IRIS

GAGLIARDI, MONICA

GAGLIARDI, MONICA  

Dipartimento di Scienze Mediche e Chirurgiche  

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A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies 1-gen-2020 Musumeci, O.; Ferlazzo, E.; Rodolico, C.; Gambardella, A.; Gagliardi, M.; Aguglia, U.; Toscano, A.
A new CHCHD2 mutation identified in a southern Italy patient with multiple system atrophy 1-gen-2018 Nicoletti, G; Gagliardi, M; Procopio, R; Iannello, G; Morelli, M; Annnesi, G; Quattrone, A.
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification 1-gen-2015 Gagliardi, M; Morelli, M; Annesi, G; Nicoletti, G; Perrotta, P; Pustorino, G; Iannello, G; Tarantino, P; Gambardella, A; Quattrone, A.
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification. 1-gen-2015 Gagliardi, M; Annesi, G; Nicoletti, G; Perrotta, P; Pustorino, G; Iannello, G; Tarantino, P; Gambardella, A; Quattrone, A; Morelli, M
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.
A SLC20A2 mutation identified in an asymptomatic patient with brain calcification 1-gen-2017 Gagliardi, M; Morelli, M; Iannello, G; Colica, C; Annesi, G; Quattrone, A. (The first two authors contributed equally to this work).
Aceruloplasminemia: a multimodal imaging study in an Italian family with a novel mutation 1-gen-2022 Salsone, M.; Arabia, G.; Annesi, G.; Gagliardi, M.; Nistico, R.; Novellino, F.; Ferini-Strambi, L.; Quattrone, A.; Quattrone, A.
Aceruloplasminemia: A novel splicing mutation preserving the globus pallidus from Iron accumulation 1-gen-2021 Salsone, Maria; Arabia, Gennarina; Annesi, Grazia; Gagliardi, Monica; Nisticò, Rita; Novellino, Fabiana; Ferini-Strambi, Luigi; Quattrone, Andrea; Quattrone, Aldo
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.
AKT1E17K is oncogenic in mouse lung and cooperates with chemical carcinogens in inducing lung cancer 1-gen-2016 Malanga, D.; Belmonte, S.; Colelli, F.; Scarfo, M.; De Marco, C.; Oliveira, D. M.; Mirante, T.; Camastra, C.; Gagliardi, M.; Rizzuto, A.; Mignogna, C.; Paciello, O.; Papparella, S.; Fagman, H.; Viglietto, G.
An exome study of Parkinson’s disease in Sardinia, a Mediterranean genetic isolate 1-gen-2015 Quadri, M.; Yang, X.; Cossu, G.; Olgiati, S.; Saddi, V. M.; Breedveld, G. J.; Ouyang, L.; Hu, J.; Xu, N.; Graafland, J.; Ricchi, V.; Murgia, D.; Guedes, L. C.; Mariani, C.; Marti, M. J.; Tarantino, P.; Asselta, R.; Valldeoriola, F.; Gagliardi, M.; Pezzoli, G.; Ezquerra, M.; Quattrone, A.; Ferreira, J.; Annesi, G.; Goldwurm, S.; Tolosa, E.; Oostra, B. A.; Melis, M.; Wang, J.; Bonifati, V.
An italian family with Fahr disease caused by SLC20A2 new mutation 1-gen-2014 Tarantino, P; Morelli, M; Gagliardi, M; Perrotta, P; Pustorino, G; Iannello, G; Annesi, G; Quattrone, A.
Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria 1-gen-2017 Gagliardi, M.; Iannello, G.; Colica, C.; Annesi, G.; Quattrone, A.
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.
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.
Assessment of Mitochondrial DNA Copy Number in Progressive Supranuclear Palsy Patients: Evidence From a Pilot Study 1-gen-2026 Citrigno, L.; Cerantonio, A.; Gagliardi, M.; Procopio, R.; Felicetti, A.; Aureli, A.; Morelli, M.; Annesi, G.