Sarajlija A - Search Results

1

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: sarajlija a. 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

2

Pulmonary involvement in siblings with Gaucher disease type III.

Djordjević M, Minić P, Sarajlija A, Djuricic SM, Djokić D, Marković O. Djordjević M, et al. Among authors: sarajlija a. Vojnosanit Pregl. 2011 Dec;68(12):1071-4. Vojnosanit Pregl. 2011. PMID: 22352271

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: sarajlija a. 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

Vitamin D deficiency in Serbian patients with Rett syndrome.

Sarajlija A, Djuric M, Tepavcevic DK, Grkovic S, Djordjevic M. Sarajlija A, et al. J Clin Endocrinol Metab. 2013 Dec;98(12):E1972-8. doi: 10.1210/jc.2013-2627. Epub 2013 Oct 8. J Clin Endocrinol Metab. 2013. PMID: 24106287

5

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: sarajlija a. J Pediatr Endocrinol Metab. 2015 Mar;28(3-4):477-80. doi: 10.1515/jpem-2014-0297. J Pediatr Endocrinol Metab. 2015. PMID: 25418970

6

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. 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.

7

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: sarajlija a. Clin Genet. 2016 Sep;90(3):252-7. doi: 10.1111/cge.12751. Epub 2016 Mar 4. Clin Genet. 2016. PMID: 26830710

8

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. Congenit Anom (Kyoto). 2017 Mar;57(2):64-65. doi: 10.1111/cga.12194. Congenit Anom (Kyoto). 2017. PMID: 27649480 No abstract available.

9

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

10

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

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