Djordjevic M - Search Results

1

Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib.

Sarajlija A, Djordjevic M, Kecman B, Skakic A, Pavlovic S, Pasic S, Stojiljkovic M. Sarajlija A, et al. Among authors: djordjevic m. Eur J Med Genet. 2020 Mar;63(3):103767. doi: 10.1016/j.ejmg.2019.103767. Epub 2019 Sep 16. Eur J Med Genet. 2020. PMID: 31536830

2

Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients.

Sarajlija A, Milenkovic T, Djordjevic M, Mitrovic K, Todorovic S, Kecman B, Hussain K. Sarajlija A, et al. Among authors: djordjevic m. J Clin Res Pediatr Endocrinol. 2016 Jun 5;8(2):228-31. doi: 10.4274/jcrpe.2436. Epub 2015 Dec 18. J Clin Res Pediatr Endocrinol. 2016. PMID: 26759084 Free PMC article.

3

CRISPR/Cas9 genome editing of SLC37A4 gene elucidates the role of molecular markers of endoplasmic reticulum stress and apoptosis in renal involvement in glycogen storage disease type Ib.

Skakic A, Andjelkovic M, Tosic N, Klaassen K, Djordjevic M, Pavlovic S, Stojiljkovic M. Skakic A, et al. Among authors: djordjevic m. Gene. 2019 Jun 30;703:17-25. doi: 10.1016/j.gene.2019.04.002. Epub 2019 Apr 3. Gene. 2019. PMID: 30951856

4

Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II.

Dvorakova L, Vlaskova H, Sarajlija A, Ramadza DP, Poupetova H, Hruba E, Hlavata A, Bzduch V, Peskova K, Storkanova G, Kecman B, Djordjevic M, Baric I, Fumic K, Barisic I, Reboun M, Kulhanek J, Zeman J, Magner M. Dvorakova L, et al. Among authors: djordjevic m. Clin Genet. 2017 May;91(5):787-796. doi: 10.1111/cge.12927. Epub 2017 Mar 17. Clin Genet. 2017. PMID: 27883178

5

Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants.

Skakic A, Djordjevic M, Sarajlija A, Klaassen K, Tosic N, Kecman B, Ugrin M, Spasovski V, Pavlovic S, Stojiljkovic M. Skakic A, et al. Among authors: djordjevic m. Clin Genet. 2018 Feb;93(2):350-355. doi: 10.1111/cge.13093. Epub 2017 Dec 11. Clin Genet. 2018. PMID: 28685844

6

New PAH gene promoter KLF1 and 3'-region C/EBPalpha motifs influence transcription in vitro.

Klaassen K, Stankovic B, Kotur N, Djordjevic M, Zukic B, Nikcevic G, Ugrin M, Spasovski V, Srzentic S, Pavlovic S, Stojiljkovic M. Klaassen K, et al. Among authors: djordjevic m. J Appl Genet. 2017 Feb;58(1):79-85. doi: 10.1007/s13353-016-0359-0. Epub 2016 Jul 22. J Appl Genet. 2017. PMID: 27447460

7

Functional Characterization of Novel Phenylalanine Hydroxylase p.Gln226Lys Mutation Revealed Its Non-responsiveness to Tetrahydrobiopterin Treatment in Hepatoma Cellular Model.

Klaassen K, Djordjevic M, Skakic A, Desviat LR, Pavlovic S, Perez B, Stojiljkovic M. Klaassen K, et al. Among authors: djordjevic m. Biochem Genet. 2018 Oct;56(5):533-541. doi: 10.1007/s10528-018-9858-5. Epub 2018 Apr 13. Biochem Genet. 2018. PMID: 29654578

8

Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia.

Raicevic M, Milenkovic T, Hussain K, Djordjevic M, Martic J, Todorovic S, Mitrovic K, Sarajlija A, Vukovic R. Raicevic M, et al. Among authors: djordjevic m. Eur J Pediatr. 2021 Sep;180(9):2815-2821. doi: 10.1007/s00431-021-04051-w. Epub 2021 Mar 26. Eur J Pediatr. 2021. PMID: 33770274

9

Molecular Genetics and Genotype-Based Estimation of BH4-Responsiveness in Serbian PKU Patients: Spotlight on Phenotypic Implications of p.L48S.

Djordjevic M, Klaassen K, Sarajlija A, Tosic N, Zukic B, Kecman B, Ugrin M, Spasovski V, Pavlovic S, Stojiljkovic M. Djordjevic M, et al. JIMD Rep. 2013;9:49-58. doi: 10.1007/8904_2012_178. Epub 2012 Oct 13. JIMD Rep. 2013. PMID: 23430547 Free PMC article.

10

Molecular and phenotypic characteristics of patients with phenylketonuria in Serbia and Montenegro.

Stojiljkovic M, Jovanovic J, Djordjevic M, Grkovic S, Cvorkov Drazic M, Petrucev B, Tosic N, Karan Djurasevic T, Stojanov L, Pavlovic S. Stojiljkovic M, et al. Among authors: djordjevic m. Clin Genet. 2006 Aug;70(2):151-5. doi: 10.1111/j.1399-0004.2006.00650.x. Clin Genet. 2006. PMID: 16879198

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