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Titolo Data di pubblicazione Autore(i) File
PCDH19 mutations in female patients from Southern Italy. 1-gen-2015 Gagliardi, M; Annesi, G; Sesta, M; Tarantino, P; Conti, P; Labate, A; Di Rosa, G; Quattrone, A; Gambardella, A
Marinesco-Sjögren syndrome caused by a new SIL1 frameshift mutation 1-gen-2015 Cerami, C.; Tarantino, P.; Cupidi, C.; Annesi, G.; Lo Re, V.; Gagliardi, M.; Piccoli, T.; Quattrone, A.
Marinesco-Sjögren syndrome caused by a new SIL1 frameshift mutation 1-gen-2015 Cerami, Chiara; Tarantino, Patrizia; Cupidi, Chiara; Annesi, Grazia; Lo Re, Vincenzina; Gagliardi, Monica; Piccoli, Tommaso; Quattrone, Aldo
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.
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.
Two new SCL20A2 mutations identified in two southern Italy families with primary familial brain calcification 1-gen-2016 Scannapieco, S; Gagliardi, M; Annesi, G; Morelli, M; Iannello, G; Nicoletti, G; Gambardella, A; Quattrone, A.
Next-generation sequencing in multiple-system atrophy 1-gen-2016 Annesi, G; Gagliardi, M; Iannello, G; Nicoletti, G; Morelli, M; Donato, A; Malanga, D; Viglietto, G; 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.
FTH1P3, a Novel H-Ferritin Pseudogene Transcriptionally Active, Is Ubiquitously Expressed and Regulated during Cell Differentiation. 1-gen-2016 Di Sanzo, M; Aversa, I; Santamaria, G; Gagliardi, M; Panebianco, M; Biamonte, F; Zolea, F; Faniello, C; Cuda, G; Costanzo, F
Mutational analysis of COASY in an Italian patient with NBIA 1-gen-2016 Annesi, G.; Gagliardi, M.; Iannello, G.; Quattrone, A.
Voxel-based morphometry to detect effect of APOE on brain gray matter changes in Parkinson's Disease 1-gen-2016 Nicoletti, G.; Manners, D. N.; Novellino, F.; Testa, C.; Gagliardi, M.; Tonon, C.; Lodi, R.; Quattrone, A.
FTH1P3, a Novel H-Ferritin Pseudogene Transcriptionally Active, Is Ubiquitously Expressed and Regulated during Cell Differentiation 1-gen-2016 Di Sanzo, Maddalena; Aversa, Ilenia; Santamaria, Gianluca; Gagliardi, Monica; Panebianco, Mariafranca; Biamonte, Flavia; Zolea, Fabiana; Faniello, Maria Concetta; Cuda, Giovanni; Costanzo, Francesco
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).
Mutations in TMEM230 are not a common cause of Parkinson’s disease in southern Italy 1-gen-2017 Annesi, G; Gagliardi, M; Iannello, G; Procopio, R; Nicoletti, G; Morelli, M; Quattrone, A.
Identification of one novel mutation in GRN gene associated with frontotemporal dementia 1-gen-2017 Garcea, T; Manna, I; Morelli, M; Mancini, M; Arabia, G; Manfredini, Li; Lupo, A; Barbagallo, G; Salsone, M; Novellino, F; Nicoletti, G; Annesi, G; Gagliardi, M; Chiriaco, C; Rocca, F; Nisticò, R; 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.
DNAJC13 mutation screening in patients with Parkinson's disease from South Italy 1-gen-2018 Gagliardi, M; Annesi, G; Procopio, R; Morelli, M; Iannello, G; Bonapace, G; Mancini, M; Nicoletti, 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.
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.
Neuropsychological heterogeneity in patients with primary familial brain calcification due to a novel mutation in SLC20A2 1-gen-2018 Chiriaco, C; Novellino, F; Salsone, M; Gagliardi, M; Morelli, M; Quattrone, A.
Mostrati risultati da 21 a 40 di 75
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