Brunetti Sara (Sara Brunetti)

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 4

Top Topics

Transcription Factor

Cerebrospinal Fluid

Intellectual Disability

Top Venues

Movement disorders clinical practice

Epileptic disorders : international epilepsy journal with videotape

American journal of medical genetics. Part A

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

Publications

Brunetti Sara, Cocco Isabella, Damioli Simona, Accorsi Patrizia, Tassi Laura, Giordano Lucio
Epileptic Nystagmus as clinical manifestation of self-limited focal epilepsy: rethinking etiology and prognostic value and literature review. Epileptic disorders : international epilepsy journal with videotape (2023)
Brunetti Sara, Serena Micheletti, Ilaria Palmieri, Enza Maria Valente, Elisa Fazzi
Benign Hereditary Chorea as a Manifestation of HPCA Mutation. Movement disorders clinical practice 10 (1) (2022)
Brunetti Sara, Serena Micheletti, Ilaria Palmieri, Enza Maria Valente, Elisa Fazzi
Benign Hereditary Chorea as a Manifestation of HPCA Mutation. Movement disorders clinical practice 10 (1) (2022)
Brunetti Sara, Laura Malerba, Lucio Giordano, Elena Parrini, Renzo Guerrini, Giovanni Palumbo, Cecilia Parazzini, Ilaria Bestetti, Patrizia Accorsi
Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 gene. American journal of medical genetics. Part A 185 (8) (2021)