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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Michaela Auer-Grumbach

Institute of Medical Biology and Human Genetics

Karl-Franzens University Graz

Harrachgasse 21/8

A-8010 Graz



Name/email consistency: high



  • Institute of Medical Biology and Human Genetics, Karl-Franzens University Graz, Harrachgasse 21/8, A-8010 Graz, Austria. 2003
  • Department of Neurology, Karl-Franzens-University, Austria. 1999 - 2000
  • Department of Neurology, Karl-Franzens University, Institute of Medical Biology and Human Genetics, Austria. 2000


  1. Autosomal dominant inherited neuropathies with prominent sensory loss and mutilations: a review. Auer-Grumbach, M., De Jonghe, P., Verhoeven, K., Timmerman, V., Wagner, K., Hartung, H.P., Nicholson, G.A. Arch. Neurol. (2003) [Pubmed]
  2. Late onset Charcot-Marie-Tooth 2 syndrome caused by two novel mutations in the MPZ gene. Auer-Grumbach, M., Strasser-Fuchs, S., Robl, T., Windpassinger, C., Wagner, K. Neurology (2003) [Pubmed]
  3. Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci. Auer-Grumbach, M., Wagner, K., Timmerman, V., De Jonghe, P., Hartung, H.P. Neurology (2000) [Pubmed]
  4. Phenotypic and genotypic heterogeneity in hereditary motor neuronopathy type V: a clinical, electrophysiological and genetic study. Auer-Grumbach, M., Löscher, W.N., Wagner, K., Petek, E., Körner, E., Offenbacher, H., Hartung, H.P. Brain (2000) [Pubmed]
  5. Clinical predominance of proximal upper limb weakness in CMT1A syndrome. Auer-Grumbach, M., Wagner, K., Strasser-Fuchs, S., Löscher, W.N., Fazekas, F., Millner, M., Hartung, H.P. Muscle. Nerve (2000) [Pubmed]
  6. Proximal Charcot-Marie-Tooth syndrome with duplication on chromosome 17p11.2. Auer-Grumbach, M., Wagner, K., Payer, F., Hartung, H.P. Ann. N. Y. Acad. Sci. (1999) [Pubmed]
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