Brockmann, K., S. Dreha-Kulaczewski, P. Dechent, C. Bonnemann, G. Helms, M. Kyllermann, W. Brueck, J. Frahm, K. Huehne, J. Gaertner and B. Rautenstrauss: Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations.. In: Journal of Neurology 255, 7, 1049-1058, Seq. No.: DOI: 10.1007/s00415-008-0847-1 (2008).
url: http://www.springerlink.com/content/0175p4p845245ql6/fulltext.pdf
Dreha-Kulaczewski, S. F., P. Dechent, J. Finsterbusch, K. Brockmann, J. Gaertner, J. Frahm and V. Hanefeld: Early reduction of total N-acetyl-aspartate-compounds in patients with classical vanishing white matter disease. A long-term follow-up MRS study.. In: Pediatric Research 63, 4, 444-449 (2008).
url: http://www.pedresearch.org/pt/re/pedresearch/pdfhandler.00006450-200804000-00022.pdf;jsessionid=JLhf9lnFTQ1vlMY6JyRJznFvHvPhNzvD70bWnf8Lrh47NwFhnry4!-256325120!181195629!8091!-1
Brockmann, K., P. Dechent, C. Boennemann, G. Schreiber, J. Frahm and F. Hanefeld: Quantitative proton MRS of cerebral metabolites in laminin α2 chain deficiency. In: Brain & Development 29, 6, 357-364 (2007).
url: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6T50-4MK611T-3-7&_cdi=4988&_user=38661&_orig=browse&_coverDate=07%2F31%2F2007&_sk=999709993&view=c&wchp=dGLbVzz-zSkWA&md5=a2b469e4bd4c26d889928d03c53141fa&ie=/sdarticle.pdf
Dreha-Kulaczewski, S., P. Dechent, G. Helms, J. Frahm, J. Gaertner and K. Brockmann: Cerebral metabolic and structural alterations in hereditary spastic paraplegia with thin corpus callosum assessed by MRS and DTI. In: Neuroradiology 48, 12, 893-898 (2006).
url: http://www.springerlink.com/content/e0p6240r188t1276/fulltext.html
Groeschel, S., K. Brockmann, P. Dechent, E. Wilichowski, J. Frahm and F. Hanefeld: Magnetic resonance imaging and proton magnetic resonance spectroscopy of megalencephaly and dilated Virchow-Robin spaces.. In: Pediatric Neurology 34, 1, 35-40 (2006).
url: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6TBD-4HVDR00-8-7&_cdi=5140&_user=38661&_orig=search&_coverDate=01%2F31%2F2006&_sk=999659998&view=c&wchp=dGLbVzz-zSkzV&md5=2e48117bfb9ae2e33462e801f16f4d77&ie=/sdarticle.pdf
Hanefeld, F., K. Brockmann, P. J. W. Pouwels, B. Wilken, J. Frahm and P. Dechent: Quantitative proton MRS of Pelizaeus-Merzbacher disease - Evidence of dys- and hypomyelination. In: Neurology 65, 5, 701-706 (2005).
url: http://www.neurology.org/cgi/reprint/65/5/701
Brockmann, K., J. Finsterbusch, U. Schara, E. Wilichowski, J. Frahm and F. Hanefeld: Stroke-like pattern in DTI and MRS of childhood mitochondrial leukoencephalopathy. In: Neuroradiology 46, 4, 267-271 (2004).
url: http://www.springerlink.com/content/3ldu3cdcrxbkdv1p/fulltext.html
Wilken, B., P. Dechent, K. Brockmann, J. Finsterbusch, M. Baumann, W. Ebell, G. C. Korenke, P. J. W. Pouwels, F. Hanefeld and J. Frahm: Quantitative proton magnetic resonance spectroscopy of children with adrenoleukodystrophy before and after hematopoietic stem cell transplantation. In: Neuropediatrics 34, 5, 237-246 (2003).
url: https://www.thieme-connect.de/ejournals/pdf/neuropediatrics/doi/10.1055/s-2003-43254.pdf
Brockmann, K., P. Dechent, B. Wilken, O. Rusch, J. Frahm and F. Hanefeld: Proton MRS profile of cerebral metabolic abnormalities in Krabbe disease. In: Neurology 60, 5, 819-825 (2003).
url: http://www.neurology.org/cgi/reprint/60/5/819
Brockmann, K., P. Dechent, M. Meins, M. Haupt, J. Sperner, U. Stephani, J. Frahm and F. Hanefeld: Cerebral proton magnetic resonance spectroscopy in infantile Alexander disease. In: Journal of Neurology 250, 3, 300-306 (2003).
url: http://springerlink.metapress.com/content/71qahag2uw1crb0v/fulltext.pdf
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