Carmine Ungaro
Rende, 87036, Italy
Last Updated: 09/26/2026
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Found 16 publications
Atmospheric mercury monitoring data across Italy: A multi-year national dataset (2020 - 2023).
Journal: Data in brief
Published: December 19, 2025
Genetic investigation of amyotrophic lateral sclerosis patients in south Italy: a two-decade analysis.
Journal: Neurobiology of aging
Published: April 28, 2020
A Systems Biology Approach for Personalized Medicine in Refractory Epilepsy.
Journal: International journal of molecular sciences
Published: June 27, 2019
Alternative Splicing of ALS Genes: Misregulation and Potential Therapies.
Journal: Cellular and molecular neurobiology
Published: April 09, 2019
A novel S379A TARDBP mutation associated to late-onset sporadic ALS.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: March 13, 2019
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report.
Journal: BMC medical genetics
Published: January 02, 2019
ALS and CHARGE syndrome: a clinical and genetic study.
Journal: Acta neurologica Belgica
Published: September 07, 2018
Horizontal gaze palsy with progressive scoliosis: is scoliosis linked to ROBO3 mutations?
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: April 11, 2018
Horizontal Gaze Palsy With Progressive Scoliosis: Two Novel ROBO3 Mutations in a Compound Heterozygous Sporadic Case.
Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society
Published: December 08, 2017
Notch3 protein expression in skin fibroblasts from CADASIL patients.
Journal: Journal of the neurological sciences
Published: November 23, 2017
Dynamic measurement of speed of sound in n-Heptane by ultrasonics during fuel injections.
Journal: Ultrasonics
Published: February 02, 2017
Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum.
Journal: European journal of neurology
Published: July 22, 2013
Last Updated: 09/26/2026