AAAAAA
Results: 26-31/31
Authors:
Timmerman, V
De Jonghe, P
Ceuterick, C
De Vriendt, E
Lofgren, A
Nelis, E
Warner, LE
Lupski, JR
Martin, JJ
Van Broeckhoven, C
Citation: V. Timmerman et al., Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotype, NEUROLOGY, 52(9), 1999, pp. 1827-1832
Authors:
Stogbauer, F
Young, P
Kuhlenbaumer, G
Kiefer, R
Timmerman, V
Ringelstein, EB
Wang, JF
Schroder, JM
Van Broeckhoven, C
Weis, J
Citation: F. Stogbauer et al., Autosomal dominant burning feet syndrome, J NE NE PSY, 67(1), 1999, pp. 78-81
Authors:
Bahr, M
Andres, F
Timmerman, V
Nelis, ME
Van Broeckhoven, C
Dichgans, J
Citation: M. Bahr et al., Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin32 gene, J NE NE PSY, 66(2), 1999, pp. 202-206
Authors:
De Jonghe, P
Timmerman, V
Ceuterick, C
Nelis, E
De Vriendt, E
Lofgren, A
Vercruyssen, A
Verellen, C
Van Maldergem, L
Martin, JJ
Van Broeckhoven, C
Citation: P. De Jonghe et al., The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene isassociated with a clinically distinct Charcot-Marie-Tooth phenotype, BRAIN, 122, 1999, pp. 281-290
Authors:
De Jonghe, P
Timmerman, V
Nelis, E
De Vriendt, E
Lofgren, A
Ceuterick, C
Martin, JJ
Van Broeckhoven, C
Citation: P. De Jonghe et al., A novel type of hereditary motor and sensory neuropathy characterized by amild phenotype, ARCH NEUROL, 56(10), 1999, pp. 1283-1288
Authors:
Kuhlenbaeumer, G
Meuleman, J
Schirmacher, A
Stoegbauer, F
Ringelstein, EB
Wehnert, M
Hoeltzenbein, M
Van Broeckhoven, C
Timmerman, V
Citation: G. Kuhlenbaeumer et al., Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicingfactor gene and the c-myb ET-locus in two families with hereditary neuralgic amyotrophy (HNA), ANN HUM GEN, 62, 1998, pp. 397-400