Search Results - "ANDREJEVIĆ, SLADJANA"
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Celiac disease-specific and inflammatory bowel disease-related antibodies in patients with recurrent aphthous stomatitis
Published in Immunobiology (1979) (01-01-2019)“…The etiology of recurrent aphthous stomatitis (RAS) remains unknown. RAS can be presented as primary, idiopathic condition and as a secondary RAS, which is…”
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The Diagnostic Importance of Recombinant Allergen IgE Testing in Patients with Hymenoptera Venom Allergy: Comparison of Two Methods
Published in Iranian journal of allergy, asthma, and immunology (07-08-2021)“…Adults with systemic anaphylactic reactions (SAR) to insect sting show often multiple-positivity of serum-specific IgE (sIgE) to Hymenoptera venoms…”
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The Different Clinical Courses of Legionnaires' Disease in Newborns from the Same Maternity Hospital
Published in Medicina (Kaunas, Lithuania) (24-08-2022)“…In children, the incidence of Legionnaires' disease (LD) is unknown, hospital-acquired LD is associated with clinical risk factors and environmental risk, and…”
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Coexistence of Autoantibodies against the Golgi Complex and Ro52 Antigen in a Patient with Nonspecific Interstitial Pneumonia
Published in Internal Medicine (01-01-2016)“…Nonspecific interstitial pneumonia (NSIP) is often associated with connective tissue diseases (CTD). The diagnosis of NSIP was confirmed in a 63-year-old man…”
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Serum B cell activating factor and interleukin 10 levels in common variable immunodeficiency: Relationship with clinical findings
Published in Vojnosanitetski pregled (2019)“…Background/Aim. Common variable immunodeficiency (CVID) is an immunologically and clinically heterogeneous disorder. Disturbed cytokine production is…”
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Triple IgE-positivity to hornet, wasp and bee venom in the patient with anaphylaxis: Diagnostic and therapeutic approach
Published in Vojnosanitetski pregled (2019)“…Introduction. Triple-positivity (TP) or double-positivity (DP) for serum-specific immunoglobulin E (sIgE) antibodies against hornet venom (HV), wasp venom (WV)…”
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High Procalcitonin in a Patient with Drug Hypersensitivity Syndrome
Published in Internal Medicine (01-01-2009)“…We present a patient who developed carbamazepine (CBZ)-induced Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) syndrome associated with high serum…”
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Hashimoto's encephalopathy: a long-lasting remission induced by intravenous immunoglobulins
Published in Vojnosanitetski pregled (01-05-2011)“…Hashimoto's encephalopathy (HE) is a rare autoimmune syndrome characterized by various neuropsychiatric manifestations, responsive to steroid treatment and…”
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Systemic mastocytosis: case report with literature review
Published in Srpski arhiv za celokupno lekarstvo (01-01-2012)“…Mastocytosis is a clonal neoplastic disorder of the mast cells. The clinical signs and symptoms of mastocytosis are heterogeneous ranging from indolent disease…”
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Aquaporin4-IgG seropositivity significantly increases the risk of comorbid autoimmune diseases in NMOSD patients: population-based registry data
Published in Journal of neurology (01-12-2024)“…Background The aim of our study was to estimate the frequency of autoimmune comorbidities, in NMOSD patients from the national Serbian NMOSD Registry. Methods…”
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Watermelon stomach in a patient with primary Sjögren's syndrome
Published in Vojnosanitetski pregled (01-03-2010)“…Watermelon stomach (WS) or gastric antral vascular ectasia (GAVE) is a rare cause of upper gastrointestinal bleeding described in a variety of autoimmune…”
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International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency
Published in Allergy (01-02-2017)“…Background The consensus documents published to date on hereditary angioedema with C1 inhibitor deficiency (C1‐INH‐HAE) have focused on adult patients. Many of…”
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Recombinant human C1 esterase inhibitor for prophylaxis of hereditary angio-oedema: a phase 2, multicentre, randomised, double-blind, placebo-controlled crossover trial
Published in The Lancet (British edition) (30-09-2017)“…Hereditary angio-oedema is a recurrent, oedematous disorder caused by deficiency of functional C1 inhibitor. Infusions of plasma-derived C1 esterase inhibitor…”
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Immunoserological parameters in SLE: high-avidity anti-dsDNA detected by ELISA are the most closely associated with the disease activity
Published in Clinical rheumatology (01-11-2013)“…We assessed the relationship between the serum levels of antibodies against double-stranded DNA (dsDNA), C1q, nucleosomes, histones, C3 and C4 complement…”
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Serum DNase I activity in systemic lupus erythematosus: correlation with immunoserological markers, the disease activity and organ involvement
Published in Clinical chemistry and laboratory medicine (01-05-2013)“…Decreased activity of serum desoxyribonuclease I (DNase I) in systemic lupus erythematosus (SLE) has been reported, but its role as a biomarker in SLE is still…”
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Autoantibodies to GP2, the major zymogen granule membrane glycoprotein, in patients with gluten-sensitive enteropathy: A possible serological trap
Published in Clinica chimica acta (11-04-2012)“…► IgA and IgG antibodies to GP2 may be elevated in gluten-sensitive enteropathy (GSE). ► Comparing with ulcerative colitis and GSE, anti-GP2 were not…”
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Prolonged infections associated with antineutrophil cytoplasmic antibodies specific to proteinase 3 and myeloperoxidase: diagnostic and therapeutic challenge
Published in Clinical rheumatology (01-08-2010)“…Chronic infections may mimic antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV). We investigated which markers may help in the diagnosis…”
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Recombinant human C1 esterase inhibitor as short-term prophylaxis in patients with hereditary angioedema
Published in The journal of allergy and clinical immunology in practice (Cambridge, MA) (01-02-2020)“…Hereditary angioedema (HAE), an inherited deficiency of functional C1 esterase inhibitor (C1-INH), is characterized by recurrent episodes of disabling and…”
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International Consensus on the Use of Genetics in the Management of Hereditary Angioedema
Published in The journal of allergy and clinical immunology in practice (Cambridge, MA) (01-03-2020)“…Hereditary angioedema (HAE) is becoming much more genetically complex than was initially considered. Thus, the role of HAE genetics is expanding beyond…”
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