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Results: 1-6 |
Results: 6

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: Bruck, W Herms, J Brockmann, K Schulz-Schaeffer, W Hanefeld, F
Citation: W. Bruck et al., Myelinopathia centralis diffusa (vanishing white matter disease): Evidenceof apoptotic oligodendrocyte degeneration in early lesion development, ANN NEUROL, 50(4), 2001, pp. 532-536

Authors: Brockmann, K Hanefeld, F
Citation: K. Brockmann et F. Hanefeld, Progressive elevation of liver enzymes in a child treated with sulthiame, NEUROPEDIAT, 32(3), 2001, pp. 165-166

Authors: Pouwels, PJW Brockmann, K Kruse, B Wilken, B Wick, M Hanefeld, F Frahm, J
Citation: Pjw. Pouwels et al., Regional age dependence of human brain metabolites from infancy to adulthood as detected by quantitative localized proton MRS, PEDIAT RES, 46(4), 1999, pp. 474-485

Authors: Schutt, WA Muradali, F Mondol, N Joseph, K Brockmann, K
Citation: Wa. Schutt et al., Behavior and maintenance of captive white-winged vampire bats, Diaemus youngi, J MAMMAL, 80(1), 1999, pp. 71-81

Authors: Mursch, K Brockmann, K Lang, JK Markakis, E Behnke-Mursch, J
Citation: K. Mursch et al., Visually evoked potentials in 52 children requiring operative repair of craniosynostosis, PED NEUROS, 29(6), 1998, pp. 320-323
Risultati: 1-6 |