PROCOPIO, RADHA
PROCOPIO, RADHA
Dipartimento di Scienze Mediche e Chirurgiche
A novel phenotype in an Italian family with a rare progranulin mutation
2022-01-01 Russillo, M. C.; Sorrentino, C.; Scarpa, A.; Vinciguerra, C.; Cicarelli, G.; Cuoco, S.; Gagliardi, M.; Talarico, M.; Procopio, R.; Quattrone, A.; Barone, P.; Pellecchia, M. T.
Admixture analysis to define late onset Parkinson's disease: Moderating effect of the APOE gene
2023-01-01 De Luca, V.; Nicoletti, G.; Gagliardi, M.; Procopio, R.; Annesi, G.
Analysis of the LRP10 gene in patients with Parkinson’s disease and dementia with Lewy bodies from Southern Italy
2021-01-01 Gagliardi, M.; Procopio, R.; Nicoletti, G.; Morelli, M.; D'Amelio, M.; Quattrone, A.; Annesi, G.
Analysis of the TMEM230 gene in familial Parkinson's disease from south Italy
2019-01-01 Procopio, R.; Gagliardi, M.; Nicoletti, G.; Morelli, M.; Annesi, G.; Quattrone, A.
Analysis of the TMEM230 gene in patients with multiple system atrophy
2018-01-01 Procopio, R.; Gagliardi, M.; Brighina, L.; Nicoletti, G.; Morelli, M.; Piatti, M.; Annesi, G.; Quattrone, A.
ANXA1 mutation analysis in Italian patients with early onset PD
2023-01-01 Gagliardi, M.; Procopio, R.; Talarico, M.; Quattrone, A.; Arabia, G.; Morelli, M.; D'Amelio, M.; Malanga, D.; Bonapace, G.; Quattrone, A.; Annesi, G.
ANXA1 mutation analysis in Italian patients with early onset PD
2023-01-01 Gagliardi, M.; Procopio, R.; Talarico, M.; Quattrone, A.; Arabia, G.; Morelli, M.; D'Amelio, M.; Malanga, D.; Bonapace, G.; Quattrone, A.; Annesi, G.
Corrigendum to “A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy” [J. Neurol. Sci. 381C (2017) 209–212] (S0022510X17337528) (10.1016/j.jns.2017.08.3260))
2018-01-01 Iannello, G.; Graziano, C.; Cenacchi, G.; Cordelli, D. M.; Zuntini, R.; Papa, V.; Magista, A. M.; Gagliardi, M.; Procopio, R.; Quattrone, A.; Annesi, G.
DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB
2020-01-01 Procopio, R.; Gagliardi, M.; D'Amelio, M.; Brighina, L.; Nicoletti, G.; Morelli, M.; Bonapace, G.; Quattrone, A.; Annesi, G.
Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophy
2019-01-01 Procopio, R.; Gagliardi, M.; Brighina, L.; Nicoletti, G.; Morelli, M.; Ferrarese, C.; Annesi, G.; Quattrone, A.
Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant
2024-01-01 Giugno, A.; Falcone, E.; Fortunato, F.; Sammarra, I.; Procopio, R.; Gagliardi, M.; Bauleo, A.; de Stefano, L.; Martino, I.; Gambardella, A.
Idiopathic generalized epilepsy in a family with SCN4A-related myotonia
2024-01-01 Talarico, M.; Fortunato, F.; Labalme, A.; Januel, L.; Chatron, N.; Sanlaville, D.; Sammarra, I.; Gagliardi, M.; Procopio, R.; Valentino, P.; Annesi, G.; Lesca, G.; Gambardella, A.
Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by Fragile X Tremor Ataxia Syndrome
2019-01-01 Bonapace, G; Gullace, R; Concolino, D; Iannello, G; Procopio, R; Gagliardi, M; Arabia, G; Barbagallo, G; Lupo, A; Manfredini, Li; Annesi, G; Quattrone, A
Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patients
2022-01-01 Bonapace, G.; Gagliardi, M.; Procopio, R.; Morelli, M.; Quattrone, A.; Brighina, L.; Quattrone, A.; Annesi, G.
Mutation analysis of the ATP13A2 gene in patients with PD and MSA from Italy
2021-01-01 Gagliardi, M.; Procopio, R.; Nicoletti, G.; Morelli, M.; Brighina, L.; Quattrone, A.; Bonapace, G.; Malanga, D.; Quattrone, A.; Annesi, G.
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria
2018-01-01 Gagliardi, M; Arabia, G; Nisticò, R; Iannello, G; Procopio, R; Manfredini, L; Annesi, G; Quattrone, A.
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria
2018-01-01 Gagliardi, M.; Arabia, G.; Nistico, R.; Iannello, G.; Procopio, R.; Manfredini, L.; Annesi, G.; Quattrone, A.
Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis
2022-01-01 Bono, Francesco; Rapisarda, Laura; Bombardieri, Caterina; Gagliardi, Monica; Procopio, Radha; Demonte, Giulio; Tosto, Federico; Bruno, Pietro A; Gambardella, Antonio; Annesi, Grazia
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia
2024-01-01 Procopio, Radha; Fortunato, Francesco; Gagliardi, Monica; Talarico, Mariagrazia; Sammarra, Ilaria; Sarubbi, Maria Chiara; Malanga, Donatella; Annesi, Grazia; Gambardella, Antonio
Selectivity of the CUBAN domain in the recognition of ubiquitin and NEDD8
2019-01-01 Castagnoli, L.; Mandaliti, W.; Nepravishta, R.; Valentini, E.; Mattioni, A.; Procopio, R.; Iannuccelli, M.; Polo, S.; Paci, M.; Cesareni, G.; Santonico, E.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A novel phenotype in an Italian family with a rare progranulin mutation | 1-gen-2022 | Russillo, M. C.; Sorrentino, C.; Scarpa, A.; Vinciguerra, C.; Cicarelli, G.; Cuoco, S.; Gagliardi, M.; Talarico, M.; Procopio, R.; Quattrone, A.; Barone, P.; Pellecchia, M. T. | |
| Admixture analysis to define late onset Parkinson's disease: Moderating effect of the APOE gene | 1-gen-2023 | De Luca, V.; Nicoletti, G.; Gagliardi, M.; Procopio, R.; Annesi, G. | |
| Analysis of the LRP10 gene in patients with Parkinson’s disease and dementia with Lewy bodies from Southern Italy | 1-gen-2021 | Gagliardi, M.; Procopio, R.; Nicoletti, G.; Morelli, M.; D'Amelio, M.; Quattrone, A.; Annesi, G. | |
| Analysis of the TMEM230 gene in familial Parkinson's disease from south Italy | 1-gen-2019 | Procopio, R.; Gagliardi, M.; Nicoletti, G.; Morelli, M.; Annesi, G.; Quattrone, A. | |
| Analysis of the TMEM230 gene in patients with multiple system atrophy | 1-gen-2018 | Procopio, R.; Gagliardi, M.; Brighina, L.; Nicoletti, G.; Morelli, M.; Piatti, M.; Annesi, G.; Quattrone, A. | |
| ANXA1 mutation analysis in Italian patients with early onset PD | 1-gen-2023 | Gagliardi, M.; Procopio, R.; Talarico, M.; Quattrone, A.; Arabia, G.; Morelli, M.; D'Amelio, M.; Malanga, D.; Bonapace, G.; Quattrone, A.; Annesi, G. | |
| ANXA1 mutation analysis in Italian patients with early onset PD | 1-gen-2023 | Gagliardi, M.; Procopio, R.; Talarico, M.; Quattrone, A.; Arabia, G.; Morelli, M.; D'Amelio, M.; Malanga, D.; Bonapace, G.; Quattrone, A.; Annesi, G. | |
| Corrigendum to “A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy” [J. Neurol. Sci. 381C (2017) 209–212] (S0022510X17337528) (10.1016/j.jns.2017.08.3260)) | 1-gen-2018 | Iannello, G.; Graziano, C.; Cenacchi, G.; Cordelli, D. M.; Zuntini, R.; Papa, V.; Magista, A. M.; Gagliardi, M.; Procopio, R.; Quattrone, A.; Annesi, G. | |
| DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB | 1-gen-2020 | Procopio, R.; Gagliardi, M.; D'Amelio, M.; Brighina, L.; Nicoletti, G.; Morelli, M.; Bonapace, G.; Quattrone, A.; Annesi, G. | |
| Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophy | 1-gen-2019 | Procopio, R.; Gagliardi, M.; Brighina, L.; Nicoletti, G.; Morelli, M.; Ferrarese, C.; Annesi, G.; Quattrone, A. | |
| Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant | 1-gen-2024 | Giugno, A.; Falcone, E.; Fortunato, F.; Sammarra, I.; Procopio, R.; Gagliardi, M.; Bauleo, A.; de Stefano, L.; Martino, I.; Gambardella, A. | |
| Idiopathic generalized epilepsy in a family with SCN4A-related myotonia | 1-gen-2024 | Talarico, M.; Fortunato, F.; Labalme, A.; Januel, L.; Chatron, N.; Sanlaville, D.; Sammarra, I.; Gagliardi, M.; Procopio, R.; Valentino, P.; Annesi, G.; Lesca, G.; Gambardella, A. | |
| Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by Fragile X Tremor Ataxia Syndrome | 1-gen-2019 | Bonapace, G; Gullace, R; Concolino, D; Iannello, G; Procopio, R; Gagliardi, M; Arabia, G; Barbagallo, G; Lupo, A; Manfredini, Li; Annesi, G; Quattrone, A | |
| Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patients | 1-gen-2022 | Bonapace, G.; Gagliardi, M.; Procopio, R.; Morelli, M.; Quattrone, A.; Brighina, L.; Quattrone, A.; Annesi, G. | |
| Mutation analysis of the ATP13A2 gene in patients with PD and MSA from Italy | 1-gen-2021 | Gagliardi, M.; Procopio, R.; Nicoletti, G.; Morelli, M.; Brighina, L.; Quattrone, A.; Bonapace, G.; Malanga, D.; Quattrone, A.; Annesi, G. | |
| Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria | 1-gen-2018 | Gagliardi, M; Arabia, G; Nisticò, R; Iannello, G; Procopio, R; Manfredini, L; Annesi, G; Quattrone, A. | |
| Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria | 1-gen-2018 | Gagliardi, M.; Arabia, G.; Nistico, R.; Iannello, G.; Procopio, R.; Manfredini, L.; Annesi, G.; Quattrone, A. | |
| Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis | 1-gen-2022 | Bono, Francesco; Rapisarda, Laura; Bombardieri, Caterina; Gagliardi, Monica; Procopio, Radha; Demonte, Giulio; Tosto, Federico; Bruno, Pietro A; Gambardella, Antonio; Annesi, Grazia | |
| Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia | 1-gen-2024 | Procopio, Radha; Fortunato, Francesco; Gagliardi, Monica; Talarico, Mariagrazia; Sammarra, Ilaria; Sarubbi, Maria Chiara; Malanga, Donatella; Annesi, Grazia; Gambardella, Antonio | |
| Selectivity of the CUBAN domain in the recognition of ubiquitin and NEDD8 | 1-gen-2019 | Castagnoli, L.; Mandaliti, W.; Nepravishta, R.; Valentini, E.; Mattioni, A.; Procopio, R.; Iannuccelli, M.; Polo, S.; Paci, M.; Cesareni, G.; Santonico, E. |