Enrico Fratto

Catanzaro, Italy

Last Updated: 09/26/2026

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Found 15 publications

Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic models.

Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic models.

Journal: Journal of neurogenetics

Published: May 18, 2026

The bidirectional association of epilepsy with Alzheimer's disease and other neurodegenerative dementias: A longitudinal observational study on the UK Biobank.

The bidirectional association of epilepsy with Alzheimer's disease and other neurodegenerative dementias: A longitudinal observational study on the UK Biobank.

Journal: Journal of Alzheimer's disease : JAD

Published: May 14, 2026

Impact of Age on the Diagnostic Yield of Routine EEG in People With Childhood or Juvenile Absence Epilepsy: A Cross-Sectional Study.

Impact of Age on the Diagnostic Yield of Routine EEG in People With Childhood or Juvenile Absence Epilepsy: A Cross-Sectional Study.

Journal: Annals of clinical and translational neurology

Published: March 30, 2026

Risk of epilepsy in people with adult-onset hydrocephalus: insights from the UK Biobank.

Risk of epilepsy in people with adult-onset hydrocephalus: insights from the UK Biobank.

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

Published: March 17, 2026

Plasma NfL and GFAP in the preclinical stages of neurodegenerative diseases: insights from the UK Biobank.

Plasma NfL and GFAP in the preclinical stages of neurodegenerative diseases: insights from the UK Biobank.

Journal: Journal of neurology

Published: September 15, 2025

In Vivo Tau and Neurodegeneration Imaging in a Family With the Presenilin 1 Met146Leu Pathogenic Variant.

In Vivo Tau and Neurodegeneration Imaging in a Family With the Presenilin 1 Met146Leu Pathogenic Variant.

Journal: Neurology

Published: November 25, 2024

Hereditary Spastic Paraplegia Associated with Ultra-Rare Variant Enrichment Encompassing the SYNE1, CAPN1 and PGAP1 Genes.

Hereditary Spastic Paraplegia Associated with Ultra-Rare Variant Enrichment Encompassing the SYNE1, CAPN1 and PGAP1 Genes.

Journal: Cerebellum (London, England)

Published: November 18, 2024

Tremor as an intrinsic feature of juvenile myoclonic epilepsy.

Tremor as an intrinsic feature of juvenile myoclonic epilepsy.

Journal: Epilepsia

Published: October 21, 2024

Challenges in diagnosing vascular parkinsonism: the pitfalls of an old tale.

Challenges in diagnosing vascular parkinsonism: the pitfalls of an old tale.

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

Published: August 02, 2024

Eyes wide shut: Horizontal direction changing nystagmus in a left cerebellar-medullary stroke. Favourable outcome after thrombolysis.

Eyes wide shut: Horizontal direction changing nystagmus in a left cerebellar-medullary stroke. Favourable outcome after thrombolysis.

Journal: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association

Published: February 01, 2024

Painful tonic limb spasms at the presentation of acute lenticulo-capsular stroke.

Painful tonic limb spasms at the presentation of acute lenticulo-capsular stroke.

Journal: Acta neurologica Belgica

Published: October 14, 2023

Should we consider including cerebral amyloid angiopathy-related inflammation in the cerebral amyloid angiopathy diagnostic criteria?

Should we consider including cerebral amyloid angiopathy-related inflammation in the cerebral amyloid angiopathy diagnostic criteria?

Journal: Journal of the neurological sciences

Published: July 22, 2023

Showing 1-12 of 15

Last Updated: 09/26/2026