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Results: 1-8 |
Results: 8
Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus
Authors: Voit, T Kutz, P Leube, B Neuen-Jacob, E Schroder, JM Cavallotti, D Vaccario, ML Schaper, J Broich, P Cohn, R Baethmann, M Gohlich-Ratmann, G Scoppetta, C Herrmann, R
Citation: T. Voit et al., Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus, NEUROMUSC D, 11(1), 2001, pp. 11-19
Sleep-disordered breathing and respiratory failure in acid maltase deficiency
Authors: Mellies, U Ragette, R Schwake, C Baethmann, M Voit, T Teschler, H
Citation: U. Mellies et al., Sleep-disordered breathing and respiratory failure in acid maltase deficiency, NEUROLOGY, 57(7), 2001, pp. 1290-1295
Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries
Authors: 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, RHM 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
Citation: D. Chandler et al., Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries, NEUROMUSC D, 10(8), 2000, pp. 584-591
Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolatereductase deficiency
Authors: Baethmann, M Wendel, U Hoffmann, GF Gohlich-Ratmann, G Kleinlein, B Seiffert, P Blom, H Voit, T
Citation: M. Baethmann et al., Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolatereductase deficiency, NEUROPEDIAT, 31(6), 2000, pp. 314-317
Congenital defects of glucose transport
Authors: Klepper, J Santer, R Baethmann, M De Vivo, DC Voit, T
Citation: J. Klepper et al., Congenital defects of glucose transport, MONATS KIND, 148(1), 2000, pp. 2-11
Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene
Authors: Budde, SMS van den Heuvel, LPWJ Janssen, AJ Smeets, RJP Buskens, CAF DeMeirleir, L Van Coster, R Baethmann, M Voit, T Trijbels, JMF Smeitink, JAM
Citation: Sms. Budde et al., Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene, BIOC BIOP R, 275(1), 2000, pp. 63-68
New knowledge on neurometabolic diseases in childhood
Authors: Baethmann, M Voit, T
Citation: M. Baethmann et T. Voit, New knowledge on neurometabolic diseases in childhood, AKT NEUROL, 26(4), 1999, pp. 152-164
Localization of laminin isoforms in the guinea pig cochlea
Authors: Weinberger, DG ten Cate, WJ Lautermann, J Baethmann, M
Citation: Dg. Weinberger et al., Localization of laminin isoforms in the guinea pig cochlea, LARYNGOSCOP, 109(12), 1999, pp. 2001-2004
Risultati: 1-8 |