| Title : Treatment of myasthenia gravis in france: A retrospective claims database study (STAMINA) - Tard_2024_J.Neurol__ |
| Author(s) : Tard C , Laforet P , de Pouvourville G , Crochard A , Chollet G , Nevoret C , Bouee S , Salort-Campana E |
| Ref : Journal of Neurology , : , 2024 |
| Abstract : |
| PubMedSearch : Tard_2024_J.Neurol__ |
| PubMedID: 39387949 |
| Title : Epidemiology of myasthenia gravis in France: A retrospective claims database study (STAMINA) - Salort-Campana_2023_Rev.Neurol.(Paris)__ |
| Author(s) : Salort-Campana E , Laforet P , de Pouvourville G , Crochard A , Chollet G , Nevoret C , Emery C , Bouee S , Tard C |
| Ref : Rev Neurol (Paris) , : , 2023 |
| Abstract : |
| PubMedSearch : Salort-Campana_2023_Rev.Neurol.(Paris)__ |
| PubMedID: 37945494 |
| Title : PNPLA2 mutation: a paediatric case with early onset but indolent course - Perrin_2013_Neuromuscul.Disord_23_986 |
| Author(s) : Perrin L , Feasson L , Furby A , Laforet P , Petit FM , Gautheron V , Chabrier S |
| Ref : Neuromuscular Disorders , 23 :986 , 2013 |
| Abstract : |
| PubMedSearch : Perrin_2013_Neuromuscul.Disord_23_986 |
| PubMedID: 24074500 |
| Title : [Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy - The French national Congenital Myasthenic Syndrome network experience] - Eymard_2013_Rev.Neurol.(Paris)_169 Suppl 1_S45 |
| Author(s) : Eymard B , Stojkovic T , Sternberg D , Richard P , Nicole S , Fournier E , Behin A , Laforet P , Servais L , Romero N , Fardeau M , Hantai D |
| Ref : Rev Neurol (Paris) , 169 Suppl 1 :S45 , 2013 |
| Abstract : |
| PubMedSearch : Eymard_2013_Rev.Neurol.(Paris)_169 Suppl 1_S45 |
| PubMedID: 23452772 |
| Title : The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy - Fischer_2007_Nat.Genet_39_28 |
| Author(s) : Fischer J , Lefevre C , Morava E , Mussini JM , Laforet P , Negre-Salvayre A , Lathrop M , Salvayre R |
| Ref : Nat Genet , 39 :28 , 2007 |
| Abstract : |
| PubMedSearch : Fischer_2007_Nat.Genet_39_28 |
| PubMedID: 17187067 |