Kecman B - Search Results

1

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: kecman b. Clin Genet. 2017 May;91(5):787-796. doi: 10.1111/cge.12927. Epub 2017 Mar 17. Clin Genet. 2017. PMID: 27883178

2

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.

3

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.

4

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

5

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.

6

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

7

Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency.

Sarajlija A, Magner M, Djordjevic M, Kecman B, Grujic B, Tesarova M, Minic P. Sarajlija A, et al. Among authors: kecman b. Congenit Anom (Kyoto). 2017 Mar;57(2):64-65. doi: 10.1111/cga.12194. Congenit Anom (Kyoto). 2017. PMID: 27649480 No abstract available.

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

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

10

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

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