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| Title : MuSK-Associated Myasthenia Gravis: Clinical Features and Management - Rodolico_2020_Front.Neurol_11_660 |
| Author(s) : Rodolico C , Bonanno C , Toscano A , Vita G |
| Ref : Front Neurol , 11 :660 , 2020 |
| Abstract : Rodolico_2020_Front.Neurol_11_660 |
| ESTHER : Rodolico_2020_Front.Neurol_11_660 |
| PubMedSearch : Rodolico_2020_Front.Neurol_11_660 |
| PubMedID: 32793097 |
| Title : Severe congenital myasthenic syndrome associated with novel biallelic mutation of the CHRND gene - Bonanno_2020_Neuromuscul.Disord__ |
| Author(s) : Bonanno C , Rodolico C , Topf A , Foti FM , Liu WW , Beeson D , Toscano A , Lochmuller H |
| Ref : Neuromuscular Disorders , : , 2020 |
| Abstract : Bonanno_2020_Neuromuscul.Disord__ |
| ESTHER : Bonanno_2020_Neuromuscul.Disord__ |
| PubMedSearch : Bonanno_2020_Neuromuscul.Disord__ |
| PubMedID: 32360402 |
| Title : Italian recommendations for the diagnosis and treatment of myasthenia gravis - Evoli_2019_Neurol.Sci_40_1111 |
| Author(s) : Evoli A , Antonini G , Antozzi C , DiMuzio A , Habetswallner F , Iani C , Inghilleri M , Liguori R , Mantegazza R , Massa R , Pegoraro E , Ricciardi R , Rodolico C |
| Ref : Neurol Sci , 40 :1111 , 2019 |
| Abstract : Evoli_2019_Neurol.Sci_40_1111 |
| ESTHER : Evoli_2019_Neurol.Sci_40_1111 |
| PubMedSearch : Evoli_2019_Neurol.Sci_40_1111 |
| PubMedID: 30778878 |
| Title : Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations - Guergueltcheva_2012_J.Neurol_259_838 |
| Author(s) : Guergueltcheva V , Muller JS , Dusl M , Senderek J , Oldfors A , Lindbergh C , Maxwell S , Colomer J , Mallebrera CJ , Nascimento A , Vilchez JJ , Muelas N , Kirschner J , Nafissi S , Kariminejad A , Nilipour Y , Bozorgmehr B , Najmabadi H , Rodolico C , Sieb JP , Schlotter B , Schoser B , Herrmann R , Voit T , Steinlein OK , Najafi A , Urtizberea A , Soler DM , Muntoni F , Hanna MG , Chaouch A , Straub V , Bushby K , Palace J , Beeson D , Abicht A , Lochmuller H |
| Ref : Journal of Neurology , 259 :838 , 2012 |
| Abstract : Guergueltcheva_2012_J.Neurol_259_838 |
| ESTHER : Guergueltcheva_2012_J.Neurol_259_838 |
| PubMedSearch : Guergueltcheva_2012_J.Neurol_259_838 |
| PubMedID: 21975507 |
| Title : Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations - Schara_2010_Eur.J.Paediatr.Neurol_14_326 |
| Author(s) : Schara U , Christen HJ , Durmus H , Hietala M , Krabetz K , Rodolico C , Schreiber G , Topaloglu H , Talim B , Voss W , Pihko H , Abicht A , Muller JS , Lochmuller H |
| Ref : Eur J Paediatr Neurol , 14 :326 , 2010 |
| Abstract : Schara_2010_Eur.J.Paediatr.Neurol_14_326 |
| ESTHER : Schara_2010_Eur.J.Paediatr.Neurol_14_326 |
| PubMedSearch : Schara_2010_Eur.J.Paediatr.Neurol_14_326 |
| PubMedID: 19900826 |
| Title : Limb-girdle myasthenia: clinical, electrophysiological and morphological features in familial and autoimmune cases - Rodolico_2002_Neuromuscul.Disord_12_964 |
| Author(s) : Rodolico C , Toscano A , Autunno M , Messina S , Nicolosi C , Aguennouz M , Laura M , Girlanda P , Messina C , Vita G |
| Ref : Neuromuscular Disorders , 12 :964 , 2002 |
| Abstract : Rodolico_2002_Neuromuscul.Disord_12_964 |
| ESTHER : Rodolico_2002_Neuromuscul.Disord_12_964 |
| PubMedSearch : Rodolico_2002_Neuromuscul.Disord_12_964 |
| PubMedID: 12467753 |