Publications by authors named "Giulia Straccia"

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Dominant VPS16 Pathogenic Variants: Not Only Isolated Dystonia.
Edoardo Monfrini, Laura Avanzino, Giovanni Palermo, Giulia Bonato, Gloria Brescia, Giulia Straccia

Mov Disord Clin Pract· January 2024

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Unraveling Autonomic Dysfunction in GBA-Related Parkinson's Disease.
Grazia Devigili, Giulia Straccia, Emanuele Cereda, Barbara Garavaglia, Alessandro Fedeli

Mov Disord Clin Pract· November 2023

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Magnetic Resonance-Guided Focused Ultrasound Thalamotomy May Spare Dopaminergic Therapy in Early-Stage Tremor-Dominant Parkinson's Disease: A Pilot Study.
Nico Golfrè Andreasi, Roberto Cilia, Luigi Michele Romito, Salvatore Bonvegna, Giulia Straccia

Mov Disord· November 2022

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ACTB gene mutation in combined Dystonia-Deafness syndrome with parkinsonism: Expanding the phenotype and highlighting the long-term GPi DBS outcome.
Giulia Straccia, Chiara Reale, Massimo Castellani, Isabel Colangelo, Eva Orunesu

Parkinsonism Relat Disord· November 2022

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Precision Medicine in Parkinson's Disease: From Genetic Risk Signals to Personalized Therapy.
Giulia Straccia, Fabiana Colucci, Roberto Eleopra, Roberto Cilia

Brain Sci· September 2022

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Cerebrospinal fluid neuropathological biomarkers in beta-propeller protein-associated neurodegeneration, with complicated parkinsonian phenotype.
Roberta Bonomo, Antonio E Elia, Roberto Cilia, Luigi M Romito, Nico Golfrè Andreasi, Giulia Straccia

Parkinsonism Relat Disord· May 2022

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AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonism.
Barbara Garavaglia, Sadeq Vallian, Luigi M Romito, Giulia Straccia, Marianna Capecci

Parkinsonism Relat Disord· April 2022

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Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network.
Salvatore Rossi, Anna Rubegni, Vittorio Riso, Melissa Barghigiani, Maria Teresa Bassi, Giulia Straccia

Neurol Genet· April 2022

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Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement.
Alessandro Vaisfeld, Giorgia Bruno, Martina Petracca, Anna Rita Bentivoglio, Serenella Servidei, Giulia Straccia

Genes (Basel)· February 2021

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Telemedicine in Parkinson's Disease: How to Ensure Patient Needs and Continuity of Care at the Time of COVID-19 Pandemic.
Giuseppina Miele, Giulia Straccia, Marcello Moccia, Letizia Leocani, Gioacchino Tedeschi

Telemed J E Health· December 2020

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Parkinsonism and Nigrostriatal Damage Secondary to CSF1R-Related Primary Microgliopathy.
Salvatore Bonvegna, Giulia Straccia, Nico Golfrè Andreasi, Antonio Emanuele Elia, Gianluca Marucci

Mov Disord· December 2020

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Effects of COVID-19 on Parkinson's Disease Clinical Features: A Community-Based Case-Control Study.
Roberto Cilia, Salvatore Bonvegna, Giulia Straccia, Nico Golfrè Andreasi, Antonio E Elia

Mov Disord· August 2020

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Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders.
Teresa Giugliano, Claudia Santoro, Annalaura Torella, Francesca Del Vecchio Blanco, Anna Grandone, Giulia Straccia

Genes (Basel)· July 2019

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A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient.
Mariano Oliva, Guglielmo Capaldo, Alessandra D'Amico, Davide Colavito, Andrea Elefante, Giulia Straccia

Neurol Sci· June 2019

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