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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 : Salort-Campana_2023_Rev.Neurol.(Paris)__ |
ESTHER : Salort-Campana_2023_Rev.Neurol.(Paris)__ |
PubMedSearch : Salort-Campana_2023_Rev.Neurol.(Paris)__ |
PubMedID: 37945494 |
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 : Eymard_2013_Rev.Neurol.(Paris)_169 Suppl 1_S45 |
ESTHER : Eymard_2013_Rev.Neurol.(Paris)_169 Suppl 1_S45 |
PubMedSearch : Eymard_2013_Rev.Neurol.(Paris)_169 Suppl 1_S45 |
PubMedID: 23452772 |
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 : Perrin_2013_Neuromuscul.Disord_23_986 |
ESTHER : Perrin_2013_Neuromuscul.Disord_23_986 |
PubMedSearch : Perrin_2013_Neuromuscul.Disord_23_986 |
PubMedID: 24074500 |
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 : Fischer_2007_Nat.Genet_39_28 |
ESTHER : Fischer_2007_Nat.Genet_39_28 |
PubMedSearch : Fischer_2007_Nat.Genet_39_28 |
PubMedID: 17187067 |