Matija Rijavec - Dissemin

Papers authored by Matija Rijavec

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2017 Peter Korosec, Paul J. Turner, Mira Silar, Peter Kopac, Mitja Kosnik, Bernhard F. Gibbs, Mohamed H. Shamji, Adnan Custovic, Matija Rijavec

Basophils, high-affinity IgE receptors, and CCL2 in human anaphylaxis

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K. Dežman, P. Korošec, H. Rupnik, M. Rijavec

SPINK5 is associated with early-onset and CHI3L1 with late-onset atopic dermatitis

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Tanja Planinsek Rucigaj, Matija Rijavec

, Jovan Miljkovic, Julij Selb, Peter Korosec

A novel mutation in the FOXC2 gene: a heterozygous insertion of adenosine (c.867insA) in a family with lymphoedema of lower limbs without distichiasis

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Ana Koren, Matija Rijavec

, Eva Sodja, Izidor Kern, Aleksander Sadikov, Viljem Kovac, Peter Korosec, Tanja Cufer

HighBMI1mRNA expression in peripheral whole blood is associated with favorable prognosis in advanced non-small cell lung cancer patients

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L. Karadža-Lapić, M. Rijavec

, K. Kralik, A. Đ. Hadžibegović, S. Delin, I. Prkačin, J. J. Zlatović, M. Košnik, M. Odak, D. Cikojević

Improvement in the management of rare diseases in Croatia based on the protocol for hereditary angioedema,Poboljšanje zbrinjavanja bolesnika s rijetkim bolestima u Hrvatskoj-temeljeno na protokolu za hereditarni angioedem

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2016 Mateja Žavbi, Peter Korošec, Matjaž Fležar, Sabina Škrgat Kristan, Mateja Marc Malovrh, Matija Rijavec

Polymorphisms and haplotypes of the chromosome locus 17q12-17q21.1 contribute to adult asthma susceptibility in Slovenian patients

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Ljerka Karadža-Lapić, Peter Korošec, Mira Šilar, Mitja Košnik, Draško Cikojević, Bernarda Lozić, Matija Rijavec

Frequent life-threatening laryngeal attacks in two Croatian families with hereditary angioedema due to C1 inhibitor deficiency harbouring a novel frameshift mutation in SERPING1

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Ana Koren

, Matija Rijavec

, Izidor Kern, Eva Sodja, Peter Korosec, Tanja Cufer

BMI1,ALDH1A1, andCD133Transcripts Connect Epithelial-Mesenchymal Transition to Cancer Stem Cells in Lung Carcinoma

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2015 Slađana Andrejević, Peter Korošec, Mira Šilar, Mitja Košnik, Radovan Mijanović, Branka Bonači-Nikolić, Matija Rijavec

Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association

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Ana Koren, Eva Sodja, Matija Rijavec

, Mojca Jez, Viljem Kovac, Peter Korosec, Tanja Cufer

Prognostic value of cytokeratin-7 mRNA expression in peripheral whole blood of advanced lung adenocarcinoma patients

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Peter Korošec, Klemen Žiberna, Mira Šilar, Manca Dežman, Nina Čelesnik Smodiš, N. Čelesnik Smodiš, Matija Rijavec

, Peter Kopač, Renato Eržen, Nika Lalek, Nissera Bajrović, Mitja Košnik, Mihaela Zidarn

Immunological and clinical factors associated with adverse systemic reactions during the build-up phase of honeybee venom immunotherapy

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Eva Sodja, Matija Rijavec

, Ana Koren, Aleksander Sadikov, Peter Korošec, Tanja Cufer

The prognostic value of whole blood SOX2, NANOG and OCT4 mRNA expression in advanced small-cell lung cancer

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H. Rupnik, M. Rijavec

, P. Korošec

Filaggrin loss-of-function mutations are not associated with atopic dermatitis that develops in late childhood or adulthood

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2014 Katarina Osolnik, Matija Rijavec

, Peter Korosec

Disposal of iNKT cell deficiency and an increase in expression of SLAM signaling factors characterizes sarcoidosis remission: a 4-year longitudinal study

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Matija Rijavec

, Peter Korošec, Mateja Zavbi, Izidor Kern, Mateja Marc Malovrh

Let-7a is differentially expressed in bronchial biopsies of patients with severe asthma

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Nina Čelesnik Smodiš, Mira Šilar, Mira Silar, Renato Eržen, Matija Rijavec

, Mitja Košnik, Peter Korošec

Down-Regulation of FcεRI-Mediated CD63 Basophil Response during Short-Term VIT Determined Venom-Nonspecific Desensitization

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2013 Anton Lopert, Matija Rijavec

, Mateja Žavbi, Peter Korošec, Matjaž Fležar

Asthma treatment outcome in adults is associated with rs9910408 in TBX21 gene

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Matija Rijavec

, Peter Korošec, Mira Šilar, Mira Silar, Mihaela Zidarn

, Jovan Miljković, Mitja Košnik

Hereditary Angioedema Nationwide Study in Slovenia Reveals Four Novel Mutations in SERPING1 Gene

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M. Balantič, M. Rijavec

, M. Fležar, T. Camlek, I. Hudoklin, M. Košnik, P. Korošec, S. Šuškovič

A polymorphism in ORMDL3 is associated not only with asthma without rhinitis but also with chronic obstructive pulmonary disease

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E. Mušič, P. Korošec, M. Šilar, K. Adamič, M. Košnik, M. Rijavec

Serum diamine oxidase activity as a diagnostic test for histamine intolerance

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Papers authored by Matija Rijavec