Kuntzer T

References (5)

Title : Acetylcholinesterase inhibitor treatment for myasthenia gravis - Mehndiratta_2014_Cochrane.Database.Syst.Rev_10_CD006986
Author(s) : Mehndiratta MM , Pandey S , Kuntzer T
Ref : Cochrane Database Syst Rev , 10 :CD006986 , 2014
Abstract :
PubMedSearch : Mehndiratta_2014_Cochrane.Database.Syst.Rev_10_CD006986
PubMedID: 25310725

Title : Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations - Wargon_2012_Neuromuscul.Disord_22_318
Author(s) : Wargon I , Richard P , Kuntzer T , Sternberg D , Nafissi S , Gaudon K , Lebail A , Bauche S , Hantai D , Fournier E , Eymard B , Stojkovic T
Ref : Neuromuscular Disorders , 22 :318 , 2012
Abstract :
PubMedSearch : Wargon_2012_Neuromuscul.Disord_22_318
PubMedID: 22088788

Title : Acetylcholinesterase inhibitor treatment for myasthenia gravis - Mehndiratta_2011_Cochrane.Database.Syst.Rev__CD006986
Author(s) : Mehndiratta MM , Pandey S , Kuntzer T
Ref : Cochrane Database Syst Rev , :CD006986 , 2011
Abstract :
PubMedSearch : Mehndiratta_2011_Cochrane.Database.Syst.Rev__CD006986
PubMedID: 21328290

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 :
PubMedSearch : Huze_2009_Am.J.Hum.Genet_85_155
PubMedID: 19631309

Title : [Myasthenia-like syndromes: current and future treatments]. [French] - Kuntzer_1995_Schweiz.Rundsch.Med.Prax_84_1042
Author(s) : Kuntzer T , Pedrazzi P
Ref : Schweiz Rundsch Med Prax , 84 :1042 , 1995
Abstract :
PubMedSearch : Kuntzer_1995_Schweiz.Rundsch.Med.Prax_84_1042
PubMedID: 7481303