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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  
Naslov The Variants in the 3 ' Untranslated Region of the Matrix Metalloproteinase 9 Gene as Modulators of Treatment Outcome in Children with Asthma (Article)
Autori Dragicevic Sandra  Kosnik Mitja  Divac-Rankov Aleksandra  Rijavec Matija  Milosevic Katarina  Korosec Peter  Skerbinjek-Kavalar Maja  Nikolic Aleksandra M 
Info LUNG, (2018), vol. 196 br. 3, str. 297-303
Projekat Slovenian Research Agency [P3-0360]; Ministry of Education, Science and Technological Development of the Republic of Serbia [173008]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype (Article)
Autori Grivcheva-Panovska Vesna  Kosnik Mitja  Korosec Peter  Andrejevic Sladjana B  Karadza-Lapic Ljerka  Rijavec Matija 
Info ANNALS OF MEDICINE, (2018), vol. 50 br. 3, str. 269-276
Projekat Public Agency for Research Activities of the Republic of Slovenia [P3-0360]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association (Article)
Autori Andrejevic Sladjana B  Korosec Peter  Silar Mira  Kosnik Mitja  Mijanovic Radovan  Bonaci-Nikolic Branka M  Rijavec Matija 
Info PLOS ONE, (2015), vol. 10 br. 11, str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov LSC 2012 abstract - Down-regulated let-7b and mir-126 in tumors and surrounding tissue correlate with high microvessel density and poor survival outcomes in non-small-cell lung cancer patients (Meeting Abstract)
Autori Jusufovic Edin  Rijavec Matija  Keser Dragan  Korosec Peter  Sodja Eva  Iljazovic Ermina  Radojevic Zorica  Kosnik Mitja 
Info EUROPEAN RESPIRATORY JOURNAL, (2012), vol. 40 br. , Suppl. 56, str. -
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov let-7b and miR-126 Are Down-Regulated in Tumor Tissue and Correlate with Microvessel Density and Survival Outcomes in Non-Small-Cell Lung Cancer (Article)
Autori Jusufovic Edin  Rijavec Matija  Keser Dragan  Korosec Peter  Sodja Eva  Iljazovic Ermina  Radojevic Zorica  Kosnik Mitja 
Info PLOS ONE, (2012), vol. 7 br. 9, str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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