Kecman B - Search Results

1

Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies.

Andjelkovic M, Klaassen K, Skakic A, Marjanovic I, Kravljanac R, Djordjevic M, Vucetic Tadic B, Kecman B, Pavlovic S, Stojiljkovic M. Andjelkovic M, et al. Among authors: kecman b. Mol Diagn Ther. 2024 Sep;28(5):645-663. doi: 10.1007/s40291-024-00720-2. Epub 2024 Jul 14. Mol Diagn Ther. 2024. PMID: 39003674 Free PMC article.

2

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: kecman b. Clin Genet. 2018 Feb;93(2):350-355. doi: 10.1111/cge.13093. Epub 2017 Dec 11. Clin Genet. 2018. PMID: 28685844

3

Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier.

Klaassen K, Djordjevic M, Skakic A, Kecman B, Drmanac R, Pavlovic S, Stojiljkovic M. Klaassen K, et al. Among authors: kecman b. Mol Genet Metab Rep. 2021 Nov 19;29:100822. doi: 10.1016/j.ymgmr.2021.100822. eCollection 2021 Dec. Mol Genet Metab Rep. 2021. PMID: 34900593 Free PMC article.

4

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. Among authors: kecman b. JIMD Rep. 2013;9:49-58. doi: 10.1007/8904_2012_178. Epub 2012 Oct 13. JIMD Rep. 2013. PMID: 23430547 Free PMC article.

5

Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias.

Stojiljkovic M, Klaassen K, Djordjevic M, Sarajlija A, Brasil S, Kecman B, Grkovic S, Kostic J, Rodriguez-Pombo P, Desviat LR, Pavlovic S, Perez B. Stojiljkovic M, et al. Among authors: kecman b. Clin Genet. 2016 Sep;90(3):252-7. doi: 10.1111/cge.12751. Epub 2016 Mar 4. Clin Genet. 2016. PMID: 26830710

6

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: kecman b. 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

7

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: kecman b. 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.

8

Appendiceal involvement in a patient with Gaucher disease.

Kocic M, Djuricic SM, Djordjevic M, Savic D, Kecman B, Sarajlija A. Kocic M, et al. Among authors: kecman b. Blood Cells Mol Dis. 2018 Feb;68:109-111. doi: 10.1016/j.bcmd.2016.09.002. Epub 2016 Sep 30. Blood Cells Mol Dis. 2018. PMID: 27717752

9

X-linked adreno leukodistrophy: 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, Djordjevic-Denic G, Kecman B. Grkovic S, et al. Among authors: kecman b. Indian J Clin Biochem. 2007 Sep;22(2):118-22. doi: 10.1007/BF02913328. Indian J Clin Biochem. 2007. PMID: 23105697 Free PMC article.

10

Tetrahydrobiopterin deficiency among Serbian patients presenting with hyperphenylalaninemia.

Stojiljkovic M, Klaassen K, Djordjevic M, Sarajlija A, Kecman B, Ugrin M, Zukic B, Desviat LR, Pavlovic S, Perez B. Stojiljkovic M, et al. Among authors: kecman b. J Pediatr Endocrinol Metab. 2015 Mar;28(3-4):477-80. doi: 10.1515/jpem-2014-0297. J Pediatr Endocrinol Metab. 2015. PMID: 25418970

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