EULAR/PReS endorsed consensus criteria for the classification of childhood vasculitides von Ozen, S, Ruperto, N, Dillon, M J, Bagga, A, Barron, K, Davin, J C, Kawasaki, T, Lindsley, C, Petty, R E, Prieur, A M, Ravelli, A, Woo, P

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Reactive haemophagocytic syndrome in children with inflammatory disorders. A retrospective study of 24 patients von Stéphan, J. L., Koné‐Paut, I., Galambrun, C., Mouy, R., Bader‐Meunier, B., Prieur, A.‐M.

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Classification of Human Chromosome 21 Gene-Expression Variations in Down Syndrome: Impact on Disease Phenotypes von Aït Yahya-Graison, E., Aubert, J., Dauphinot, L., Rivals, I., Prieur, M., Golfier, G., Rossier, J., Personnaz, L., Créau, N., Bléhaut, H., Robin, S., Delabar, J.M., Potier, M.-C.

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CARD15 mutations in Blau syndrome von Miceli-Richard, Corinne, Lesage, Suzanne, Rybojad, Michel, Prieur, Anne-Marie, Manouvrier-Hanu, Sylvie, Häfner, Renate, Chamaillard, Mathias, Zouali, Habib, Thomas, Gilles, Hugot, Jean-Pierre

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Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders von Jacquemont, M-L, Sanlaville, D, Redon, R, Raoul, O, Cormier-Daire, V, Lyonnet, S, Amiel, J, Le Merrer, M, Heron, D, de Blois, M-C, Prieur, M, Vekemans, M, Carter, N P, Munnich, A, Colleaux, L, Philippe, A

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Initial presentation of childhood-onset systemic lupus erythematosus: A French multicenter study von Bader-Meunier, B., Armengaud, J.B., Haddad, E., Salomon, R., Deschênes, G., Koné-Paut, I., Leblanc, T., Loirat, C., Niaudet, P., Piette, J.C., Prieur, A.M., Quartier, P., Bouissou, F., Foulard, M., Leverger, G., Lemelle, I., Pilet, P., Rodière, M., Sirvent, N., Cochat, P., the French pediatric-onset SLE study group

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Autologous stem cell transplantation for refractory juvenile idiopathic arthritis: analysis of clinical effects, mortality, and transplant related morbidity von de Kleer, I M, Brinkman, D M C, Ferster, A, Abinun, M, Quartier, P, van der Net, J, ten Cate, R, Wedderburn, L R, Horneff, G, Oppermann, J, Zintl, F, Foster, H E, Prieur, A M, Fasth, A, van Rossum, M A J, Kuis, W, Wulffraat, N M

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The effect of expertise in gymnastics on postural control von Vuillerme, N, Danion, F, Marin, L, Boyadjian, A, Prieur, J.M, Weise, I, Nougier, V

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Can vision compensate for a lower limbs muscular fatigue for controlling posture in humans? von Vuillerme, Nicolas, Nougier, Vincent, Prieur, Jean-Michel

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A recently recognised chronic inflammatory disease of early onset characterised by the triad of rash, central nervous system involvement and arthropathy von PRIEUR, A.-M

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Efficacy of cyclosporine A in the treatment of macrophage activation syndrome in juvenile arthritis: Report of five cases von Mouy, Richard, Stephan, Jean-Louis, Pillet, Pascal, Haddad, Elie, Hubert, Philippe, Prieur, Anne-Marie

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La continuité des soins en rhumatologie pédiatrique von Prieur, A.-M., Deslandre, C., Lemelle, I.

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Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study von Ryan, A K, Goodship, J A, Wilson, D I, Philip, N, Levy, A, Seidel, H, Schuffenhauer, S, Oechsler, H, Belohradsky, B, Prieur, M, Aurias, A, Raymond, F L, Clayton-Smith, J, Hatchwell, E, McKeown, C, Beemer, F A, Dallapiccola, B, Novelli, G, Hurst, J A, Ignatius, J, Green, A J, Winter, R M, Brueton, L, Brøndum-Nielsen, K, Scambler, P J

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Development of Crohn Disease During Anti–TNF-α Therapy in a Child With Juvenile Idiopathic Arthritis von Ruemmele, F. M, Prieur, A-M, Talbotec, C, Goulet, O, Schmitz, J

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Spectrum of NSD1 mutations in Sotos and Weaver syndromes von Rio, M, Clech, L, Amiel, J, Faivre, L, Lyonnet, S, Le Merrer, M, Odent, S, Lacombe, D, Edery, P, Brauner, R, Raoul, O, Gosset, P, Prieur, M, Vekemans, M, Munnich, A, Colleaux, L, Cormier-Daire, V

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Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations von Luciani, J J, de Mas, P, Depetris, D, Mignon-Ravix, C, Bottani, A, Prieur, M, Jonveaux, P, Philippe, A, Bourrouillou, G, de Martinville, B, Delobel, B, Vallee, L, Croquette, M-F, Mattei, M-G

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The Relationship Between Left and Right Pericardial Pressures in Humans: An Intraoperative Study von Hamilton, Douglas R., MD, PhD, MSc, EEng, Sas, Rozsa, MD, Semlacher, Roy A., MD, Kieser Prieur, Teresa M., MD, Tyberg, John V., MD, PhD

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New Natural Inactivating Mutations of the Follicle-Stimulating Hormone Receptor: Correlations between Receptor Function and Phenotype von Touraine, P, Beau, I, Gougeon, A, Meduri, G, Desroches, A, Pichard, C, Detoeuf, M, Paniel, B, Prieur, M, Zorn, J-R, Milgrom, E, Kuttenn, F, Misrahi, M

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Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes von Feldmann, Jérôme, Prieur, Anne-Marie, Quartier, Pierre, Berquin, Patrick, Certain, Stéphanie, Cortis, Elisabetta, Teillac-Hamel, Dominique, Fischer, Alain, Basile, Geneviève de Saint

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Accuracy of spatial localization depending on head posture in a perturbed gravitoinertial force field von PRIEUR, J.-M, BOURDIN, C, VERCHER, J.-L, SARES, F, BLOUIN, J, GAUTHIER, G. M

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