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Browsing by Author Kavečan, Ivana

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Issue DateTitleAuthor(s)TypeМp-cat.
2016A case of 47,XYY in asscociation with congenital anomalies in teenage coupleKavečan, Ivana  ; Jovanović-Privrodski, Jadranka ; Redžek-Mudrinić, Tatjana  ; Obrenović, Milan Conference Paper
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2016A case of craniorachischisis totalisKavečan, Ivana  ; Jovanović-Privrodski, Jadranka ; Redžek-Mudrinić, Tatjana  ; Obrenović, Milan Conference Paper
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2015A case of infant hot water epilepsy: A clinical commentary with video sequencesRedzek-Mudrinic, Tatjana B; Kavecan, Ivana I  ; Pericin-Starcevic, Ivana; Stojadinovic, AleksandraContribution to periodical
22M22
2012Accessory Scrotum Attached to a Peduncular Perineal LipomaKavecan, Ivana I  ; Jovanovic-Privrodski, Jadranka; Dobanovacki, Dusanka S; Obrenovic, Milan RArticle
22M22
2021Analysis of mtDNA sequence in patients with mitochondriopathiesDawod, Phepy Gamal AmvarDoctoral theses
70M70
2017Approach to Pregnancy in Niemann Pick Disease Type B PatientAgic, Danijela D  ; Dinic-Uzurov, Vera; Milosevic, Ivana D  ; Rankov, Olivera; Milosevic, Pavle; Mitic, Gorana P  ; Kavecan, Ivana I  ; Stojic, SinisaConference Paper
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2021Assessment of intellectual impairment, health-related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registryKeller, Mareike; ...; Kavecan, Ivana I  ; ...; Stevanovic, Galina B; (broj, koautora 39)Article
21M21
2009Autism and hypoplastic corpus callosum in a case of monocentric marker chromosome 15Jovanović Privrodski, Jadranka; Kavečan, Ivana  ; Obrenović, Milan R.; Buonadonna, Lucia A.; Bukvić, Nenad M.Article
22M22
2021Birth of a healthy child fathered by a man with Klinefelter's syndrome after preimplantation genetic testingTrninic-Pjevic, Aleksandra M  ; Milatovic, Stevan V  ; Havrljenko, Jelena; Kavecan, Ivana I  ; Kopitovic, Aleksandar  Article
23M23
2011CCFDN sindromRadovanov, D; Jovanović-Privrodski, Jadranka ; Petrovacki Balj, B; Kavečan, Ivana  Conference Paper
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2022Characteristics and quality of life of substance users and their caregiversMaksimovic, Jadranka M  ; Sbutega, Olivera B; Pavlovic, Aleksandar D; Vlajinac, Hristina D ; Kavecan, Ivana I  ; Vujcic, Isidora S  ; Sipetic-Grujicic, Sandra BArticle
21M21
2019Clinical and genetic aspects of overgrowth spectrum syndromesKavečan, Ivana  Conference Paper
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2023Clinical manifestations of Johanson-Blizzard syndrome in patient with nucleotide variants in UBR1 geneJojkić-Pavkov, Danijela  ; Tošić, Jela  ; Kavečan, Ivana  ; Plazačić, MilicaArticle
23M23
2012Complete androgen insensitivity syndrome: Review of four casesDobanovacki, Dusanka; Jokić, Radoica  ; Vučković, Nada  ; Jovanović Privrodski, Jadranka ; Katanic, Dragan; Tatić, Milanka  ; Skeledzija, Miskovic Sanja; Kavečan, Ivana  Article
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2022Could COVID19 cause hemifacial microsomia?Maksimović, Jadranka  ; Kavečan, Ivana  ; Maksimović, Miloš  ; Bojadzieva-Stojanoska, Biljana; Obrenović, Milan Conference Paper
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2008Deficit 21-hidroksilaze kao uzrok kongenitalne nadbubrežne hiperplazije : prikaz slučajaVlaški, Jovan; Katanić, Dragan ; Kavečan, Ivana  ; Dautović, Slavica; Vorgučin, Ivana  Article
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2022Detekcija i karakterizacija genomskih abnormalnosti kod novorođenčadi sa kritično teškim urođenim srčanim manamaMiletić, AleksandraDoctoral theses
70M70
2018Duchenne and Becker Muscular Dystrophy and EpilepsyRedzek-Mudrinic, Tatjana B; Kavecan, Ivana I  ; Knezevic-Pogancev, Marija FConference Paper
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2017Early recurrent pregnancy lost caused by paternal translocation t(3;8)(q13;q24)Kavečan, Ivana  ; Privrodski, Boris; Obrenovic, Milan ; Redžek-Mudrinić, Tatjana  Conference Paper
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2015EpigenetikaKavečan, Ivana  ; Obrenović, Milan Article
52M52