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2. A multicenter analysis of individuals with a 47,XXY/46,XX karyotype

3. Assessing Machine Learning for Diagnostic Classification of Hypertension Types Identified by Ambulatory Blood Pressure Monitoring

4. Alpha 1-acid glycoprotein is upregulated in severe COVID-19 patients and decreases neutrophil NETs in SARS-CoV-2 infection

6. MMP-2 and MMP-9 levels in plasma are altered and associated with mortality in COVID-19 patients

9. Assessing Machine Learning for Diagnostic Classification of Hypertension Types Identified by Ambulatory Blood Pressure Monitoring

10. Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld‐Rieger Syndrome

15. Abstract P114: Differential Expression Of Angiotensin Ii Receptors In Aorta Of Ela2ko Mice With Abdominal Aortic Aneurysm.

18. Predictive Accuracy and Clinical Utility of Machine Learning Prediction for Classifying Blood Pressure Status

19. Abstract P108: Inflammatory Factors And Metalloproteinases Levels Are Elevated In Aorta Of Patients With Abdominal Aortic Aneurysm

21. CARDIOVASCULAR RISK PROFILE IN YOUNG PATIENTS WITH EPILEPSY

25. Metabolomic Signature of Early Vascular Aging (EVA) in Hypertension

26. Telomere Length and Risk of Major Adverse Cardiac Events and Cancer in Obstructive Sleep Apnea Patients

27. Untargeted Metabolomics Provides Insight into the Mechanisms Underlying Resistant Hypertension

31. Co-occurrence of a maternally inherited DNMT3A duplication and a paternally inherited pathogenic variant in EZH2 in a child with growth retardation and severe short stature: atypical Weaver syndrome or evidence of a DNMT3A dosage effect?

35. Reference values for local arterial stiffness. Part B: femoral artery

36. Reference values for local arterial stiffness. Part A: carotid artery

42. Reference intervals for common carotid intima-media thickness measured with echotracking: relation with risk factors

44. Comprehensive Analysis of TEK Variants in Patients With Vascular Malformations.

45. Modified Rules for Classification of Variants Associated With Disorders of Somatic Mosaicism.

47. Co-occurrence of a maternally inherited DNMT3A duplication and a paternally inherited pathogenic variant in EZH2 in a child with growth retardation and severe short stature: atypical Weaver syndrome or evidence of a DNMT3A dosage effect?

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