Pregled po CROSBI profilu: Ingeborg Barišić (CROSBI Profil: 13659, MBZ: 168183)
Pronađeno 523 radova
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451.Petković, Iskra; Barišić, IngeborgUnusual mosaicism due to non-homologous postzygotic recombination involving chromosomes 6 and 10 in the mother, and 46,Xder(X)t(X;6) in her daughter // European Journal of Human Genetics, 9 (2001), 1. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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452.Barišić, Ingeborg; Clementi, Maurizio; Haeusler, Martin; Gjergja, Romana; Kern, Josipa; Stoll, ClaudeEvaluation of prenatal ultrasound diagnosis of fetal abdominal wall defects by 19 European registries // Ultrasound in Obstetrics and Gynecology, 18 (2001), 4; 309-316 (međunarodna recenzija, članak, znanstveni)
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453.Hećimović, Silva; Vlašić, Jelena; Barišić, Ingeborg; Marković, Dubravko; Čulić, Vida; Pavelić, KrešimirA simple and rapid analysis of triplet repeat diseases by Expand Long PCR // Clinical Chemistry and Laboratory Medicine, 39 (2001), 12; 1259-1262 (međunarodna recenzija, članak, znanstveni)
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454.Primorac, Dragan; Rowe, David, W; Mottes, Monica; Barišić, Ingeborg; Antičević, Darko; Mirandola, Stefania; Gomez Lira, Macarena; Kalajzić, Ivo; Kušec, Vesna; Glorieux, Francis, HOsteogenesis imperfecta at the beginning of bone and joint decade // Croatian Medical Journal, 42 (2001), 4; 393-415 (podatak o recenziji nije dostupan, pregledni rad, ostalo)
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455.Ligutić, Ivo; Barišić, Ingeborg; Antičević, Darko; Vrdoljak, Javor; Primorac, Dragan;Koštane displazije - specifična zdravstvena skrb djece s hondrodisplazijama // Paediatria Croatica, 45 (2001), 1; 19-26 (podatak o recenziji nije dostupan, pregledni rad, stručni)
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456.Barišić, Ingeborg; Haeusler, Martin; Clementi, Maurizio; Gjergja-Matejić, Romana; Stoll, ClaudePrenatal ultrasound detection of abdominal wall defects: associated malformations, chromosomal abnormalities and pregnancy outcome // European journal of human genetics, 1 (2000), 8. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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457.Petković, Iskra; Barišić, IngeborgChromosome inactivation pattern study in an unbalanced X;6 translocation // European journal of human genetics, 1 (2000), 8. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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458.Barišić, Ingeborg; Clementi, Maurizio; Haeusler, Martin; Gjergja-Matejić, RomanaEvaluation of routine prenatal ultrasound detection of fetal gastrointestinal malformations: European multicentric study // Ultrasound in obstetrics & gynecology, 16 (2000), 1. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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459.Barišić, Ingeborg; Clementi, Maurizio; Haeusler, Martin; Gjergja, Romana; Modrušan-Mozetič, Zlata; Žužek, Adele; Stanojević, Milan; Beer, Zlata; Stoll, Claude; EUROSCAN Study GroupEvaluacija prenatalnog otkrivanja dijafragmalnih hernija rutinskim ultrazvučnim pregledom u 19 europskih centara // Paediatria Croatica, 44 (2000), 3. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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460.Barišić, Ingeborg; Stoll, Claude; Clementi, Maurizio; Haeusler, Martin; Gjergja-Matejić, Romana; Modrušan-Mozetič, Zlata; Žužek, Adele; Stanojević, Milan; Beer, Zlata; EUROSCAN Study GroupUčinkovitost prenatalnog ultrazvučnog otkrivanja kongenitalnih malformacija: europsko multicentrično ispitivanje // Paediatria Croatica, 44 (2000), 3. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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461.Barišić, Ingeborg; Clementi, Maurizio; Haeusler, Martin; Gjergja, Romana; Modrušan-Mozetič, Zlata; Žužek, Adele, Stanojević, Milan; Beer, Zlata; Stoll, Claude; EUROSCAN Study GroupEvaluation of prenatal ultrasound detection of fetal abdominal wall defects: European multicentric study // Proceedings of the XXII Alpe Adria Meeting of Perinatal Medicine ( XIV Congress) / Dražančić, Ante; Elkaz, B. (ur.).
Čakovec: Zrinski, dd, 2000. (predavanje, međunarodna recenzija, sažetak, znanstveni) -
462.Barišić, Ingeborg; Petković, Iskra; Mrsić, Sanja; Gjergja-Matejić, RomanaCitogenetička i FISH analiza u dječaka sa sindromom 48, XXYY // Paediatria Croatica, 44 (2000), 1-2; 65-68 (podatak o recenziji nije dostupan, članak, stručni)
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463.Tanacković, Goranka; Barišić, Ingeborg; Gjergja-Matejić, Romana; Hećimović, Silva; Pavelić, JasminkaThe incidence of cystic fibrosis (CF) mutations among patients from Croatia // Clinical Genetics, 58 (2000), 4; 333-335 (međunarodna recenzija, članak, znanstveni)
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464.Barišić, I; Marušić–Dellamarina, B; Hećimović, S; Lujić, L; Gjergja-Matejić, R.Etičko promišljanje liječnika - nekad i danas // Paediatria Croatica, 43 (1999), 1. (međunarodna recenzija, pregledni rad, znanstveni)
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465.Barišić, IngeborgOsnove humane genetike // Paediatria Croatica, 43 (1999), suppl 2; 65-66 (podatak o recenziji nije dostupan, kongresno priopcenje, stručni)
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466.Barišić, Ingeborg; Hećimović, Silva; Pavelić, KrešimirGenetic screening for the fragile X syndrome in population at risk: clinical preselection notably improves cost-effectiveness of fragile X population studies // EUROCAT-ICBDMS International Symposium on Registration and Prevention of Congenital Anomalies - September 25-26, 1998 - Firenze, Italy - Abstract. Reproductive Toxicology. 13(4):321-340, 1999
Firenca, Italija, 1999. str. 330-330 (poster, sažetak, znanstveni) -
467.Barišić, Ingeborg; Juretić, Emilija; Peter, Branimir; Mikecin, Lili; Gjergja-Matejić RomanaToriello-Carey syndrome in two siblings: further delineation and confirmation of an autosomal recessive inheritance // European Journal of Human Genetics, 7 (1999), 1-2. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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468.Tanacković, Goranka; Barišić, Ingeborg; Pavelić, KrešimirThe occurrence of the most common CFTR mutations among Croatian cystic fibrosis patients // European Journal of Human Genetics, 7 (1999), Suppl 1. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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469.Barišić, Ingeborg; Petković, Iskra; Morožin, LeonaDe novo interstitial deletion of 8p21-p23 in a patient with dysmorphic features and normal development // Cytogenetics and Cell Genetics, 85 (1999), 1-2. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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470.Barišić, Ingeborg; Lasan, Ružica; Petković, Iskra; Morožin, LeonaInterstitial del(11)(q14q21) associated with severe malformation syndrome // Cytogenetics and Cell Genetics, 85 (1999), 1-2. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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471.Barišić, Ingeborg; Marušić-Della Marina, Branka; Hećimović, Silva; Lujić, Lucija; Gjergja-Matejić, RomanaEpilepsija i EEG zapisi u bolesnika s mutacijomm u FMR1 genu // Paediatria Croatica, 43 (1999), 3; 105-110 (međunarodna recenzija, članak, znanstveni)
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472.Petković, Iskra; Barišić, Ingeborg; Lasan, RužicaProximal 6p trisomy due to unbalanced (X ; 6) translocation: clinical and cytogenetic characterization // 30th Annual Meeting of the European Society of Human Genetics - Lisabon, Portugal - 10-13 May 1998 - Final Programme and Abstracts. European Journal of Human Genetics. 6(Suppl 1), 1998
Lisabon, Portugal, 1998. (poster, sažetak, znanstveni) -
473.Barišić, Ingeborg; Petković, Iskra; Lasan, RužicaDeletion (8)(p21.1): clinical description of a new patient with mild phenotypic manifestations and normal development // 30th Annual Meeting of the European Society of Human Genetics - Lisabon, Portugal - 10-13 May 1998 - Final Programme and Abstracts. European Journal of Human Genetics. 6(Suppl 1), 1998
Lisabon, Portugal, 1998. (poster, sažetak, znanstveni) -
474.Barišić, Ingeborg; Hećimović, Silva; Pavelić, KrešimirGenetic screening for the fragile X syndrome in population at risk: clinical preselection notably improves cost-effectiveness of fragile X population studies // EUROCAT-ICBDMS International Symposium on Registration and Prevention of Congenital Anomalies - Programme and Abstracts / - (ur.).
Firenza : München: -, 1998. str. 21-21 (poster, međunarodna recenzija, sažetak, znanstveni) -
475.Hrešić Kršulović, Vilka; Löffler Badžek, Dagmar; Percl, Mirjana; Barišić, Ingeborg; Herceg Čavrak, Vesna; Grgić Jandriš, Dunja; Barčot, Lj.; Vukmanić, D.; Cetinić, L.Bolničko i ambulantno zbrinjavanje bolesnika s cističnom fibrozom u našoj ustanovi // Paediatria Croatica, 42 (1998), Suppl 2. (podatak o recenziji nije dostupan, kongresno priopcenje, stručni)
