Silvia Romano | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Reworking GWAS data to understand the role of nongenetic factors in MS etiopathogenesis	GENES	2020
Listening to the neurological teams for multiple sclerosis. the SMART project	NEUROLOGICAL SCIENCES	2020
Frataxin deficiency in Friedreich's ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survival	HUMAN MOLECULAR GENETICS ONLINE	2020
Functional changes of mentalizing network in SCA2 patients: novel insights into understanding the social cerebellum	CEREBELLUM	2020
Considering patient clinical history impacts performance of machine learning models in predicting course of multiple sclerosis	PLOS ONE	2020
Association between toll-like receptor 4 (TLR4) and triggering receptor expressed on myeloid cells 2 (TREM2) genetic variants and clinical progression of Huntington's disease	MOVEMENT DISORDERS	2020
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders	JOURNAL OF MEDICAL GENETICS	2020
Detection of disability worsening in relapsing-remitting multiple sclerosis patients: a real-world roving Expanded Disability Status Scale reference analysis from the Italian Multiple Sclerosis Register	EUROPEAN JOURNAL OF NEUROLOGY	2020
DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease	ANNALS OF NEUROLOGY	2019
Genome-Wide Multiple Sclerosis Association Data and Coagulation	FRONTIERS IN NEUROLOGY	2019
Drug holiday of interferon beta 1b in multiple sclerosis: A Pilot, Randomized, Single Blind Study of Non-inferiority	FRONTIERS IN NEUROLOGY	2019
The contribution of gut barrier changes to multiple sclerosis pathophysiology	FRONTIERS IN IMMUNOLOGY	2019
Exit strategies for "needle fatigue" in multiple sclerosis: a propensity score-matched comparison study	JOURNAL OF NEUROLOGY	2019
La neurologia della Sapienza		2019
Intestinal Permeabiliy in Relapsing-Remitting Multiple Sclerosis	NEUROTHERAPEUTICS	2018
Structural cerebellar correlates of cognitive functions in spinocerebellar Ataxia type 2	JOURNAL OF NEUROLOGY	2018
Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegia	CLINICAL NEUROLOGY AND NEUROSURGERY	2018
Perinatal insults and neurodevelopmental disorders may impact Huntington's disease age of diagnosis	PARKINSONISM & RELATED DISORDERS	2018
Suicidal ideation and suicidal behavior according to the C-SSRS in a European cohort of Huntington's disease gene expansion carriers	JOURNAL OF AFFECTIVE DISORDERS	2018
Does arterial hypertension influence the onset of Huntington’s disease?	PLOS ONE	2018

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