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European Journal of Human Genetics : EJHG|November 13, 2004
MVK mutations and associated clinical features in Italian patients affected with autoinflammatory disorders and recurrent feverAndrea D'Osualdo, Paolo Picco, Francesco Caroli, et al.
Annals of the Rheumatic Diseases|May 3, 2013
Whole-body MRI in the assessment of disease activity in juvenile dermatomyositisClara Malattia, Maria Beatrice Damasio, Annalisa Madeo, et al.
Journal of Clinical Immunology|May 31, 2019
Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI SyndromeStefano Volpi, Antonella Insalaco, Roberta Caorsi, et al.
Annals of the Rheumatic Diseases|May 20, 2017
ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national studyRoberta Caorsi, Federica Penco, Alice Grossi, et al.
Nature Communications|July 29, 2015
Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndromePeter E Thijssen, Yuya Ito, Giacomo Grillo, et al.
The Journal of Rheumatology|April 17, 2015
Dissecting the heterogeneity of macrophage activation syndrome complicating systemic juvenile idiopathic arthritisFrancesca Minoia, Sergio Davì, AnnaCarin Horne, et al.
Blood|September 27, 2018
T-cell defects in patients with <i>ARPC1B</i> germline mutations account for combined immunodeficiencyImmacolata Brigida, Matteo Zoccolillo, Maria Pia Cicalese, et al.
Nature Communications|December 21, 2017
Type I interferon-mediated autoinflammation due to DNase II deficiencyMathieu P Rodero, Alessandra Tesser, Eva Bartok, et al.
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