Silvia Romano | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Treatment modifiers across different regimens of natalizumab treatment in MS: An Italian real-world experience	NEUROTHERAPEUTICS	2024
Disentangling multiple sclerosis phenotypes through Mendelian disorders: A network approach	MULTIPLE SCLEROSIS	2024
Multiple Sclerosis Progression and Relapse Activity in Children	JAMA NEUROLOGY	2024
Co-existence of Myelin Oligodendrocyte Glycoprotien Antibody-associated Disease (MOGAD) and Spinocerebellar Ataxia type 1 (SCA1): A case report	NEUROLOGICAL SCIENCES	2024
Case report: A novel mutation of glial fibrillary acidic protein gene causing juvenile-onset Alexander disease	FRONTIERS IN NEUROLOGY	2024
Disease-modifying therapies in managing disability worsening in paediatric-onset multiple sclerosis: a longitudinal analysis of global and national registries	THE LANCET CHILD & ADOLESCENT HEALTH	2024
A comparison of natalizumab and ocrelizumab on disease progression in multiple sclerosis	ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY	2024
Long-Term Follow-Up before and during Riluzole Treatment in Six Patients from Two Families with Spinocerebellar Ataxia Type 7	THE CEREBELLUM	2024
Disability trajectories by progression independent of relapse activity status differ in pediatric, adult and late-onset multiple sclerosis	JOURNAL OF NEUROLOGY	2024
[Registers as central real world data source: the experience of the Italian Multiple Sclerosis and Related Disorders Register]	EPIDEMIOLOGIA E PREVENZIONE	2024
Sex contribution to average age at onset of Huntington's disease depends on the number of (CAG)n repeats	SCIENTIFIC REPORTS	2024
Peripheral Biomarkers in Manifest and Premanifest Huntington’s Disease	INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES	2023
Relapse-associated worsening in a real-life multiple sclerosis cohort: The role of age and pyramidal phenotype	EUROPEAN JOURNAL OF NEUROLOGY	2023
Hematopoietic Stem Cell Transplantation in People With Active Secondary Progressive Multiple Sclerosis	NEUROLOGY	2023
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias	AMERICAN JOURNAL OF HUMAN GENETICS	2023
Multimodal Ophthalmic Imaging in Spinocerebellar Ataxia Type 7	LIFE	2023
Evaluation of drivers of treatment switch in relapsing multiple sclerosis: a study from the Italian MS Registry	JOURNAL OF NEUROLOGY	2023
Tominersen in Adults with Manifest Huntington's Disease	THE NEW ENGLAND JOURNAL OF MEDICINE	2023
Data monitoring roadmap. The experience of the Italian Multiple Sclerosis and Related Disorders Register	NEUROLOGICAL SCIENCES	2023
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network	NEUROLOGY. GENETICS	2022

ERC

LS5_11

Interessi di ricerca

Diagnosi, terapia e classificazione fenotipica delle atassie cerebellari ereditarie
Diagnosi, terapia e classificazione fenotipica idelle paraparesi spastiche ereditarie
Diagnosi, terapia e classificazione fenotipica idelle malattie monogeniche dei piccoli vasi (CADASIL, CARASIL)
Ricerca di biomarcatori circolanti nella Malattia di Huntington