Zobrazeno 1 - 10 of 20 pro vyhledávání: '"Kooi, A.J. van der"'
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Comprehensive overview of autoantibody isotype and subclass distribution
Autor: Volkov, M., Coppola, M., Huizinga, R., Eftimov, F., Huizinga, T.W.J., Kooi, A.J. van der, Oosten, L.E.M., Raaphorst, J., Rispens, T., Sciarrillo, R., Titulaer, M.J., Wieske, L., Toes, R.E.M., Huijbers, M.G.M., Schie, K.A. van, Woude, D. van der, T2B Consortium
Publikováno v: T2B Consortium 2022, ' Comprehensive overview of autoantibody isotype and subclass distribution ', Journal of Allergy and Clinical Immunology, vol. 150, no. 5, pp. 999-1010 . https://doi.org/10.1016/j.jaci.2022.05.023
Journal of Allergy and Clinical Immunology, 150(5), 999-1010. MOSBY-ELSEVIER
The presence of autoreactive antibodies is a hallmark of many autoimmune diseases. The effector functions of (auto)antibodies are determined by their constant domain, which defines the antibody isotype and subclass. The most prevalent isotype in seru
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59192b959ff488b389e565b96a42d84b
https://hdl.handle.net/1887/3512518
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4
Breakthrough infections with the SARS-CoV-2 omicron (B.1.1.529) variant in patients with immune-mediated inflammatory diseases
Autor: Stalman, E.W., Wieske, L., Dam, K.P.J. van, Kummer, L.Y., Kempen, Z.L.E. van, Killestein, J., Volkers, A.G., Tas, S.W., Boekel, L., Wolbink, G.J., Kooi, A.J. van der, Raaphorst, J., Lowenberg, M., Takkenberg, R.B., D'Haens, G.R.A.M., Spuls, P.I., Bekkenk, M.W., Musters, A.H., Post, N.F., Bosma, A.L., Hilhorst, M.L., Vegting, Y., Bemelman, F.J., Voskuyl, A.E., Broens, B., Sanchez, A.P., Els, C.A.C.M. van, Wit, J. de, Rutgers, A., Leeuw, K. de, Horvath, B., Verschuuren, J.J.G.M., Ruiter, A.M., Ouwerkerk, L. van, Woude, D. van der, Allaart, C.F., Teng, O.Y.K., Paassen, P. van, Busch, M.H., Jallah, P.B.P., Brusse, E., Doorn, P.A. van, Baars, A.E., Hijnen, D.J., Schreurs, C.R.G., Pol, W.L. van der, Goedee, H.S., Steenhuis, M., Keijzer, S., Keijser, J.B.D., Boogaard, A., Cristianawati, O., Brinke, A. ten, Verstegen, N.J.M., Zwinderman, K.A.H., Rispens, T., Ham, S.M. van, Kuijpers, T.W., Eftimov, F., T2B Immunity Against SARS Co
Publikováno v: Annals of the Rheumatic Diseases, 81(12):222904, 1757-1766. BMJ Publishing Group
Annals of the rheumatic diseases, 81(12):222904, 1757-1766. BMJ Publishing Group
Annals of the Rheumatic Diseases, 81, 1757-1766. BMJ PUBLISHING GROUP
Annals of the Rheumatic Diseases, 81(12), 1757-1766. BMJ Publishing Group
Stalman, E W, Wieske, L, van Dam, K P J, Kummer, L Y, van Kempen, Z L E, Killestein, J, Volkers, A G, Tas, S W, Boekel, L, Wolbink, G J, van der Kooi, A J, Raaphorst, J, Löwenberg, M, Takkenberg, R B, D'Haens, G R A M, Spuls, P I, Bekkenk, M W, Musters, A H, Post, N F, Bosma, A L, Hilhorst, M L, Vegting, Y, Bemelman, F J, Voskuyl, A E, Broens, B, Parra Sanchez, A, van Els, C C A C M, Wit, J D, Rutgers, A, de Leeuw, K, Horváth, B, Verschuuren, J J G M, Ruiter, A M, van Ouwerkerk, L, van der Woude, D, Allaart, C F, Teng, O Y K, van Paassen, P, Busch, M H, Jallah, P B P, Brusse, E, van Doorn, P A, Baars, A E, Hijnen, D J, Schreurs, C R G, van der Pol, W L, Goedee, H S, Steenhuis, M, Keijzer, S, Keijser, J B D, Boogaard, A, Cristianawati, O, ten Brinke, A, Verstegen, N J M, Zwinderman, K A H, Rispens, T, van Ham, S M, Kuijpers, T W & Eftimov, F 2022, ' Breakthrough infections with the SARS-CoV-2 omicron (B.1.1.529) variant in patients with immune-mediated inflammatory diseases ', Annals of the Rheumatic Diseases, vol. 81, no. 12, 222904, pp. 1757-1766 . https://doi.org/10.1136/ard-2022-222904
Annals of the Rheumatic Diseases, 81(12). BMJ PUBLISHING GROUP
ObjectivesTo compare the cumulative incidence and disease severity of reported SARS-CoV-2 omicron breakthrough infections between patients with immune-mediated inflammatory diseases (IMID) on immunosuppressants and controls, and to investigate determ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19dc8c343aa3a7c58690faa029528df1
https://pure.eur.nl/en/publications/95be4c3a-8d51-4bec-a116-f9d40c9a985a
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5
Predicting Outcome in Guillain-Barre Syndrome International Validation of the Modified Erasmus GBS Outcome Score
Autor: Doets, A.Y., Lingsma, H.F., Walgaard, C., Islam, B., Papri, N., Davidson, A., Yamagishi, Y., Kusunoki, S., Dimachkie, M.M., Waheed, W., Kolb, N., Islam, Z., Mohammad, Q.D., Harbo, T., Sindrup, S.H., Chavada, G., Willison, H.J., Casasnovas, C., Bateman, K., Miller, J.A.L., Berg, B. van den, Verboon, C., Roodbol, J., Leonhard, S.E., Benedetti, L., Kuwabara, S., Bergh, P. van den, Monges, S., Marfia, G.A., Shahrizaila, N., Galassi, G., Pereon, Y., Burmann, J., Kuitwaard, K., Kleyweg, R.P., Marchesoni, C., Tous, M.J.S., Querol, L., Illa, I., Wang, Y.Z., Nobile-Orazio, E., Rinaldi, S., Schenone, A., Pardo, J., Vermeij, F.H., Lehmann, H.C., Granit, V., Cavaletti, G., Gutierrez-Gutierrez, G., Barroso, F.A., Visser, L.H., Katzberg, H.D., Dardiotis, E., Attarian, S., Kooi, A.J. van der, Eftimov, F., Wirtz, P.W., Samijn, J.P.A., Gilhuis, H.J., Hadden, R.D.M., Holt, J.K.L., Sheikh, K.A., Karafiath, S., Vytopil, M., Antonini, G., Feasby, T.E., Faber, C.G., Gijsbers, C.J., Busby, M., Roberts, R.C., Silvestri, N.J., Fazio, R., Dijk, G.W. van, Garssen, M.P.J., Straathof, C.S.M., Gorson, K.C., Jacobs, B.C., IGOS Consortium
Publikováno v: Neurology, 98(5), E518-E532. Lippincott Williams and Wilkins
Neurology, 98(5), E518-E532. LIPPINCOTT WILLIAMS & WILKINS
Neurology, 98(5), E518-E532. Lippincott Williams & Wilkins
Doets, A Y, Lingsma, H F, Walgaard, C, Islam, B, Papri, N, Davidson, A, Yamagishi, Y, Kusunoki, S, Dimachkie, M M, Waheed, W, Kolb, N, Islam, Z, Mohammad, Q D, Harbo, T, Sindrup, S H, Chavada, G, Willison, H J, Casasnovas, C, Bateman, K, Miller, J A L, van den Berg, B, Verboon, C, Roodbol, J, Leonhard, S E, Benedetti, L, Kuwabara, S, van den Bergh, P, Monges, S, Marfia, G A, Shahrizaila, N, Galassi, G, Péréon, Y, Bürmann, J, Kuitwaard, K, Kleyweg, R P, Marchesoni, C, Sedano Tous, M J, Querol, L, Illa, I, Wang, Y, Nobile-Orazio, E, Rinaldi, S, Schenone, A, Pardo, J, Vermeij, F H, Lehmann, H C, Granit, V, Cavaletti, G, Gutiérrez-Gutiérrez, G, Barroso, F A & the IGOS consortium 2022, ' Predicting Outcome in Guillain-Barré Syndrome : International Validation of the Modified Erasmus GBS Outcome Score ', Neurology, vol. 98, no. 5, pp. E518-E532 . https://doi.org/10.1212/WNL.0000000000013139
Doets, A Y, Lingsma, H F, Walgaard, C, Islam, B, Papri, N, Davidson, A, Yamagishi, Y, Kusunoki, S, Dimachkie, M M, Waheed, W, Kolb, N, Islam, Z, Mohammad, Q D, Harbo, T, Sindrup, S H, Chavada, G, Willison, H J, Casasnovas, C, Bateman, K, Miller, J A L, van den Berg, B, Verboon, C, Roodbol, J, Leonhard, S E, Benedetti, L, Kuwabara, S, van den Bergh, P, Monges, S, Marfia, G A, Shahrizaila, N, Galassi, G, Péréon, Y, Bürmann, J, Kuitwaard, K, Kleyweg, R P, Marchesoni, C, Sedano Tous, M J, Querol, L, Illa, I, Wang, Y, Nobile-Orazio, E, Rinaldi, S, Schenone, A, Pardo, J, Vermeij, F H, Lehmann, H C, Granit, V, Cavaletti, G, Gutiérrez-Gutiérrez, G, Barroso, F A & the IGOS Consortium 2022, ' Predicting Outcome in Guillain-Barré Syndrome International Validation of the Modified Erasmus GBS Outcome Score ', Neurology, vol. 98, no. 5, pp. E518-E532 . https://doi.org/10.1212/WNL.0000000000013139
Neurology
Background and ObjectivesThe clinical course and outcome of the Guillain-Barré syndrome (GBS) are diverse and vary among regions. The modified Erasmus GBS Outcome Score (mEGOS), developed with data from Dutch patients, is a clinical model that predi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37779cf9507298a6202d42c62178d160
https://hdl.handle.net/1887/3495929
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6
Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samples
Autor: Straathof, C.S., Heusden, D. Van, Ippel, P.F., Post, J.G., Voermans, N.C., Visser, M. de, Brusse, E., Bergen, J.C. van den, Kooi, A.J. van der, Verschuuren, J.J., Ginjaar, H.B.
Publikováno v: Muscle & nerve, 53(1), 44-48. John Wiley and Sons Inc.
Muscle & Nerve, 53(1), 44. John Wiley and Sons Inc.
Muscle and Nerve, 53, 44-8
Muscle & Nerve, 53(1), 44-48. John Wiley & Sons Inc.
Muscle and Nerve, 53, 1, pp. 44-8
Item does not contain fulltext INTRODUCTION: The phenotype of Becker muscular dystrophy (BMD) is highly variable, and the disease may be underdiagnosed. We searched for new mutations in the DMD gene in a cohort of previously undiagnosed patients who
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7f952fb48b193831d1e74b03f44eb03b
https://hdl.handle.net/2066/167723
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10
UBQLN2 in familial amyotrophic lateral sclerosis in The Netherlands
Autor: Doormaal, P.T. van, Rheenen, W. van, Blitterswijk, M. van, Schellevis, R.D., Schelhaas, H.J., Visser, M. de, Kooi, A.J. van der, Veldink, J.H., Berg, L.H. van den
Publikováno v: Neurobiology of Aging, 33, 9, pp. 2233.e7-2233.e8
Neurobiology of Aging, 33, 2233.e7-2233.e8
Item does not contain fulltext Recently it was discovered that mutations in the UBQLN2 gene were a cause of an X-linked dominant type of familial amyotrophic lateral sclerosis (ALS). We investigated the frequency of mutations in this gene in a cohort
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e8ad91c3453a3781b53524ee1ca0e9ad
https://hdl.handle.net/2066/110084
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