MONGINI, Tiziana Enrica

MONGINI, Tiziana Enrica  

NEUROSCIENZE "RITA LEVI MONTALCINI"  

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208th ENMC International Workshop: Formation of a European Network to develop a European data sharing model and treatment guidelines for Pompe disease Naarden, The Netherlands, 26-28 September 2014 2015 Schoser, Benedikt; Laforêt, Pascal; Kruijshaar, Michelle E.; Toscano, Antonio; van Doorn, Pieter A.; van der Ploeg, Ans T.; Angelini, Corrado; van der Beek, Nadine A.M.E.; Van den Bergh, Peter; Broomfield, Alexander; Desnuelle, Claude; Hahn, Andreas; Lachmann, Robin; Mengel, Eugen; Mongini, Tiziana; Müller-Felber, Wolfgang; Padberg, George; Parenti, Giancarlo; Pascual, Ignacio Pascual; Pijnappel, W.W.M. Pim; Roberts, Mark; Talim, Beril; Treur, Wilma; Vissing, John
A 5-year clinical follow-up study from the Italian National Registry for FSHD 2021 Vercelli L.; Mele F.; Ruggiero L.; Sera F.; Tripodi S.; Ricci G.; Vallarola A.; Villa L.; Govi M.; Maranda L.; Di Muzio A.; Scarlato M.; Bucci E.; Maggi L.; Rodolico C.; Moggio M.; Filosto M.; Antonini G.; Previtali S.; Angelini C.; Berardinelli A.; Pegoraro E.; Siciliano G.; Tomelleri G.; Santoro L.; Mongini T.; Tupler R.
The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boys 2014 Pane, Marika; Mazzone, Elena Stacy; Sivo, Serena; Fanelli, Lavinia; De Sanctis, Roberto; D'Amico, Adele; Messina, Sonia; Battini, Roberta; Bianco, Flaviana; Scutifero, Marianna; Petillo, Roberta; Frosini, Silvia; Scalise, Roberta; Vita, Gian Luca; Bruno, Claudio; Pedemonte, Marina; Mongini, Tiziana; Pegoraro, Elena; Brustia, Francesca; Gardani, Alice; Berardinelli, Angela; Lanzillotta, Valentina; Viggiano, Emanuela; Cavallaro, Filippo; Sframeli, Maria; Bello, Luca; Barp, Andrea; Busato, Fabio; Bonfiglio, Serena; Rolle, Enrica; Colia, Giulia; Bonetti, Annamaria; Palermo, Concetta; Graziano, Alessandra; D'Angelo, Grazia; Pini, Antonella; Corlatti, Alice; Gorni, Ksenija; Baranello, Giovanni; Antonaci, Laura; Bertini, Enrico; Politano, Luisa; Mercuri, Eugenio
6 minute walk test in Duchenne MD patients with different mutations: 12 month changes. 2014 Pane M;Mazzone ES;Sormani MP;Messina S;Vita GL;Fanelli L;Berardinelli A;Torrente Y;D'Amico A;Lanzillotta V;Viggiano E;D'Ambrosio P;Cavallaro F;Frosini S;Bello L;Bonfiglio S;Scalise R;De Sanctis R;Rolle E;Bianco F;Van der Haawue M;Magri F;Palermo C;Rossi F;Donati MA;Alfonsi C;Sacchini M;Arnoldi MT;Baranello G;Mongini T;Pini A;Battini R;Pegoraro E;Previtali SC;Napolitano S;Bruno C;Politano L;Comi GP;Bertini E;Morandi L;Gualandi F;Ferlini A;Goemans N;Mercuri E
A case of to treatment with piridostigmine bromide: a new phenotype? 2011 L. Vercelli; S. Benedetti; E. Vittonatto ; L. Chiadò-Piat; E. Pilati; T. Mongini.
A new method for myofibrillar Ca++-ATPase reaction based on the use of metachromatic dyes: its advantages in muscle fibre typing. 1983 DORIGUZZI C ;MONGINI T ;PALMUCCI L ;SCHIFFER D
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency 2000 SILVESTRI G; MONGINI T; ODOARDI F; MODONI A; DEROSA G; DORIGUZZI C; L. PALMUCCI; TONALI P; SERVIDEI S
A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) gene 2000 PIRULLI D; ZEZLINA S; VATTA L; DI STEFANO P; BONIOTTO M; G. TARONE; MONGINI T; UGO I; PALMUCCI L; AMOROSO A; CROVELLA S
A peculiar case of LGMD with rimmed vacuoles 2016 Ponzalino V., Vercelli L., Chiadò-Piat L., Vittonatto E., Boschi S., Bortolani S., Xu L., Lek M., Johnson K., Topf A., MacArthur D., Straub V., Mongini T.
A young boy with a new mutation in lamin A/C gene responsive to treatment with ACHE inhibitors 2011 Vercelli, L; Benedetti, S; Vittonatto, E; Chiado'-Piat, L; Pilati, E; Pinessi, L; Mongini, T
Absence of dystrophin in two patients with Becker type Xp21 muscular dystrophy. 1992 MONGINI T ;PALMUCCI L ;DORIGUZZI C ;CHIADOÒ-PIAT L ;RESTAGNO G
Acute neuromuscular failure related to long-term botulinum toxin therapy. 2004 Coletti Moja M;Dimanico U;Mongini T;Cavaciocchi V;Gerbino Promis PC;Grasso E
Adapted physical activity and therapeutic exercise in late-onset Pompe disease (LOPD): a two-step rehabilitative approach 2020 Iolascon G.; Vitacca M.; Carraro E.; Chisari C.; Fiore P.; Messina S.; Mongini T.; Moretti A.; Sansone V.A.; Toscano A.; Siciliano G.
Adult onset nemaline myopathy: a distinct nosologic entity? 1993 PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L
Adult-onset mitochondrial movement disorders: a national picture from the Italian Network 2022 Montano V.; Orsucci D.; Carelli V.; La Morgia C.; Valentino M.L.; Lamperti C.; Marchet S.; Musumeci O.; Toscano A.; Primiano G.; Santorelli F.M.; Ticci C.; Filosto M.; Rubegni A.; Mongini T.; Tonin P.; Servidei S.; Ceravolo R.; Siciliano G.; Mancuso M.
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria. 2002 MONGINI T; DORIGUZZI C; BOSONE I; CHIADÒ-PIAT L; HOFFMAN EP; L. PALMUCCI
Analysis of CHCHD2 and CHCHD10 genes in patients with Parkinson’s disease and mitochondrial myopathy. 2017 E. Rubino; S. Boschi; M. Zhang; L. Brusa; F. Govone; A. Vacca; A. Gai; L. Lopiano; E. Rogaeva; T. Mongini; M. Giordana; I. Rainero;
Analysis of dystrophin expression after activation of myogenesis in amniocytes, chorionic-villus cells, and fibroblasts. A new method for diagnosing Duchenne's muscular dystrophy. 1993 Sancho S; Mongini T; Tanji K;Tapscott SJ; Walker WF; Weintraub H; Miller AD; Miranda AF
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel 2018 Altamura C.; Lucchiari S.; Sahbani D.; Ulzi G.; Comi G.P.; D'Ambrosio P.; Petillo R.; Politano L.; Vercelli L.; Mongini T.; Dotti M.T.; Cardani R.; Meola G.; Lo Monaco M.; Matthews E.; Hanna M.G.; Carratu M.R.; Conte D.; Imbrici P.; Desaphy J.-F.
Approccio clinico e riabilitativo alle miopatie 2008 T Mongini; L Palmucci; C Doriguzzi