Carla Battisti

Siena, Italy

Last Updated: 09/26/2026

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Found 55 publications

Bridging the Gap: Baló Concentric Sclerosis-Like Leukoencephalopathy in Chronic Cocaine Use: A 1-Year Clinical and Imaging Follow-Up of 2 Cases.

Bridging the Gap: Baló Concentric Sclerosis-Like Leukoencephalopathy in Chronic Cocaine Use: A 1-Year Clinical and Imaging Follow-Up of 2 Cases.

Journal: Neurology
Published: May 08, 2026

Neural network plasticity in Parkinson's disease: the impact of exercise-driven modulation.

Neural network plasticity in Parkinson's disease: the impact of exercise-driven modulation.

Journal: Frontiers in rehabilitation sciences
Published: April 19, 2026

From Guillain-Barré-Like Neuropathy to EGPA: ANCA Testing and Kidney Biopsy as Diagnostic Turning Points.

From Guillain-Barré-Like Neuropathy to EGPA: ANCA Testing and Kidney Biopsy as Diagnostic Turning Points.

Journal: Nephrology (Carlton, Vic.)
Published: February 06, 2026

Supervised-not voluntary-upper limb exercise enhances vestibular function in Parkinson's disease.

Supervised-not voluntary-upper limb exercise enhances vestibular function in Parkinson's disease.

Journal: Frontiers in neurology
Published: April 26, 2025

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

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

FOLR1 Gene Variation With Adult-Onset Cerebral Folate Deficiency and Stable Clinical and MRI Features up to 2 Years.

FOLR1 Gene Variation With Adult-Onset Cerebral Folate Deficiency and Stable Clinical and MRI Features up to 2 Years.

Journal: Neurology. Genetics
Published: July 21, 2023

A case report of FAVA syndrome in a young woman carrying a mutation in the PIK3CA gene.

A case report of FAVA syndrome in a young woman carrying a mutation in the PIK3CA gene.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: March 28, 2023

Early-onset motor polyneuropathy associated with a novel dominant NAGLU mutation.

Early-onset motor polyneuropathy associated with a novel dominant NAGLU mutation.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: December 28, 2022

Diagnosis, treatment, and follow-up of patients with cerebral amyloid angiopathy-related inflammation.

Diagnosis, treatment, and follow-up of patients with cerebral amyloid angiopathy-related inflammation.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: March 11, 2022

Clinical Features and Outcome of the Guillain-Barre Syndrome: A Single-Center 11-Year Experience.

Clinical Features and Outcome of the Guillain-Barre Syndrome: A Single-Center 11-Year Experience.

Journal: Frontiers in neurology
Published: January 16, 2022

A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis.

A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: August 17, 2021
Showing 1-12 of 55

Last Updated: 09/26/2026