Pregled po CROSBI profilu: Ivona Sansović (CROSBI Profil: 30909, MBZ: 328473)
Pronađeno 30 radova
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1.Bašković, Marko; Zaninović, Luca; Sansović, Ivona; Meašić, Ana Maria; Katušić Bojanac, Ana; Ježek, DavorTrends in the treatment of undescended testes: a pediatric tertiary care center experience from Croatia // World Journal of Pediatric Surgery, 5 (2022), 4; e000461, 6 doi:10.1136/wjps-2022-000461 (međunarodna recenzija, članak, znanstveni)
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2.Bašković, Marko; Zaninović, Luca; Sansović, Ivona; Meašić, Ana Maria; Katušić Bojanac, Ana; Ježek, DavorDo we treat undescended testes on a time!? // Frontiers in Pediatrics, Event abstracts (2022)
online ; Barcelona, Španjolska, 2022. str. 3594-3595 (poster, međunarodna recenzija, sažetak, znanstveni) -
3.Bašković, Marko; Zaninović, Luca; Sansović, Ivona; Meašić, Ana Maria; Katušić Bojanac, Ana; Ježek, DavorDo we treat undescended testes on a time!? // 7th World Congress of Pediatric Surgery
Prag, Češka Republika, 2022. (poster, međunarodna recenzija, neobjavljeni rad, znanstveni) -
4.Vulin, Katarina; Odak, Ljubica; Morožin Pohovski, Leona; Đaković, Ivana; Tripalo Batoš, Ana; Meašić, Ana-Maria; Kero, Mijana; Sansović, Ivona; Bobinec, Adrana; Barišić, IngeborgChromosomal microarray in clinical diagnosis of cerebral palsy // Journal of Bioanthropology ; vol.2, no.1, 2022. Program and abstracts: The Twelfth ISABS Conference on Forensic and Anthropological Genetics and Mayo Clinic Lectures in Individualized Medicine ; June 22-27, 2022, Dubrovnik, Croatia. / Marjanović, D (ur.).
Zagreb: Institute for Anthropological Research, 2022. str. 308-308 doi:10.54062/jb (predavanje, međunarodna recenzija, sažetak, znanstveni) -
5.Morozin Pohovski, Leona; Bobinec, Adriana; Measic, Ana-Maria; Sansovic, Ivona; Barisic, IngeborgA new case of intragenic deletion of the TCF4 gene without features of Pitt-Hopkins syndrome // Molecular and experimental biology in medicine, 3 (2020), 2; 56-58 doi:10.33602/mebm.3.2.8 (recenziran, članak, stručni)
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6.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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7.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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8.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) -
9.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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10.Ivankov, Ana-Maria; Bobinec, Adriana; Boban, Ljubica; Sansović, Ivona; Barišić, IngeborgMikrodelecija 8q23.3-q24.11 povezana sa sindromima Langer- Giedion i Cornelia de Lange-4 // Paediatria Croatica, 60 (2016), 3; 106-110 (domaća recenzija, članak, stručni)
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11.Bobinec, Adriana; Ivankov, Ana-Maria; Čule, Marina; Sansović, Ivona; Barišić, IngeborgSekvenca kaudalne regresije i delecija 7q34-q36.3 // Paediatria Croatica, 60 (2016), 3; 112-115 doi:10.13112/PC.2016.17 (domaća recenzija, članak, stručni)
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12.Ivona Vrkić Boban, Ingeborg Barišić, Ivona Sansović, Vjekoslav Krželj, Bernarda LozićTeško globalno zaostajanje, epilepsija, hipospadija s kriptorhizmom i bulozna epidermoliza povezane s de novo delecijom 2q22.2-q22.3: prikaz slučaja // Paediatria Croatica. Supplement / Barišić, Ingeborg (ur.).
Zagreb: Klinika za dječje bolesti Zagreb, 2016. str. 152-153 (poster, domaća recenzija, sažetak, stručni) -
13.Sansović, Ivona; Dumić Kubat, Katja; Barišić, IngeborgMetoda višestrukog umnažanja vezanih sondi u dijagnostici kongenitalne adrenalne hiperplazije uzrokovane deficitom 21-hidroksilaze // Pediatria Croatica Supplement
Dubrovnik, Republika Hrvatska, 2014. str. 109-109 (poster, domaća recenzija, sažetak, znanstveni) -
14.Sansović, I; Morožin Pohovski, L; Barišić, IMicroduplication of Xp22.31 region involving the STS gene in two males with intellectual disability // European journal of human genetics
Milano, Italija: Nature Publishing Group, 2014. str. 163-164 (poster, međunarodna recenzija, sažetak, znanstveni) -
15.Sansović, IvonaMetoda višestrukog umnažanja vezanih sondi u molekularnoj dijagnostici cistične fibroze // „Dani humane genetike. prof. dr. sc. Ljiljane Zergollern –Čupak“
Zagreb, Hrvatska, 2014. (predavanje, neobjavljeni rad, stručni) -
16.Sansović, Ivona; Morožin Pohovski, Leona; Barišić, IngeborgMicroduplication of Xp22.31 region involving the STS gene in two males with intellectual disability // European Journal of Human Genetics, Volume 22, Supplement 1, May 2014 / G-J B van Ommen (ur.).
Milano, Italija: Nature Publishing Group, 2014. str. 163-164 (poster, međunarodna recenzija, sažetak, znanstveni) -
17.Sansović, Ivona; Dumić Kubat, Katja; Barišić, IngeborgMetoda višestrukog umnažanja vezanih sondi u dijagnostici kongenitalne adrenalne hiperplazije uzrokovane deficitom 21-hidroksilaze // PAEDIATRIA CROATICA, Vol. 58, Suppl 2 / Prof.dr.sc. Ingeborg Barišić, dr.med. (ur.).
Zagreb, 2014. str. 111-111 (poster, domaća recenzija, sažetak, stručni) -
18.Sansović, Ivona; Dumić Kubat, Katja; Barišić, IngeborgMolekularna analiza gena MECP2 u bolesnica sa sindromom Rett // Paediatria Croatica, 57 (2013), 4; 408-415 doi:10.13112/PC.2013.14 (međunarodna recenzija, članak, znanstveni)
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19.Kero, Mijana; Morožin Pohovski, Leona; Sansović, Ivona; Odak, Ljubica; Dumić, Katja; Barišić, IngeborgCongenital anomalies in patients with submicroscopic chromosome abnormalities // Book of abstracts of 12th European Symposium on Congenital Anomalies
Zagreb: European Surveillance of Congenital Anomalies Association, 2013. str. 69-69 (poster, međunarodna recenzija, sažetak, ostalo) -
20.Sansović, Ivona; Barišić, IngeborgMolecular testing of FGFR3 gene in patients with achondroplasia and hypochondroplasia from Croatia // Book of abstracts of 12th European Symposium on Congenital Anomalies /
Zagreb: European Surveillance of Congenital Anomalies Association, 2013. str. 72-72 (poster, međunarodna recenzija, sažetak, znanstveni) -
21.Sansović, Ivona; Barišić, IngeborgDetection of full mutation FMR1 and AFF2 alleles by Methylation- Specific Multiplex Ligation-dependent Probe Amplification method in male patients with intellectual disability // European Journal of Human Genetics
Paris, Francuska: Nature Publishing Group, 2013. str. 171-171 (poster, međunarodna recenzija, sažetak, znanstveni) -
22.Sansović, Ivona; Barišić, Ingeborg; Dumić Kubat, KatjaImproved detection of deletions and duplications in the DMD gene using the multiplex ligation-dependent probe amplification (MLPA) method // Biochemical genetics, 51 (2013), 3/4; 189-201 doi:10.1007/s10528-012-9554-9 (međunarodna recenzija, članak, znanstveni)
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23.Sansović, Ivona; Barišić, IngeborgImproved detection of deletions/duplications in the DMD gene using the multiplex-ligation-dependent probe amplification (MLPA) method // 7th ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine Book of Abstracts
Zagreb: ISABS – International Society for Applied Biological Sciences, 2011. str. 268-268 (predavanje, međunarodna recenzija, sažetak, znanstveni) -
24.Sansović, Ivona; Barišić, Ingeborg; Dumić, KatjaNovel triple deletion of the MECP2 gene in atypical Rett syndrome patient // European journal of human genetics. Supplement 2
Amsterdam: Nature Publishing Group, 2011. str. 118-118 (poster, međunarodna recenzija, sažetak, znanstveni) -
25.Odak, Ljubica; Barišić, Ingeborg; Morožin Pohovski, Leona; Sansović, Ivona; Dumić, Katja; Jakušić, Nenad; Klobučar, Aleksandra; Grgurić, JosipDiagnostic algorithm for children with autism // 7th ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine Book of Abstracts
Zagreb: ISABS – International Society for Applied Biological Sciences, 2011. str. 261-261 (predavanje, međunarodna recenzija, sažetak, stručni)
