Andrea Mignarri

Siena, Italy

Last Updated: 09/26/2026

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Found 68 publications

TMS-EEG Reveals Distinct Cortical Signatures in Non-Fluent PPA.

TMS-EEG Reveals Distinct Cortical Signatures in Non-Fluent PPA.

Journal: medRxiv : the preprint server for health sciences

Published: December 25, 2025

Miglustat in Alzheimer's Disease Associated With Heterozygous NPC1 Mutation: Exploratory Case Series and Preliminary Findings.

Miglustat in Alzheimer's Disease Associated With Heterozygous NPC1 Mutation: Exploratory Case Series and Preliminary Findings.

Journal: European journal of neurology

Published: July 07, 2025

Palatal tremor as the clue sign of POLG-related syndrome.

Palatal tremor as the clue sign of POLG-related syndrome.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: January 16, 2025

An atypical case of Creutzfeldt-Jakob disease mimicking frontotemporal dementia: genotypic influence and clinical implications.

An atypical case of Creutzfeldt-Jakob disease mimicking frontotemporal dementia: genotypic influence and clinical implications.

Journal: BMC geriatrics

Published: November 27, 2024

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

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

Journal: Journal of neurology

Published: November 05, 2024

Case report: Multiple approach analysis in a case of clinically assessed myotonia congenita.

Case report: Multiple approach analysis in a case of clinically assessed myotonia congenita.

Journal: Frontiers in genetics

Published: August 29, 2024

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

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

Journal: Journal of neurology

Published: April 22, 2024

Oculomotor features in SCA27B patients.

Oculomotor features in SCA27B patients.

Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology

Published: December 01, 2023

Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review.

Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review.

Journal: Journal of neurology

Published: February 16, 2023

Familial Alzheimer's disease associated with heterozygous NPC1 mutation.

Familial Alzheimer's disease associated with heterozygous NPC1 mutation.

Journal: Journal of medical genetics

Published: February 14, 2023

Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies.

Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies.

Journal: Genes

Published: November 25, 2022

24S-Hydroxycholesterol and Cerebellar Degeneration: Insights from SCA2.

24S-Hydroxycholesterol and Cerebellar Degeneration: Insights from SCA2.

Journal: Cerebellum (London, England)

Published: July 13, 2022

Showing 1-12 of 68

Last Updated: 09/26/2026