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Arthritis & Rheumatology (Hoboken, N.J.)|March 27, 2015
Brief Report: Childhood-Onset Systemic Necrotizing Vasculitides: Long-Term Data From the French Vasculitis Study Group RegistryMichele Iudici, Xavier Puéchal, Christian Pagnoux, et al.
Clinical Immunology (Orlando, Fla.)|February 14, 2004
Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiencyPierre Quartier, Jacinta Bustamante, Ozden Sanal, et al.
Expert Opinion on Biological Therapy|March 20, 2019
Expert opinion on the use of biological therapy in non-infectious uveitisSara Touhami, Eléonore Diwo, Pascal Sève, et al.
Arthritis Research & Therapy|March 20, 2025
The needed daily dose of colchicine in patients with Familial Mediterranean Fever may be higher in women: a study on behalf of the JIR cohortIlenia Di Cola, Alessandra Bartoli, Léa Savey, et al.
The Journal of Rheumatology|November 16, 2020
Development and Testing of Reduced Versions of the Manual Muscle Test-8 in Juvenile DermatomyositisSilvia Rosina, Giulia C Varnier, Angela Pistorio, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|September 19, 2022
De Novo Gain-Of-Function Variations in LYN Associated With an Early-Onset Systemic Autoinflammatory DisorderCamille Louvrier, Elma El Khouri, Martine Grall Lerosey, et al.
The Journal of Allergy and Clinical Immunology|September 19, 2012
Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiencyFabian Hauck, Clotilde Randriamampita, Emmanuel Martin, et al.
The Journal of Rheumatology|June 17, 2020
Inflammatory Bowel Disease in Children With Systemic Juvenile Idiopathic ArthritisJustine Maller, Emily Fox, K T Park, et al.
The Journal of Experimental Medicine|July 19, 2017
Protein kinase D at the Golgi controls NLRP3 inflammasome activationZhirong Zhang, Gergö Meszaros, Wan-Ting He, et al.
Pediatrics|June 29, 2011
Mevalonate kinase deficiency: a survey of 50 patientsBrigitte Bader-Meunier, Benoit Florkin, Jean Sibilia, et al.
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