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Features
Assistant
AI grounded in research
Search
Full-text citation search
Collections
Organize and monitor papers
All Features →
Integrations
MCP
Connect AI agents to Scite
API
Programmatic data access
Holdings
Full-text via your library
Zotero Plugin
Citation data in Zotero
Browser Extension
Citation badges anywhere
All Integrations →
Data
Rankings
Pricing
Log In
Start Free Trial
Alessia Perna
Sign up to set email alerts
93
Publications
604
Citation Statements Received
2,661
Citation Statements Given
How they've been cited
762
32
562
10
How they cite others
2,902
137
2,512
12
Affiliations
Università Cattolica del Sacro Cuore
,
Agostino Gemelli University Polyclinic
Publications
Order By: Most citations
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study
D’Amore
1
,
Tessa
2
,
Casali
3
et al.
2018
Front. Neurol.
Abstract
Show
90
6
64
4
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Cite
Cardiac Magnetic Resonance in HCM Phenocopies: From Diagnosis to Risk Stratification and Therapeutic Management
Licordari
1
,
Trimarchi
2
,
Teresi
3
et al.
2023
JCM
Abstract
Show
63
0
73
1
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Cite
Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional study
Rossi
1
,
Della Marca
2
,
Ricci
3
et al.
2019
Journal of the Neurological Sciences
44
3
42
0
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Cite
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients
Piano
1
,
Di Stasio
2
,
Primiano
3
et al.
2020
Front. Neurol.
Abstract
Show
30
1
36
1
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Cite
Abnormal Cortical Thickness Is Associated With Deficits in Social Cognition in Patients With Myotonic Dystrophy Type 1
Serra
1
,
Bianchi
2
,
Bruschini
3
et al.
2020
Front. Neurol.
Abstract
Show
30
1
27
0
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Cite
High Prevalence and Gender-Related Differences of Gastrointestinal Manifestations in a Cohort of DM1 Patients: A Perspective, Cross-Sectional Study
Perna
1
,
Maccora
2
,
Rossi
3
et al.
2020
Front. Neurol.
Abstract
Show
31
0
25
0
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Cite
Hereditary spastic paraplegia: Novel mutations and expansion of the phenotype variability in SPG56
Masciullo
1
,
Tessa
2
,
Perazza
3
et al.
2016
European Journal of Paediatric Neurology
37
1
25
0
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Cite
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials
Garibaldi
1
,
Nicoletti
2
,
Bucci
3
et al.
2021
Euro J of Neurology
Abstract
Show
26
1
20
2
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Cite
1
2
3
4
5