Report for Voit T

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References (5)

Title : Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations - Guergueltcheva_2012_J.Neurol_259_838
Author(s) : Guergueltcheva V , Muller JS , Dusl M , Senderek J , Oldfors A , Lindbergh C , Maxwell S , Colomer J , Mallebrera CJ , Nascimento A , Vilchez JJ , Muelas N , Kirschner J , Nafissi S , Kariminejad A , Nilipour Y , Bozorgmehr B , Najmabadi H , Rodolico C , Sieb JP , Schlotter B , Schoser B , Herrmann R , Voit T , Steinlein OK , Najafi A , Urtizberea A , Soler DM , Muntoni F , Hanna MG , Chaouch A , Straub V , Bushby K , Palace J , Beeson D , Abicht A , Lochmuller H
Ref : Journal of Neurology , 259 :838 , 2012
Abstract : Guergueltcheva_2012_J.Neurol_259_838
ESTHER : Guergueltcheva_2012_J.Neurol_259_838
PubMedSearch : Guergueltcheva_2012_J.Neurol_259_838
PubMedID: 21975507

Title : Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease - Hunter_2003_Hum.Mutat_22_129
Author(s) : Hunter M , Bernard R , Freitas E , Boyer A , Morar B , Martins IJ , Tournev I , Jordanova A , Guergelcheva V , Ishpekova B , Kremensky I , Nicholson G , Schlotter B , Lochmuller H , Voit T , Colomer J , Thomas PK , Levy N , Kalaydjieva L
Ref : Hum Mutat , 22 :129 , 2003
Abstract : Hunter_2003_Hum.Mutat_22_129
ESTHER : Hunter_2003_Hum.Mutat_22_129
PubMedSearch : Hunter_2003_Hum.Mutat_22_129
PubMedID: 12872253
Gene_locus related to this paper: human-NDRG1

Title : Hereditary motor and sensory neuropathy--Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries - Chandler_2000_Neuromuscul.Disord_10_584
Author(s) : Chandler D , Angelicheva D , Heather L , Gooding R , Gresham D , Yanakiev P , de Jonge R , Baas F , Dye D , Karagyozov L , Savov A , Blechschmidt K , Keats B , Thomas PK , King RH , Starr A , Nikolova A , Colomer J , Ishpekova B , Tournev I , Urtizberea JA , Merlini L , Butinar D , Chabrol B , Voit T , Baethmann M , Nedkova V , Corches A , Kalaydjieva L
Ref : Neuromuscular Disorders , 10 :584 , 2000
Abstract : Chandler_2000_Neuromuscul.Disord_10_584
ESTHER : Chandler_2000_Neuromuscul.Disord_10_584
PubMedSearch : Chandler_2000_Neuromuscul.Disord_10_584
PubMedID: 11053686

Title : HMSNL in a 13-year-old Bulgarian girl - Baethmann_1998_Neuromuscul.Disord_8_90
Author(s) : Baethmann M , Gohlich-Ratmann G , Schroder JM , Kalaydjieva L , Voit T
Ref : Neuromuscular Disorders , 8 :90 , 1998
Abstract : Baethmann_1998_Neuromuscul.Disord_8_90
ESTHER : Baethmann_1998_Neuromuscul.Disord_8_90
PubMedSearch : Baethmann_1998_Neuromuscul.Disord_8_90
PubMedID: 9608562

Title : Multisystem triglyceride storage disorder without ichthyosis in two siblings - Wessalowski_1994_Acta.Paediatr_83_93
Author(s) : Wessalowski R , Schroten H , Neuen-Jacob E , Reichmann H , Melnik BC , Lenard HG , Voit T
Ref : Acta Paediatr , 83 :93 , 1994
Abstract : Wessalowski_1994_Acta.Paediatr_83_93
ESTHER : Wessalowski_1994_Acta.Paediatr_83_93
PubMedSearch : Wessalowski_1994_Acta.Paediatr_83_93
PubMedID: 8193482