Pregled po CROSBI profilu: Ingeborg Barišić (CROSBI Profil: 13659, MBZ: 168183)
Pronađeno 523 radova
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101.Petković, Giorgie; Barišić, IngeborgFetal alcohol syndrome prevalence in rural Krapinsko –Zagorska county // The Eighth ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine, Book of Abstracts
Split, Hrvatska, 2013. str. 318-318 (poster, međunarodna recenzija, sažetak, ostalo) -
102.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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103.Kero, Mijana; Dumić Kubat, Katja; Antičević, Darko; Barišić, IngeborgSindrom poplitealnog pterigija // Paediatria Croatica
Zagreb, Hrvatska, 2013. str. 303-303 (predavanje, domaća recenzija, sažetak, ostalo) -
104.Boban, Ljubica; Barišić, Ingeborg; Loane, Maria; Garne, Ester; Wellesley, Diana; Calzolari, Elisa; Dolk, Helen; EUROCAT Working groupBeckwith Wiedemannov sindrom - europska epidemiologijska studija // Paediatria Croatica
Zagreb, Hrvatska, 2013. str. 308-308 (predavanje, domaća recenzija, sažetak, ostalo) -
105.Morožin Pohovski, Leona; Barišić, IngeborgProbir mikrodelecijskih/mikroduplikacijskih sindroma tehnikom višestrukog umnožavanja vezanih sondi (MLPA) // Paediatria Croatica
Zagreb, Hrvatska, 2013. str. 301-301 (predavanje, domaća recenzija, sažetak, ostalo) -
106.Odak, Ljubica; Barišić, Ingeborg; Loane, M; Garne, E; Wellesley, D; Calzolari, E; Dolk, H; EUROCAT Working GroupAdvancing rare disease research: the use of network of congenital anomaly registries in the study of rare genetic syndromes // Book of abstracts of 12th European Symposium on Congenital Anomalies
Zagreb: European Surveillance of Congenital Anomalies Association, 2013. str. 89-89 (poster, međunarodna recenzija, sažetak, ostalo) -
107.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) -
108.Odak, Ljubica; Mahulja Stamenković, V; Vondraček, N; Magaš, K; Milevoj Ražem, M; Jurković, M; Kmet, R; Barišić, IngeborgEpidemiology of orofacial clefts in Northern Croatia // Book of abstracts of 12th European Symposium on Congenital Anomalies /
Zagreb: European Surveillance of Congenital Anomalies Association, 2013. str. 51-51 (poster, međunarodna recenzija, sažetak, ostalo) -
109.Odak, LJubica; Mahulja Stamenković, V; Vondraček, N; Magaš, K; Milevoj Ražem, M; Jurković, M; Kmet, R; Barišić, IngeborgA study on congenital limb anomalies in Northern Croatia // Book of abstracts of 12th European Symposium on Congenital Anomalies /
Zagreb: European Surveillance of Congenital Anomalies Association, 2013. str. 50-50 (poster, međunarodna recenzija, sažetak, ostalo) -
110.Dumić Kubat, Katja; Grubić, Zorana; Krnić, Nevena; Škrabić, Veselin; Stipančić, Gordana; Kušec, Vesna; Štingl, Katarina; Barišić, IngeborgClassical Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency in Croatia Between 1995 and 2012 // Book of abstracts of 12th European Symposium on Congenital Anomalies /
Zagreb: European Surveillance of Congenital Anomalies Association, 2013. str. 95-96 (poster, međunarodna recenzija, sažetak, ostalo) -
111.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) -
112.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
Pariz, Francuska: Nature Publishing Group, 2013. str. 171-171 (poster, međunarodna recenzija, sažetak, znanstveni) -
113.Dimopoulou, A.; Fischer, B.; Gardeitchik, T.; Schröter, P.; Kayserili, H.; Schlack, C.; Li, Y.; Brum, J.M.; Barišić, Ingeborg; Castori, M. et al.Genotype-phenotype spectrum of PYCR1-related autosomal recessive cutis laxa // Molecular genetics and metabolism, 110 (2013), 3; 352-361 doi:10.1016/j.ymgme.2013.08.009 (međunarodna recenzija, članak, znanstveni)
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114.Petković, Giorgie; Barišić, IngeborgPrevalence of fetal alcohol syndrome and maternal characteristics in a sample of schoolchildren in rural province of Croatia // International journal of environmental research and public health, 10 (2013), 4; 1547-1561 doi:10.3390/ijerph10041547 (međunarodna recenzija, članak, znanstveni)
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115.Wijers, C.H.V.; van Rooij, I.; Bakker, M.; Marcelis, C.; Addor, M.; Barišić, Ingeborg; Béres, J.; Bianca, S.; Bianchi, F.; Calzolari, E. et al.Anorectal malformations and pregnancy-related disorders : a registry-based case-control study in 17 European regions // BJOG, 120 (2013), 9; 1066-1074 doi:10.1111/1471-0528.12235 (međunarodna recenzija, članak, znanstveni)
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116.Jones, S.A.; Parini, R.; Harmatz, P.; Giugliani, R.; Fang, J.; Mendelsohn, N.J.; ...; Barić, Ivo; Barišić, Ingeborg; ...The effect of idursulfase on growth in patients with Hunter syndrome : data from the Hunter Outcome Survey (HOS) // Molecular genetics and metabolism, 109 (2013), 1; 41-48 doi:10.1016/j.ymgme.2013.03.001 (međunarodna recenzija, članak, znanstveni)
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117.Barišić, Ingeborg; Odak, Ljubica; Loane, M.; Garne, E.; Wellesley, D.; Calzolari, E.; Dolk, H.; Addor, M.C.; Arriola, L.; Bergman, J. et al.Fraser syndrome : epidemiological study in a European population // American journal of medical genetics. Part A, 161A (2013), 5; 1012-1018 doi:10.1002/ajmg.a.35839 (međunarodna recenzija, članak, znanstveni)
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118.Morožin-Pohovski, Leona; Dumić Kubat, Katja, Odak, Ljubica; Barišić, IngeborgMultiplex ligation-dependent probe amplification workflow for the detection of submicroscopic chromosomal abnormalities in patients with developmental delay/intellectual disability // Molecular cytogenetics, 6 (2013), 1; 7-7 (međunarodna recenzija, članak, znanstveni)
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119.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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120.Khoshnood, B.; Loane, M.; Garne, E.; Addor, M.C.; Arriola, L.; Bakker, M.; Barišić, Ingeborg; Bianca, S.; Boyd, P.; Calzolari, E. et al.Recent decrease in the prevalence of congenital heart defects in Europe // Journal of pediatrics, 162 (2013), 1; 108-113 doi:10.1016/j.jpeds.2012.06.035 (međunarodna recenzija, članak, znanstveni)
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121.Mejaški-Bošnjak, Vlatka; Grgurić, Josip; Barišić, Ingeborg; Zakanj, Zora; Miličić, Gordana; Marn, Borut; Kolaček, Sanja; Jakušić, Nenad; Popović, Ljiljana; Vrcić, Mladenka et al.Pedijatrijska laboratorijska medicina. U: Zdravstvena zaštita dojenčadi i male djece, Poslijediplomski studij "Obiteljska medicina" (Izabrana poglavlja) Medicinskog fakulteta Sveučilišta u Zagrebu / Mejaški-Bošnjak, Vlatka (ur.).
Zagreb: Medicinski fakultet Sveučilišta u Zagrebu, 2013 -
122.Barišić, IAutistički spektar poremećaja // Zbornik radova XIII. simpozija preventivne pedijatrije
Skrad, Hrvatska, 2012. str. 18-24 (predavanje, domaća recenzija, sažetak, ostalo) -
123.Dumić Kubat, KatjaKliničke, molekularne i biokemijske karakteristike bolesnka s kongenitalnoma adrenalnom hiperplazijom zbog nedostatka 21- hidroksilaze, 2012., doktorska disertacija, Medicinski fakultet, Zagreb
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124.Jadrešin, Oleg; Jaklin Kekez, Alemka; Jakovljević, Gordana; Lohse, P; Mišak, Zrinjka; Hojsak, Iva; Barišić, Ingeborg; Kolaček, SanjaSindrom Shwachman-Diamond – serija slučajeva // Paediatria Croatica
Pula, Hrvatska, 2012. str. 97-97 (poster, domaća recenzija, sažetak, ostalo) -
125.Dumić Kubat, Katja; Barišić, IngeborgDvije nove mutacije (c133delG i R151Q) i R448H mutacija gena CYP11B u bolesnika s kongenitalnom adrenalnom hiperplazihjom zbog manjka 11beta-hidroksilaze // Paediatria Croatica
Pula, Hrvatska, 2012. str. 226-226 (poster, domaća recenzija, sažetak, ostalo) -
126.Morožin Pohovski, Leona; Barišić, IngeborgMLPA as screening method in detection of submicroscopic rearrangements detected in patients with developmental delay/intellectual disability // European Journal of Human Genetics
Nürnberg, Njemačka: Nature Publishing Group, 2012. str. 123-123 (poster, međunarodna recenzija, sažetak, ostalo) -
127.Barišić, Ingeborg; Dumić Kubat, Katja; Morožin Pohovski, Leona; Petković, Iskra; Riegel M, Schinzel, AlbertArray CGH characterisation of ring chromosome 9 formation due to inverted duplication and terminal deletion in a patient with sex- reversal // European Journal of Human Genetics
Nürnberg, Njemačka, 2012. str. 127-127 (poster, međunarodna recenzija, sažetak, ostalo) -
128.Barišić, Ingeborg; Loane, M; Curran, R; Garne, E; Vrijeheid Taruscio, D; Morris, J; Bakker, M; Irgent, L; Calzolari, E; Khoshnood, B et al.Joint Action EUROCAT 2011-2013 Funded by the Public Health Programme 2008-2013 of the European Commission // Hrvatski časopis za javno zdravstvo, 8 (2012), 31; 21-24 (podatak o recenziji nije dostupan, pregledni rad, stručni)
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129.Morožin Pohovski, Leona; Barišić, IngeborgProbir aberacija subtelomera i mikrodelecijskih sindroma u bolesnika s razvojnim /intelektualnim smetnjama metodom MLPA // Paediatria Croatica, 56 (2012), 2; 18-21 (međunarodna recenzija, članak, znanstveni)
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130.Garne, E.; Loane, M.; Dolk, H.; Barišić, Ingeborg; Addor, M.C.; Arriola, L.; Bakker, M.; Calzolari, E.; Matias Dias, C.; Doray, B. et al.Spectrum of congenital anomalies in pregnancies with pregestational diabetes // Birth defects research. Part A. Clinical and molecular teratology, 94 (2012), 3; 134-140 doi:10.1002/bdra.22886 (međunarodna recenzija, članak, znanstveni)
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131.Jadrešin, Oleg; Jaklin Kekez, Alemka; Jakovljević, Gordana; Lohse P; Mišak, Zrinjka; Hojsak, Iva; Barišić, Ingeborg; Kolaček, Sanja.Sindrom Shwachman-Diamond – serija slučajeva // Paediatria Croatica
Pula, Hrvatska, 2012. (poster, domaća recenzija, sažetak, stručni) -
132.Jaklin Kekez, Alemka; Batinica, Maja; Voskresensky Baričić, Tamara; Gagro, Alenka; Barišić, Ingeborg; Dumić, Katja; Kapović, Agneza Marija; La Grasta Sabolić, LaviniaStečena generalizirana lipodistrofija povezana s panikulitisom i autoimunim poremećajima – prikaz slučaja // Paediatria Croatica, 56 (2012), 115-116 (podatak o recenziji nije dostupan, ostalo, stručni)
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133.Petković, GiorgieUčestalost fetalnog alkoholnog sindroma u školske djece sjeverozapadne Hrvatske, 2012., doktorska disertacija, Medicinski fakultet, Zagreb
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134.Mastroiacovo, Pierpaolo; ...; Barišić, Ingeborg; ...; Zhuchenko, Ludmila A.Prevalence at birth of cleft lip with or without cleft palate : data from the International Perinatal Database of Typical Oral Clefts (IPDTOC) // Cleft palate-craniofacial journal, 48 (2011), 1; 66-81 doi:10.1597/09-217 (međunarodna recenzija, članak, znanstveni)
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135.Barišić, IngeborgEtički aspekti genetičkog testiranja u djece // Bioetika i dijete / Čović, Ante ; Radonić, Marija (ur.).
Zagreb: Pergamena, 2011. str. 121-140 -
136.Bulić-Jakuš Floriana; Barišić IngeborgEmeryeve osnove medicinske genetike, 2011. (podatak o recenziji nije dostupan, izvještaj).
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137.Odak, Ljubica; Barišić, Ingeborg; Loane, M; Calzolari, E; Garne, E; Wellesley, D; Dolk, HPrenatal ultrasound diagnosis of oculoauriculovertebral spectrum disorder // Facts, Views & Vision in obGyn, Book of Abstracts
Antwerpen, Belgija, 2011. str. 32-32 (poster, međunarodna recenzija, sažetak, znanstveni) -
138.Dumić, Katja; Barišić, Ingeborg; Garg, AA patient with atypical progeria syndrome due to heterozygous E159 mutation in LMNA gene // 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. (poster, međunarodna recenzija, sažetak, znanstveni) -
139.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) -
140.Morožin Pohovski, LeonaProbir aberantnih subtelomera u dijagnostici razvojnog zaostajanja/mentalne retardacije primjenom metode višestrukog umnožavanja vezanih sondi (MLPA), 2011., doktorska disertacija, Prirodoslovno-matematički fakultet, Biološki odsjek, Zagreb
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141.Roganović, Jelena; Barišić, Ingeborg; Jonjić, NivesAngiokeratoma in Fabry disease: diagnostic but not treatment effectiveness marker // 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. 266-266 (predavanje, međunarodna recenzija, sažetak, ostalo) -
142.Morožin Pohovski, Leona; Barišić, IngeborgScreening of patients with mental retardation using subtelomeric MLPA assay // 7th ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine Book of Abstracts
Zagreb: SABS – International Society for Applied Biological Sciences, 2011. str. 258-258 (predavanje, međunarodna recenzija, sažetak, stručni) -
143.Dumić, Katja; Krnić, Nevena; Škrabć, Veselin; Stipančić, Gordana; Kušec, Vesna; Štingl, Katarina; Barišić, IngeborgClassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia between 1995 and 2010 // 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. 252-252 (predavanje, međunarodna recenzija, sažetak, stručni) -
144.Dumić, Katja; Morožin-Pohovski, Leona; Barišić, IngeborgDuplication of pseudoautosomal region 1 and SHOX gene could be linked with characteristic phenotype // Europan Journal of Human Genetics. Supplement 2
Amsterdam: Nature Publishing Group, 2011. str. 121-121 (poster, međunarodna recenzija, sažetak, ostalo) -
145.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) -
146.Odak, Ljubica; Barišić, Ingeborg; Loane, M; Calzolari, E; Garne, E; Wellesley, D; Dolk, HEpidemiological study of Beckwith Wiedemann syndrome in European population // European Journal of Human Genetics. Supplement 2
Amsterdam: Nature Publishing Group, 2011. str. 329-329 (poster, međunarodna recenzija, sažetak, znanstveni) -
147.Odak, Ljubica; Barišić, Ingeborg, Petković, Iskra; Riegel, M; Schinzel, AClinical and cytogenetic findings in a girl with dup16 (q12.1q21) // European journal of human genetics. Supplement 2
Amsterdam: Nature Publishing Group, 2011. str. 84-84 (poster, međunarodna recenzija, sažetak, znanstveni) -
148.Barišić, Ingeborg; Petković, GiorgieFetal alcohol syndrome in urban schools // Pregnancy and Alcohol Consumption / Hoffman, Joshua D (ur.).
New York (NY): Nova Science Publishers, 2011. str. 281-298 -
149.Odak, Ljubica; Barišić, Ingeborg; Morožin Pohovski, Leona; Riegel, Mariluce; Schinzel, AlbertA novel de novo dir dup (16) (q12.1-q21) in a girl with behavioral disorder, mild cognitive impairment, speech delay, and dysmorphic features: case report and review of the literature // 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. 295-295 (poster, međunarodna recenzija, sažetak, stručni) -
150.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) -
151.Odak, Ljubica; Barišić, Ingeborg; Loane, M; Calzolari, E; Garne, E; Wellesey, D; Dolk, H; EUROCAT Working groupBeckwith Wiedemann syndrome: clinical and epidemiological study of a large series of patients in Europe // 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. 294-294 (poster, međunarodna recenzija, sažetak, znanstveni) -
152.Dumić, Katja; Barišić, Ingeborg; Poročki, Kristina; Sansović, IvonaHypochondroplasia due to FGFR3 gene mutation (N540K) and mosaic form of Down syndrome in the same patient // Journal of applied genetics, 52 (2011), 2; 209-212 doi:10.1007/s13353-010-0024-y (podatak o recenziji nije dostupan, prikaz, znanstveni)
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153.Dolk, H.; Loane, M.; Garne, E.; EUROCAT Working Group; Barišić, IngeborgCongenital heart defects in Europe : prevalence and perinatal mortality, 2000 to 2005 // Circulation, 123 (2011), 8; 841-849 doi:10.1161/CIRCULATIONAHA.110.958405 (međunarodna recenzija, pregledni rad, znanstveni)
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154.Greenlees, Ruth; Neville, Amanda; Addor, Marie-Claude; Amar, Emmanuelle; Arriola, Larraitz; Bakker, Marian; Barišić, Ingeborg; Boyd, Patricia A; Calzolari, Elisa; Doray, Berenice et al.Paper 6: EUROCAT member registries: organization and activities // Birth defects research. Part A. Clinical and molecular teratology, 91 (2011), Supp 1; S51-S100 doi:10.1002/bdra.20775 (međunarodna recenzija, pregledni rad, znanstveni)
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155.Khoshnood, B.; Greenlees, R.; Loane, M.; Dolk, H.; EUROCAT Project Management Committee; EUROCAT Working Group; Barišić, IngeborgPaper 2 : EUROCAT public health indicators for congenital anomalies in Europe // Birth defects research. Part A. Clinical and molecular teratology, 91 (2011), Sp.Issue; S16-S22 doi:10.1002/bdra.20776 (međunarodna recenzija, pregledni rad, znanstveni)
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156.Loane, M.; Dolk, H.; Kelly, A.; Teljeur, C..; Greenlees, R; Densem, J.; EUROCAT Working Group; Barišić, IngeborgPaper 4 : EUROCAT statistical monitoring: identification and investigation of ten year trends of congenital anomalies in Europe // Birth defects research. Part A. Clinical and molecular teratology, 91 (2011), Sp.Issue; S31-S43 doi:10.1002/bdra.20778 (međunarodna recenzija, pregledni rad, znanstveni)
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157.Garne, Ester; Dolk, Helen; Loane, Maria; Wellesley, Diana; Barišić, Ingeborg; Calzolari, Elisa; Densem, James; EUROCAT Working GroupPaper 5 : Surveillance of multiple congenital anomalies: implementation of a computer algorithm in European registers for classification of cases // Birth defects research. Part A. Clinical and molecular teratology, 91 (2011), Supp 1; S44-S50 doi:10.1002/bdra.20777 (međunarodna recenzija, pregledni rad, znanstveni)
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158.Loane, M.; Dolk, H.; Garne, E.; Greenlees, R.; EUROCAT Working Group; Barišić, IngeborgPaper 3 : EUROCAT data quality indicators for population-based registries of congenital anomalies // Birth defects research. Part A. Clinical and molecular teratology, 91 (2011), Sp. Issue; S23-S30 doi:10.1002/bdra.20779 (međunarodna recenzija, pregledni rad, znanstveni)
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159.Boyd, P.A.; Haeusler, M.; Barišić, Ingeborg, Loane, M.; Garne, E.; Dolk, H.Paper 1 : The EUROCAT network-organization and processes // Birth defects research. Part A. Clinical and molecular teratology, 91 (2011), Sp.Issue; S2-S15 doi:10.1002/bdra.20780 (međunarodna recenzija, pregledni rad, znanstveni)
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160.Boyd, P.A.; Haeusler, M.; Barišić, IngeborgEUROCAT Report 9: Surveillance of congenital anomalies in Europe 1980-2008 // Birth defects research. Part A. Clinical and molecular teratology, 91 (2011), Sp.I.; S1-S1 (podatak o recenziji nije dostupan, uvodnik, znanstveni)
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161.Burton, B.K.; Whiteman, D.A.; HOS investigators; Barišić, Ingeborg; Barić, IvoIncidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS) // Molecular genetics and metabolism, 103 (2011), 2; 113-120 doi:10.1016/j.ymgme.2011.02.018 (međunarodna recenzija, članak, znanstveni)
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162.Odak, Ljubica; Barišić, Ingeborg; Morožin Pohovski, Leona; Riegl, M.; Schinzel, AlbertNovel duplication on chromosome 16 (q12.1-q21) associated with behavioral disorder, mild cognitive impairment, speech delay, and dysmorphic features: case report // Croatian Medical Journal, 52 (2011), 3; 415-422 doi:10.3325/cmj.2011.52.415 (podatak o recenziji nije dostupan, prikaz, znanstveni)
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163.Emeryeve osnove medicinske genetike (14. izdanje) / Bulić Jakuš, Floriana ; Barišić, Ingeborg (ur.). Zagreb: Medicinska naklada, 2011 (Udžbenik)
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164.Petković, Iskra; Barišić, Ingeborg; Petković, GiorgieFISH screening for subtelomeric rearrangements revealed 4 different chromosomal anomalies in 55 children with intellectual deficit // Chromosome Research / Macgregor, Herbert (ur.).
Dordrecht: Springer, 2011. str. S48-S49 (poster, međunarodna recenzija, sažetak, znanstveni) -
165.Barišić, IGenetičko savjetovanje - stajalište Hrvatskog društva za humanu genetiku Hrvatskog liječničkog zbora // Paediatria Croatica, 54 (2010), 213-216 (međunarodna recenzija, članak, znanstveni)
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166.Odak, Ljubica; Barišić, Ingeborg; Loane, M; Calzolari, E; Garne, E; Wellesey, D; Dolk, H; EUROCAT Working groupTreacher Collins syndrome- multicentrična studija u europskoj populaciji // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb: Denona, 2010. str. 54-54 (poster, domaća recenzija, sažetak, znanstveni) -
167.Odak, Ljubica; Milevoj Ražem, Mirna; Mahulja Stamenković, Vesna; Vondraček, Nenad; Magaš, Karmen; Barišić, IngeborgPrirođene srčane grješke u sjeverozapadnoj Hrvatskoj // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb: Denona, 2010. str. 82-83 (poster, domaća recenzija, sažetak, ostalo) -
168.Odak, Ljubica; Milevoj Ražem, Mirna; Mahulja Stamenković, Vesna; Vondraček, Nenad; Magaš, Karmen; Barišić, IngeborgPrenatalna dijagnoza Downovog sindroma u četiri Hrvatske regije // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb: Denona, 2010. str. 82-83 (poster, domaća recenzija, sažetak, znanstveni) -
169.Dumić, Katja; Morožin Pohovski, Leona; Barišić, IngeborgKlinička i molekularna analiza nasljedne duplikacije gena SHOX i evolucijski očuvane sekvence u SHOX3' regiji // Paediatria Croatica. Supplement 2. / Barišić, Ingeborg (ur.).
Zagreb: Denona, 2010. str. 80-80 (poster, domaća recenzija, sažetak, znanstveni) -
170.Morožin Pohovski, Leona; Ciglar, Željka; Barišić, IngeborgDe novo mikrodelecija 4p16.3 u bolesnice s blagim fenotipom // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb: Denona, 2010. str. 81-81 (poster, domaća recenzija, sažetak, znanstveni) -
171.Sansović, Ivona; Barišić, IngeborgMLPA( multiplex ligation probe amplification) metoda u otkrivanju delecije gena MECP2-prikaz slučaja // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb: Denona, 2010. str. 82-82 (poster, domaća recenzija, sažetak, znanstveni) -
172.De Souza, E.; Morris, J.K.; EUROCAT Working Group; Barišić, IngeborgCase-control analysis of paternal age and trisomic anomalies // Archives of disease in childhood, 95 (2010), 11; 893-897 doi:10.1136/adc.2009.176438 (međunarodna recenzija, članak, znanstveni)
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173.Burton, B.K.; Guffon, N.; Roberts, J.; van der Ploeg, A.T.; Jones, S.A.; on behalf of the HOS investigators: Guelbert, N. ...; Barić, Ivo; Barišić, Ingeborg; ...; Ibrahim, J.Home treatment with intravenous enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II - data from the Hunter Outcome Survey // Molecular genetics and metabolism, 101 (2010), 2/3; 123-129 doi:10.1016/j.ymgme.2010.06.011 (međunarodna recenzija, članak, znanstveni)
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174.Mendelsohn, N.J.; Harmatz, P.; Bodamer, O.; Burton, B.K.; Giugliani, R.; Jones, S.A.; Lampe, C.; Malm, G.; Steiner, R.D.; Parini, R. et al.Importance of surgical history in diagnosing mucopolysaccharidosis type II (Hunter syndrome) : data from the Hunter Outcome Survey // Genetics in medicine, 12 (2010), 12; 816-822 doi:10.1097/GIM.0b013e3181f6e74d (međunarodna recenzija, članak, znanstveni)
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175.(EUROCAT Antiepileptic Study Working Group) Jentink, J.; Dolk, H.; Loane, M. A.; Morris, J. K.; Wellesley, D.; Garne, E.; de Jong-van den Berg, L.Intrauterine exposure to carbamazepine and specific congenital malformations: systematic review and case-control study // BMJ. British medical journal, 341 (2010), c6581, 7 doi:10.1136/bmj.c6581 (međunarodna recenzija, pregledni rad, znanstveni)
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176.Sansović, Ivona; Barišić, Ingeborg; Pavelić, JasminkaAnaliza MLPA u dijagnostici DFNB1 gluhoće // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb: Denona, 2010. str. 82-82 (poster, domaća recenzija, sažetak, znanstveni) -
177.Jakovljević, Gordana; Kardum-Skelin, Ika; Rogošić, Srđan; Čulić, Srđana; Stepan, Jasminka; Gagro, Alenka; Škarić, Ivančica; Mikecin, Lili; Bonevski, Aleksandra; Barišić, Ingeborg; Nakić, MelitaFamilial Hemophagocytic Lymphohistiocytosis in a 6-Week-Old Male Infan : case report // Collegium antropologicum, 34 (2010), 2; 631-634 (međunarodna recenzija, članak, znanstveni)
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178.Dumić, Katja; Potočki, Kristina; Sansović, Ivona; Barišić, IngeborgDownov sindrom i hipohondroplazija // Paediatria croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb: Denona, 2010. str. 80-80 (poster, domaća recenzija, sažetak, znanstveni) -
179.Palčić, Iva; Petković, Giorgie; Cvitković Roić, Andrea; Barišić, Ingeborg; Roić, Goran; Bastić, Mislav; Đelmiš, Jasna; Angelini FDentova bolest tip 1-prikaz dvaju bolesnika i nove H731P mutacije // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb: Denona, 2010. str. 80-80 (poster, domaća recenzija, sažetak, znanstveni) -
180.Jentink, Janneke; Loane, Maria; Dolk, Helen; Barišić, Ingeborg; Garne, Ester; Morris, Joan; de Jong-van den Berg, Lolkje; EUROCAT Antiepileptic Drug Working GroupValproic acid monotherapy in pregnancy and major congenital malformations // The New England journal of medicine, 362 (2010), 23; 2185-2193 doi:10.1056/NEJMoa0907328 (međunarodna recenzija, članak, znanstveni)
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181.Petković, Giorgie; Barišić, IngeborgFAS prevalence in a sample of urban schoolchildren in Croatia // Reproductive toxicology, 29 (2010), 2; 237-241 doi:10.1016/j.reprotox.2009.11.006 (međunarodna recenzija, članak, znanstveni)
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182.Garne, Ester; Loane, Maria; Addor, Marie-Claude; Boyd, Patricia; Barišić, Ingeborg; Dolk, HelenCongenital hydrocephalus - prevalence, prenatal diagnosis and outcome of pregnancy in four European regions // European journal of paediatric neurology, 14 (2010), 2; 150-155 doi:10.1016/j.ejpn.2009.03.005 (međunarodna recenzija, članak, znanstveni)
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183.Odak, Ljubica; Barišić, Ingeborg; Loane, M; Bianchi, F; Calzolari, EPrenatal ultrasound diangosis of genetic syndromes. // 10th European Symposium on Prevention of Congenital Anomalies, Book of Abstracts
Bilbao, 2009. str. 62-62 (poster, međunarodna recenzija, sažetak, znanstveni) -
184.Barišić, IngeborgEUROCAT – Epidemiological surveillance of congenital malformations in Europe // International Regional Conference on Medical Genetics, Book of Abstracts
Beograd, 2009. (poster, sažetak, ostalo) -
185.Barišić, IngeborgGenetics in Croatia // International Regional Conference on Medical Genetics, Book of Abstracts
Beograd, 2009. (poster, sažetak, znanstveni) -
186.Jones, S.A.; Almássy, Z.; Beck, Miroslav; Burt, K.; Clarke, J.T.; Giugliani, R.; Hendriksz, C.; Kroepfl, T.; Lavery, L.; Lin, S.P. et al.Mortality and cause of death in mucopolysaccharidosis type II-a historical review based on data from the Hunter Outcome Survey (HOS) // Journal of inherited metabolic disease, 32 (2009), 4; 534-543 doi:10.1007/s10545-009-1119-7 (međunarodna recenzija, članak, znanstveni)
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187.Loane, Maria; Dolk, Helen; Morris, Joan; EUROCAT working group. Collaborators(23) Haeusler, Martin; Nelen, Vera; Barišić, Ingeborg; Garne, Ester; de Vigan, Catherine; Doray, Berenice; Queisser-Luft, Annette et al.Maternal age-specific risk of non-chromosomal anomalies // Bjog-an international journal of obstetrics and gynaecology, 116 (2009), 8; 1111-1119 (međunarodna recenzija, članak, znanstveni)
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188.Barišić, Ingeborg; EUROCAT Working GroupEUROCAT- Epidemiological surveillance of congenital anomalies in Europe // Zdravniški vestnik, 78 (2009), 1; 175-79 (recenziran, pregledni rad, stručni)
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189.Barišić, Ingeborg; Petković, GiorgieMukopolisaharidoza tip VI (MPS VI), 2009. (podatak o recenziji nije dostupan, popularni rad).
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190.Sansović, Ivona; Knežević, Jelena; Musani, Vesna; Seeman, Pavel; Barišić, Ingeborg; Pavelić, JasminkaGJB2 mutations in patients with non-syndromic hearing loss from Croatia // Genetic Testing and Molecular Biomarkers, 13 (2009), 5; 693-699 doi:10.1089/gtmb.2009.0073 (međunarodna recenzija, članak, znanstveni)
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191.Petković, Iskra; Barišić, IngeborgDe novo unbalanced whole arm translocation resulting in 18p- syndrome // Chromosome Research / Macgregor, Herbert (ur.).
Dordrecht: Springer, 2009. str. S34-S34 (poster, međunarodna recenzija, sažetak, znanstveni) -
192.Jakovljević, Gordana; Gagro, Alenka; Barišić, Ingeborg; Stepan, Jasminka; Bonevski, Aleksandra; Rimac, Milan; Mikecin, Lily; Škarić, Ivančica; Nakić, MelitaFamilial hemophagocytic lymphohistiocytosis type 3 due to UNC13D mutation // Paediatria Croatica, Supplement 2 / Ingeborg Barišić (ur.).
Zagreb: Denona, 2009. str. 42-42 (poster, međunarodna recenzija, sažetak, ostalo) -
193.Sansović, Ivona; Barišić, IngeborgRecessive mutations at the DFNB1 locus in patients with non-syndromic hearing loss from Croatia // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb, 2009. str. 74-74 (poster, međunarodna recenzija, sažetak, znanstveni) -
194.Morožin Pohovski, Leona; Sansović, Ivona; Barišić, IngeborgEvaluation of subtelomere imbalance in patients with mental retardation detected by MLPA screening // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb, 2009. str. 71-71 (poster, međunarodna recenzija, sažetak, ostalo) -
195.Petković, Giorgie; Barišić, IngeborgEnzyme replacement therapy (ERT) in two patients with MPS VI // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb, 2009. str. 48-48 (poster, međunarodna recenzija, sažetak, znanstveni) -
196.Kušec, Vesna; Barišić, Ingeborg; Rešić, Arnes; Huzjak, Nevenka; Antičević, DarkoOsteogenesis imperfecta patient group - longitudinal follow up by bone markers // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb, 2009. str. 45-45 (poster, međunarodna recenzija, sažetak, znanstveni) -
197.Đapić, Tomislav; Antičević, Darko; Barišić, IngeborgDeformity correction in vitamin D resistant hypophosphatemic rickets // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb, 2009. str. 42-42 (poster, međunarodna recenzija, sažetak, ostalo) -
198.Petković, Giorgie; Barišić, IngeborgEnzyme replacement therapy in three patients with MPS II // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb, 2009. str. 48-48 (poster, međunarodna recenzija, sažetak, znanstveni) -
199.Roganović, Jelena; Barišić, Ingeborg; Fumić, Ksenija; Jonjić, NivesFabry disease-case report // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb, 2009. str. 40-40 (poster, međunarodna recenzija, sažetak, znanstveni) -
200.Antičević, Darko; Đapić, Tomislav; Barišić, IngeborgOrthopaedic management of the most common skeletal dysplasia // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb, 2009. str. 40-40 (poster, međunarodna recenzija, sažetak, znanstveni)
