Browsing eNauka
Browsing by Author Kecman, B.
Showing results 1 to 7 of 7
Issue Date | Title | Author(s) | Type | Мp-cat. |
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2006 | Diagnosis of inborn errors of metabolism in Serbian children a referral centre experience | Đorđević, Maja S.; Grković, Sanja; Đurić, Milena; Janković, Borisav; Šumarac, Zorica; Kecman, B.; Stojanov, Lj. | Conference Paper | Mp. category will be shown later |
2018 | Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants![]() | Skakić, Anita ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 21M21 |
2016 | Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias | Stojiljković, Maja ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 21M21 |
2012 | Molecular genetics and genotype-based estimation of BH4-responsiveness in serbian PKU patients: Spotlight on phenotypic implications of p.L48S![]() | Đorđević, M. ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | Mp. category will be shown later |
2021 | Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier![]() | Klaassen, Kristel ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 22M22 |
2007 | X-linked adrenoleukodistrophy: Profiles of very long chain fatty acids in plasma and fibroblasts in eigth Serbian patients![]() | Grkovic, S.; Nikolic, R.; Djordjevic, M.; Stojanov, L.; Zivancevic-Simonovic, S. ![]() ![]() | Article | Mp. category will be shown later |
2006 | X-linked adrenoleukodystrophy: Diagnosis, pathogenesis and prenatal diagnosis![]() | Grković, S.; Nikolić, R.; Dordević, M.; Živančević-Simonović, S. ![]() ![]() | Article | Mp. category will be shown later |