Sfoglia per ???browse.type.metadata.typeResearch??? AREA06 - SCIENZE MEDICHE
Muscular dystrophy: new challenges and review of the current clinical trials
2013 Mercuri, Eugenio Maria; Muntoni, F.
Musculoskeletal Aging and Sarcopenia in the Elderly
2022 Marzetti, E.
Musculoskeletal manifestations in children with Behçet's syndrome: data from the AIDA Network Behçet's Syndrome Registry
2023 Gaggiano, C; Maselli, A; Sfikakis, Pp; Laskari, K; Ragab, G; Hegazy, Mt; Laymouna, Ah; Lopalco, G; Almaghlouth, Ia; Asfina, Kn; Alahmed, O; Giardini Mayrink, Ha; Parente de Brito Antonelli, I; Cattalini, M; Piga, M; Sota, J; Gentileschi, S; Maggio, Mc; Opris-Belinski, D; Hatemi, G; Insalaco, A; Olivieri, An; Tufan, A; Karadeniz, H; Kardaş, Rc; La Torre, F; Cardinale, F; Marino, A; Guerriero, S; Ruscitti, P; Tarsia, M; Vitale, A; Caggiano, V; Telesca, S; Iannone, F; Parretti, V; Frassi, M; Aragona, E; Ciccia, F; Wiesik-Szewczyk, E; Ionescu, R; Şahin, A; Akkoç, N; Hinojosa-Azaola, A; Tharwat, S; Hernández-Rodríguez, J; Espinosa, G; Conti, G; Del Giudice, E; Govoni, M; Emmi, G; Fabiani, C; Balistreri, A; Frediani, B; Rigante, Donato; Cantarini, L
Musculoskeletal manifestations of childhood cancer and differential diagnosis with juvenile idiopathic arthritis (ONCOREUM): a multicentre, cross-sectional study
2021 Civino, A; Alighieri, G; Prete, E; Caroleo, Am; Magni-Manzoni, S; Vinti, L; Romano, M; Santoro, N; Filocamo, G; Belotti, T; Santarelli, F; Gorio, C; Ricci, F; Colombini, A; Pastore, S; Cesaro, S; Barone, P; Verzegnassi, F; Olivieri, An; Ficara, M; Miniaci, A; Russo, G; Gallizzi, R; Pericoli, R; Breda, L; Mura, R; Podda, R; Onofrillo, D; Lattanzi, B; Tirtei, E; Maggio, Mc; De Santis, R; Consolini, R; Arlotta, A; La Torre, F; Messina, C; Pelagatti, Ma; Coassin, E; Capolsini, I; Burnelli, R; Tornesello, A; Soscia, F; De Fanti, A; Rigante, Donato; Pizzato, C; De Fusco, C; Abate, Me; Roncadori, A; Rossi, E; Stabile, G; Biondi, A; Lepore, L; Conter, V; Rondelli, R; Pession, A; Ravelli, A
Musculoskeletal symptoms at the onset of pediatric tumors and predictive features in the differential diagnosis with juvenile idiopatic arthritis: preliminary analysis of a multicenter, prospective, observational study
2017 Civino, A; Alighieri, G; Davì, S; Rondelli, R; Martino, S; Filocamo, G; Magnolato, A; Ricci, F; Gallizzi, R; Olivieri, A; Gerloni, V; Lattanzi, B; Soscia, F; De Fanti, A; Magni Manzoni, S; Citiso, S; Quartulli, L; La Torre, F; Rigante, Donato; Maggio, Mc; Marsili, M; Pelagatti, Ma; Conter, V; Fagioli, F; Lepore, L; Pession, A; Ravelli, A.
Musculoskeletal ultrasound in systemic lupus erythematosus: Systematic literature review by the lupus task force of the OMERACT ultrasound working group
2019 Wong, P. C.; Lee, G.; Delle Sedie, A.; Hanova, P.; Inanc, N.; Jousse-Joulin, S.; Ohrndorf, S.; Stoenoiu, M. S.; Keen, H. I.; Terslev, L.; D'Agostino, Maria Antonietta; Bruyn, G. A.
Musculoskeletal ultrasound including definitions for ultrasonographic pathology
2005 Wakefield, Richard J; Balint, Peter V; Szkudlarek, Marcin; Filippucci, Emilio; Backhaus, Marina; D'Agostino, Maria-Antonietta; Sanchez, Esperanza Naredo; Iagnocco, Annamaria; Schmidt, Wolfgang A; Bruyn, George A W; Bruyn, George; Kane, David; O'Connor, Philip J; Manger, Bernhard; Joshua, Fred; Koski, Juhani; Grassi, Walter; Lassere, Marissa N D; Swen, Nanno; Kainberger, Franz; Klauser, Andrea; Ostergaard, Mikkel; Brown, Andrew K; Machold, Klaus P; Conaghan, Philip G
Musculo‑skeletal phenotype of Costello syndrome and cardio‑facio‑cutaneous syndrome: insights on the functional assessment status.
2021 Leoni, Chiara; Romeo, Domenico Marco; Pelliccioni, M; Di Già, M; Onesimo, R; Giorgio, Valentina; Flex, E; Tedesco, Marta; Tartaglia, M; Rigante, Donato; Valassina, A; Zampino, Giuseppe
Music exposure differentially alters the levels of brain-derived neurotrophic factor and nerve growth factor in the mouse hypothalamus.
2007 Angelucci, Francesco; Ricci, Enzo; Padua, Luca; Sabino, Andrea; Tonali, Pietro Attilio
Music identification skills of children with specific language impairment
2015 Mari, G; Scorpecci, Alessandro; Reali, L; D'Alatri, Lucia
Musical training software for children with cochlear implants
2015 Di Nardo, W; Schinaia, L; Anzivino, R; De Corso, E; Ciacciarelli, A; Paludetti, G
Musical training software for children with cochlear implants [Software di training musicale per bambini con impianto cocleare]
2015 Di Nardo, Walter; Schinaia, Lorenzo; Anzivino, Roberta; De Corso, Eugenio; Ciacciarelli, A; Paludetti, Gaetano
MuSK autoantibodies in myasthenia gravis detected by cell based assay-A multinational study
2015 Evoli Stampanoni-B, Amelia; Tsonis, A; Zisimopoulou, P; Matsigkou, E; Lazaridis, K; Tzartos, J; Zouvelou, Vasiliki; Mantegazza, Renato; Antozzi, Carlo; Deymeer, Feza; Saruhan Direskeneli, G; Durmus, H; Brenner, T; Vaknin, A; Behin, A; Berrih Aknin, S; Sharshar, T; De Baets, Mark; Martinez Martinez, P; Losen, Mario; Zamba Papanicolaou, E; Kleopa, Ka; Kyriakides, T; Kostera Pruszczyk, A; Szczudlik, P; Szyluk, B; Lavrnic, D; Basta, I; Peric, S; Tallaksen, Chantal; Maniaol, A; Casasnovas Pons, C; Pitha, J; Jakubíkova, M; Hanisch, F; Tzartos, Sj; Andreetta, F
Mutant human β4 subunit identified in amyotrophic lateral sclerosis patients impairs nicotinic receptor function.
2011 Moriconi, S; Di Angeloantonio, S; Sabatelli, Mario; Grassi, F.
Mutation analysis and X-inactivation studies in the galactosidase A gene
2002 Morrone, A; Cavicchi, C; Bardelli, T; Antuzzi, D; Rigante, Donato; Parini, R; Di Rocco, M; Feriozzi, S; Gabrielli, O; Barone, R; Aricò, M; Ricci, Roberta; Zammarchi, E.
Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia
2007 Kratz, C P; Niemeyer, C M; Thomas, C; Bauhuber, S; Matejas, V; Bergsträsser, E; Flotho, C; Flores, N J; Haas, O; Hasle, H; van den Heuvel-Eibrink, M M; Kucherlapati, R S; Lang, P; Roberts, A E; Starý, J; Strahm, B; Swanson, K D; Trebo, M; Zecca, M; Neel, B; Locatelli, Franco; Loh, M L; Zenker, M
Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth
2005 Cecconi, Maurizio; Forzano, F.; Milani, Daniela; Cavani, S.; Baldo, C.; Selicorni, Angelo; Pantaleoni, C.; Silengo, M.; Ferrero, G. B.; Scarano, Gioacchino; Della Monica, M.; Fischetto, R.; Grammatico, P.; Majore, S.; Zampino, Giuseppe; Memo, Luigi; Cordisco, E. L.; Neri, Giovanni; Pierluigi, M.; Bricarelli, F. D.; Grasso, M.; Faravelli, F.
Mutation identification of Fabry disease in families with other lysosomal storage disorders
2012 Zampetti, Anna; Fania, L; Antuzzi, D; Giurdanella, F; Gnarra, M; Bertola, F; Lualdi, S; Filocamo, M; Morrone, A; Feliciani, Claudio
MUTATION OF SHOC2 PROMOTES ABERRANT PROTEIN N-MYRISTOYLATION AND CAUSES NOONAN-LIKE SUNDROME WITH LOOSE ANAGEN HAIR.
2009 Cordeddu, V; Di Schiavi, E; Zampino, Giuseppe; Dallapiccola, Bruno; Gelb, Bd; Tartaglia, Marco
Mutation profile of BBS genes in patients with Bardet-Biedl syndrome: An Italian study
2019 Manara, E.; Paolacci, S.; D'Esposito, F.; Abeshi, A.; Ziccardi, L.; Falsini, Benedetto; Colombo, L.; Iarossi, G.; Pilotta, A.; Boccone, L.; Guerri, Giulia; Monica, M.; Marta, B.; Maltese, P. E.; Buzzonetti, Luca; Rossetti, Lodovico; Bertelli, M.
Data di pubblicazione | Titolo | Autore(i) | File |
---|---|---|---|
1-gen-2013 | Muscular dystrophy: new challenges and review of the current clinical trials | Mercuri, Eugenio Maria; Muntoni, F. | |
1-gen-2022 | Musculoskeletal Aging and Sarcopenia in the Elderly | Marzetti, E. | |
1-gen-2023 | Musculoskeletal manifestations in children with Behçet's syndrome: data from the AIDA Network Behçet's Syndrome Registry | Gaggiano, C; Maselli, A; Sfikakis, Pp; Laskari, K; Ragab, G; Hegazy, Mt; Laymouna, Ah; Lopalco, G; Almaghlouth, Ia; Asfina, Kn; Alahmed, O; Giardini Mayrink, Ha; Parente de Brito Antonelli, I; Cattalini, M; Piga, M; Sota, J; Gentileschi, S; Maggio, Mc; Opris-Belinski, D; Hatemi, G; Insalaco, A; Olivieri, An; Tufan, A; Karadeniz, H; Kardaş, Rc; La Torre, F; Cardinale, F; Marino, A; Guerriero, S; Ruscitti, P; Tarsia, M; Vitale, A; Caggiano, V; Telesca, S; Iannone, F; Parretti, V; Frassi, M; Aragona, E; Ciccia, F; Wiesik-Szewczyk, E; Ionescu, R; Şahin, A; Akkoç, N; Hinojosa-Azaola, A; Tharwat, S; Hernández-Rodríguez, J; Espinosa, G; Conti, G; Del Giudice, E; Govoni, M; Emmi, G; Fabiani, C; Balistreri, A; Frediani, B; Rigante, Donato; Cantarini, L | |
1-gen-2021 | Musculoskeletal manifestations of childhood cancer and differential diagnosis with juvenile idiopathic arthritis (ONCOREUM): a multicentre, cross-sectional study | Civino, A; Alighieri, G; Prete, E; Caroleo, Am; Magni-Manzoni, S; Vinti, L; Romano, M; Santoro, N; Filocamo, G; Belotti, T; Santarelli, F; Gorio, C; Ricci, F; Colombini, A; Pastore, S; Cesaro, S; Barone, P; Verzegnassi, F; Olivieri, An; Ficara, M; Miniaci, A; Russo, G; Gallizzi, R; Pericoli, R; Breda, L; Mura, R; Podda, R; Onofrillo, D; Lattanzi, B; Tirtei, E; Maggio, Mc; De Santis, R; Consolini, R; Arlotta, A; La Torre, F; Messina, C; Pelagatti, Ma; Coassin, E; Capolsini, I; Burnelli, R; Tornesello, A; Soscia, F; De Fanti, A; Rigante, Donato; Pizzato, C; De Fusco, C; Abate, Me; Roncadori, A; Rossi, E; Stabile, G; Biondi, A; Lepore, L; Conter, V; Rondelli, R; Pession, A; Ravelli, A | |
1-gen-2017 | Musculoskeletal symptoms at the onset of pediatric tumors and predictive features in the differential diagnosis with juvenile idiopatic arthritis: preliminary analysis of a multicenter, prospective, observational study | Civino, A; Alighieri, G; Davì, S; Rondelli, R; Martino, S; Filocamo, G; Magnolato, A; Ricci, F; Gallizzi, R; Olivieri, A; Gerloni, V; Lattanzi, B; Soscia, F; De Fanti, A; Magni Manzoni, S; Citiso, S; Quartulli, L; La Torre, F; Rigante, Donato; Maggio, Mc; Marsili, M; Pelagatti, Ma; Conter, V; Fagioli, F; Lepore, L; Pession, A; Ravelli, A. | |
1-gen-2019 | Musculoskeletal ultrasound in systemic lupus erythematosus: Systematic literature review by the lupus task force of the OMERACT ultrasound working group | Wong, P. C.; Lee, G.; Delle Sedie, A.; Hanova, P.; Inanc, N.; Jousse-Joulin, S.; Ohrndorf, S.; Stoenoiu, M. S.; Keen, H. I.; Terslev, L.; D'Agostino, Maria Antonietta; Bruyn, G. A. | |
1-gen-2005 | Musculoskeletal ultrasound including definitions for ultrasonographic pathology | Wakefield, Richard J; Balint, Peter V; Szkudlarek, Marcin; Filippucci, Emilio; Backhaus, Marina; D'Agostino, Maria-Antonietta; Sanchez, Esperanza Naredo; Iagnocco, Annamaria; Schmidt, Wolfgang A; Bruyn, George A W; Bruyn, George; Kane, David; O'Connor, Philip J; Manger, Bernhard; Joshua, Fred; Koski, Juhani; Grassi, Walter; Lassere, Marissa N D; Swen, Nanno; Kainberger, Franz; Klauser, Andrea; Ostergaard, Mikkel; Brown, Andrew K; Machold, Klaus P; Conaghan, Philip G | |
1-gen-2021 | Musculo‑skeletal phenotype of Costello syndrome and cardio‑facio‑cutaneous syndrome: insights on the functional assessment status. | Leoni, Chiara; Romeo, Domenico Marco; Pelliccioni, M; Di Già, M; Onesimo, R; Giorgio, Valentina; Flex, E; Tedesco, Marta; Tartaglia, M; Rigante, Donato; Valassina, A; Zampino, Giuseppe | |
1-gen-2007 | Music exposure differentially alters the levels of brain-derived neurotrophic factor and nerve growth factor in the mouse hypothalamus. | Angelucci, Francesco; Ricci, Enzo; Padua, Luca; Sabino, Andrea; Tonali, Pietro Attilio | |
1-gen-2015 | Music identification skills of children with specific language impairment | Mari, G; Scorpecci, Alessandro; Reali, L; D'Alatri, Lucia | |
1-gen-2015 | Musical training software for children with cochlear implants | Di Nardo, W; Schinaia, L; Anzivino, R; De Corso, E; Ciacciarelli, A; Paludetti, G | |
1-gen-2015 | Musical training software for children with cochlear implants [Software di training musicale per bambini con impianto cocleare] | Di Nardo, Walter; Schinaia, Lorenzo; Anzivino, Roberta; De Corso, Eugenio; Ciacciarelli, A; Paludetti, Gaetano | |
1-gen-2015 | MuSK autoantibodies in myasthenia gravis detected by cell based assay-A multinational study | Evoli Stampanoni-B, Amelia; Tsonis, A; Zisimopoulou, P; Matsigkou, E; Lazaridis, K; Tzartos, J; Zouvelou, Vasiliki; Mantegazza, Renato; Antozzi, Carlo; Deymeer, Feza; Saruhan Direskeneli, G; Durmus, H; Brenner, T; Vaknin, A; Behin, A; Berrih Aknin, S; Sharshar, T; De Baets, Mark; Martinez Martinez, P; Losen, Mario; Zamba Papanicolaou, E; Kleopa, Ka; Kyriakides, T; Kostera Pruszczyk, A; Szczudlik, P; Szyluk, B; Lavrnic, D; Basta, I; Peric, S; Tallaksen, Chantal; Maniaol, A; Casasnovas Pons, C; Pitha, J; Jakubíkova, M; Hanisch, F; Tzartos, Sj; Andreetta, F | |
1-gen-2011 | Mutant human β4 subunit identified in amyotrophic lateral sclerosis patients impairs nicotinic receptor function. | Moriconi, S; Di Angeloantonio, S; Sabatelli, Mario; Grassi, F. | |
1-gen-2002 | Mutation analysis and X-inactivation studies in the galactosidase A gene | Morrone, A; Cavicchi, C; Bardelli, T; Antuzzi, D; Rigante, Donato; Parini, R; Di Rocco, M; Feriozzi, S; Gabrielli, O; Barone, R; Aricò, M; Ricci, Roberta; Zammarchi, E. | |
1-gen-2007 | Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia | Kratz, C P; Niemeyer, C M; Thomas, C; Bauhuber, S; Matejas, V; Bergsträsser, E; Flotho, C; Flores, N J; Haas, O; Hasle, H; van den Heuvel-Eibrink, M M; Kucherlapati, R S; Lang, P; Roberts, A E; Starý, J; Strahm, B; Swanson, K D; Trebo, M; Zecca, M; Neel, B; Locatelli, Franco; Loh, M L; Zenker, M | |
1-gen-2005 | Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth | Cecconi, Maurizio; Forzano, F.; Milani, Daniela; Cavani, S.; Baldo, C.; Selicorni, Angelo; Pantaleoni, C.; Silengo, M.; Ferrero, G. B.; Scarano, Gioacchino; Della Monica, M.; Fischetto, R.; Grammatico, P.; Majore, S.; Zampino, Giuseppe; Memo, Luigi; Cordisco, E. L.; Neri, Giovanni; Pierluigi, M.; Bricarelli, F. D.; Grasso, M.; Faravelli, F. | |
1-gen-2012 | Mutation identification of Fabry disease in families with other lysosomal storage disorders | Zampetti, Anna; Fania, L; Antuzzi, D; Giurdanella, F; Gnarra, M; Bertola, F; Lualdi, S; Filocamo, M; Morrone, A; Feliciani, Claudio | |
1-gen-2009 | MUTATION OF SHOC2 PROMOTES ABERRANT PROTEIN N-MYRISTOYLATION AND CAUSES NOONAN-LIKE SUNDROME WITH LOOSE ANAGEN HAIR. | Cordeddu, V; Di Schiavi, E; Zampino, Giuseppe; Dallapiccola, Bruno; Gelb, Bd; Tartaglia, Marco | |
1-gen-2019 | Mutation profile of BBS genes in patients with Bardet-Biedl syndrome: An Italian study | Manara, E.; Paolacci, S.; D'Esposito, F.; Abeshi, A.; Ziccardi, L.; Falsini, Benedetto; Colombo, L.; Iarossi, G.; Pilotta, A.; Boccone, L.; Guerri, Giulia; Monica, M.; Marta, B.; Maltese, P. E.; Buzzonetti, Luca; Rossetti, Lodovico; Bertelli, M. |
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