COMPARISON OF DIFFERENT DIAGNOSTIC GUIDELINES FOR THE DIAGNOSIS OF MACROPHAGE ACTIVATION SYNDROME COMPLICATING SYSTEMIC JUVENILE IDIOPATHIC ARTHRITIS: SINGLE CENTRE EXPERIENCE

por Jelušić, Marija, Kronja, Matea, Frković, Marijan, Sršen, Saša, Huljev Frković, Sanda, Štekić Novački, Ksenija
Publicado 2018

Vascular Ehlers-Danlos syndrome, an often unrecognized clinical entity: a case report of a novel mutation in the COL3A1 gene

por Huljev Frković, Sanda, Marija Slišković, Ana, Toivonen, Mia, Crkvenac Gregorek, Andrea, Šutalo, Ana, Vrkić Kirhmajer, Majda
Publicado 2022

Two sides of the same coin: a complex presentation of autosomal dominant tubulointerstitial kidney diseases: a literature review and case reports

por Fistrek Prlic, Margareta, Huljev Frkovic, Sanda, Beck, Bodo, Tonkovic Durisevic, Ivana, Bulimbasic, Stela, Coric, Marijana, Lamot, Lovro, Ivandic, Ema, Vukovic Brinar, Ivana
Publicado 2023