Author Hoffmann, Katrin

1 to 4 of 4 Items
  • 2010 | Journal Article
    ​ ​Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy​
    Cirak, S.; von Deimling, F.; Sachdev, S.; Errington, W. J.; Herrmann, R.; Boennemann, C. & Brockmann, K. et al.​ (2010) 
    Brain, 133 pp. 2123​-2135​.​ DOI: https://doi.org/10.1093/brain/awq108 
    ​Details  DOI  PMID  PMC  WoS 
  • 2015 | Journal Article | 
    ​ ​Impact of neo-adjuvant Sorafenib treatment on liver transplantation in HCC patients - a prospective, randomized, double-blind, phase III trial​
    Hoffmann, K.; Ganten, T. M.; Gotthardtp, D.; Radeleff, B.; Settmacher, U.; Kollmar, O. & Nadalin, S. et al.​ (2015) 
    BMC Cancer, 15 art. 392​.​ DOI: https://doi.org/10.1186/s12885-015-1373-z 
    ​Details  DOI  PMID  PMC  WoS 
  • 2018 | Journal Article | 
    ​ ​Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence​
    Bonnin, E.; Cabochette, P.; Filosa, A.; Jühlen, R.; Komatsuzaki, S.; Hezwani, M. & Dickmanns, A. et al.​ (2018) 
    PLOS Genetics, 14(12) art. e1007845​.​ DOI: https://doi.org/10.1371/journal.pgen.1007845 
    ​Details  DOI  PMID  PMC 
  • 2019 | Journal Article
    ​ ​SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy​
    Fischer-Zirnsak, B.; Koenig, R.; Alisch, F.; Güneş, N.; Hausser, I.; Saha, N. & Beck-Woedl, S. et al.​ (2019) 
    Journal of Human Genetics, 64(7) pp. 609​-616​.​ DOI: https://doi.org/10.1038/s10038-019-0602-8 
    ​Details  DOI  PMID  PMC 

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