Showing 1 - 8 results of 8 for search 'Guergueltcheva V', query time: 0.06s
Refine Results
-
1
Association Between Loss of Dp140 and Cognitive Impairment in Duchenne and Becker Dystrophies by Chamova T, Guergueltcheva V, Raycheva M, Todorov T, Genova J, Bichev S, Bojinova V, Mitev V, Tournev I, Todorova A
Published 2013-06-01
Article -
2
Molecular Diagnostics of Duchenne/Becker Muscular Dystrophy Patients by Multiplex Ligation-Dependent Probe Amplification Analysis and Direct Sequencing by Todorova A, Guergueltcheva V, Genova J, Mihaylova V, Todorov T, Tchamova T, Georgieva B, Kremensky I, Tournev I, Mitev V
Published 2009-01-01
Article -
3
Pyridostigmine-responsive limb-girdle congenital myasthenic syndrome with frequent tubular aggregates by Mueller, J, Senderek, J, Dusl, M, Guergueltcheva, V, Laval, S, Bushby, K, Straub, V, Beeson, D, Abicht, A, Lochmueller, H
Published 2011Conference item -
4
THE CLINICAL PHENOTYPIC SPECTRUM OF GFPT1 ASSOCIATED CONGENITAL MYASTHENIC SYNDROME by Chaouch, A, Mueller, J, Guergueltcheva, V, Muntoni, F, Bushby, K, Straub, V, Palace, J, Beeson, D, Abicht, A, Lochmuller, H
Published 2012Conference item -
5
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect. by Senderek, J, Müller, J, Dusl, M, Strom, T, Guergueltcheva, V, Diepolder, I, Laval, S, Maxwell, S, Cossins, J, Krause, S, Muelas, N, Vilchez, J, Colomer, J, Mallebrera, C, Nascimento, A, Nafissi, S, Kariminejad, A, Nilipour, Y, Bozorgmehr, B, Najmabadi, H, Rodolico, C, Sieb, J, Steinlein, O, Schlotter, B, Schoser, B
Published 2011Journal article -
6
Mutation history of the roma/gypsies. by Morar, B, Gresham, D, Angelicheva, D, Tournev, I, Gooding, R, Guergueltcheva, V, Schmidt, C, Abicht, A, Lochmuller, H, Tordai, A, Kalmar, L, Nagy, M, Karcagi, V, Jeanpierre, M, Herczegfalvi, A, Beeson, D, Venkataraman, V, Warwick Carter, K, Reeve, J, de Pablo, R, Kucinskas, V, Kalaydjieva, L
Published 2004Journal article -
7
Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations. by Guergueltcheva, V, Müller, J, Dusl, M, Senderek, J, Oldfors, A, Lindbergh, C, Maxwell, S, Colomer, J, Mallebrera, C, Nascimento, A, Vilchez, J, Muelas, N, Kirschner, J, Nafissi, S, Kariminejad, A, Nilipour, Y, Bozorgmehr, B, Najmabadi, H, Rodolico, C, Sieb, J, Schlotter, B, Schoser, B, Herrmann, R, Voit, T, Steinlein, O
Published 2011Journal article -
8
Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations by Guergueltcheva, V, Müller, J, Dusl, M, Senderek, J, Oldfors, A, Lindbergh, C, Maxwell, S, Colomer, J, Mallebrera, C, Nascimento, A, Vilchez, J, Muelas, N, Kirschner, J, Nafissi, S, Kariminejad, A, Nilipour, Y, Bozorgmehr, B, Najmabadi, H, Rodolico, C, Sieb, J, Schlotter, B, Schoser, B, Herrmann, R, Voit, T, Steinlein, O
Published 2011Journal article