Prof. Dr. Dr. Robert Steinfeld

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  • 2018 | Journal Article
    ​ ​Cathepsin D Polymorphism C224T in Childhood-Onset Neurodegenerative Disorders: No Impact for Childhood Dementia​
    Ohlenbusch, A. ; Jung, K. ; Steinfeld, R. ; Gärtner, J.   & Kettwig, M.​ (2018) 
    Journal of Pediatric Genetics, 07(01) pp. 014​-018​.​ DOI: https://doi.org/10.1055/s-0037-1607341 
    ​Details  DOI 
  • 2016 | Journal Article
    ​ ​Late-Onset Metachromatic Leukodystrophy with Early Onset Dementia Associated with a Novel Missense Mutation in the Arylsulfatase A Gene​
    Stoeck, K.; Psychogios, M. N. ; Ohlenbusch, A. ; Steinfeld, R.   & Schmidt, J. ​ (2016) 
    Journal of Alzheimer's Disease, 51(3) pp. 683​-687​.​ DOI: https://doi.org/10.3233/JAD-150819 
    ​Details  DOI  PMID  PMC  WoS 
  • 2014 | Journal Article | Research Paper
    ​ ​The expanding clinical and genetic spectrum of ATP1A3-related disorders​
    Rosewich, H. ; Ohlenbusch, A. ; Huppke, P. ; Schlotawa, L.; Baethmann, M.; Carrilho, I. & Fiori, S. et al.​ (2014) 
    Neurology, 82(11) pp. 945​-955​.​ DOI: https://doi.org/10.1212/WNL.0000000000000212 
    ​Details  DOI  PMID  PMC  WoS 
  • 2009 | Journal Article | Research Paper | 
    ​ ​RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection​
    Henneke, M.; Diekmann, S.; Ohlenbusch, A. ; Kaiser, J.; Engelbrecht, V.; Kohlschuetter, A. & Kraetzner, R.  et al.​ (2009) 
    Nature Genetics, 41(7) pp. 773​-775​.​ DOI: https://doi.org/10.1038/ng.398 
    ​Details  DOI  PMID  PMC  WoS 

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Contributor:  Ohlenbusch, Andreas

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https://publications.goettingen-research-online.de URI: /cris/rp/rp10435
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