Author Burkhardt, Harald

1 to 16 of 16 Items
  • 2000 Journal Article
    ​ ​I-123-antileukoproteinase scintigraphy reveals microscopic cartilage alterations in the contralateral knee joint of rats with "monarticular" antigen-induced arthritis​
    Meyer, P.; Burkhardt, H.; Palombo-Kinne, E.; Grunder, W.; Brauer, R.; Stiller, K. J. & Kalden, J. R. et al.​ (2000) 
    Arthritis & Rheumatism43(2) pp. 298​-310​.​ DOI: https://doi.org/10.1002/1529-0131(200002)43:2<298::AID-ANR9>3.0.CO;2-G 
    Details  DOI  PMID  PMC  WoS 
  • 2006 Journal Article
    ​ ​Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients​
    Huffmeier, U.; Steffens, M.; Burkhardt, H.; Lascorz, J.; Schurmeier-Horst, F.; Stander, M. & Kelsch, R. et al.​ (2006) 
    Journal of Medical Genetics43(6) pp. 517​-522​.​ DOI: https://doi.org/10.1136/jmg.2005.037515 
    Details  DOI  PMID  PMC  WoS 
  • 2007 Conference Abstract
    ​ ​Tumor necrosis factor polymorphisms in psoriatic arthritis: association with the promoter polymorphism TNF-857 independent of the PSORS1 risk allele​
    Reich, K.; Hueffmeier, U.; Koenig, I. R.; Lascorz, J.; Lohmann, J.; Wendler, J. & Traupe, H. et al.​ (2007)
    Arthritis Research & Therapy9 ​6th Global Arthritis Research Network Meeting (GARN)​, Zurich, SWITZERLAND.
    London​: Biomed Central Ltd. DOI: https://doi.org/10.1186/ar2244 
    Details  DOI  WoS 
  • 2007 Conference Abstract
    ​ ​TNF, LTA and TNF receptor polymorphisms in psoriasis vulgaris and psoriatic arthritis: Evidence for an association of psoriatic arthritis with the promoter polymorphism TNF-857 independent of the PSORS1 risk allele​
    Reich, K.; Hueffmeier, U.; Koenig, I. R.; Lascorz, J.; Lohmann, J.; Wendler, J. & Traupe, H. et al.​ (2007)
    Experimental Dermatology16(3) pp. 204​-205. ​34th Annual Meeting of the Arbeitsgemeinschaft-Dermatologische-Forschung​, Freiburg, GERMANY.
    Oxford​: Blackwell Publishing.
    Details  WoS 
  • 2007 Journal Article
    ​ ​TNF polymorphisms in psoriasis - Association of psoriatic arthritis with the promoter polymorphism TNF -857 independent of the PSORS1 risk allele​
    Reich, K.; Hueffmeier, U.; Koenig, I. R.; Lascorz, J.; Lohmann, J.; Wendler, J. & Traupe, H. et al.​ (2007) 
    Arthritis & Rheumatism56(6) pp. 2056​-2064​.​ DOI: https://doi.org/10.1002/art.22590 
    Details  DOI  PMID  PMC  WoS 
  • 2008 Conference Abstract
    ​ ​Variants of genes coding for IL-12 beta ? and for IL-23R are associated with psoriasis vulgaris and psoriatic arthritis in large German study groups​
    Hueffmeier, U.; Lascorz, J.; Boehm, B.; Lohmann, J.; Wendler, J.; Moessner, R. & Reich, K. et al.​ (2008)
    Experimental Dermatology17(3) ​35th Annual Meeting of the Arbeitsgemeinschaft-Dermatolog-Forschung​, Eriangen, GERMANY.
    Oxford​: Blackwell Publishing.
    Details  WoS 
  • 2009 Journal Article
    ​ ​Genetic Variants of the IL-23R Pathway: Association with Psoriatic Arthritis and Psoriasis Vulgaris, but No Specific Risk Factor for Arthritis​
    Hueffmeier, U.; Lascorz, J.; Boehm, B.; Lohmann, J.; Wendler, J.; Moessner, R. & Reich, K. et al.​ (2009) 
    Journal of Investigative Dermatology129(2) pp. 355​-358​.​ DOI: https://doi.org/10.1038/jid.2008.233 
    Details  DOI  PMID  PMC  WoS 
  • 2010 Conference Abstract
    ​ ​Deletion of LCE3C and LCE3B genes at PSORS4 contributes to susceptibility to psoriasis vulgaris but not to psoriatic arthritis in German patients​
    Hueffmeier, U.; Traupe, H.; Moessner, R.; Reich, K.; Kurrat, W.; Estivill, X. & Riveira-Munoz, E. et al.​ (2010)
    Experimental Dermatology19(2) ​37th Annual Meeting of the Arbeitsgemeinschaft-Dermatologishche-Forschung​, Luebeck, GERMANY.
    Malden​: Wiley-blackwell Publishing, Inc.
    Details  WoS 
  • 2010 Conference Abstract
    ​ ​A Tissue-Specific Nf-Kappa B Inhibitor Ameliorates Inflammatory Joint Diseases​
    Sehnert, B.; Burkhardt, H.; Nimmerjahn, F.; Pohle, S.; Wessels, J. T.; Vestweber, D. & Zwerina, J. et al.​ (2010)
    Annals of the Rheumatic Diseases69 ​30th European Workshop for Rheumatology Research​, Bamberg, GERMANY.
    London​: B M J Publishing Group. DOI: https://doi.org/10.1136/ard.2010.129635e 
    Details  DOI  WoS 
  • 2014 Conference Abstract
    ​ ​Palmoplantar pustular psoriasis is associated with a missense variant in CARD14 in European patients​
    Moessner, R.; Frambach, Y.; Wilsmann-Theis, D.; Loehr, S.; Jacobi, A.; Weyergraf, A. J. & Mueller, M. et al.​ (2014)
    British Journal of Dermatology171(6) ​7th International Congress of Psoriasis - From Gene to Clinic​, London, ENGLAND.
    Hoboken​: Wiley-blackwell.
    Details  WoS 
  • 2015 Journal Article | Letter Note
    ​ ​Palmoplantar Pustular Psoriasis Is Associated with Missense Variants in CARD14, but Not with Loss-of-Function Mutations in IL36RN in European Patients​
    Moessner, R.; Frambach, Y.; Wilsmann-Theis, D.; Loehr, S.; Jacobi, A.; Weyergraf, A. J. & Mueller, M. et al.​ (2015) 
    Journal of Investigative Dermatology135(10) pp. 2538​-2541​.​ DOI: https://doi.org/10.1038/jid.2015.186 
    Details  DOI  PMID  PMC  WoS 
  • 2016 Journal Article
    ​ ​Vasoactive Therapy in Systemic Sclerosis: Real-life Therapeutic Practice in More Than 3000 Patients​
    Moinzadeh, P.; Riemekasten, G.; Siegert, E.; Fierlbeck, G.; Henes, J.; Blank, N. & Melchers, I. et al.​ (2016) 
    The Journal of Rheumatology43(1) pp. 66​-74​.​ DOI: https://doi.org/10.3899/jrheum.150382 
    Details  DOI  PMID  PMC  WoS 
  • 2019 Journal Article
    ​ ​Analyses of association of psoriatic arthritis and psoriasis vulgaris with functional NCF1 variants​
    Löhr, S.; Ekici, A. B; Uebe, S.; Büttner, C.; Köhm, M.; Behrens, F. & Böhm, B. et al.​ (2019) 
    Rheumatology58(5) pp. 915​-917​.​ DOI: https://doi.org/10.1093/rheumatology/key448 
    Details  DOI 
  • 2020 Journal Article
    ​ ​Rare Loss-of-Function Mutation in SERPINA3 in Generalized Pustular Psoriasis​
    Frey, S.; Sticht, H.; Wilsmann-Theis, D.; Gerschütz, A.; Wolf, K.; Löhr, S. & Haskamp, S. et al.​ (2020) 
    Journal of Investigative Dermatology140(7) pp. 1451​-1455.e13​.​ DOI: https://doi.org/10.1016/j.jid.2019.11.024 
    Details  DOI 
  • 2020 Journal Article | 
    ​ ​Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups​
    Assmann, G.; Köhm, M.; Schuster, V.; Behrens, F.; Mössner, R. ; Magnolo, N. & Oji, V. et al.​ (2020) 
    BMC Medical Genetics21(1).​ DOI: https://doi.org/10.1186/s12881-020-01037-7 
    Details  DOI 
  • 2021 Journal Article
    ​ ​Genetic Analysis of MPO Variants in Four Psoriasis Subtypes in Patients from Germany​
    Haskamp, S.; Horowitz, J. S.; Oji, V.; Philipp, S.; Sticherling, M.; Schäkel, K. & Schuhmann, S. et al.​ (2021) 
    Journal of Investigative Dermatology141(8) pp. 2079​-2083​.​ DOI: https://doi.org/10.1016/j.jid.2021.01.017 
    Details  DOI 

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