Pregled po CROSBI profilu: Feodora Stipoljev (CROSBI Profil: 27291, MBZ: 231504)
Pronađeno 88 radova
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1.M. Požgaj Šepec, L. La Grasta Sabolić, H. Karnaš, F. Stipoljev, G. Stipančić.A rare case of male sex reversal syndrome (46,XX) with negative SRY gene: a disorder of sexual differentiation (DSD) // Horm Res Paediatr 20122 ; 95(Suppl 2):1-616. ESPE (European Society for Pediatric Endocrinology) 60th Annual Meeting, Rome, Italy 15th – 17th September 2022.
Rim, Italija, 2022. str. 378-378 (poster, međunarodna recenzija, sažetak, znanstveni) -
2.Oroz, Maja; Vičić, Ana; Požgaj Šepec, Marija; Karnaš, Helena; Stipančić, Gordana; Stipoljev, FeodoraThe smallest dislocated microduplication of Xq27.1 harboring SOX3 gene associated with XX male phenotype // Journal of Pediatric Endocrinology and Metabolism, 36 (2022), 1; 86-90 doi:10.1515/jpem-2022-0324 (međunarodna recenzija, prikaz, znanstveni)
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3.Stipovljev, Feodora; Stipančić, GordanaMedicinska genetika // Pedijatrija / Stipančić, Gordana ; Miahtov Štefanović, Iva ; Žaja, Orjena (ur.).
Jasrebarsko: Naklada Slap, 2022. str. 133-157 -
4.Logara Klarić, Monika; Trgovec-Greif, Lovro; Žunić, Lucija; Rokić, Filip; Vičić, Ana; Marić, Tihana; Merkler, Ana; Katušić Bojanac, Ana; Belužić, Robert; Stipoljev, Feodora et al.Genetic analysis of azoospermic men by an integrated NGS panel // European journal of human genetics, 30 (2022), Suppl 1
online, 2022. str. 90-90 doi:10.1038/s41431-021-01026-1 (poster, međunarodna recenzija, sažetak, stručni) -
5.Huljev Frković, Sanda; Vičić, Ana; Crkvenac Gornik, Kristina; Kulišić, Dinko; Stipoljev, FeodoraPrenatally detected encephalocele associated with a novel pathogenic TCTN3 variant: A case report and literature review // American journal of medical genetics. Part A, 188 (2022), 6; 1826-1830 doi:10.1002/ajmg.a.62684 (međunarodna recenzija, prikaz, znanstveni)
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6.Stipoljev, Feodora; Vujisić, Sanja; Ježek, Davor; Vičić, Ana; Radmanić, Leona; Papić, Neven; Židovec Lepej, SnježanaMid trimester amniotic fluid soluble receptor tunica interna endothelial cell kinase-2 levels and risk for preeclampsia // Pregnancy Hypertension-An International Journal of Womens Cardiovascular Health, 27 (2022), 69-73 doi:10.1016/j.preghy.2021.12.009 (međunarodna recenzija, članak, znanstveni)
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7.Vicic, Ana; Skaro, Vedrana; Projic, Petar; Korac, Petra; Gjergja-Juraski, Romana; Stipoljev, FeodoraAntenatal detection of chromosomal abnormalities combining QF-PCR and cytogenetic analysis // Molecular and experimental biology in medicine, 3 (2020), 1; 34-43 doi:10.33602/mebm.3.1.6 (recenziran, članak, znanstveni)
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8.Stipoljev, Feodora; Barbalić, Maja; Logara, Monika; Vicic, Ana; Vulic, Marko; Zekic Tomas, Sandra; Gjergja Juraski, RomanaFETAL CYSTIC HYGROMA ASSOCIATED WITH TERMINAL 2p25.1 DUPLICATION AND TERMINAL 3p25.3 DELETION: CYTOGENETIC, FLUORESCENT IN SITU HYBRIDIZATION AND MICROARRAY FAMILIAL CHARACTERIZATION OF TWO DIFFERENT CHROMOSOMAL STRUCTURAL REARRANGEMENTS // Balkan journal of medical genetics, 23 (2020), 2; 1-7 doi:10.2478/BJMG-2020-0023 (međunarodna recenzija, članak, znanstveni)
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9.Gjergja Juraški, Romana; Turkalj, Mirjana; Plavec, Davor; Nogalo, Boro; Marušić, Ivana; Miloš, Marija; Anzić, Srđan Ante; Kovač Šižgorić, Matilda; Stipoljev, FeodoraSleep phenotype in children with Down syndrome – altered sleep architecture and sleep- disordered breathing // Paediatria Croatica, 63 (2019), 4; 179-184 doi:10.13112/pc.2019.37 (međunarodna recenzija, članak, ostalo)
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10.Shkelzen, Elezaj; Paić, Frane; Stipoljev, Feodora; Gashi, Zafer; Zeqiraj, Afrim; Lila, Albert; Nikuševa Martić, TamaraThe frequency of follicle-stimulating hormone receptor 2039A>G gene polymorphism and the risk of male infertility in albanian population // Acta clinica Croatica, 59 (2019), 1; 37-48 doi:10.20471/acc.2020.59.01.05 (međunarodna recenzija, članak, znanstveni)
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11.Juretić, NestijaAnaliza sekvenci kromosoma Y u Turnerovom sindromu, 2018., diplomski rad, diplomski, Zagreb
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12.Stipoljev, Feodora; Lasan-Trcic Ruzica; Vicic, AnaPrenatal diagnosis of trisomy 21 mosaicism // Molecular and experimental biology in medicine, 1 (2018), 1; 36-41 (recenziran, članak, znanstveni)
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13.Stipoljev Feodora; Miric-Tesanic Danka; Hafner Tomislav; Barbalic Maja; Logara Monika; Lasan-Trcic Ruzica; Vicic Ana; Gjergja- Juraski RomanaPrenatal diagnosis of complex phenotype in a 13-week-old fetus with an interstitial multigene deletion 20q13.13.-q13.2 by chromosomal microarray // European journal of medical genetics, 60 (2017), 11; 589-594 doi:10.1016/j.ejmg.2017.08.010 (međunarodna recenzija, članak, znanstveni)
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14.Vicic, A; Hafner, Tomislav; Bekavac Vlatkovic, Ivanka; Korac, P; Habek, D; Stipoljev, FeodoraPrenatal diagnosis of Down syndrome: A 13-year retrospective study. // Taiwanese Journal of Obstetrics & Gynecology, 4 (2017), 731-735 doi:10.1016/j.tjog.2017.10.004 (međunarodna recenzija, članak, znanstveni)
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15.Gjergja-Juraski , Romana; Turkalj , Mirjana; Plavec , Davor; Nogalo , Boro; Nenadic- Baranasic , Natasa; Stipoljev , Feodora; Marusic , Ivana; Ordulj-Anicic , Darija; Miloš , Marija; Anzic , Ante.ALTERED SLEEP STRUCTURE AND BREATHING IN CHILDREN WITH DOWN SYNDROME – A NEED FOR ROUTINE POLYSOMNOGRAPHIC STUDIES // 10th ISABS Conference
Dubrovnik, Hrvatska, 2017. (poster, međunarodna recenzija, sažetak, znanstveni) -
16.Vičić, Ana; Škaro, Vedrana; Projić, Petar; Korać, Petra; Gjergja-Juraški, Romana; Stipoljev, FeodoraAntenatal Detection of Chromosomal Abnormalities Combining QF-PCR and Cytogenetic Analysis // Tenth ISABS Conference on Forensic and Anthropologic Genetics and Mayo Clinic Lectures in Individualized Medicine ; program and abstracts / Primorac, Dragan ; Schanfield, Moses ; Vuk-Pavlović, Stanimir ; Manfred, Kayser ; Tamás Ördög (ur.).
Zagreb: ISABS - International Society for Applied Biological Sciences, 2017. str. 270-270 (poster, međunarodna recenzija, sažetak, znanstveni) -
17.Stipoljev, Feodora; Crkvenac-Gornik, Kristina; Huljev Frković, Sanda; Gjergja-Juraški, Romana; Brajenović-Milić, BojanaSeven false-positive cases from non-invasive cell- free fetal DNA testing: Data obtained from three referring centres in Croatia // 4th Central Eastern European Symposium on Free Nucleic Acids in Non-Invasive Prenatal Diagnosis / Paediatria Croatica, 60(Suppl.2) / Barišić, Ingeborg (ur.).
Zagreb: Klinika za dječje bolesti Zagreb, 2016. str. 24-24 (predavanje, sažetak, stručni) -
18.Arbanasić, Haidi, Galov, Ana, Vranković, Lana, Stipoljev, Sunčica, Šprem, Nikica, Bujanić, Miljenko, Konjević, DeanVariability of major histocompatibility complex class II DRB1 locus in wild boar (Sus scrofa l.) from Croatia – preliminary observations // 3rd International VETIstanbul group congress 2016 Book of Abstracts
Sarajevo: Veterinarski fakultet Sarajevo, 2016. str. 213-213 (poster, međunarodna recenzija, sažetak, znanstveni) -
19.Stipoljev, FeodoraBiopsija korionskih resica // Genetičko informiranje u praksi / Čulić, Vida ; Pavelić, Jasminka ; Radman, Maja. (ur.).
Zagreb: Medicinska naklada, 2016. str. 281-283 -
20.Stipoljev, Feodora; Projić, Petar; Škaro, Vedrana; Vičić, Ana; Lauc, GordanBrzi probir najčešćih aneuploidija analizom STR lokusa // Gynaecologia et Perinatologia / Đelmiš, Josip ; Juras, Josip (ur.).
Zagreb: Hrvatski liječnički zbor - Hrvatsko društvo za perinatalnu medicinu, 2015. str. 96-97 (poster, sažetak, znanstveni) -
21.Stipoljev, Feodora; Projić, Petar; Škaro, Vedrana; Crkvenac-Gornik, Kristina; Hafner, Tomislav; Habek, Dubravko; Vičić, Ana; Lauc, GordanKariotipizacija i određivanje zigociteta blizanačkih trudnoća // Gynaecologia et Perinatologia / Đelmiš, Josip ; Juras, Josip (ur.).
Zagreb: Hrvatski liječnički zbor - Hrvatsko društvo za perinatalnu medicinu, 2015. str. 96-96 (poster, sažetak, znanstveni) -
22.Stipoljev, Feodora; Karlović, Dalibor; Ćelić, Ivan; Sertić, JadrankaSindrom fragilnog X kromosoma // klinička kemija i molekularna dijagnostika u kliničkoj praksi / Sertić, Jadranka (ur.).
Zagreb: Medicinska naklada, 2015. str. 161-164 -
23.Stipoljev, Feodora; Vičić, AnaPrednosti i ograničenja invazivne prenatalne dijagnostike // Paediatria Croatica, 59 (2015), 130-137 (međunarodna recenzija, članak, znanstveni)
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24.Vlatkovic Bekavac, Ivanka; Hafner Tomislav; Miskovic BerIVOJ; Vicic A; Poljak B; Stipoljev FeodoraPrenatal diagnosis of sex chromosome aneuploidies and disorders of sex development--a retrospective analysis of 11-year data. // Journal of perinatal medicine, 5 (2014), 529-534 doi:10.1515/jpm-2013-0279 (međunarodna recenzija, pregledni rad, znanstveni)
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25.Spittel, Hannes; Kubek, Florian; Kreskowski, Katharina; Ziegler, Monika; Klein, Elisabeth; Hamid Ahmed, B.; Kosyakova, Nadezda; Radhakrishnan, Gopakumar; Junge, Annelore; Kozlowski, Peter et al.Mitotic stability of small supernumerary marker chromosomes: a study based on 93 imortalized cell lines // Cytogenetic and genome research, 142 (2014), 3; 151-160 doi:10.1159/000360776 (međunarodna recenzija, članak, znanstveni)
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26.Stipoljev, Feodora; Vičić, Ana; Matijević, RatkoPrenatal diagnosis of pericentric inversion homozygosity for chromosome 9 // Journal of obstetrics and gynaecology, 32 (2014), 2; 189-190 doi:10.3109/01443615.2013.837038 (međunarodna recenzija, kratko priopcenje, znanstveni)
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27.Vlatković Bekavac, Ivanka; Hafner, Tomislav; Mišković, Berivoj; Vičić, Ana; Poljak, Borna; Stipoljev, FeodoraPrenatal diagnosis of sex chromosome aneuploidies and disorders of sex development-a retrospective analysis of 11-year data // Journal of perinatal medicine, 42 (2014), 4; 529-534 doi:10.1515/jpm-2013-0279 (međunarodna recenzija, članak, znanstveni)
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28.Vičić, Ana; Hafner, Tomislav; Wagner, Jasenka; Stipoljev, FeodoraPrenatal Diagnosis of 18p Deletion and Isochromosome 18q Mosaicism in a Fetus with a Cystic Hygroma // Collegium antropologicum, 38 (2014), 3; 1059-1062 (recenziran, članak, stručni)
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29.Škrlec, Ivana; Wagner, Jasenka; Pušeljić, Silvija; Heffer, Marija; Stipoljev, FeodoraPartial Monosomy 2p and Partial Trisomy 4q due to Paternal Translocation t(2 ; 4)(p25.1 ; q31.3) // Collegium antropologicum, 38 (2014), 2; 762-762 (podatak o recenziji nije dostupan, prikaz, znanstveni)
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30.Škrlec, Ivana; Wagner, Jasenka; Pušeljić, Silvija; Heffer, Marija; Stipoljev, FeodoraDe novo case of a partial trisomy 4p and a partial monosomy 8p // Collegium antropologicum, 38 (2014), 1; 319-323 (podatak o recenziji nije dostupan, prikaz, znanstveni)
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31.Vičić, Ana; Stipoljev, FeodoraBiopsija korionskih resica // Paediatria Croatica, 57 (2013), 392-399 (podatak o recenziji nije dostupan, članak, ostalo)
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32.Vičić, Ana; Zudenigob, Damir; Korać, Petra; Liehre, Thomas; Stipoljev, FeodoraPrenatally detected interstitial deletion 13q12.3– q22 in a fetus with a cystic hygroma // Gene, 531 (2013), 1; 90-91 doi:10.1016/j.gene.2013.08.029 (međunarodna recenzija, kratko priopcenje, znanstveni)
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33.Vičić, Ana; Mišković, B; Korać, Petra; Jandrić, D; Stipoljev, FeodoraPrenatally diagnosed case of mosaic trisomy 13 associated with Currarino triad // European Journal of Human Genetics / ESHG (ur.).
Pariz: Nature Publishing Group, 2013. str. 584-584 (poster, međunarodna recenzija, sažetak, znanstveni) -
34.Tislarić-Medenjak D; Kosec V; Tonković-Durisević I; Zec I; Sabolović-Rudman S; Kuna K; Herman R; Ivicević-Bakulić T; Soljacić-Vranes H; Tuckar N et al.Biochemical screening of fetal aneuploidies and neural tube defects by "double-test" in Croatia: a 10 years' experience // Collegium antropologicum, 35 (2011), 3; 957-962 (međunarodna recenzija, članak, znanstveni)
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35.Wagner, Jasenka; Stipoljev, Feodora; Pušeljić, Silvija; Škrlec, Ivana; Heffer, Marija; Liehr, ThomasCharacterization of a familial case with complex chromosome rearrangement involving chromosomes 1, 10, 11, 13 and 18 // Chromosome research
Porto, Portugal, 2011. str. S87-S88 (poster, međunarodna recenzija, sažetak, stručni) -
36.Škrlec, Ivana; Wagner, Jasenka; Pušeljić, Silvija; Heffer, Marija; Stipoljev, FeodoraDe novo case of a partial trisomy 4p and a partial monosomy 8p // Chromosome Research
Porto, Portugal, 2011. str. S58-S58 (poster, međunarodna recenzija, sažetak, stručni) -
37.Tišlarić-Medenjak, Dubravka; Košec, Vesna; Tonković-Đurišević, Ivana; Zec, Ivana; Sabolović- Rudman, Senka; Kuna, Krunoslav; Herman, Radoslav; Ivičević-Bakulić, Tomislav; Soljačić-Vraneš, Hrvojka; Tučkar, Neven et al.Biochemical Screening of Fetal Aneuploidies and Neural Tube Defects by »Double-Test« in Croatia: A 10 Years’ Experience // Collegium Antropologicum, 35 (2011), 3; 957-962 (međunarodna recenzija, pregledni rad, znanstveni)
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38.Škrlec, Ivana; Wagner, Jasenka; Pušeljić, Silvija; Heffer, Marija; Stipoljev, FeodoraPartial monosomy 2p and partial trisomy 4q due to paternal translocation t(2 ; 4)(p25.1 ; q31.3) // 2nd ‘AnEUploidy’ Workshop
Split, Hrvatska, 2010. str. 68-68 (poster, međunarodna recenzija, sažetak, stručni) -
39.Wagner, J; Dorner, S; Stipoljev, F; Skrlec, I; Lauc, G; Weise, A; Mrasek, K; Liehr, T; Brecevic, LPartial monosomy 4q and partial trisomy 13q: phenotype and molecular mapping of the breakpoints // Chromosome Research / Herbert C. Macgregor (ur.).
Stockholm, Švedska: Springer, 2009. str. S32-S32 (poster, međunarodna recenzija, sažetak, znanstveni) -
40.Petković Ramadža, Danijela; Stipoljev, Feodora; Sarnavka, Vladimir; Begović, Davor; Potočki, Kristina; Fumić, Ksenija; Mornet, Etienne; Barić, Ivo.Hypophosphatasia: phenotypic variability and possible Croatian origin of the c.1402G>A mutation of TNSALP gene // Collegium antropologicum, 33 (2009), 4; 1255-1260 (međunarodna recenzija, članak, znanstveni)
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41.Vičić, Ana; Roje, Damir; Strinić, Tomislav; Stipoljev, FeodoraTrisomy 1 in an early pregnancy failure // American journal of medical genetics. Part A, 146 (2008), 18; 2439-2441 (podatak o recenziji nije dostupan, pismo, stručni)
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42.Misković, B; Stipoljev, F; Hadzisejdić, I; Grahovac; BPrenatal genotyping of the RhD locus by polymerase chain reaction in fetus at risk of hemolytic disease // Liječnički vjesnik, 130 (2008), 1-2; 4-6 (međunarodna recenzija, članak, znanstveni)
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43.Mišković, Berivoj; Sertić, Jadranka; Stavljenić- Rukavina, Ana; Stipoljev, FeodoraAssociation of angiotensin-converting enzyme insertion-deletion polymorphism with preeclampsia // Collegium antropologicum, 32 (2008), 2; 339-343 (recenziran, članak, stručni)
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44.Tišlarić-Medenjak, Dubravka; Košec, Vesna; Kos, Milan; Latin, Višnja; Harni, Vesna; Lovrić, Boris; Tučkar, Neven; Sabolović-Rudman, Senka; Herman, Radoslav; Končar, Mišo et al.Kombinirani ultrazvučno-biokemijski probir fetalnih aneuploidija od 10. – 14. tjedna trudnoće: prvi rezultati primjene testa u Hrvatskoj // Gynaecologia et perinatologia : journal for gynaecology, perinatology, reproductive medicine and ultrasonic diagnostics, 17 (2008), 4; 195-200 (međunarodna recenzija, članak, znanstveni)
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45.Pavlinić, Dinko; Džijan, Snježana; Stipoljev, Feodora; Wagner, Jasenka; Ćurić, Goran; Lauc, GordanQuantitative Fluorescent PCR : A Rapid Approach to Prenatal Diagnostics of Common Autosomal Aneuploidies // Croatica Chemica Acta, 81 (2008), 1; 219-222 (međunarodna recenzija, članak, znanstveni)
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46.Stipoljev, FeodoraGenetski uzroci neplodnosti // Medicina : glasilo Hrvatskoga liječničkoga zbora, Podružnica Rijeka, 43 (2007), 279-284 (podatak o recenziji nije dostupan, članak, stručni)
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47.Canki-Klain, Nina; Quijano-Roy, Susana; Antun Sasso; Telarović, Srđana; Lessel, Davor; Stiglmayer, Neda; Juri, Jelena; Žagar, Marija; Gjergja, Romana; Stipoljev, Feodora et al.PRAKTIČKI ASPEKTI GENETSKOG SAVJETOVANJA / Canki-Klain, Nina (ur.).
Zagreb: COPY SERVIS, Kranjčevićeva 25, Zagreb, 2007 -
48.Canki-Klain, Nina; Bošnjak, Ivan; Kvakić, Milka; Sepčić, Juraj; Marković, Dubravko; Gjergja Juraški, Romana; Jokić-Begić, Nataša; Stipoljev, Feodora; Lessel, Davor; Vranješ, Davorka et al.Praktični aspekti genetskog savjetovanja / Canki-Klain, Nina (ur.).
Zagreb: COPY SERVIS, 2007 -
49.Wagner, Jasenka; Škrlec, Ivana; Štibi, Sanela; Viljetić, Barbara; Pušeljić, Silvija; Stipoljev, Feodora; Heffer-Lauc, MarijaSindrom potpune neosjetljivosti na androgene // Medicinski vjesnik, 39 (2007), 1-4; 35-44 (recenziran, pregledni rad, stručni)
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50.Stipoljev, Feodora; Vujisić, Sanja; Parazajder, Josip; Hafner, Daria; Ježek, Davor; Sertić, JadrankaCytogenetic analysis of azoospermic patients : karyotype comparison of peripheral blood lymphocytes and testicular tissue // European journal of obstetrics, gynecology, and reproductive biology, 124 (2006), 2; 197-203 doi:10.1016/j.ejogrb.2005.05.020 (međunarodna recenzija, članak, znanstveni)