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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

  Published: 9 July 2019

  1090

  PDF: 785
• 

  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

  Published: 31 March 2015

  2051

  PDF: 956
• 

  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

  Published: 10 April 2020

  1454

  PDF: 1049

• 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

  Published: 24 June 2024

  1026

  PDF: 366

• The enthesopathy of vitamin D-resistant osteomalacia in adults

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

  52-56

  Published:

  1340

  PDF: 1622