CASELLA, ANTONELLA

CASELLA, ANTONELLA  

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A clinico-genetical study in a large cohort of patients with spastic paraplegia type 4 (SPG4) 2016 Orlacchio, Antonio; Mearini, M; Pedace, L; Casella, A; Montecchiani, C; Gaudiello, F; Miele, M; Massa, R; Caltagirone, C; Munhoz, Rp; Pedroso, Jl; Barsottini, Ogp; Kawarai, T
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease 2016 Montecchiani, Celeste; Pedace, Lucia; Lo Giudice, Temistocle; Casella, Antonella; Mearini, Marzia; Gaudiello, Fabrizio; Pedroso José, L; Terracciano, Chiara; Caltagirone, Carlo; Massa, Roberto; St George-Hyslop Peter, H; Barsottini Orlando, Gp; Kawarai, Toshitaka; Orlacchio, Antonio
Clinical and genetic study in a large cohort of patients with spastic paraplegia 2016 Casella, A; Pedace, L; Mearini, M; Montecchiani, C; Gaudiello, F; Miele, M; Massa, R; Caltagirone, C; Munhoz, Rp; Pedroso, Jl; Barsottini, Ogp; Kawarai, T; Orlacchio, Antonio
Clinical and genetic study of a large SPG4 Italian family with hereditary spastic paraplegia and early-onset familial Alzheimer’s disease 2015 Lo Giudice, T; Casella, A; Mearini, M; Montecchiani, C; Miele, M; Kawarai, T; Orlacchio, Antonio
Epidemiological, clinical, and genetic study in a large cohort of patients with spastic paraplegia 2016 Pedace, L; Montecchiani, C; Casella, A; Gaudiello, F; Miele, M; Massa, R; Caltagirone, C; Munhoz, Rp; Pedroso, Jl; Barsottini, Ogp; Kawarai, T; Orlacchio, Antonio
Hereditary spastic paraplegia and Alzheimer's disease: hypothesis of a founder effect of a SPG4/SPAST mutation 2016 Pedace, L; Mearini, M; Casella, A; Montecchiani, C; Miele, M; Caltagirone, C; Kawarai, T; Orlacchio, Antonio
Hereditary Spastic Paraplegia Type 4 (SPG4): A Clinico-Genetic Study in a Large Cohort of Patients with Spastic Paraplegia 2016 Mearini, M; Pedace, L; Casella, A; Montecchiani, C; Gaudiello, F; Miele, M; Massa, R; Caltagirone, C; Munhoz, R; Pedroso, Jl; Barsottini, Ogp; Kawarai, T; Orlacchio, Antonio
Identification of ALS5/SPG11/KIAA1840 Mutations in Patients with Autosomal Recessive Form of Charcot-Marie-Tooth Disease Type 2 2016 Montecchiani, C; Pedace, L; Lo Giudice, T; Casella, A; Mearini, M; Gaudiello, F; Pedroso, Jl; Terracciano, C; Caltagirone, C; Massa, R; St George-Hyslop, Ph; Barsottini, Ogp; Kawarai, T; Orlacchio, Antonio
SPG11 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease 2015 Lo Giudice, T; Montecchiani, C; Di Lullo, M; Mearini, M; Casella, A; Gaudiello, F; Terracciano, C; Massa, R; Rogaeva, E; St George-Hyslop, Ph; Pedroso, Jl; Barsottini, Ogp; Kawarai, T; Orlacchio, Antonio
sPlot – A new tool for global vegetation analyses 2019 Bruelheide, H.; Dengler, J.; Jimenez-Alfaro, B.; Purschke, O.; Hennekens, S. M.; Chytry, M.; Pillar, V. D.; Jansen, F.; Kattge, J.; Sandel, B.; Aubin, I.; Biurrun, I.; Field, R.; Haider, S.; Jandt, U.; Lenoir, J.; Peet, R. K.; Peyre, G.; Sabatini, F. M.; Schmidt, M.; Schrodt, F.; Winter, M.; Acic, S.; Agrillo, E.; Alvarez, M.; Ambarli, D.; Angelini, P.; Apostolova, I.; Arfin Khan, M. A. S.; Arnst, E.; Attorre, F.; Baraloto, C.; Beckmann, M.; Berg, C.; Bergeron, Y.; Bergmeier, E.; Bjorkman, A. D.; Bondareva, V.; Borchardt, P.; Botta-Dukat, Z.; Boyle, B.; Breen, A.; Brisse, H.; Byun, C.; Cabido, M. R.; Casella, L.; Cayuela, L.; Cerny, T.; Chepinoga, V.; Csiky, J.; Curran, M.; Custerevska, R.; Dajic Stevanovic, Z.; De Bie, E.; de Ruffray, P.; De Sanctis, M.; Dimopoulos, P.; Dressler, S.; Ejrnaes, R.; El-Sheikh, M. A. E. -R. M.; Enquist, B.; Ewald, J.; Fagundez, J.; Finckh, M.; Font, X.; Forey, E.; Fotiadis, G.; Garcia-Mijangos, I.; de Gasper, A. L.; Golub, V.; Gutierrez, A. G.; Hatim, M. Z.; He, T.; Higuchi, P.; Holubova, D.; Holzel, N.; Homeier, J.; Indreica, A.; Isik Gursoy, D.; Jansen, S.; Janssen, J.; Jedrzejek, B.; Jirousek, M.; Jurgens, N.; Kacki, Z.; Kavgaci, A.; Kearsley, E.; Kessler, M.; Knollova, I.; Kolomiychuk, V.; Korolyuk, A.; Kozhevnikova, M.; Kozub, L.; Krstonosic, D.; Kuhl, H.; Kuhn, I.; Kuzemko, A.; Kuzmic, F.; Landucci, F.; Lee, M. T.; Levesley, A.; Li, C. -F.; Liu, H.; Lopez-Gonzalez, G.; Lysenko, T.; Macanovic, A.; Mahdavi, P.; Manning, P.; Marceno, C.; Martynenko, V.; Mencuccini, M.; Minden, V.; Moeslund, J. E.; Moretti, M.; Muller, J. V.; Munzinger, J.; Niinemets, U.; Nobis, M.; Noroozi, J.; Nowak, A.; Onyshchenko, V.; Overbeck, G. E.; Ozinga, W. A.; Pauchard, A.; Pedashenko, H.; Penuelas, J.; Perez-Haase, A.; Peterka, T.; Petrik, P.; Phillips, O. L.; Prokhorov, V.; Rasomavicius, V.; Revermann, R.; Rodwell, J.; Ruprecht, E.; Rusina, S.; Samimi, C.; Schaminee, J. H. J.; Schmiedel, U.; Sibik, J.; Silc, U.; Skvorc, Z.; Smyth, A.; Sop, T.; Sopotlieva, D.; Sparrow, B.; Stancic, Z.; Svenning, J. -C.; Swacha, G.; Tang, Z.; Tsiripidis, I.; Turtureanu, P. D.; Ugurlu, E.; Uogintas, D.; Valachovic, M.; Vanselow, K. A.; Vashenyak, Y.; Vassilev, K.; Velez-Martin, E.; Venanzoni, R.; Vibrans, A. C.; Violle, C.; Virtanen, R.; von Wehrden, H.; Wagner, V.; Walker, D. A.; Wana, D.; Weiher, E.; Wesche, K.; Whitfeld, T.; Willner, W.; Wiser, S.; Wohlgemuth, T.; Yamalov, S.; Zizka, G.; Zverev, A.
Trans-crocetin improves amyloid-β degradation in monocytes from Alzheimer's Disease patients 2017 Tiribuzi, Roberto; Crispoltoni, Lucia; Chiurchiù, Valerio; Casella, Antonella; Montecchiani, Celeste; DEL PINO, Alberto Marco; Maccarrone, Mauro; Palmerini, Carlo Alberto; Caltagirone, Carlo; Kawarai, Toshitaka; Orlacchio, Aldo; Orlacchio, Antonio