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Gabriella Silvestri

Ricercatore Universitario

Università Cattolica del Sacro Cuore Facoltà di Medicina e Chirurgia

Italy

Research Interests

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Professors in Italy

Articles (18)

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2024

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Collaborators (15)

Ludger Schöls

Section head

Eberhard Karls Universität Tübingen

GERMANY

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Vincent Huin

Associate Professor

Université de Lille

FRANCE

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Franco Taroni

Head

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Angelo Minucci

University of Padova

ITALY

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Alessandra Rufa

Docenti di ruolo di IIa fascia

University of Siena

ITALY

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Daniela Di Bella

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Elena Rossini

Sapienza University of Rome

ITALY

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Pietro Chiurazzi

Università Cattolica del Sacro Cuore

ITALY

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Anna ladogana

Head of research

Istituto Superiore di Sanità

ITALY

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MARIA TERESA PELLECCHIA

Associate Professor of Neurology

University of Salerno

ITALY

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Mauro Monforte

Agostino Gemelli University Polyclinic

ITALY

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Fiorella Piemonte

Head of Enzymology and Biochemistry Section

ITALY

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Giovanni Pennisi

Catholic University of the Sacred Heart

ITALY

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Maria Laura Manca

Dirigente Ep in convenzione con Azienda Ospedaliero-universitaria Pisana

University of Pisa

ITALY

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Luis Pereira de Almeida

Associate Professor

University of Coimbra

PORTUGAL

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Gabriella Silvestri

Research Interests

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Articles (18)

Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease

Correction to: Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia—experience from an Italian cohort (Journal of Neurology, (2024), 271, 8, (5478-5488), 10.1007/s00415-024-12506-x)

Creutzfeldt-Jakob disease in a man surviving COVID-19: disentangling a casual or causal association by neuropathology

Differential Gene Expression in Late-Onset Friedreich Ataxia: A Comparative Transcriptomic Analysis Between Symptomatic and Asymptomatic Sisters

Hospital admissions from the emergency department of adult patients affected by myopathies

Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia—experience from an Italian cohort

Role of Circulating X-Chromosome Inactivation and <i>Xist</i> as Biomarkers in Female Carriers of Fabry Disease

Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene

Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literature

Isolated pontocerebellar leukoencephalopathy in HIV-related PML: focus on the “shrimp sign”

Consensus Recommendations for Clinical Outcome Assessments and Registry Development in Ataxias: Ataxia Global Initiative (AGI) Working Group Expert Guidance

Triple Genetic Diagnosis in a Patient with Late-Onset Leukodystrophy and Mild Intellectual Disability

Clinical Reasoning: A Young Man with Subacute Onset of Spastic Paraparesis

Fluid Biomarkers of Central Nervous System (CNS) Involvement in Myotonic Dystrophy Type 1 (DM1)

Myotonic Dystrophies

Neurological Erdheim–Chester Disease Manifesting with Subacute or Progressive Cerebellar Ataxia: Novel Case Series and Review of the Literature

Power of NGS-based tests in HSP diagnosis: analysis of massively parallel sequencing in clinical practice

Unusual case of long survival patient with leptomeningeal carcinomatosis from breast cancer

Collaborators (15)

Ludger Schöls

Vincent Huin

Franco Taroni

Angelo Minucci

Alessandra Rufa

Daniela Di Bella

Elena Rossini

Pietro Chiurazzi

Anna ladogana

MARIA TERESA PELLECCHIA

Mauro Monforte

Fiorella Piemonte

Giovanni Pennisi

Maria Laura Manca

Luis Pereira de Almeida

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