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Results: 1-6 |
Results: 6

Authors: Ramaekers, VT Senderek, J Hausler, M Haring, M Abeling, N Zerres, K Bergmann, C Heimann, G Blau, N
Citation: Vt. Ramaekers et al., A novel neurodevelopmental syndrome responsive to 5-hydroxytryptophan and carbidopa, MOL GEN MET, 73(2), 2001, pp. 179-187

Authors: Hausler, MG Jaeken, J Monch, E Ramaekers, VT
Citation: Mg. Hausler et al., Phenotypic heterogeneity and adverse effects of serine treatment in 3-phosphoglycerate dehydrogenase deficiency: Report on two siblings, NEUROPEDIAT, 32(4), 2001, pp. 191-195

Authors: Senderek, J Ramaekers, VT Zerres, K Rudnik-Schoneborn, S Schroder, JM Bergmann, C
Citation: J. Senderek et al., Phenotypic variation of a novel nonsense mutation in the P0 intracellular domain, J NEUR SCI, 192(1-2), 2001, pp. 49-51

Authors: Kolker, S Ramaekers, VT Zschocke, J Hoffmann, GF
Citation: S. Kolker et al., Acute encephalopathy despite early therapy in a patient with homozygosity for E365K in the glutaryl-coenzyme A dehydrogenase gene, J PEDIAT, 138(2), 2001, pp. 277-279

Authors: Muller, HD Mugler, M Ramaekers, VT Schroder, JM
Citation: Hd. Muller et al., Hereditary motor and sensory neuropathy with absence of large myelinated fibers due to absence of large neurons in dorsal root ganglia and anterior horns, clinically associated with deafness, mental retardation, and epilepsy(HMSN-ADM), J PERIPH N, 5(3), 2000, pp. 147-157

Authors: Senderek, J Hermanns, B Bergmann, C Boroojerdi, B Bajbouj, M Hungs, M Ramaekers, VT Quasthoff, S Karch, D Schroder, JM
Citation: J. Senderek et al., X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations, J NEUR SCI, 167(2), 1999, pp. 90-101
Risultati: 1-6 |