silvia Ferranti (S Ferranti)

Publication Activity (10 Years)

Years Active: 2018-2020
Publications (10 Years): 7

Top Topics

Cerebrospinal Fluid

Helicobacter Pylori

Congenital Heart Disease

Top Venues

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Clinical genetics

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

Publications

Gianni Coriolani, Silvia Ferranti, Giulia Squarci, Salvatore Grosso
A case of Bickerstaff encephalitis associated with Mycoplasma pneumoniae infection. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 41 (6) (2020)
Maria Rosaria Curcio, Silvia Ferranti, Federica Lotti, Salvatore Grosso
Coffin-Siris syndrome and epilepsy. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 42 (2) (2020)
Silvia Ferranti, Caterina Lo Rizzo, Alessandra Renieri, Paolo Galluzzi, Salvatore Grosso
Focus on progressive myoclonic epilepsy in Berardinelli-Seip syndrome. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 41 (11) (2020)
Chiara Romano, Silvia Ferranti, Maria Antonietta Mencarelli, Ilaria Longo, Alessandra Renieri, Salvatore Grosso
17p13.3 microdeletion including YWHAE and CRK genes: towards a clinical characterization. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 41 (8) (2020)
Gianni Coriolani, Silvia Ferranti, Filippo Biasci, Federica Lotti, Salvatore Grosso
Acute flaccid myelitis temporally associated with rhinovirus infection: just a coincidence? Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 41 (2) (2019)
Valentina Pelliccia, Silvia Ferranti, Rosa Mostardini, Salvatore Grosso
A case of Friedreich ataxia in an adolescent with 16p11.2 microdeletion syndrome. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 41 (3) (2019)
G Capecchi, M Baldassarri, Silvia Ferranti, E Guidoni, M Cioni, P Nürnberg, M A Mencarelli, Alessandra Renieri, S Grosso
CKAP2L mutation confirms the diagnosis of Filippi syndrome. Clinical genetics 93 (5) (2018)