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European Journal of Endocrinology|July 1, 1997
Variability of endocrinological dysfunction in 55 patients with X-linked adrenoleucodystrophy: clinical, laboratory and genetic findingsG C Korenke, C Roth, E Krasemann, et al.Neuropediatrics|October 9, 2002
Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patientsM Meins, K Brockmann, S Yadav, et al.Developmental Medicine and Child Neurology|March 4, 2000
Foix-Chavany-Marie (anterior operculum) syndrome in childhood: a reappraisal of Worster-Drought syndromeH J Christen, F Hanefeld, E Kruse, et al.American Journal of Human Genetics|April 20, 2001
MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal originR Trappe, F Laccone, J Cobilanschi, et al.European Journal of Pediatrics|January 1, 1995
Glyceroltrioleate/glyceroltrierucate therapy in 16 patients with X-chromosomal adrenoleukodystrophy/adrenomyeloneuropathy: effect on clinical, biochemical and neurophysiological parametersG C Korenke, D H Hunneman, J Kohler, et al.Medical and Pediatric Oncology|January 1, 1980
Changes of CSF-protein pattern in children with acute lymphoblastic leukemia during prophylactic CNS therapy (Berlin protocol)H Siemes, D Rating, M Siegert, et al.Journal of Neurology|December 1, 1993
Alterations of brain metabolites in metachromatic leukodystrophy as detected by localized proton magnetic resonance spectroscopy in vivoB Kruse, F Hanefeld, H J Christen, et al.Neuropediatrics|April 1, 1994
Giant axonal neuropathy: a generalized disorder of intermediate filaments with longitudinal grooves in the hairS Treiber-Held, H Budjarjo-Welim, D Reimann, et al.Pediatric Research|October 6, 1999
Regional age dependence of human brain metabolites from infancy to adulthood as detected by quantitative localized proton MRSP J Pouwels, K Brockmann, B Kruse, et al.Annals of Neurology|November 1, 1995
Monocyte/macrophage differentiation in early multiple sclerosis lesionsW Brück, P Porada, S Poser, et al.Pageof 15