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; 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.
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.
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation 1-gen-2015 Gagliardi, M.; Annesi, G.; Lesca, G.; Broussolle, E.; Iannello, G.; Vaiti, V.; Gambardella, A.; Quattrone, A.
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation. 1-gen-2015 Gagliardi, M; Annesi, G; Lesca, G; Broussolle, E; Iannello, G; Vaiti, V; Gambardella, A; Quattrone, A.
Ceruloplasmin gene variations in patients with different neurological diseases 1-gen-2015 Scannapieco, S; Morelli, M; Iannello, G; Gagliardi, M; Salvino, D; Fratto, A; Novellino, F; Nicoletti, G; Annesi, G; Quattrone, A.
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.