Ljerka Karadža-Lapić

1. KARADŽA-LAPIĆ, Ljerka, RIJAVEC, Matija, KRALIK, Kristina, ĐANIĆ HAĐIBEGOVIĆ, Ana, DELIN, Sanja, PRKAČIN, Ingrid, JOVIĆ ZLATOVIĆ, Josipa, KOŠNIK, Mitja, ODAK, Marija, CIKOJEVIĆ, Draško. 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. Acta medica Croatica : časopis Hrvatske akademije medicinskih znanosti. 2017, vol. 71, str. 157-162. ISSN 1330-0164. [COBISS.SI-ID 33517785]

2. KARADŽA-LAPIĆ, Ljerka. Učestalost otekline grkljana oboljelih od hereditarnog angioedema : doktorska disertacija. Osijek: [L. Karadža-Lapić], 2017. III, 60 f., [10] f. barvnih pril., ilustr. [COBISS.SI-ID 2048239473]

3. RIJAVEC, Matija, KOROŠEC, Peter, ANDREJEVIĆ, Slađana, KARADŽA-LAPIĆ, Ljerka, GRIVČEVA-PANOVSKA, Vesna, KOŠNIK, Mitja. Hereditary angioedema due to C1-inhibitor deficiency : heterogeneity of SERPING1 mutations, and genetic factors modifying the clinical phenotype. In: SKOČAJ, Matej (ed.). Genetika 2018 : book of abstracts. 8th Congress of the Genetics Society of Slovenia [and] 8th Meeting of the Slovenian Society of Human Genetics, September 19-21, 2018. Ljubljana: Slovensko genetsko društvo: = Genetics Society of Slovenia, 2018. Str. 25. ISBN 978-961-93545-5-1. http://genetika2018.alfa-faktor.si/. [COBISS.SI-ID 2048358257]

4. GRIVČEVA-PANOVSKA, Vesna, KOŠNIK, Mitja, KOROŠEC, Peter, ANDREJEVIĆ, Slađana, KARADŽA-LAPIĆ, Ljerka, RIJAVEC, Matija. Hereditary angioedema due to C1-inhibitor deficiency in Macedonia : clinical characteristics, novel SERPING1 mutations, and genetic factors modifying the clinical phenotype. Annals of medicine. 2018, vol. 50, iss. 3, str. 269-276, tabele. ISSN 1365-2060. https://www.tandfonline.com/doi/abs/10.1080/07853890.2018.1449959?journalCode=iann20, DiRROS - Digitalni repozitorij raziskovalnih organizacij Slovenije, DOI: 10.1080/07853890.2018.1449959. [COBISS.SI-ID 2048261745]

5. RIJAVEC, Matija, KOŠNIK, Mitja, ANDREJEVIĆ, Slađana, KARADŽA-LAPIĆ, Ljerka, GRIVČEVA-PANOVSKA, Vesna, KOROŠEC, Peter. The functional promoter F12-46C/T variant predicts the asymptomatic phenotype of C1-INH-HAE. Clinical & experimental allergy. [Online ed.]. Nov. 2019, vol. 49, iss. 11, str. 1520-1522, ilustr. ISSN 1365-2222. https://onlinelibrary.wiley.com/doi/abs/10.1111/cea.13470, DOI: 10.1111/cea.13470. [COBISS.SI-ID 2048522609]

6. KARADŽA-LAPIĆ, Ljerka, BAREŠIĆ, Marko, VRSALOVIĆ, Renata, IVKOVIĆ-JUREKOVIĆ, Irena, SRŠEN, Saša, PRKAČIN, Ingrid, RIJAVEC, Matija, CIKOJEVIĆ, Draško. Hereditary angioedema due to C1-inhibitor deficiency in pediatric patients in Croatia : first national study, diagnostic and prophylactic challenges. Acta clinica Croatica. 2019, vol. 58, no. 1, str. 139-146, ilustr. ISSN 1333-9451. https://hrcak.srce.hr/file/322489, DiRROS - Digitalni repozitorij raziskovalnih organizacij Slovenije, DOI: 10.20471/acc.2019.58.01.18. [COBISS.SI-ID 2048524657]

7. RIJAVEC, Matija, KOŠNIK, Mitja, ZIDARN, Mihaela, ANDREJEVIĆ, Slađana, KARADŽA-LAPIĆ, Ljerka, CIKOJEVIĆ, Draško, GRIVČEVA-PANOVSKA, Vesna, KOROŠEC, Peter. Hereditary angioedema due to C1-inhibitor deficiency in south-eastern Europe : SERPING1 mutations and genetic factors modifying the clinical phenotype. In: ESHG 2019. Gothenburg: European Society of Human Genetics, 2019. https://www.abstractsonline.com/pp8/#!/7874/presentation/1675. [COBISS.SI-ID 2048520049]