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1. Effect of standardized Aronia Melanocarpa extract on oxidative stress and antioxidant status in patient with cronic myeloid leukemia treated with imatinib

2. Identification of the DNA methylation signature of Mowat-Wilson syndrome

3. The detection of a strong episignature for Chung–Jansen syndrome, partially overlapping with Börjeson–Forssman–Lehmann and White–Kernohan syndromes

5. CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature

6. Active Learning and Novel Model Calibration Measurements for Automated Visual Inspection in Manufacturing

9. Microduplications of ARID1A and ARID1B cause a novel clinical and epigenetic distinct BAFopathy

10. Enriching Artificial Intelligence Explanations with Knowledge Fragments

11. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

12. Venous thromboembolism characteristics and outcomes among RIETE patients tested and untested for inherited thrombophilia

13. Streaming Machine Learning and Online Active Learning for Automated Visual Inspection

14. Active Learning for Automated Visual Inspection of Manufactured Products

15. Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes

16. DNA methylation analysis in patients with neurodevelopmental disorders improves variant interpretation and reveals complexity

17. Identification of DNA methylation episignature for the intellectual developmental disorder, autosomal dominant 21 syndrome, caused by variants in the CTCF gene

19. Age-Related Differences in the Presentation, Management, and Clinical Outcomes of 100,000 Patients With Venous Thromboembolism in the RIETE Registry

22. Debasement Language as a Subset of Political Incivility: Characteristics and Effects

23. The Gig Economy in the Post-COVID Era

24. DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorder

25. Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype

26. Comparative roadmaps of reprogramming and oncogenic transformation identify Bcl11b and Atoh8 as broad regulators of cellular plasticity

28. PB2273: EFFICACY OF OBINUTUZUMAB - BASED REGIMENS IN PATIENTS WITH PREVIOUSLY UNTREATED FOLLICULAR LYMPHOMA: A RETROSPECTIVE OBSERVATIONAL SINGLE-CENTER STUDY

30. Autoimmune lymphoproliferative syndrome identified through reverse phenotyping

31. de novo TINF2 C.845G>A: Pathogenic Variant in Patient with Dyskeratosis Congenita

32. Blepharophimosis with intellectual disability and Helsmoortel‐Van Der Aa Syndrome share episignature and phenotype.

33. Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases

34. An Overview of the North Macedonian Non-discrimination Law

39. Negotiating Identity During the Macedonia’s Name Change Period in Media Discourse

40. Safety and efficacy of teriflunomide in paediatric multiple sclerosis (TERIKIDS): a multicentre, double-blind, phase 3, randomised, placebo-controlled trial

41. Extranodal Diffuse Large B-Cell Lymphoma of the Small Bowel in Female Patient Causing Intestinal Obstruction: A Case Report

43. Molecular Aspects in Chronic Lymphocytic Leukemia patients with Autoimmune Cytopenias: single center experience

47. TIPS AND TRICKS TO PROTECT PREGNANCY FROM LISTERIA.

48. Early-Onset Colorectal Cancer in a Young Woman with Type 1 Gaucher Disease

50. Effect of standardized Aronia Melanocarpa extract on oxidative stress and antioxidant status in patient with chronic myeloid leukemia treated with imatinib

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