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Browsing by Author Kecman, Božica
Showing results 1 to 15 of 15
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2018 | Appendiceal involvement in a patient with Gaucher disease![]() | Kocić, Marija; Đuričić, Slaviša M.; Đorđević, Maja | Article | 22M22 |
| 2024 | Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies![]() | Anđelković, Marina | Article | 21M21 |
| 2024 | CHARACTERIZATION OF 16 NOVEL GENETIC VARIANTS IN GENES ASSOCIATED WITH EPILEPSY | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
| 2024 | Characterization of 16 novel genetic variants in genes associated with paediatric epilepsy: implications for targeted therapeutic strategies![]() | Anđelković, Marina | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2016 | Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients![]() | Sarajlija, Adrijan | Article | 22M22 |
| 2017 | Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II![]() | Dvorakova, L.; Vlaskova, H.; Sarajlija, Adrijan | Article | 21M21 |
| 2020 | Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib![]() | Sarajlija, Adrijan | Article | 22M22 |
| 2010 | Inborn errors of metabolism in neonatal and pediatric intensive care unit: five year expirience![]() | Đorđević, Maja S | Conference Paper | Mp. category will be shown later |
| 2017 | Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency![]() | Sarajlija, Adrijan | Contribution to periodical | 22M22 |
| 2025 | MITOCHONDRIAL MYOPATHY CAUSED BY MT-ND5 VARIANT: INTEGRATING WES AND MITOCHONDRIAL DNA ANALYSIS | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2016 | Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias![]() | Stojiljković, Maja | Научни чланак | 21M21 - Водећи међународни часопис категорије M21 |
| 2023 | Molecular basis of phenylketonuria in Serbia: an update![]() | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2024 | MOLECULAR BASIS OF PHENYLKETONURIA IN SERBIAN PAEDIATRIC COHORT | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2015 | Molecular characterization of mutations in Serbian patients with glycogen storage diseases - an NGS approach![]() | Skakic, Anita | Conference Paper | Mp. category will be shown later |
| 2015 | Non-renal indications for the continuous renal replacement therapy in the intensive care unit of terciary care center: eleven years of experience![]() | Stajić, Nataša; Putnik, Jovana; Paripović, Aleksandra; Đorđević, Maja
Bogdanović, Radovan;
| Conference Paper | Mp. category will be shown later |
