37 results on '"Novakovic, Ivana"'
Search Results
2. Clinical exome sequencing in Serbian patients with movement disorders: Single centre experience
3. Analysis of “clinical exome” panel in Serbian patients with cognitive disorders
4. PPARGC1A gene polymorphism and its association with obesity-related metabolic traits in Serbian adolescent population
5. The importance of direct genetic testing to determine female carriers in dystrophinopathies
6. Impact of the fetuin gene polymorphisms in coronary artery calcification and mortality of patients with chronic kidney disease and renal transplant
7. C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population
8. Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies
9. Novel PANK2 mutation identified in patient with pantothenate kinase-associated neurodegeneration
10. GLUT1 deficiency syndrome: A case report with a novel SLC2A1 mutation
11. Phenotypic expression and founder effect of PANK2 c.1583C>T (p.T528M) mutation in Serbian pantothenate kinase-associated neurodegeneration patients
12. Significance of KIT and PDGFRA mutations in gastric gist imatinib - naive surgically treated patients
13. Analysis of T-786C and 4a/b endothelial nitric oxide synthase gene polymorphisms in retinopathy of prematurity
14. Analysis of association between polymorphisms of MTHFR, MTHFD1 and RFC1 genes and efficacy and toxicity of methotrexate in rheumatoid arthritis patients
15. Prospective study of perinatal outcome in pregnancies with primary antiphospholipid syndrome
16. Possible influence of MTHFR C677T polymorphism on serum lipid levels in Serbian school children
17. The effect of Ni on concentration of the most abundant essential cations in several Brassica species
18. 657del5 mutation of the NBS1 gene in myelodysplastic syndrome
19. Distribution of apolipoprotein E gene polymorphism in students and in high-educated elderly from Serbia
20. Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia
21. Quantitative analysis of the dystrophin gene by real-time PCR
22. Epilepsy in a child with Wolf-Hirschhorn syndrome
23. NPM1 gene mutations in children with Myelodysplastic syndromes
24. Anthropometric and lipid parameters trends in school children: One decade of YUSAD study
25. STR loci D19S216, D20S502 and D20S842 analysis in the Serbian population using dentin DNA
26. Investigation of Balkan endemic nephropathy in Serbia: How to proceed?
27. Genetic clues to the etiology of Balkan endemic nephropathy: Investigating the role of ACE and AT1R polymorphisms
28. Radiotherapeutical chromosomal aberrations in laryngeal cancer patients
29. Mowat-Wilson syndrome: A case report
30. Alterations of c-Myc and c-erbB-2 genes in ovarian tumours
31. Mutation status of p53 gene in oral squamous cell carcinoma
32. Analysis of microsatellite markers D18S70 and d20S116 in DNA isolated from dentin: Use in forensic medicine
33. Y chromosome microdeletions in infertile male candidates for microfertilization
34. Determination of titratable acidity in white wine
35. Determination of fluoride content in drinking water and tea infusions using fluoride ion selective electrode
36. Analysis of the anti-apoptotic protein bcl-2 in oral squamous cell carcinoma
37. Analysis of loss of heterozygosity of the tumor suppressor genes p53 and BRCA1 in ovarial carcinomas
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.