Radivojevic D - Search Results

1

Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature.

Aguilera C, Viñas-Jornet M, Baena N, Gabau E, Fernández C, Capdevila N, Cirkovic S, Sarajlija A, Miskovic M, Radivojevic D, Ruiz A, Guitart M. Aguilera C, et al. Among authors: radivojevic d. BMC Med Genet. 2017 Nov 21;18(1):137. doi: 10.1186/s12881-017-0500-x. BMC Med Genet. 2017. PMID: 29162042 Free PMC article. Review.

2

Lower incidence of deletions in the survival of motor neuron gene and the neuronal apoptosis inhibitory protein gene in children with spinal muscular atrophy from Serbia.

Miskovic M, Lalic T, Radivojevic D, Cirkovic S, Vlahovic G, Zamurovic D, Guc-Scekic M. Miskovic M, et al. Among authors: radivojevic d. Tohoku J Exp Med. 2011 Nov;225(3):153-9. doi: 10.1620/tjem.225.153. Tohoku J Exp Med. 2011. PMID: 21971302 Free article.

3

Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from Serbia.

Miskovic M, Lalic T, Radivojevic D, Cirkovic S, Ostojic S, Guc-Scekic M. Miskovic M, et al. Among authors: radivojevic d. Int J Gynaecol Obstet. 2014 Jan;124(1):55-8. doi: 10.1016/j.ijgo.2013.07.025. Epub 2013 Oct 5. Int J Gynaecol Obstet. 2014. PMID: 24144239

4

Newborn screening for cystic fibrosis in Serbia: a pilot study.

Radivojevic D, Sovtic A, Minic P, Grkovic S, Guc-Scekic M, Lalic T, Miskovic M. Radivojevic D, et al. Pediatr Int. 2013 Apr;55(2):181-4. doi: 10.1111/ped.12009. Epub 2013 Feb 27. Pediatr Int. 2013. PMID: 23163630

5

Deletion and duplication screening in the DMD gene using MLPA.

Lalic T, Vossen RH, Coffa J, Schouten JP, Guc-Scekic M, Radivojevic D, Djurisic M, Breuning MH, White SJ, den Dunnen JT. Lalic T, et al. Among authors: radivojevic d. Eur J Hum Genet. 2005 Nov;13(11):1231-4. doi: 10.1038/sj.ejhg.5201465. Eur J Hum Genet. 2005. PMID: 16030524

6

Molecular analysis of ring y chromosome in a 10-year-old boy with mixed gonadal dysgenesis and growth hormone deficiency.

Milenkovic T, Guc-Scekic M, Zdravkovic D, Topic V, Liehr T, Joksic G, Radivojevic D, Lakic N. Milenkovic T, et al. Among authors: radivojevic d. Balkan J Med Genet. 2011 Dec;14(2):71-6. doi: 10.2478/v10034-011-0049-5. Balkan J Med Genet. 2011. PMID: 24052714 Free PMC article.

7

[Deletions in the dystrophin gene and its phenotype expression].

Lalić T, Guć-Sćekić M, Djurisić M, Radivojević D, Zamurović D, Todorović S. Lalić T, et al. Among authors: radivojevic d. Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:3-5. Srp Arh Celok Lek. 2001. PMID: 15637982 Serbian.

8

[Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].

Radivojević D, Guć-Sćekić M, Djurisić M, Lalić T, Minić P, Kanavakis E. Radivojević D, et al. Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:6-9. Srp Arh Celok Lek. 2001. PMID: 15637983 Serbian.

9

LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients.

Kosac A, Pesovic J, Radenkovic L, Brkusanin M, Radovanovic N, Djurisic M, Radivojevic D, Mladenovic J, Ostojic S, Kovacevic G, Kravljanac R, Savic Pavicevic D, Milic Rasic V. Kosac A, et al. Among authors: radivojevic d. Genes (Basel). 2022 Aug 4;13(8):1385. doi: 10.3390/genes13081385. Genes (Basel). 2022. PMID: 36011296 Free PMC article.

10

Spectrum of cystic fibrosis mutations in Serbia and Montenegro and strategy for prenatal diagnosis.

Radivojevic D, Djurisic M, Lalic T, Guc-Scekic M, Savic J, Minic P, Antoniadi T, Tzetis M, Kanavakis E. Radivojevic D, et al. Genet Test. 2004 Fall;8(3):276-80. doi: 10.1089/gte.2004.8.276. Genet Test. 2004. PMID: 15727251

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