Full name : Fardeau Michel
First name : Michel
Mail : Inserm 153, 17 rue du Fer-a-Moulin, 75005 Parts
Zip Code :
City :
Country : France
Email :
Phone : (33) 1 43 36 46 31
Fax : (33) 1 43 37 85 22
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Directory :
| 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 : Peripheral nerve hyperexcitability with preterminal nerve and neuromuscular junction remodeling is a hallmark of Schwartz-Jampel syndrome - Bauche_2013_Neuromuscul.Disord_23_998 |
| Author(s) : Bauche S , Boerio D , Davoine CS , Bernard V , Stum M , Bureau C , Fardeau M , Romero NB , Fontaine B , Koenig J , Hantai D , Gueguen A , Fournier E , Eymard B , Nicole S |
| Ref : Neuromuscular Disorders , 23 :998 , 2013 |
| Abstract : Bauche_2013_Neuromuscul.Disord_23_998 |
| ESTHER : Bauche_2013_Neuromuscul.Disord_23_998 |
| PubMedSearch : Bauche_2013_Neuromuscul.Disord_23_998 |
| PubMedID: 24011702 |
| Title : Identification of an agrin mutation that causes congenital myasthenia and affects synapse function - Huze_2009_Am.J.Hum.Genet_85_155 |
| Author(s) : Huze C , Bauche S , Richard P , Chevessier F , Goillot E , Gaudon K , Ben Ammar A , Chaboud A , Grosjean I , Lecuyer HA , Bernard V , Rouche A , Alexandri N , Kuntzer T , Fardeau M , Fournier E , Brancaccio A , Ruegg MA , Koenig J , Eymard B , Schaeffer L , Hantai D |
| Ref : American Journal of Human Genetics , 85 :155 , 2009 |
| Abstract : Huze_2009_Am.J.Hum.Genet_85_155 |
| ESTHER : Huze_2009_Am.J.Hum.Genet_85_155 |
| PubMedSearch : Huze_2009_Am.J.Hum.Genet_85_155 |
| PubMedID: 19631309 |
| Title : Mutations in MUSK cause congenital myasthenic syndrome - |
| Author(s) : Chevessier F , Faraut B , Ravel-Chapuis A , Richard P , Gaudon K , Bauche S , Prioleau C , Herbst R , Goillot E , Ioos C , Azulay J-P , Attarian S , Leroy J-P , Fournier E , Legay C , Schaeffer L , Koenig J , Fardeau M , Eymard B , Pouget J , Hantai D |
| Ref : Journal de Physiologie (Paris) , 99 :256 , 2006 |
| PubMedID: |
| Title : Expression of matrix metalloproteinases 2 and 9 in regenerating skeletal muscle: a study in experimentally injured and mdx muscles - Kherif_1999_Dev.Biol_205_158 |
| Author(s) : Kherif S , Lafuma C , Dehaupas M , Lachkar S , Fournier JG , Verdiere-Sahuque M , Fardeau M , Alameddine HS |
| Ref : Developmental Biology , 205 :158 , 1999 |
| Abstract : Kherif_1999_Dev.Biol_205_158 |
| ESTHER : Kherif_1999_Dev.Biol_205_158 |
| PubMedSearch : Kherif_1999_Dev.Biol_205_158 |
| PubMedID: 9882504 |
| Title : Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic) - Donger_1998_Am.J.Hum.Genet_63_967 |
| Author(s) : Donger C , Krejci E , Serradell AP , Eymard B , Bon S , Nicole S , Chateau D , Gary F , Fardeau M , Massoulie J , Guicheney P |
| Ref : American Journal of Human Genetics , 63 :967 , 1998 |
| Abstract : Donger_1998_Am.J.Hum.Genet_63_967 |
| ESTHER : Donger_1998_Am.J.Hum.Genet_63_967 |
| PubMedSearch : Donger_1998_Am.J.Hum.Genet_63_967 |
| PubMedID: 9758617 |
| Title : Acrylamide neuropathy and changes in the axonal transport and muscular content of the molecular forms of acetylcholinesterase - Couraud_1982_Muscle.Nerve_5_302 |
| Author(s) : Couraud JY , Di Giamberardino L , Chretien M , Souyri F , Fardeau M |
| Ref : Muscle & Nerve , 5 :302 , 1982 |
| Abstract : Couraud_1982_Muscle.Nerve_5_302 |
| ESTHER : Couraud_1982_Muscle.Nerve_5_302 |
| PubMedSearch : Couraud_1982_Muscle.Nerve_5_302 |
| PubMedID: 6178969 |