| Title : The European LEMS Registry: Baseline Demographics and Treatment Approaches - Mantegazza_2015_Neurol.Ther_4_105 |
| Author(s) : Mantegazza R , Meisel A , Sieb JP , Le Masson G , Desnuelle C , Essing M |
| Ref : Neurol Ther , 4 :105 , 2015 |
| Abstract : |
| PubMedSearch : Mantegazza_2015_Neurol.Ther_4_105 |
| PubMedID: 26525537 |
| Title : The European LEMS Registry: Baseline Demographics and Treatment Approaches - Mantegazza_2015_Neurol.Ther_4_105 |
| Author(s) : Mantegazza R , Meisel A , Sieb JP , Le Masson G , Desnuelle C , Essing M |
| Ref : Neurol Ther , 4 :105 , 2015 |
| Abstract : |
| PubMedSearch : Mantegazza_2015_Neurol.Ther_4_105 |
| PubMedID: 26525537 |
| Title : The European LEMS Registry: Baseline Demographics and Treatment Approaches - Mantegazza_2015_Neurol.Ther_4_105 |
| Author(s) : Mantegazza R , Meisel A , Sieb JP , Le Masson G , Desnuelle C , Essing M |
| Ref : Neurol Ther , 4 :105 , 2015 |
| Abstract : |
| PubMedSearch : Mantegazza_2015_Neurol.Ther_4_105 |
| PubMedID: 26525537 |
| Title : The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa - Richard_2008_Neurology_71_1967 |
| Author(s) : Richard P , Gaudon K , Haddad H , Ammar AB , Genin E , Bauche S , Paturneau-Jouas M , Muller JS , Lochmuller H , Grid D , Hamri A , Nouioua S , Tazir M , Mayer M , Desnuelle C , Barois A , Chabrol B , Pouget J , Koenig J , Gouider-Khouja N , Hentati F , Eymard B , Hantai D |
| Ref : Neurology , 71 :1967 , 2008 |
| Abstract : |
| PubMedSearch : Richard_2008_Neurology_71_1967 |
| PubMedID: 19064877 |
| Title : The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa - Richard_2008_Neurology_71_1967 |
| Author(s) : Richard P , Gaudon K , Haddad H , Ammar AB , Genin E , Bauche S , Paturneau-Jouas M , Muller JS , Lochmuller H , Grid D , Hamri A , Nouioua S , Tazir M , Mayer M , Desnuelle C , Barois A , Chabrol B , Pouget J , Koenig J , Gouider-Khouja N , Hentati F , Eymard B , Hantai D |
| Ref : Neurology , 71 :1967 , 2008 |
| Abstract : |
| PubMedSearch : Richard_2008_Neurology_71_1967 |
| PubMedID: 19064877 |
| Title : The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa - Richard_2008_Neurology_71_1967 |
| Author(s) : Richard P , Gaudon K , Haddad H , Ammar AB , Genin E , Bauche S , Paturneau-Jouas M , Muller JS , Lochmuller H , Grid D , Hamri A , Nouioua S , Tazir M , Mayer M , Desnuelle C , Barois A , Chabrol B , Pouget J , Koenig J , Gouider-Khouja N , Hentati F , Eymard B , Hantai D |
| Ref : Neurology , 71 :1967 , 2008 |
| Abstract : |
| PubMedSearch : Richard_2008_Neurology_71_1967 |
| PubMedID: 19064877 |