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Pregled prema Autor Đorđević-Milošević, Maja
Prikaz rezultata 1 do 20 od 45
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| Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
|---|---|---|---|---|
| 2021 | Ambiguous Genitalia and Lissencephaly in a 46,xy Neonate with a Novel Variant of Aristaless Gene![]() | Basa, Mihail; Vuković, Rade; Sarajlija, Adrijan | Naučni članak | 23M23 - Međunarodni časopis kategorije M23 |
| 2018 | Appendiceal involvement in a patient with Gaucher disease![]() | Kocić, Marija; Đuričić, Slaviša M.; Đorđević, Maja | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 2010 | Biohemijska dijagnostika urođenih poremećaja metaboizma organskih kiselina | Đorđević, Maja | Poglavlje u monografiji | Mp kategorija će biti prikazana naknadno. |
| 2011 | Biomarkers in Serbian patients with Gaucher disease![]() | Šumarac, Zorica; Suvajdzić, Nada | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2019 | Case report of parathyroid carcinoma in a pediatric patient![]() | Živaljević, Vladan R. | Article | 22M22 |
| 2020 | Case-control study of primary hyperparathyroidism in juvenile vs. adult patients![]() | Jovanović, Milan D.; Paunović, Ivan R. | Article | 22M22 |
| 2024 | Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies![]() | Anđelković, Marina | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 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. |
| 2025 | Chorea in Hereditary Leukodystrophies - Overview of Two Cases![]() | Milovanović, Andona | Article | 22M22 |
| 2021 | Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia![]() | Raičević, Maja; Milenković, Tatjana; Hussain, Khalid; Đorđević, Maja | Article | 21aM21a |
| 2026 | Current Status of Newborn Screening in Southeastern and Central Europe![]() | Požun, Nika; ...; Baša, Mihail I.; ...; Brkušanin, Miloš | Article | 21aM21a |
| 2019 | Decreased plasma L-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment![]() | Molema, Femke; ...; Đorđević, Maja S. | Article | 21M21 |
| 2020 | Differences in primary hyperparathyroidism characteristics between children and adolescents![]() | Živaljević, Vladan R. | Article | 21M21 |
| 2016 | Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients![]() | Sarajlija, Adrijan | Article | 22M22 |
| 2013 | Etiology, clinical features and outcome of epilepsia partialis continua in cohort of 51 children![]() | Kravljanac, Ružica | Article | 22M22 |
| 2019 | Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry![]() | Molema, Femke; ...; Đorđević, Maja S. | Article | 21M21 |
| 2011 | Fanconijev sindrom | Đorđević, Maja | Book parts | Mp. category will be shown later |
| 2014 | Flow cytometric assessment of lymphocyte subsets in Gaucher type 1 patients![]() | Rodić, Predrag | Article | 22M22 |
| 2003 | Fulminant subacute sclerosing panencephalitis: Two cases with atypical presentation![]() | Marjanović, Borivoj; Stojanov, Ljubomir; Zamurović, Dragan; Pašić, Srđan | Article | 22M22 |
| 2013 | Gammopathy and B lymphocyte clonality in patients with Gaucher type I disease![]() | Rodić, Predrag | Article | 22M22 |
