Researchers

Results 21-40 of 87
Issue DateTitleAuthor(s)TypeМp-cat.
2022Natural Evolution of Morquio: A Syndrome Caused by Two Heterozygous Mutations of the GALNS GenePajic, Milos D  ; Kavecan, Ivana I  ; Maksimovic, Jadranka M  ; Babovic, Sinisa S  ; Bojadzieva Stojanoska, Biljana TArticle
21M21
2022Febrile and afebrile seizures associated with mild acute gastroenteritis in childhoodPajić, Jasmina; Redžek-Mudrinić, Tatjana  ; Kavečan, Ivana  ; Vijatov-Đurić, Gordana  ; Milanović, Borko  ; Vorgučin, Ivana  Article
51M51
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
2021Insights into the expanding phenotypic spectrum of inherited disorders of biogenic aminesKuseyri Hübschmann, Oya; Horvath, Gabriella; Cortès-Saladelafont, Elisenda; Yıldız, Yılmaz; Mastrangelo, Mario; Pons, Roser; Friedman, Jennifer; Mercimek-Andrews, Saadet; Wong, Suet-Na; Pearson, Toni S.;
Zafeiriou, Dimitrios I.; Kulhánek, Jan; Kurian, Manju A.; López-Laso, Eduardo; Oppebøen, Mari; Kılavuz, Sebile; Wassenberg, Tessa; Goez, Helly; Scholl-Bürgi, Sabine; Porta, Francesco; Honzík, Tomáš; Santer, René; Burlina, Alberto; Sivri, H. Serap; Leuzzi, Vincenzo; Hoffmann, Georg F.; Jeltsch, Kathrin; Hübschmann, Daniel; Garbade, Sven F.; Assmann, Birgit; Fung, Cheuk-Wing; Guder, Philipp; Hong, Stacey Tay Kiat; Karall, Daniela; Kato, Mitsuhiro; Kavečan, Ivana  ; Koht, Jeanette Aimee; Kuster, Alice; Lücke, Thomas; Manti, Filippo; Mir, Pablo; Mühlhausen, Chris; Önenli Mungan, Halise Neslihan; Palacios, Natalia Alexandra Julia; Ramos, Joaquín Alejandro Fernández; Steel, Dora; Stevanović, Galina; Sykut-Cegielska, Jolanta; Verbeek, Marcel M.; García-Cazorla, Angeles; Opladen, Thomas;
Article
21a+M21a+
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
2021Metachromatic Leukodystrohy - Late infantile TypeKavečan, Ivana  ; Maksimovic, Jadranka  ; Obrenovic, Milan Conference Paper
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2021Factors associated with smoking habits among undergraduate medical students: a cross-sectional studyMaksimovic, Jadranka M  ; Pavlovic, Aleksandar D; Vlajinac, Hristina D ; Vujcic, Isidora S  ; Sipetic-Grujicic, Sandra B; Maris, Slavica R; Maksimovic, Milos Z  ; Obrenovic, Milan R ; Kavecan, Ivana I  Article
23M23
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
2020Pedijatrija : za studente medicineBarišić, Nenad  ; Cvejić, Aleksandar; Doronjski, Aleksandra  ; Đapić, Milesa; Georgijević, Ljubica; Jojkić-Pavkov, Danijela  ; Katanić, Dragan ; Kavečan, Ivana  ; Knežević-Pogančev, Marija  ; Kolarović, Jovanka  ;
Konstantinidis, Georgios  ; Konstantinidis, Nada; Ljuština-Pribić, Radmila; Milankov, Olgica; Milošević, Biljana ; Pavlović, Vesna ; Petrović, Slobodanka; Redžek-Mudrinić, Tatjana  ; Ristivojević, Anđelka; Saravolac-Stefanović, Svetlana; Spasojević, Slobodan  ; Stojadinović, Aleksandra  ; Stojanović, Vesna  ; Velisavljev-Filipović, Gordana  ; Vijatov-Đurić, Gordana  ; Vlaški, Jovan; Vorgučin, Ivana  ; Vukavić, Tamara ; Jovanović-Privrodski, Jadranka ;
Text book
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2020Klinička genetikaJovanović-Privrodski, Jadranka ; Kavečan, Ivana  Monograph
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2019Hypothyroidism and Down syndromeKavečan, Ivana  ; Jovanović-Privrodski, Jadranka ; Obrenovic, Milan ; Privrodski, Boris  ; Redžek-Mudrinić, Tatjana  Conference Paper
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2019Prenatally detected case of CCAM type 1 associated with deficiency of alpha 1 antitrypsinKavečan, Ivana  ; Obrenovic, Milan ; Bogavac, Mirjana  Conference Paper
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2019Clinical and genetic aspects of overgrowth spectrum syndromesKavečan, Ivana  Conference Paper
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2019Evolution of Partially Involuting Congenital Hemangiomas of the FaceKavecan, Ivana I  ; Jovanovic-Privrodski, Jadranka ; Obrenovic, Milan R ; Privrodski, Boris K  ; Redzek-Mudrinic, Tatjana B  ; Savic, Radojica NArticle
22M22
2019Unilateral Type of Macrodystrophia Lipomatosa of the Thumb, Index Finger, and ThenarKavecan, Ivana I  ; Obrenovic, Milan R ; Privrodski, Boris K  ; Erdes-Kavecan, Djerdji  ; Golusin, Zoran  Article
22M22
2018Pachydermodactyly: A Rare Type of Macrodactyly as a Dermatological Sign of Compulsive Behavior and Repetitive Minor Trauma; a Case Report and Review of the LiteratureKavecan, Ivana  ; Pajic, Milos  ; Vučković, Nada  ; Redzek, Mudrinic Tatjana  ; Bjelica, Artur  ; Velisavljev Filipovic, Gordana  ; Stojsic-Milosavljevic, Anastazija  ; Vijatov-Djuric, Gordana  ; Stojsic, Mirjana  ; Erdes-Kavecan, Djerdji  ;
Savic, Radojica; Katanic, Jasmina  ; Hrnjak Ilic, Helena;
Reviews
22M22
2018Preventivna medicinska epigenetikaObrenović, Milan ; Kavečan, Ivana  ; Privrodski, Boris  ; Redžek-Mudrinić, Tatjana  Article
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2018Late Infantile Type of Metachromatic Leukodystrophy Caused by Novel Combination of Heterozygous Arsa MutationsKavecan, Ivana I  ; Obrenovic, Milan R ; Privrodski, Boris K  ; Savic, Radojica NContribution to periodical
23M23
2018Parasitic Twin Presenting Rudimentary Upper Limbs Causes a Unique Spectrum of Anomalies of AutositeKavecan, Ivana I  ; Obrenovic, Milan R ; Jovanovic-Privrodski, Jadranka ; Privrodski, Boris K  ; Jeckovic, MihajloArticle
22M22
2018Duchenne and Becker Muscular Dystrophy and EpilepsyRedzek-Mudrinic, Tatjana B  ; Kavecan, Ivana I  ; Knezevic-Pogancev, Marija F  Conference Paper
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