Researchers
Kavečan, Ivana
Results 21-40 of 87
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2022 | Natural Evolution of Morquio: A Syndrome Caused by Two Heterozygous Mutations of the GALNS Gene![]() | Pajic, Milos D | Article | 21M21 |
| 2022 | Febrile and afebrile seizures associated with mild acute gastroenteritis in childhood![]() | Pajić, Jasmina; Redžek-Mudrinić, Tatjana | Article | 51M51 |
| 2022 | Characteristics and quality of life of substance users and their caregivers![]() | Maksimovic, Jadranka M | Article | 21M21 |
| 2021 | Insights into the expanding phenotypic spectrum of inherited disorders of biogenic amines![]() | Kuseyri 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
| Article | 21a+M21a+ |
| 2021 | Birth of a healthy child fathered by a man with Klinefelter's syndrome after preimplantation genetic testing![]() | Trninic-Pjevic, Aleksandra M | Article | 23M23 |
| 2021 | Metachromatic Leukodystrohy - Late infantile Type![]() | Kavečan, Ivana | Conference Paper | Mp. category will be shown later |
| 2021 | Factors associated with smoking habits among undergraduate medical students: a cross-sectional study![]() | Maksimovic, Jadranka M | Article | 23M23 |
| 2021 | Assessment of intellectual impairment, health-related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registry![]() | Keller, Mareike; ...; Kavecan, Ivana I | Article | 21M21 |
| 2020 | Pedijatrija : za studente medicine![]() | Barišić, Nenad
Konstantinidis, Georgios
| Text book | Mp. category will be shown later |
| 2020 | Klinička genetika![]() | Jovanović-Privrodski, Jadranka | Monograph | Mp. category will be shown later |
| 2019 | Hypothyroidism and Down syndrome![]() | Kavečan, Ivana | Conference Paper | Mp. category will be shown later |
| 2019 | Prenatally detected case of CCAM type 1 associated with deficiency of alpha 1 antitrypsin![]() | Kavečan, Ivana | Conference Paper | Mp. category will be shown later |
| 2019 | Clinical and genetic aspects of overgrowth spectrum syndromes![]() | Kavečan, Ivana | Conference Paper | Mp. category will be shown later |
| 2019 | Evolution of Partially Involuting Congenital Hemangiomas of the Face![]() | Kavecan, Ivana I | Article | 22M22 |
| 2019 | Unilateral Type of Macrodystrophia Lipomatosa of the Thumb, Index Finger, and Thenar![]() | Kavecan, Ivana I | Article | 22M22 |
| 2018 | Pachydermodactyly: A Rare Type of Macrodactyly as a Dermatological Sign of Compulsive Behavior and Repetitive Minor Trauma; a Case Report and Review of the Literature![]() | Kavecan, Ivana | Reviews | 22M22 |
| 2018 | Preventivna medicinska epigenetika![]() | Obrenović, Milan | Article | Mp. category will be shown later |
| 2018 | Late Infantile Type of Metachromatic Leukodystrophy Caused by Novel Combination of Heterozygous Arsa Mutations![]() | Kavecan, Ivana I | Contribution to periodical | 23M23 |
| 2018 | Parasitic Twin Presenting Rudimentary Upper Limbs Causes a Unique Spectrum of Anomalies of Autosite![]() | Kavecan, Ivana I | Article | 22M22 |
| 2018 | Duchenne and Becker Muscular Dystrophy and Epilepsy![]() | Redzek-Mudrinic, Tatjana B | Conference Paper | Mp. category will be shown later |
