Hanefeld, Folker

Creatine deficiency in the brain: A new, treatable inborn error of metabolism

Stöckler, S., Holzbach, U., Hanefeld, F., Marquardt, I., Helms, G., Requart, M., Hänicke, W., & Frahm, J. (1994) · Pediatric Research

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 417

Creatine replacement therapy in guanidineoacetate methyltransferase deficiency, a novel inborn error of metabolism

Stöckler, S., Hanefeld, F., & Frahm, J. (1996) · The Lancet

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 240

Virchow-Robin spaces on magnetic resonance images: normative data, their dilatation, and a review of the literature

Groeschel, S., Chong, W. K., Surtees, R., & Hanefeld, F. (2006) · Neuroradiology

Cerebrospinal fluid and hydrocephalusAdvanced MRI Techniques and Applications

Cited by 230

Increase of total creatine in human brain after oral supplementation of creatine-monohydrate

Dechent, P., Pouwels, P. J. W., Wilken, B., Hanefeld, F., & Frahm, J. (1999) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology

Muscle metabolism and nutritionAdvanced MRI Techniques and Applications

Cited by 221

Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotype

Korenke, G. C., Wilichowski, E., Hunneman, D. H., Hanefeld, F., Fuchs, S., Krasemann, E., & Doerr, H. G. (1996) · Annals of Neurology

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 117

Succinate in dystrophic white matter: a proton magnetic resonance spectroscopy finding characteristic for complex II deficiency

Brockmann, K., Bjornstad, A., Dechent, P., Korenke, C. G., Smeitink, J., Trijbels, J. M. F., Athanassopoulos, S., Villagran, R., Skjeldal, O. H., Wilichowski, E., et al. (2002) · Annals of Neurology

Metabolism and Genetic DisordersMitochondrial Function and Pathology

Cited by 81

Haematopoietic stem cell transplantation in 12 patients with cerebral X-linked adrenoleukodystrophy

Baumann, M., Korenke, C., Weddige-Diedrichs, A., Wilichowski, E., Hunneman, D., Wilken, B., Brockmann, K., Klingebiel, T., Niethammer, D., Kühl, J., et al. (2003) · European Journal of Pediatrics

Lysosomal Storage Disorders ResearchMetabolism and Genetic Disorders

Cited by 47

Arrested cerebral adrenoleukodystrophy: A clinical and proton magnetic resonance spectroscopy study in three patients

Korenke, G. C., Pouwels, P. J. W., Frahm, J., Hunneman, D. H., Stoeckler, S., Krasemann, E., Jost, W., & Hanefeld, F. (1996) · Pediatric Neurology

Metabolism and Genetic DisordersNeurological diseases and metabolism

Cited by 39

Variability of endocrinological dysfunction in 55 patients with X-linked adrenoleucodystrophy: clinical, laboratory and genetic findings

Korenke, G., Roth, C., Krasemann, E., Hufner, M., Hunneman, D., & Hanefeld, F. (1997) · European Journal of Endocrinology

Metabolism and Genetic DisordersAdrenal Hormones and Disorders

Cited by 38

Cerebral proton magnetic resonance spectroscopy in Rett syndrome

Hanefeld, F., Christen, H.-J., Holzbach, U., Kruse, B., Frahm, J., & Hänicke, W. (1995) · Neuropediatrics

Genetics and Neurodevelopmental DisordersAdvanced MRI Techniques and Applications

Cited by 24