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Monatsschrift Fur Kinderheilkunde|February 1, 1976
[Rapidly progressive glomerulonephritis in a child. Clinical and histological observation over 3 1/2 years (author's transl)]M Brandis, P H Krause, G Hünermund, et al.Neurology|April 24, 2002
Giant axonal neuropathy (GAN): case report and two novel mutations in the gigaxonin geneG Kuhlenbäumer, P Young, C Oberwittler, et al.Journal of Neurology|November 8, 2001
Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneousG Kuhlenbäumer, J Meuleman, P De Jonghe, et al.Human Genetics|June 21, 2001
Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA)J Meuleman, G Kuhlenbäumer, D Audenaert, et al.Fortschritte Der Neurologie-Psychiatrie|February 3, 2005
[The reliability of the german version of the barthel-index and the development of a postal and telephone version for the application on stroke patients]P U Heuschmann, P L Kolominsky-Rabas, C H Nolte, et al.Neurology|June 24, 2004
Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14G Kuhlenbäumer, P Lüdemann, A Schirmacher, et al.Pageof 1