Pregled po CROSBI profilu: Ingeborg Barišić (CROSBI Profil: 13659, MBZ: 168183)
Pronađeno 523 radova
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26.Morris, Joan K; Wellesley, Diana G; Barisic, Ingeborg; Addor, Marie-Claude; Bergman, Jorieke E H; Braz, Paula; Cavero- Carbonell, Clara; Draper, Elizabeth S; Gatt, Miriam; Haeusler, Martin et al.Epidemiology of congenital cerebral anomalies in Europe: a multicentre, population-based EUROCAT study // Archives of Disease in Childhood, 104 (2019), 12; 1181-1187 doi:10.1136/archdischild-2018-316733 (međunarodna recenzija, članak, znanstveni)
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27.Santoro, Michele; Coi, Alessio; Barišić, Ingeborg; Garne, Ester; Addor, Marie-Claude; Bergman, Jorieke E.H.; Bianchi, Fabrizio; Boban, Ljubica; Braz, Paula; Cavero-Carbonell, Clara et al.Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study // Neuroepidemiology, 53 (2019), 3-4; 169-179 doi:10.1159/000501238 (međunarodna recenzija, članak, znanstveni)
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28.van de Putte, Romy; van Rooij, Iris A. L. M.; Marcelis, Carlo L. M.; Guo, Michel; Brunner, Han G.; Addor, Marie-Claude; Cavero- Carbonell, Clara; Dias, Carlos M.; Draper, Elizabeth S.; Etxebarriarteun, Larraitz et al.Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study // Pediatric Research, 87 (2019), 3; 541-549 doi:10.1038/s41390-019-0561-y (međunarodna recenzija, članak, znanstveni)
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29.Cleary, Brian; Loane, Maria; Addor, Marie-Claude; Barisic, Ingeborg; de Walle, Hermien E K; Matias Dias, Carlos; Gatt, Miriam; Klungsoyr, Kari; McDonnell, Bob; Neville, Amanda et al.Methadone, Pierre Robin sequence and other congenital anomalies: case–control study // Archives of Disease in Childhood - Fetal and Neonatal Edition, 105 (2019), 2; 151-157 doi:10.1136/archdischild-2019-316804 (međunarodna recenzija, članak, ostalo)
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30.Coi, Alessio; Santoro, Michele; Garne, Ester; Pierini, Anna; Addor, Marie‐Claude; Alessandri, Jean‐Luc; Bergman, Jorieke E. H.; Bianchi, Fabrizio; Boban, Ljubica; Braz, Paula et al.Epidemiology of achondroplasia: A population‐based study in Europe // American Journal of Medical Genetics Part A, 179 (2019), 9; 1791-1798 doi:10.1002/ajmg.a.61289 (međunarodna recenzija, članak, znanstveni)
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31.Wang, Hao; Barisic, Ingeborg; Loane, Maria; Addor, Marie-Claude; Bailey, Linda M.; Gatt, Miriam; Klungsoyr, Kari; Mokoroa, Olatz; Nelen, Vera; Neville, Amanda J. et al.Congenital clubfoot in Europe: A population-based study // American Journal of Medical Genetics Part A, 179 (2019), 4; 595-601 doi:10.1002/ajmg.a.61067 (međunarodna recenzija, članak, ostalo)
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32.Morris, Joan K.; Springett, Anna L.; Greenlees, Ruth; Loane, Maria; Addor, Marie-Claude; Arriola, Larraitz; Barisic, Ingeborg; Bergman, Jorieke E. H.; Csaky-Szunyogh, Melinda; Dias, Carlos et al.Trends in congenital anomalies in Europe from 1980 to 2012 // PLOS ONE, 13 (2018), 4; e0194986, 18 doi:10.1371/journal.pone.0194986 (međunarodna recenzija, članak, znanstveni)
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33.Garne, Ester; Rissmann, Anke; Addor, Marie-Claude; Barisic, Ingeborg; Bergman, Jorieke; Braz, Paula; Cavero-Carbonell, Clara; Draper, Elizabeth S.; Gatt, Miriam; Haeusler, Martin et al.Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age – A EUROCAT study // European Journal of Medical Genetics, 61 (2018), 9; 483-488 doi:10.1016/j.ejmg.2018.05.010 (međunarodna recenzija, članak, znanstveni)
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34.Barisic, Ingeborg; Boban, Ljubica; Akhmedzhanova, Diana; Bergman, Jorieke E.H.; Cavero-Carbonell, Clara; Grinfelde, Ieva; Materna-Kiryluk, Anna; Latos-Bieleńska, Anna; Randrianaivo, Hanitra; Zymak-Zakutnya, Natalya et al.Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe // European Journal of Medical Genetics, 61 (2018), 9; 499-507 doi:10.1016/j.ejmg.2018.05.014 (međunarodna recenzija, članak, znanstveni)
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35.O’Connor, Daniel J.; Sheean, Maria E.; Hofer, Matthias P.; Tsigkos, Stelios; Mariz, Segundo; Fregonese, Laura; Larsson, Kristina; Hivert, Virginie; Westermark, Kerstin; Naumann-Winter, Frauke et al.Defining orphan conditions in the context of the European orphan regulation: challenges and evolution // Nature Reviews Drug Discovery, 18 (2018), 7; 479-480 doi:10.1038/nrd.2018.128 (međunarodna recenzija, pregledni rad, stručni)
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36.Morris, Joan K.; Garne, Ester; Loane, Maria; Addor, Marie-Claude; Barisic, Ingeborg; Bianchi, Fabrizio; Gatt, Miriam; Lanzoni, Monica; Lynch, Catherine; Mokoroa, Olatz et al.Prevalence of valproate syndrome in Europe from 2005 to 2014: A registry based multi-centre study // European Journal of Medical Genetics, 61 (2018), 9; 479-482 doi:10.1016/j.ejmg.2018.05.008 (međunarodna recenzija, članak, znanstveni)
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37.Krnjak, Goran; Đuranović, Vlasta; Barišić, Ingeborg; Pažanin, Leo; Vulin, Katarina; Đaković, IvanaMakrofagni miofascitis u djevojčice s usporenim psihomotornim razvojem // 13. kongres Hrvatskog pedijatrijskog društva i 12. kongres Pedijatrijskog društva Hrvatske udruge medicinskih sestara / Paediatria Croatica, 62(Suppl.2) / Barišić, Ingeborg (ur.).
Zagreb: Klinika za dječje bolesti Zagreb, 2018. str. 234-234 (poster, međunarodna recenzija, sažetak, stručni) -
38.Bobinec, Adriana; Ivankov, Ana-Maria; Kero, Mijana; Sansović, Ivona; Barišić, IngeborgGenotipsko-fenotipska korelacija rijetke mikrodelecije 17q24.1-q24.3 // Paediatria Croatica, 61 (2017), 2; 84-89 doi:10.13112/PC.2017.13 (domaća recenzija, prikaz, ostalo)
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39.Ivankov, Ana-Maria; Bobinec, Adriana; Boban, Ljubica; Sansović, Ivona; Barišić, IngeborgDe novo složena kromosomska preraspodjela u regiji 2q32q35 // Paediatria Croatica, 61 (2017), 2; 78-83 doi:10.13112/PC.2017.12 (domaća recenzija, prikaz, ostalo)
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40.Dvorakova, L.; Vlaskova, H.; Sarajlija, A.; Ramadza, D. P.; Poupetova, H.; Hruba, E.; Hlavata, A.; Bzduch, V.; Peskova, K.; Storkanova, G. et al.Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II // Clinical Genetics, 91 (2017), 5; 787-796 doi:10.1111/cge.12927 (međunarodna recenzija, članak, znanstveni)
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41.Sansović, Ivona; Ivankov, Ana-Maria; Bobinec, Adriana; Kero, Mijana; Barišić, IngeborgChromosomal microarray in clinical diagnosis: a study of 337 patients with congenital anomalies and developmental delays or intellectual disability // Croatian Medical Journal, 58 (2017), 3; 231-238 doi:10.3325/cmj.2017.58.231 (recenziran, članak, znanstveni)
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42.Boyle, Breidge; Addor, Marie-Claude; Arriola, Larraitz; Barisic, Ingeborg; Bianchi, Fabrizio; Csáky-Szunyogh, Melinda; de Walle, Hermien E K; Dias, Carlos Matias; Draper, Elizabeth; Gatt, Miriam et al.Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data // Archives of Disease in Childhood - Fetal and Neonatal Edition, 103 (2017), 1; F22-F28 doi:10.1136/archdischild-2016-311845 (međunarodna recenzija, članak, znanstveni)
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43.Given, Joanne E.; Loane, Maria; Garne, Ester; Nelen, Vera; Barisic, Ingeborg; Randrianaivo, Hanitra; Khoshnood, Babak; Wiesel, Awi; Rissmann, Anke; Lynch, Catherine et al.Gastroschisis in Europe - A Case-malformed-Control Study of Medication and Maternal Illness during Pregnancy as Risk Factors // Paediatric and Perinatal Epidemiology, 31 (2017), 6; 549-559 doi:10.1111/ppe.12401 (međunarodna recenzija, članak, znanstveni)
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44.Ecker, Andrea; Mariz, Segundo; Naumann-Winter, Frauke; Norga, Koenraad; Barisic, Ingeborg; Girard, Thomas; Tomasi, Paolo; Mentzer, Dirk; Sepodes, BrunoComparative analysis of the scope of European Union paediatric investigation plans with corresponding orphan designations // Archives of Disease in Childhood, 103 (2017), 5; 427-430 doi:10.1136/archdischild-2017-313352 (međunarodna recenzija, članak, znanstveni)
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45.Bergman, Jorieke E. H.; Lutke, L. Renée; Gans, Rijk O. B.; Addor, Marie-Claude; Barisic, Ingeborg; Cavero-Carbonell, Clara; Garne, Ester; Gatt, Miriam; Klungsoyr, Kari; Lelong, Nathalie et al.Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study // Drug Safety, 41 (2017), 4; 415-427 doi:10.1007/s40264-017-0627-x (međunarodna recenzija, članak, znanstveni)
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46.Gagro, Alenka; Roić, Goran; Sansović, Ivona; Ivankov, AM; Bobinec, A; Antičević, Darko; Barišić, IngeborgInflammatory polyarthritis in patient with 18q deletion syndrome. // Program and abstracts Book of 10th ISABS Conference on Forensic and Anthropologic Genetics and Mayo Clinic lectures in Individualized Medicine.
Dubrovnik, Hrvatska, 2017. str. 309-309 (predavanje, međunarodna recenzija, sažetak, stručni) -
47.Barišić, I; Turkalj, M; Primorac, D.Osteogenesis imperfecta: klinička procjena i liječenje // Paediatria Croatica, 61 (2017), 3; 97-105 (recenziran, članak, znanstveni)
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48.Dumić, Katja K.; Grubić, Zorana; Yuen, Tony; Wilson, Robert C.; Kušec, Vesna; Barišić, Ingeborg; Stingl, Katarina; Sansović, Ivona; Škrabić, Veselin; Dumić, Miroslav; New, Maria I.Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia // Journal of steroid biochemistry and molecular biology, 165 (2017), Part A; 51-56 doi:10.1016/j.jsbmb.2016.03.035 (podatak o recenziji nije dostupan, pregledni rad, znanstveni)
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49.Sansović, Ivona; Ivankov, Ana-Maria; Bobinec, Adriana; Barišić, IngeborgRazlike u broju kopija u genomu kao uzrok razvojnih poremećaja, kongenitalnih anomalija i autističkog spektra poremećaja // Paediatria Croatica. Supplement, 60 (Suppl 3) (2016), 35-44 (domaća recenzija, članak, znanstveni)
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50.Sansović, Ivona; Ivankov, Ana-Maria; Bobinec, Adriana; Barišić, IngeborgKROMOSOMSKI MICROARRAY U KLINIČKOJ DIJAGNOSTICI OSOBA S RAZVOJNIM POREMEĆAJIMA // Paediatria Croatica. Supplement, 60 (Suppl 1) (2016), 58-64 (domaća recenzija, pregledni rad, znanstveni)
