Skoric D - Search Results

1

Wiskott-Aldrich syndrome with macrothrombocytopenia.

Skoric D, Dimitrijevic A, Cuturilo G, Ivanovski P. Skoric D, et al. Indian Pediatr. 2014 Dec;51(12):1015-6. doi: 10.1007/s13312-014-0550-5. Indian Pediatr. 2014. PMID: 25560165 Free article.

2

Improving the Diagnosis of Children with 22q11.2 Deletion Syndrome: A Single-center Experience from Serbia.

Cuturilo G, Drakulic D, Jovanovic I, Krstic A, Djukic M, Skoric D, Mijovic M, Stefanovic I, Milivojevic M, Stevanovic M. Cuturilo G, et al. Among authors: skoric d. Indian Pediatr. 2016 Sep 8;53(9):786-789. doi: 10.1007/s13312-016-0931-z. Indian Pediatr. 2016. PMID: 27771646 Free article.

3

Mitotic crossover promotes leukemogenesis in children born with TEL-AML1 via the generation of loss of heterozygosity at 12p.

Ivanovski I, Garavelli L, Djurić O, Ćirović A, Škorić D, Ivanovski PI. Ivanovski I, et al. Among authors: skoric d. Pediatr Med Chir. 2015 Jun 30;37(2):pmc.2015.112. doi: 10.4081/pmc.2015.112. Pediatr Med Chir. 2015. PMID: 26429121 Free article.

4

The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative Outcome.

Cuturilo G, Drakulic D, Jovanovic I, Ilic S, Kalanj J, Vulicevic I, Raus M, Skoric D, Mijovic M, Medjo B, Rsovac S, Stevanovic M. Cuturilo G, et al. Among authors: skoric d. Pediatr Cardiol. 2017 Dec;38(8):1680-1685. doi: 10.1007/s00246-017-1713-7. Epub 2017 Sep 22. Pediatr Cardiol. 2017. PMID: 28940032

5

Aplastic anemia and Turner syndrome.

Cuturilo G, Skoric D, Grkovic SM, Bojic V, Rodic P, Stefanovic I. Cuturilo G, et al. Among authors: skoric d. Cancer Genet Cytogenet. 2008 Jan 15;180(2):158-9. doi: 10.1016/j.cancergencyto.2007.09.021. Cancer Genet Cytogenet. 2008. PMID: 18206544 No abstract available.

6

Collection strategies and cryopreservation of umbilical cord blood.

Skoric D, Balint B, Petakov M, Sindjic M, Rodic P. Skoric D, et al. Transfus Med. 2007 Apr;17(2):107-13. doi: 10.1111/j.1365-3148.2007.00728.x. Transfus Med. 2007. PMID: 17430466

7

Diagnosis of Fanconi's Anemia by Diepoxybutane Analysis in Children from Serbia.

Cirkovic S, Guc-Scekic M, Vujic D, Ilic N, Micic D, Skoric D, Jovanovic A. Cirkovic S, et al. Among authors: skoric d. Balkan J Med Genet. 2011 Dec;14(2):65-70. doi: 10.2478/v10034-011-0048-6. Balkan J Med Genet. 2011. PMID: 24052713 Free PMC article.

8

Methylenetetrahydrofolate reductase and glutathione S-tranferase gene polymorphisms in secondary mixed phenotype acute leukemia: a case report.

Skoric D, Ivana J, Tanja R, Jovana J, Petar I, Tatjana S. Skoric D, et al. J Pediatr Hematol Oncol. 2014 Apr;36(3):e152-4. doi: 10.1097/MPH.0000000000000050. J Pediatr Hematol Oncol. 2014. PMID: 24276031

9

Hypersensitivity reactions to antiepileptic drugs in children.

Atanasković-Marković M, Janković J, Tmušić V, Gavrović-Jankulović M, Ćirković Veličković T, Nikolić D, Škorić D. Atanasković-Marković M, et al. Among authors: skoric d. Pediatr Allergy Immunol. 2019 Aug;30(5):547-552. doi: 10.1111/pai.13055. Epub 2019 May 20. Pediatr Allergy Immunol. 2019. PMID: 30951222

10

Chromosomal instability in patients with Fanconi anemia from Serbia.

Cirković S, Guć-Sćekić M, Vujić D, Mićić D, Skorić D. Cirković S, et al. Among authors: skoric d. Vojnosanit Pregl. 2014 Apr;71(4):368-72. doi: 10.2298/vsp1404368c. Vojnosanit Pregl. 2014. PMID: 24783417

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