Publications by authors named "Radha Procopio"

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Genetic analysis of GBA1 gene in a cohort of patients with Parkinson's disease.
Monica Gagliardi, Maurizio Morelli, Gennarina Arabia, Radha Procopio, Alessia Felicetti

Parkinsonism Relat Disord· October 2025

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Hereditary Transthyretin Amyloidosis: Genetic Characterization of the P.Val142Ile Variant in a Calabrian Kindred.
Francesca Dinatolo, Radha Procopio, Valentina Rocca, Elisa Lo Feudo, Adele Dattola

Genes (Basel)· August 2025

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Subhaplotypes in Different Progressive Supranuclear Palsy Phenotypes.
Monica Gagliardi, Radha Procopio, Alessia Felicetti, Grazia Annesi, Mariagrazia Talarico

Biomedicines· June 2025

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Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson's disease from Southern Italy.
Monica Gagliardi, Radha Procopio, Grazia Annesi, Jolanda Buonocore, Mariagrazia Talarico

NPJ Parkinsons Dis· March 2025

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Novel Variants Related to a Variable Phenotypic Spectrum Ranging from Epilepsy with Auditory Features to Severe Developmental and Epileptic Encephalopathies.
Mariagrazia Talarico, Radha Procopio, Monica Gagliardi, Maria Chiara Sarubbi, Francesco Fortunato

Int J Mol Sci· December 2024

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Two Novel Variants in the and Genes in Italian Patients with Febrile Seizures.
Radha Procopio, Monica Gagliardi, Mariagrazia Talarico, Francesco Fortunato, Ilaria Sammarra, Anna Caterina Procopio

Genes (Basel)· October 2024

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Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant.
Alessia Giugno, Elena Falcone, Francesco Fortunato, Ilaria Sammarra, Radha Procopio

Eur J Neurol· August 2024

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Idiopathic generalized epilepsy in a family with SCN4A-related myotonia.
Mariagrazia Talarico, Francesco Fortunato, Audrey Labalme, Louis Januel, Nicolas Chatron, Radha Procopio

Epilepsia Open· June 2024

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Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia.
Radha Procopio, Francesco Fortunato, Monica Gagliardi, Mariagrazia Talarico, Ilaria Sammarra

Int J Mol Sci· May 2024

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ANXA1 mutation analysis in Italian patients with early onset PD.
Monica Gagliardi, Radha Procopio, Mariagrazia Talarico, Andrea Quattrone, Gennarina Arabia

Neurobiol Aging· May 2023

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Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis.
Francesco Bono, Laura Rapisarda, Caterina Bombardieri, Monica Gagliardi, Radha Procopio

Neurol Sci· April 2023

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A novel phenotype in an Italian family with a rare progranulin mutation.
Maria Claudia Russillo, Cristiano Sorrentino, Alfonso Scarpa, Claudia Vinciguerra, Giulio Cicarelli, Radha Procopio

J Neurol· November 2022

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Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patients.
Giuseppe Bonapace, Monica Gagliardi, Radha Procopio, Maurizio Morelli, Andrea Quattrone

Neurobiol Aging· April 2022

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Mutation analysis of the ATP13A2 gene in patients with PD and MSA from Italy.
Monica Gagliardi, Radha Procopio, Giuseppe Nicoletti, Maurizio Morelli, Laura Brighina

J Neurol Sci· November 2021

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Analysis of the LRP10 gene in patients with Parkinson's disease and dementia with Lewy bodies from Southern Italy.
Monica Gagliardi, Radha Procopio, Giuseppe Nicoletti, Maurizio Morelli, Marco D'Amelio

Neurol Sci· January 2021

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DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB.
Radha Procopio, Monica Gagliardi, Marco D'Amelio, Laura Brighina, Giuseppe Nicoletti

Neurobiol Aging· September 2020

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Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophy.
Radha Procopio, Monica Gagliardi, Laura Brighina, Giuseppe Nicoletti, Maurizio Morelli

Gene· October 2019

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Analysis of the TMEM230 gene in familial Parkinson's disease from south Italy.
Radha Procopio, Monica Gagliardi, Giuseppe Nicoletti, Maurizio Morelli, Grazia Annesi

J Neurol Sci· September 2019

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Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome.
Giuseppe Bonapace, Rosa Gullace, Daniela Concolino, Grazia Iannello, Radha Procopio

Heliyon· June 2019

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Selectivity of the CUBAN domain in the recognition of ubiquitin and NEDD8.
Luisa Castagnoli, Walter Mandaliti, Ridvan Nepravishta, Eleonora Valentini, Anna Mattioni, Radha Procopio

FEBS J· February 2019

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DNAJC13 mutation screening in patients with Parkinson's disease from South Italy.
Monica Gagliardi, Grazia Annesi, Radha Procopio, Maurizio Morelli, Grazia Iannello

Parkinsonism Relat Disord· October 2018

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Analysis of the TMEM230 gene in patients with multiple system atrophy.
Radha Procopio, Monica Gagliardi, Laura Brighina, Giuseppe Nicoletti, Maurizio Morelli

J Neurol Sci· September 2018

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Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria.
Monica Gagliardi, Gennarina Arabia, Rita Nisticò, Grazia Iannello, Radha Procopio

J Neurol Sci· July 2018

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A new CHCHD2 mutation identified in a southern italy patient with multiple system atrophy.
Giuseppe Nicoletti, Monica Gagliardi, Radha Procopio, Grazia Iannello, Maurizio Morelli

Parkinsonism Relat Disord· February 2018

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Corrigendum to "A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy" [J. Neurol. Sci. 381C (2017) 209-212].
Grazia Iannello, Claudio Graziano, Giovanna Cenacchi, Duccio Maria Cordelli, Roberta Zuntini, Radha Procopio

J Neurol Sci· February 2018

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