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European Journal of Endocrinology|February 14, 1998
Hyperphagia in children with craniopharyngioma is associated with hyperleptinaemia and a failure in the downregulation of appetiteC Roth, B Wilken, F Hanefeld, et al.Human Genetics|January 1, 1987
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markersE Wilichowski, M Krawczak, E Seemanova, et al.Brain & Development|January 1, 1985
Rett syndrome: criteria for inclusion and exclusionB Hagberg, F Goutières, F Hanefeld, et al.Neuropediatrics|June 21, 2002
Altered methylation pattern of the G6 PD promoter in Rett syndromeP Huppke, S Bohlander, N Krämer, et al.Human Molecular Genetics|May 18, 2000
Rett syndrome: analysis of MECP2 and clinical characterization of 31 patientsP Huppke, F Laccone, N Krämer, et al.Acta Paediatrica (Oslo, Norway : 1992)|January 26, 2002
Endocrinological study on growth retardation in Rett syndromeP Huppke, C Roth, H J Christen, et al.Journal of the Neurological Sciences|July 1, 1977
Oligoclonal gamma-globulin banding of cerebrospinal fluid in patients with subacute sclerosing panencephalitis. Comparison of the electrophoretic pattern with that in multiple sclerosis and congenital infectionsH Siemes, M Siegert, F Hanefeld, et al.American Journal of Human Genetics|May 1, 1996
Guanidinoacetate methyltransferase deficiency: the first inborn error of creatine metabolism in manS Stöckler, D Isbrandt, F Hanefeld, et al.Acta Paediatrica Scandinavica|December 1, 1990
Peripheral facial palsy in childhood--Lyme borreliosis to be suspected unless proven otherwiseH J Christen, N Bartlau, F Hanefeld, et al.Annals of Neurology|October 17, 2001
Myelinopathia centralis diffusa (vanishing white matter disease): evidence of apoptotic oligodendrocyte degeneration in early lesion developmentW Brück, J Herms, K Brockmann, et al.Pageof 16