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Browsing by Author Kecman, Bozica
Showing results 1 to 11 of 11
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2010 | ABDOMINAL LYMPHADENOPATHY DURING ENZYME REPLACEMENT THERAPY: AN EMERGING CHALLENGE OF GAUCHER DISEASE? | Sarajlija, Adrijan   ; Djordjevic, Maja S; Kecman, Bozica; Djuricic, Slavisa M; Ristic, Goran G | Conference Paper | Mp. category will be shown later |
| 2025 | Clinical and Genetic Profile of 35 Patients with Glycogen Storage Disease Type 1b: A Comparative Analysis Before and During SGLT2 Inhibitor Therapy | Djordjevic-Milosevic, Maja; Skakic, Anita G ; Kecman, Bozica; Stankovic, Sara S ; Kovacevic, Ivona; Pavlovic, Sonja T ; Stojiljkovic, Maja M | Article | 21M21 |
| 2011 | Depression and Health Related Quality of Life in Caregivers of Children with Phenylketonuria | Sarajlija, Adrijan ; Djordjevic, Maja S; Kecman, Bozica | Conference Paper | Mp. category will be shown later |
| 2022 | Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire | Gruenert, Sarah C; ...; Djordjevic-Milosevic, Maja; ...; Kecman, Bozica; ...; (broj, koautora 64) | Article | 21a+M21a+ |
| 2026 | First Reported Use of Recombinant Parathyroid Hormone in Kenny–Caffey Syndrome Type 2: A Case Report and Literature Review | Milošević Đorđević, Maja; Skakić, Anita ; Anđelković, Marina ; Delgado-Vega, Angelica Maria; Thonberg, Håkan; Klaassen, Kristel ; Komazec, Jovana; Kecman, Bozica; Jocić, Nikola ; Björck, Erik;
Lindstrand, Anna; Stojiljković, Maja
; | Article | 22M22 |
| 2016 | Kliničke karakteristike i genotip bolesnika sa glikogenozom tip 1 | Adrijan Sarajlija; Đorđevic, Maja; Stojiljković, Maja ; Kecman, Bozica; Skakić, Anita ; Pavlović, Sonja | Conference Paper | Mp. category will be shown later |
| 2015 | Next generation sequencing role in diagnosis of mitochondrial disease in Serbian patient | Đorđević, Maja; Stojiljković, Maja ; Sarajlija, Adrijan; Kecman, Bozica; Skakić, Anita ; Pavlović, Sonja | Conference Paper | Mp. category will be shown later |
| 2024 | Novel deep intronic variant in GALC gene in the patient with infantile Krabbe disease | Maric, Nina; Kecman, Bozica; Ostojic, Slavica B | Conference Paper | Mp. category will be shown later |
| 2010 | NOVEL MITOCHONDRIAL DNA DELETION IN PATIENT WITH DISTINCT PRESENTATION OF PEARSON SYNDROME | Kecman, Bozica; Mayr, Johannes A; Djordjevic, Maja S; Sarajlija, Adrijan ; Stajic, Natasa | Conference Paper | Mp. category will be shown later |
| 2011 | Successful Early Treatment of Neonatal Maple Syrup Urine Disease | Djordjevic, Maja S; Sarajlija, Adrijan ; Kecman, Bozica; Stajic, Natasa; Bogdanovic, Radovan M; Jankovic, Borisav Z | Conference Paper | Mp. category will be shown later |
| 2015 | Tetrahydrobiopterin deficiency among Serbian patients presenting with hyperphenylalaninemia | Stojiljković, Maja ; Klaassen, Kristel ; Đorđević, Maja; Sarajlija, Adrijan ; Kecman, Bozica; Ugrin, Milena ; Zukić, Branka ; Desviat, Lourdes R.; Pavlović, Sonja ; Perez, Belen | Article | 23M23 |