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American Journal of Medical Genetics. Supplement|January 1, 1986
Rett syndrome--search for genetic markersF Hanefeld, U Hanefeld, E Wilichowski, 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.
Neuropediatrics|October 8, 1998
Characterization of the mitochondrial genome in childhood multiple sclerosis. I. Optic neuritis and LHON mutationsA Ohlenbusch, E Wilichowski, F Hanefeld
Neuropediatrics|February 24, 1999
Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genesE Wilichowski, A Ohlenbusch, F Hanefeld
Neuropediatrics|February 24, 1999
Characterization of the mitochondrial genome in childhood multiple sclerosis. III. Multiple sclerosis without optic neuritis and the non-LHON-associated genesA Ohlenbusch, E Wilichowski, F Hanefeld
Nucleic Acids Research|June 15, 1997
S1 nuclease hybrid analysis of mitochondrial DNA amplified by long-distance PCR: rapid screening for small-scale rearrangementsK Lundin, E Wilichowski, B P Ernst, et al.
Molecular and Cellular Probes|February 1, 1994
Deletion screening of mitochondrial DNA via multiprimer DNA amplificationB P Ernst, E Wilichowski, M Wagner, et al.
Neuropediatrics|December 22, 1999
Quantitative proton magnetic resonance spectroscopy of cerebral metabolic disturbances in patients with MELASE Wilichowski, P J Pouwels, J Frahm, et al.
European Journal of Pediatrics|May 1, 1988
DNA analysis of ornithine transcarbamylase deficiencyU Wendel, E Wilichowski, J Schmidtke, et al.
Neuroradiology|March 23, 2004
Stroke-like pattern in DTI and MRS of childhood mitochondrial leukoencephalopathyK Brockmann, J Finsterbusch, U Schara, et al.
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