Genetic susceptibility to temporomandibular joint involvement in juvenile idiopathic arthritis von Niibo, P., Nikopensius, T., Jagomägi, T., Voog, Ü., Haller, T., Tõnisson, N., Metspalu, A., Saag, M., Pruunsild, C.

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AB0994 T2T in Juvenile Idiopathic Arthritis: The Estonian Experience von Laan, M., Ilisson, J., Pruunsild, C.

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Incidence of juvenile idiopathic arthritis in children in Estonia: a prospective population-based study von Pruunsild, C., Uibo, K., Liivamägi, H., Tarraste, S., Talvik, T., Pelkonen, P.

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EULAR/PRINTO/PRES criteria for Henoch–Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Fi... von Ozen, Seza, Pistorio, Angela, Iusan, Silvia M, Bakkaloglu, Aysin, Herlin, Troels, Brik, Riva, Buoncompagni, Antonella, Lazar, Calin, Bilge, Ilmay, Uziel, Yosef, Rigante, Donato, Cantarini, Luca, Hilario, Maria Odete, Silva, Clovis A, Alegria, Mauricio, Norambuena, Ximena, Belot, Alexandre, Berkun, Yackov, Estrella, Amparo Ibanez, Olivieri, Alma Nunzia, Alpigiani, Maria Giannina, Rumba, Ingrida, Sztajnbok, Flavio, Tambic-Bukovac, Lana, Breda, Luciana, Al-Mayouf, Sulaiman, Mihaylova, Dimitrina, Chasnyk, Vyacheslav, Sengler, Claudia, Klein-Gitelman, Maria, Djeddi, Djamal, Nuno, Laura, Pruunsild, Chris, Brunner, Jurgen, Kondi, Anuela, Pagava, Karaman, Pederzoli, Silvia, Martini, Alberto, Ruperto, Nicolino

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Prevalence and short-term outcome of juvenile idiopathic arthritis : a population-based study in Estonia von PRUUNSILD, C, UIBO, K, LIIVAMÄGI, H, TARRASTE, S, TALVIK, T, PELKONEN, P

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PReS-FINAL-2034: Α1 - Antitrypsin deficiency in children with arthritis: four cases von Pruunsild, C, Ilisson, J

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High mobility group box protein 1—A prognostic marker for structural joint damage in 10-year follow-up of patients with juvenile idiopathic arthritis von Pullerits, Rille, Schierbeck, Hanna, Uibo, Karin, Liivamägi, Hille, Tarraste, Sirje, Talvik, Tiina, Sundberg, Erik, Pruunsild, Chris

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Low Serum IGF-1 in Boys with Recent Onset of Juvenile Idiopathic Arthritis von Pullerits, Rille, Pruunsild, Chris, Rebane, Tiina, Tarraste, Sirje, Uibo, Karin, Liivamägi, Hille, Bokarewa, Maria, Erlandsson, Malin C., Lundell, Anna-Carin, Talvik, Tiina

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JIA affected sibling pairs present high correlation for ANA and ILAR category von Filocamo, G, Malattia, C, Foeldvari, I, Stanevicha, V, Nielsen, S, Herlin, T, Pruunsild, C, Zulian, F, Balogh, Z, Dressler, F, Rumba, I, Alpigiani, MG, Cortis, E, Falcini, F, Trauzeddel, R, Calcagno, G, Lepore, L, Alessio, M, Glass, DN, Thompson, SD, Martini, A, Ruperto, N

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Evaluation of the danger signal HMGB1 as a potential biomarker in juvenile idiopathic arthritis (JIA): a preliminary study using the novel biobank jabba von Schierbeck, Hanna, Pullerits, Rille, Pruunsild, Chris, Fischer, Marie, Holzinger, Dirk, Palmblad, Karin, Aveberger, Ann-Charlotte, Sundberg, Erik, Harris, Helena Erlandsson

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IDENTIFICATION OF 254 FAMILIES WITH JUVENILE IDIOPATHIC ARTHRITIS AFFECTED SIBPAIRS: RESULTS OF THE PRINTO SURVEY von Malattia, C, Filocamo, G, Foeldvari, I, Michels, H, Pruunsild, C, Nielsen, S, Stanevicha, V, Espada, G, Herlin, T, Balogh, Z, Cuttica, R, Fasth, A, Garcia-Consuegra, J, Mihaylova, D, Glass, DN, Martini, A, Ruperto, N

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P001. ASSOCIATION OF CHRONIC OLIGOARTHRITIS WITH HLA CLASS II ALLELES: DRB1, DQB1 AND DQA1 IN BULGARIAN CHILDRENP002. DECREASE IN CELLULARITY AND CYTOKINE EXPRESSION BY AUTOLOGOUS... von Boykinov, I. N., Brinkman, D. M. C., Brochhausen, C., Gattorno, M., Girschick, H. J., Thomson, W., Metzler, M., Ihle, J., Kamphuis, S. S. M., de Kleer, I., Knupp, S., Frosch, M., Scola, M. P., Laurell, L., Modesto, C., Ogilvie, E., Stanevicha, V., Wedderburn, L. R., Ramanan, A. V., Tommasini, A., Picco, P., Hayata, A. L. S., Huemer, C., Kasapçopur, Ö., Smittenaar, N. M., Susic, G., Avčin, T., Muller, S., Christov, G., Cleary, A. G., Bouayed, K., Cortis, E., Epps, H. A., Shaw, K. L., Rauz, S., Gattinara, M., Schramm, I., Guillaume, S., Herlin, T., Tzimouli, V., Kuemmerle-Deschner, J. B., Legerstee, J. S., Maron, S., Mazur-Zielińska, H., Niewerth, M., Murray, K. J., Nikishina, I. P., Fantini, F., Pruunsild, C., Selvaag, A. M., Falcini, F., Haas, P. J., Tsitsami, E., Lotito, A. P. N., Avcin, T., Dijkman-Neerincx, R. H. M., Adib, N., Suess, Y. J., Kröger, L., Moura, C., Petříková, A., Astrauskiene˙, D., Grassi, A., Diógenes, A. H. M., Zulian, F., Campos, L. M. A., Gardner-Medwin, J. M., Leone, V., Pittini, C., Trapani, S., Scarazatti, M., Aypar, E., Brunner, J., Fiselier, Th, Minden, K., Ozen, S., Rietschel, C., Stuecklin-Utsch, A., Vougiouka, O., Dolezalova, P., Huppertz, H. I., Moenkemoeller, K., Sallum, A. M. E., Elst, E. F., Al-Mayouf, S. M., Bustabad, S., Cassidy, J. T., Davidson, J. E., Garay, S., Nascimento, A. P., Jakutovič, M., Lepore, L., Musiej-Nowakowska, E., Porras, O., Punaro, M., Wierzbowska, M., Trujillo, E., Silva, C. A. A., Cimaz, R., Alpigiani, M. G.

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The CB1 cannabinoid receptor signals striatal neuroprotection via a PI3K/Akt/mTORC1/BDNF pathway von Blázquez, C, Chiarlone, A, Bellocchio, L, Resel, E, Pruunsild, P, García-Rincón, D, Sendtner, M, Timmusk, T, Lutz, B, Galve-Roperh, I, Guzmán, M

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Results of NOPHO ALL2008 treatment for patients aged 1–45 years with acute lymphoblastic leukemia von Toft, N, Birgens, H, Abrahamsson, J, Griškevičius, L, Hallböök, H, Heyman, M, Klausen, T W, Jónsson, ÓG, Palk, K, Pruunsild, K, Quist-Paulsen, P, Vaitkeviciene, G, Vettenranta, K, Åsberg, A, Frandsen, T L, Marquart, H V, Madsen, H O, Norén-Nyström, U, Schmiegelow, K

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Networks of Cultured iPSC-Derived Neurons Reveal the Human Synaptic Activity-Regulated Adaptive Gene Program von Pruunsild, Priit, Bengtson, C. Peter, Bading, Hilmar

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Expression of the primate-specific LINC00473 RNA in mouse neurons promotes excitability and CREB-regulated transcription von Pruunsild, Priit, Bengtson, C. Peter, Loss, Isabel, Lohrer, Benjamin, Bading, Hilmar

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N-methyl-d-aspartate Receptor-mediated Preconditioning Mitigates Excitotoxicity in Human Induced Pluripotent Stem Cell-derived Brain Organoids von Bauersachs, Hanke Gwendolyn, Bengtson, C. Peter, Weiss, Ursula, Hellwig, Andrea, García-Vilela, Celia, Zaremba, Bastienne, Kaessmann, Henrik, Pruunsild, Priit, Bading, Hilmar

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LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia von FRANCKS, C, MAEGAWA, S, TIMMUSK, T, PRUUNSILD, P, KOPPEL, I, LIND, P. A, MATSUMOTO-ITABA, N, NICOD, J, XIONG, L, JOOBER, R, ENARD, W, KRINSKY, B, LAUREN, J, NANBA, E, RICHARDSON, A. J, RILEY, B. P, MARTIN, N. G, STRITTMATTER, S. M, MÖLLER, H.-J, RUJESCU, D, ST CLAIR, D, MUGLIA, P, ROOS, J. L, ABRAHAMS, B. S, FISHER, S. E, WADE-MARTINS, R, ROULEAU, G. A, STEIN, J. F, KARAYIORGOU, M, GESCHWIND, D. H, RAGOUSSIS, J, KENDLER, K. S, AIRAKSINEN, M. S, OSHIMURA, M, VELAYOS-BAEZA, A, DELISI, L. E, MONACO, A. P, MEDLAND, S. E, COLELLA, S, GROSZER, M, MCAULEY, E. Z, CAFFREY, T. M

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The added value of a European Reference Network on rare and complex connective tissue and musculoskeletal diseases: insights after the first 5 years of the ERN ReCONNET von Talarico, Rosaria, Aguilera, Silvia, Alexander, Tobias, Amoura, Zahir, Andersen, Janette, Arnaud, Laurent, Avcin, Tadej, Marsal Barril, Sara, Beretta, Lorenzo, Bombardieri, Stefano, Bortoluzzi, Alessandra, Bouillot, Coralie, Bulina, Inita, Burmester, Gerd R, Cannizzo, Sara, Cavagna, Lorenzo, Chaigne, Benjamin, Cornet, Alain, Corti, Paolo, Costedoat-Chalumeau, Nathalie, Dāvidsone, Zane, Doria, Andrea, Fenech, Carol, Ferraris, Alessandro, Fischer-Betz, Rebecca, Fonseca, João Eurico, Frank, Charissa, Gaglioti, Andrea, Galetti, Ilaria, Guimarães, Vera, Hachulla, Eric, Holmner, Monica, Houssiau, Frederic, Iaccarino, Luca, Jacobsen, Søren, Limper, Maarten, Malfait, Fransiska, Mariette, Xavier, Marinello, Diana, Martin, Thierry, Matthews, Lisa, Matucci-Cerinic, Marco, Meyer, Alain, Milas-Ahić, Jasminka, Moinzadeh, Pia, Montecucco, Carlomaurizio, Mouthon, Luc, Müller-Ladner, Ulf, Nagy, György, Patarata, Eunice, Pileckyte, Margarita, Pruunsild, Chris, Rednic, Simona, Romão, Vasco C, Schneider, Matthias, Scirè, Carlo Alberto, Smith, Vanessa, Sulli, Alberto, Tamirou, Farah, Tani, Chiara, Taruscio, Domenica, Taulaigo, Anna V, Tincani, Angela, Ticciati, Simone, Turchetti, Giuseppe, van Hagen, P Martin, van Laar, Jacob M, Viera, Ana, de Vries-Bouwstra, Jeska K, Zschocke, Johannes, Cutolo, Maurizio, Mosca, Marta

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Effects of germ line DHFR and FPGS variants on methotrexate metabolism and relapse of leukemia von Tulstrup, M., Moriyama, T., Jiang, C., Grosjean, M., Nersting, J., Abrahamsson, Jonas, Grell, K., Hjalgrim, L. L., Jonsson, O. G., Kanerva, J., Lund, B., Nielsen, S. N., Nielsen, R. L., Quist-Paulsen, P., Pruunsild, K., Wolthers, B. O., Zhang, H., Gupta, R., Yang, J. J., Schmiegelow, K.

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