Spectroscopic Measurements and Models of Energy Deposition in the Substrate of Quantum Circuits by Natural Ionizing Radiation
2024 Fowler, J; Szypryt, P; Bunker, R; Edwards, E; Fogarty Florang, I; Gao, J; Giachero, A; Hoogerheide, S; Loer, B; Mumm, H; Nakamura, N; O'Neil, G; Orrell, J; Scott, E; Stevens, J; Swetz, D; Vandevender, B; Vissers, M; Ullom, J
Encoding Manual Dexterity through Modulation of Intrinsic α Band Connectivity
2024 Maddaluno, O; Penna, S; Pizzuti, A; Spezialetti, M; Corbetta, M; de Pasquale, F; Betti, V
Investigating the impact of the regularization parameter on EEG resting-state source reconstruction and functional connectivity using real and simulated data
2024 Leone, F; Caporali, A; Pascarella, A; Perciballi, C; Maddaluno, O; Basti, A; Belardinelli, P; Marzetti, L; Di Lorenzo, G; Betti, V
Rewiring the evolution of the human hand: How the embodiment of a virtual bionic tool improves behavior
2024 Marucci, M; Maddaluno, O; Ryan, C; Perciballi, C; Vasta, S; Ciotti, S; Moscatelli, A; Betti, V
Gamma oscillations and auditory perception: a cluster-based statistic investigation in infants at higher likelihood of autism and developmental language disorder.
In corso di stampa Polver, S; Cantiani, C; Bulf, H; Piazza, C; Turati, C; Molteni, M; Riva, V
Second language phonolexical representations in Italian first-grade children enrolled in an English immersion program: effects of receptive vocabulary and environmental factors.
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Adult diagnosis of Cockayne syndrome
2019 Cocco, A; Calandrella, D; Carecchio, M; Garavaglia, B; Albanese, A
Long-term effect of subthalamic and pallidal deep brain stimulation for status dystonicus in children with methylmalonic acidemia and GNAO1 mutation
2019 Benato, A; Carecchio, M; Burlina, A; Paoloni, F; Sartori, S; Nosadini, M; D'Avella, D; Landi, A; Antonini, A
Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrum
2019 Iodice, A; Carecchio, M; Zorzi, G; Garavaglia, B; Spagnoli, C; Salerno, G; Frattini, D; Mencacci, N; Invernizzi, F; Veneziano, L; Mantuano, E; Angriman, M; Fusco, C
Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study
2019 Carecchio, M; Invernizzi, F; Gonzalez-Latapi, P; Panteghini, C; Zorzi, G; Romito, L; Leuzzi, V; Galosi, S; Reale, C; Zibordi, F; Joseph, A; Topf, M; Piano, C; Bentivoglio, A; Girotti, F; Morana, P; Morana, B; Kurian, M; Garavaglia, B; Mencacci, N; Lubbe, S; Nardocci, N
Pallidal deep brain stimulation in DYT6 dystonia: Clinical outcome and predictive factors for motor improvement
2019 Danielsson, A; Carecchio, M; Cif, L; Koy, A; Lin, J; Solders, G; Romito, L; Lohmann, K; Garavaglia, B; Reale, C; Zorzi, G; Nardocci, N; Coubes, P; Gonzalez, V; Roubertie, A; Collod-Beroud, G; Lind, G; Tedroff, K
Inborn errors of coenzyme a metabolism and neurodegeneration
2019 Di Meo, I; Carecchio, M; Tiranti, V
Primary brain calcification: an international study reporting novel variants and associated phenotypes
2018 Ramos, E; Carecchio, M; Lemos, R; Ferreira, J; Legati, A; Sears, R; Hsu, S; Panteghini, C; Magistrelli, L; Salsano, E; Esposito, S; Taroni, F; Richard, A; Tranchant, C; Anheim, M; Ayrignac, X; Goizet, C; Vidailhet, M; Maltete, D; Wallon, D; Frebourg, T; Pimentel, L; Geschwind, D; Vanakker, O; Galasko, D; Fogel, B; Innes, A; Ross, A; Dobyns, W; Alcantara, D; O'Driscoll, M; Hannequin, D; Campion, D; Oliveira, J; Garavaglia, B; Coppola, G; Nicolas, G
MYORG-related disease is associated with central pontine calcifications and atypical parkinsonism
2020 Chelban, V; Carecchio, M; Rea, G; Bowirrat, A; Kirmani, S; Magistrelli, L; Efthymiou, S; Schottlaender, L; Vandrovcova, J; Salpietro, V; Salsano, E; Pareyson, D; Chiapparini, L; Jan, F; Ibrahim, S; Khan, F; Qarnain, Z; Groppa, S; Bajaj, N; Balint, B; Bhatia, K; Lees, A; Morrison, P; Wood, N; Garavaglia, B; Houlden, H
High prolactin levels in dihydropteridine reductase deficiency: A sign of therapy failure or additional pathology?
2021 Vitturi, N; Lenzini, L; Luisi, C; Carecchio, M; Gugelmo, G; Francini-Pesenti, F; Avogaro, A
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A case of childhood-onset dystonia-parkinsonism due to homozygous parkin mutations and effect of globus pallidus deep brain stimulation
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