Authors: Brockmann, K Wang, D Korenke, CG von Moers, A Ho, YY Pascual, JM Kuang, K Yang, H Ma, L Kranz-Eble, P Fischbarg, J Hanefeld, F De Vivo, DC

Citation: K. Brockmann et al., Autosomal dominant Glut-1 deficiency syndrome and familial epilepsy, ANN NEUROL, 50(4), 2001, pp. 476-485

Authors: Netchine, I Sobrier, ML Krude, H Schnabel, D Maghnie, M Marcos, E Duriez, B Cacheux, V von Moers, A Goossens, M Gruters, A Amselem, S

Citation: I. Netchine et al., Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency, NAT GENET, 25(2), 2000, pp. 182-186

Authors: Kerst, B Mennerich, D Schuelke, M Stoltenburg-Didinger, G von Moers, A Gossrau, R van Landeghem, FKH Speer, A Braun, T Hubner, C

Citation: B. Kerst et al., Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Backer muscular dystrophy, NEUROMUSC D, 10(8), 2000, pp. 572-577

Authors: Endesfelder, S Krahn, A Kreuzer, KA Lass, U Schmidt, CA Jahrmarkt, C von Moers, A Speer, A

Citation: S. Endesfelder et al., Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per se, J MOL MED-J, 78(10), 2000, pp. 569-574

Authors: Pfeiffer, E von Moers, A

Citation: E. Pfeiffer et A. Von Moers, Camptocormia in an adolescent, J AM A CHIL, 39(8), 2000, pp. 944-945

Authors: Schuelke, M Finckh, B Sistermans, EA Ausems, MGEM Hubner, C von Moers, A

Citation: M. Schuelke et al., Ataxia with vitamin E deficiency: Biochemical effects of malcompliance with vitamin E therapy, NEUROLOGY, 55(10), 2000, pp. 1584-1586