Search Results - "Sršen, Saša"
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How to Treat Patients after Serious Adverse Effects Caused by TNF Inhibitors?
Published in Acta clinica Croatica (Tisak) (01-03-2020)“…Biological agents are widely used in the treatment of autoimmune rheumatic disorders. We report on serious adverse events during treatment with anti-tumor…”
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HEREDITARY ANGIOEDEMA DUE TO C1-INHIBITOR DEFICIENCY IN PEDIATRIC PATIENTS IN CROATIA - FIRST NATIONAL STUDY, DIAGNOSTIC AND PROPHYLACTIC CHALLENGES
Published in Acta clinica Croatica (Tisak) (01-03-2019)“…Hereditary angioedema (HAE) is a rare autosomal dominant disease with deficiency (type I) or dysfunction (type II) of C1 inhibitor, caused by mutations in the…”
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Comparison of Different Diagnostic Guidelines for the Diagnosis of Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: Single Centre Experience
Published in Acta clinica Croatica (Tisak) (01-06-2018)“…Macrophage activation syndrome (MAS) is a potentially fatal complication of systemic juvenile idiopathic arthritis (sJIA), caused by exaggerated but…”
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439 New candidate biomarker of nephritis risk assessment in children with Henoch-Schönlein purpura
Published in Archives of disease in childhood (11-10-2021)“…GoalHenoch-Schönlein purpura (HSP) is the most common vasculitis of the childhood. Among all possible symptoms/complications, nephritis (HSPN) is the main and…”
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435 Severe skin manifestations in patients with Henoch Schoenlein purpura (HSP) in five tertiary centres in Croatia between 2009 and 2019
Published in Archives of disease in childhood (11-10-2021)“…To evaluate characteristics of patients with severe skin manifestations of Henoch Schoenlein purpura (HSP) in five tertiary centres in Croatia in time period…”
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Erythrocyte Glutathione S-Transferase Activity as a Sensitive Marker of Kidney Function Impairment in Children with IgA Vasculitis
Published in International journal of molecular sciences (01-04-2024)“…IgA vasculitis (IgAV) is the most common childhood vasculitis. The main cause of morbidity and mortality in children with IgAV is nephritis (IgAVN), but the…”
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Insight into the Interplay of Gd-IgA1, HMGB1, RAGE and PCDH1 in IgA Vasculitis (IgAV)
Published in International journal of molecular sciences (16-04-2024)“…The pathogenesis of IgAV, the most common systemic vasculitis in childhood, appears to be complex and requires further elucidation. We aimed to investigate the…”
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Association of Glutathione Transferase M1, T1, P1 and A1 Gene Polymorphism and Susceptibility to IgA Vasculitis
Published in International journal of molecular sciences (16-07-2024)“…Endothelial cell injury is a hallmark of IgA vasculitis (IgAV), possibly associated with various factors, including oxidative stress. Certain single nucleotide…”
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HLA Polymorphisms and Clinical Manifestations in IgA Vasculitis
Published in International journal of molecular sciences (01-01-2024)“…Studies concerning the genetic background of IgA vasculitis (IgAV), a small-vessel vasculitis occurring predominantly in childhood, have confirmed that the…”
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The Impact of Vitamin D Levels on Clinical Manifestations of Multisystem Inflammatory Syndrome in Children: A Cross-Sectional Study
Published in Life (Basel, Switzerland) (01-03-2023)“…Hyperinflammatory response that resembles Kawasaki disease may develop in children after COVID-19 disease, and it is called multisystem inflammatory syndrome…”
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Gastrointestinal involvement and its association with the risk for nephritis in IgA vasculitis
Published in Therapeutic advances in musculoskeletal disease (2021)“…Background: We analysed clinical and biochemical parameters in predicting severe gastrointestinal (GI) manifestations in childhood IgA vasculitis (IgAV) and…”
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Serum Levels of S100A8/A9 as a Biomarker of Disease Activity in Patients with IgA Vasculitis
Published in Biomedicines (01-04-2024)“…S100A8/A9 protein is a well-known marker of disease activity or severity in many autoimmune and autoinflammatory diseases, but there have not been many studies…”
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Henoch-Schönleinov purpurni nefritis u djece: iskustva dvaju tercijarnih centara za pedijatrijsku i adolescentnu reumatologiju Republike Hrvatske u razdoblju od 2006. do 2017. godine
Published in Liječnički vjesnik (08-07-2019)“…Cilj istraživanja: Valjalo je utvrditi vrste bubrežnih komplikacija, indikacije za biopsiju, načine liječenja te moguće ishode u bolesnika s…”
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Hereditarni angioedem uzrokovan manjkom C1-inhibitora u pedijatrijskih bolesnika u Hrvatskoj – prvo nacionalno istraživanje, dijagnostički i profilaktički izazovi
Published in Acta clinica Croatica (Tisak) (01-03-2019)“…Hereditarni angioedem (HAE) je rijetka autosomno dominantna bolest nastala zbog mutacije gena SERPING1 za inhibitor plazmatskog proteina C1 (C1-INH). Uslijed…”
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Persistence and Severity of Cutaneous Manifestations in IgA Vasculitis Is Associated with Development of IgA Vasculitis Nephritis in Children
Published in Dermatology (Basel) (01-03-2022)“…The purpose of this study was to evaluate the prevalence and severity of skin involvement in children with IgA vasculitis (IgAV) and its relationship with…”
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Kako liječiti bolesnike nakon teških neželjenih djelovanja uzrokovanih inhibitorima TNF
Published in Acta clinica Croatica (01-03-2020)“…Biološki lijekovi se primjenjuju u liječenju brojnih autoimunih reumatskih bolesti. U ovom članku prikazujemo dva slučaja ozbiljnih nuspojava liječenja…”
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Clinical features, treatment and outcome of pediatric patients with severe cutaneous manifestations in IgA vasculitis: Multicenter international study
Published in Seminars in arthritis and rheumatism (01-08-2023)“…IgA vasculitis (IgAV) (formerly Henoch-Schönlein Purpura, HSP) rarely causes severe skin lesions in children. The purpose of the research was to determine…”
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443 Different histological classifications for IgA vasculitis nephritis – which one has the best association with the disease outcome?
Published in Archives of disease in childhood (11-10-2021)“…IntroductionIgA vasculitis nephritis (IgAVN) is almost the only cause of morbidity and mortality among children suffering from this most common…”
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Semiquantitative classification (SQC) and Oxford classifications predict poor renal outcome better than The International Study of Kidney Disease in Children (ISKDC) and Haas in patients with IgAV nephritis: a multicenter study
Published in Journal of nephrology (01-03-2023)“…Introduction Several histologic classifications are used in the evaluation of IgA vasculitis nephritis (IgAVN), however, to date, no studies have determined…”
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Usporedba različitih dijagnostičkih smjernica za dijagnozu sindroma aktivacije makrofaga koji komplicira sistemski tip juvenilnog idiopatskog artritisa: iskustvo jednog centra
Published in Acta clinica Croatica (01-06-2018)“…Sindrom aktivacije makrofaga (MAS) potencijalno je smrtonosna komplikacija sistemskog tipa juvenilnog idiopatskog artritisa (sJIA) uzrokovana prekomjernim, ali…”
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