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  A new MEFV gene mutation in an Iranian patient with familial Mediterranean fever

  S. Farjadian, F. Bonatti, A. Soriano, M. Reina, A. Adorni, C. Graziano, M. Moghtaderi, A. Percesepe, G. Romeo, D. Martorana

  85-87

  09-07-2019

  https://doi.org/10.4081/reumatismo.2019.1141

  1122

  PDF: 799
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  Ex vivo and in vitro production of pro-inflammatory cytokines in Blau syndrome

  P. Galozzi, O. Negm, E. Greco, N. Alkhattabi, A. Gava, P. Sfriso, L. Fairclough, I. Todd, P. Tighe, L. Punzi

  277-284

  31-03-2015

  https://doi.org/10.4081/reumatismo.2014.772

  2080

  PDF: 994
• 

  Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene

  E. Conticini, A. Negro, L. Magnani, R. Ugolini, B. Atienza-Mateo, B. Frediani, C. Salvarani

  67-70

  10-04-2020

  https://doi.org/10.4081/reumatismo.2020.1255

  1517

  PDF: 1085

• Novel genetic mutation associated with hyperphosphatemic familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome treated with denosumab: a case report

  G. Fabbriciani, A. Colombini, C. Messina, G. Adami

  24-06-2024

  https://doi.org/10.4081/reumatismo.2024.1687

  1083

  PDF: 413

• The enthesopathy of vitamin D-resistant osteomalacia in adults

  R. Ramonda, P. Sfriso, M. Podswiadek, F. Oliviero, C. Valvason, L. Punzi

  52-56

  https://doi.org/10.4081/reumatismo.2005.52

  1361

  PDF: 1645