Lennart Truedsson

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  1. 2020
  2. Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies

    Dezfouli, M., Bergström, S., Skattum, L., Abolhassani, H., Neiman, M., Torabi-Rahvar, M., Franco Jarava, C., Martin-Nalda, A., Ferrer Balaguer, J. M., Slade, C. A., Roos, A., Fernandez Pereira, L. M., López-Trascasa, M., Gonzalez-Granado, L. I., Allende-Martinez, L. M., Mizuno, Y., Yoshida, Y., Friman, V., Lundgren, Å., Aghamohammadi, A. & 9 others, Rezaei, N., Hernández-Gonzalez, M., von Döbeln, U., Lennart Truedsson, Hara, T., Nonoyama, S., Schwenk, J. M., Nilsson, P. & Hammarström, L., 2020 Mar 17, In : Frontiers in Immunology. 11, 455.

    Research output: Contribution to journalArticle

  3. 2019
  4. Two subgroups in systemic lupus erythematosus with features of antiphospholipid or Sjögren's syndrome differ in molecular signatures and treatment perspectives

    Idborg, H., Zandian, A., Sandberg, A. S., Nilsson, B., Elvin, K., Lennart Truedsson, Sohrabian, A., Rönnelid, J., Mo, J., Grosso, G., Kvarnström, M., Gunnarsson, I., Lehtiö, J., Nilsson, P., Svenungsson, E. & Jakobsson, P. J., 2019 Feb 18, In : Arthritis Research and Therapy. 21, 1, 62.

    Research output: Contribution to journalReview article

  5. Analysis of anti-C1q autoantibodies by western blot

    Verlemyr, A., Lennart Truedsson & Lillemor Skattum, 2019, Methods in Molecular Biology. Humana Press, p. 183-189 7 p. (Methods in Molecular Biology; vol. 1901).

    Research output: Chapter in Book/Report/Conference proceedingBook chapter

  6. 2018
  7. Inherited Classical and Alternative Pathway Complement Deficiencies in Children: A Single Center Experience

    Genel, F., Erdem, S. B., Gülez, N., Karaman, S., Nacaroglu, H. T., Lillemor Skattum & Lennart Truedsson, 2018 Dec 1, In : Iranian journal of immunology : IJI. 15, 4, p. 309-320 12 p.

    Research output: Contribution to journalArticle

  8. Age and sex-associated changes of complement activity and complement levels in a healthy caucasian population

    Da Costa, M. G., Poppelaars, F., Van Kooten, C., Mollnes, T. E., Tedesco, F., Würzner, R., Trouw, L. A., Lennart Truedsson, Daha, M. R., Roos, A. & Seelen, M. A., 2018 Nov 20, In : Frontiers in Immunology. 9, NOV, 2664.

    Research output: Contribution to journalArticle

  9. 2017
  10. Transancestral mapping and genetic load in systemic lupus erythematosus

    Langefeld, C. D., Anders A. Bengtsson, Lennart Truedsson, Vyse, T. J. & et al., 2017 Jul 17, In : Nature Communications. 8, 16021.

    Research output: Contribution to journalArticle

  11. Delayed cochlear implantation in post-meningitic deafness and hereditary complement C2 deficiency

    Di Berardino, F., Lennart Truedsson & Zanetti, D., 2017 Jan 1, In : International Journal of Pediatric Otorhinolaryngology Extra. 15, p. 4-8 5 p.

    Research output: Contribution to journalArticle

  12. 2016
  13. Prasugrel 5 mg inhibits platelet P-selectin and GPIIb–IIIa expression in very elderly and non elderly: results from the GENERATIONS trial, a pharmacodynamic study in stable CAD patients

    Wagner, H., Lood, C., Borna, C., Olof Gidlöf, Lennart Truedsson, Brown, P., Zhou, C., Winters, K., Jakubowski, J. A. & David Erlinge, 2016 Oct, In : Journal of Thrombosis and Thrombolysis. 42, 3, p. 369-375 7 p.

    Research output: Contribution to journalArticle

  14. 2015
  15. Allogeneic Hematopoietic Stem Cell Transplantation in the Treatment of Human C1q Deficiency: The Karolinska Experience.

    Olsson, R. F., Hagelberg, S., Schiller, B., Ringdén, O., Lennart Truedsson & Åhlin, A., 2015, In : Transplantation.

    Research output: Contribution to journalArticle

  16. Anti-C1q antibodies in systemic lupus erythematosus.

    Orbai, A-M., Truedsson, L., Sturfelt, G., Nived, O., Fang, H., Alarcón, G., Gordon, C., Merrill, J., Fortin, P., Bruce, I., Isenberg, DA., Wallace, D., Ramsey-Goldman, R., Bae, S-C., Hanly, J., Sanchez-Guerrero, J., Clarke, A., Aranow, C., Manzi, S., Urowitz, M. & 33 others, Gladman, D., Kalunian, K., Costner, M., Werth, V., Zoma, A., Bernatsky, S., Ruiz-Irastorza, G., Khamashta, M., Jacobsen, S., Buyon, J., Maddison, P., Dooley, M., Van Vollenhoven, R., Ginzler, E., Stoll, T., Peschken, C., Jorizzo, J., Callen, J., Lim, S., Fessler, B., Inanc, M., Kamen, D., Rahman, A., Steinsson, K., Franks, A., Sigler, L., Hameed, S., Pham, N., Brey, R., Weisman, M., McGwin, G., Magder, L. & Petri, M., 2015, In : Lupus. 24, 1, p. 42-49

    Research output: Contribution to journalArticle

  17. Classical pathway deficiencies - A short analytical review.

    Lennart Truedsson, 2015, In : Molecular Immunology. 68, 1, p. 14-19

    Research output: Contribution to journalReview article

  18. European Union funded project on the development of a whole complement deficiency screening ELISA-A story of success and an exceptional manager: Mohamed R. Daha.

    Würzner, R., Tedesco, F., Garred, P., Mollnes, T. E., Lennart Truedsson, Turner, M. W., Sommarin, Y., Wieslander, J. & Sim, R. B., 2015, In : Molecular Immunology. 68, 1, p. 63-66

    Research output: Contribution to journalReview article

  19. Heat differentiated complement factor profiling.

    Hamsten, C., Lillemor Melander Skattum, Lennart Truedsson, von Döbeln, U., Uhlén, M., Schwenk, J. M., Hammarström, L., Nilsson, P. & Neiman, M., 2015, In : Journal of Proteomics. 126, p. 155-162

    Research output: Contribution to journalArticle

  20. Marked variability in clinical presentation and outcome of patients with C1q immunodeficiency.

    van Schaarenburg, R. A., Schejbel, L., Truedsson, L., Topaloglu, R., Al-Mayouf, S. M., Riordan, A., Simon, A., Kallel-Sellami, M., Arkwright, P. D., Åhlin, A., Hagelberg, S., Nielsen, S., Shayesteh, A., Morales, A., Tam, S., Genel, F., Berg, S., Ketel, A. G., Merlijn van den Berg, J., Kuijpers, T. W. & 4 others, Olsson, R. F., Huizinga, T. W. J., Lankester, A. C. & Trouw, L. A., 2015, In : Journal of Autoimmunity. 62, Jun 25, p. 39-44

    Research output: Contribution to journalArticle

  21. Novel Genetic Mutations in the First Swedish Patient with Purine Nucleoside Phosphorylase Deficiency and Clinical Outcome After Hematopoietic Stem Cell Transplantation with HLA-Matched Unrelated Donor.

    Brodszki, N., Svensson, M., van Kuilenburg, A. B. P., Meijer, J., Zoetekouw, L., Lennart Truedsson & Toporski, J., 2015, In : JIMD Reports. 24, p. 83-9 7 p.

    Research output: Contribution to journalArticle

  22. PXK locus in systemic lupus erythematosus: fine mapping and functional analysis reveals novel susceptibility gene ABHD6

    Oparina, N. Y., Delgado-Vega, A. M., Martinez-Bueno, M., Magro-Checa, C., Fernandez, C., Ortega Castro, R., Pons-Estel, B. A., D'Alfonso, S., Sebastiani, G. D., Witte, T., Lauwerys, B. R., Endreffy, E., Kovacs, L., Escudero, A., Lopez-Pedrera, C., Vasconcelos, C., da Silva, B. M., Frostegard, J., Truedsson, L., Martin, J. & 7 others, Raya, E., Ortego-Centeno, N., de los Angeles Aguirre, M., de Ramon Garrido, E., Castillo Palma, M-J., Alarcon-Riquelme, M. E. & Kozyrev, S. V., 2015, In : Annals of the Rheumatic Diseases. 74, 3, p. e14

    Research output: Contribution to journalArticle

  23. Reversal of Immunoglobulin. A Deficiency in Children

    Lim, C. K., Dahle, C., Elvin, K., Andersson, B. A., Ronnelid, J., Melen, E., Bergstrom, A., Lennart Truedsson & Hammarstrom, L., 2015, In : Journal of Clinical Immunology. 35, 1, p. 87-91

    Research output: Contribution to journalArticle

  24. 2014
  25. Clinical phenotype associations with various types of anti-dsDNA antibodies in patients with recent onset of rheumatic symptoms. Results from a multicentre observational study.

    Michele Compagno, Rekvig, O. P., Anders Bengtsson, Sturfelt, G., Heegaard, N. H. H., Andreas Jönsen, Jacobsen, R. S., Eilertsen, G. Ø., Fenton, C. G., Lennart Truedsson, Nossent, J. C. & Jacobsen, S., 2014, In : Lupus science & medicine. 1, 1, p. e000007

    Research output: Contribution to journalArticle

  26. Miniaturization of multiplexed planar recombinant antibody arrays for serum protein profiling.

    Petersson, L., Coen, M., Amro, N. A., Lennart Truedsson, Borrebaeck, C. A. & Wingren, C., 2014, In : Bioanalysis. 6, 9, p. 1175-1185

    Research output: Contribution to journalArticle

  27. Serological assessment for celiac disease in IgA deficient adults.

    Wang, N., Lennart Truedsson, Elvin, K., Andersson, B. A., Rönnelid, J., Mincheva-Nilsson, L., Lindkvist, A., Ludvigsson, J. F., Hammarström, L. & Dahle, C., 2014, In : PLoS ONE. 9, 4, e93180.

    Research output: Contribution to journalArticle

  28. 2013
  29. Contribution of IKBKE and IFIH1 gene variants to SLE susceptibility

    Wang, C., Ahlford, A., Laxman, N., Nordmark, G., Eloranta, M-L., Gunnarsson, I., Svenungsson, E., Padyukov, L., Sturfelt, G., Andreas Jönsen, Anders Bengtsson, Lennart Truedsson, Rantapaa-Dahlqvist, S., Sjowall, C., Sandling, J. K., Ronnblom, L. & Syvanen, A-C., 2013, In : Genes and Immunity. 14, 4, p. 217-222

    Research output: Contribution to journalArticle

  30. Low diagnostic and predictive value of anti-dsDNA antibodies in unselected patients with recent onset of rheumatic symptoms: results from a long-term follow-up Scandinavian multicentre study.

    Michele Compagno, Jacobsen, S., Rekvig, O. P., Lennart Truedsson, Heegaard, N. H. H., Nossent, J., Andreas Jönsen, Jacobsen, R. S., Eilertsen, G. Ö., Sturfelt, G. & Anders Bengtsson, 2013, In : Scandinavian Journal of Rheumatology. 42, 4, p. 311-316

    Research output: Contribution to journalArticle

  31. 2012
  32. Complement in the immunopathogenesis of rheumatic disease.

    Sturfelt, G. & Lennart Truedsson, 2012, In : Nature Reviews Rheumatology. 8, 8, p. 458-468

    Research output: Contribution to journalArticle

  33. Fine mapping and conditional analysis identify a new mutation in the autoimmunity susceptibility gene BLK that leads to reduced half-life of the BLK protein

    Delgado-Vega, A. M., Dozmorov, M. G., Bernal Quiros, M., Wu, Y-Y., Martinez-Garcia, B., Kozyrev, S. V., Frostegard, J., Truedsson, L., de Ramon, E., Gonzalez-Escribano, M. F., Ortego-Centeno, N., Pons-Estel, B. A., D'Alfonso, S., Sebastiani, G. D., Witte, T., Lauwerys, B. R., Endreffy, E., Kovacs, L., Vasconcelos, C., da Silva, B. M. & 4 others, Wren, J. D., Martin, J., Castillejo-Lopez, C. & Alarcon-Riquelme, M. E., 2012, In : Annals of the Rheumatic Diseases. 71, 7, p. 1219-1226

    Research output: Contribution to journalArticle

  34. Genetic association of miRNA-146a with systemic lupus erythematosus in Europeans through decreased expression of the gene

    Lofgren, S. E., Frostegard, J., Lennart Truedsson, Pons-Estel, B. A., D'Alfonso, S., Witte, T., Lauwerys, B. R., Endreffy, E., Kovacs, L., Vasconcelos, C., Martins da Silva, B., Kozyrev, S. V. & Alarcon-Riquelme, M. E., 2012, In : Genes and Immunity. 13, 3, p. 268-274

    Research output: Contribution to journalArticle

  35. Increased IgG on cell-derived plasma microparticles in systemic lupus erythematosus is associated with autoantibodies and complement activation.

    Nielsen, C. T., Ostergaard, O., Stener, L., Iversen, L. V., Lennart Truedsson, Birgitta Gullstrand, Jacobsen, S. & Heegaard, N. H. H., 2012, In : Arthritis and Rheumatism. 64, 4, p. 1227-1236

    Research output: Contribution to journalArticle

  36. Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation

    Paixao-Cavalcante, D., Lopez-Trascasa, M., Lillemor Melander Skattum, Giclas, P. C., Goodship, T. H., Rodriguez de Cordoba, S., Lennart Truedsson, Morgan, B. P. & Harris, C. L., 2012, In : Kidney International. 82, 10, p. 1084-1092

    Research output: Contribution to journalArticle

  37. Vaccination against encapsulated bacteria in hereditary C2 deficiency results in antibody response and opsonization due to antibody-dependent complement activation.

    Jönsson, G., Lood, C., Birgitta Gullstrand, Holmström, E. M., Selander, B., Braconier, J. H., Sturfelt, G., Anders Bengtsson & Lennart Truedsson, 2012, In : Clinical Immunology. 144, 3, p. 214-227

    Research output: Contribution to journalArticle

  38. 2011
  39. A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE

    Sandling, J. K., Garnier, S., Sigurdsson, S., Wang, C., Nordmark, G., Gunnarsson, I., Svenungsson, E., Padyukov, L., Sturfelt, G., Jönsen, A., Bengtsson, A., Truedsson, L., Eriksson, C., Rantapaa-Dahlqvist, S., Malarstig, A., Strawbridge, R. J., Hamsten, A., Criswell, L. A., Graham, R. R., Behrens, T. W. & 4 others, Eloranta, M-L., Alm, G., Ronnblom, L. & Syvanen, A-C., 2011, In : European Journal of Human Genetics. 19, 4, p. 479-484

    Research output: Contribution to journalArticle

  40. Complement deficiency states and associated infections.

    Lillemor Melander Skattum, van Deuren, M., van der Poll, T. & Lennart Truedsson, 2011, In : Molecular Immunology. 48, p. 1643-1655

    Research output: Contribution to journalArticle

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