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Naslov The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency (Article)
Autori Rupar Nina  Selb Julij  Kosnik Mitja  Zidarn Mihaela  Andrejevic Sladjana B  Culav Ljerka  Grivceva-Panovska Vesna  Korosec Peter  Rijavec Matija 
Info GENE, (2024), vol. 919 br. , str. -
Projekat Slovenian Research and Inno-vation Agency [P3-0360, J3-2532]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Hereditary angioedema due to C1-inhibitor deficiency in south-eastern Europe: SERPING1 mutations and genetic factors modifying the clinical phenotype (Meeting Abstract)
Autori Rijavec Matija  Kosnik Mitja  Zidarn M  Andrejevic Sladjana B  Karadza-Lapic Ljerka  Cikojevic D  Grivceva-Panovska Vesna  Korosec Peter 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1360-1361
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov The functional promoter F12-46C/T variant predicts the asymptomatic phenotype of C1-INH-HAE (Letter)
Autori Rijavec Matija  Kosnik Mitja  Andrejevic Sladjana B  Karadza-Lapic Ljerka  Grivceva-Panovska Vesna  Korosec Peter 
Info CLINICAL AND EXPERIMENTAL ALLERGY, (2019), vol. 49 br. 11, str. 1520-1522
Projekat Javna Agencija za Raziskovalno Dejavnost RS [P3-0360]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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