437 results on '"Baas, A. F."'
Search Results
2. Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study
3. Phenotypic variability of filamin C–related cardiomyopathy: Insights from a novel Dutch founder variant
4. Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy
5. Treatment with IFB-088 Improves Neuropathy in CMT1A and CMT1B Mice
6. Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN)
7. A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial
8. Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients
9. Sudden Cardiac Death in the Young: Post-mortem Investigation and Cardiogenetic Evaluation of Victims and Their Relatives
10. Mitochondrial Cardiomyopathies
11. Genotype-phenotype correlation in pseudoxanthoma elasticum
12. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study
13. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.
14. BIO FOr CARE: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants—design and status
15. Influence of stressful life events and personality traits on PLN cardiomyopathy severity:an exploratory study
16. Influence of stressful life events and personality traits on PLN cardiomyopathy severity: an exploratory study
17. Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study
18. The Genetic Basis of Apparently Idiopathic Ventricular Fibrillation – a Retrospective Overview
19. Multi-omics integration identifies key upstream regulators of pathomechanisms in hypertrophic cardiomyopathy due to truncating MYBPC3 mutations
20. Automatic multilabel detection of ICD10 codes in Dutch cardiology discharge letters using neural networks
21. The prevalence of pseudoxanthoma elasticum: Revised estimations based on genotyping in a high vascular risk cohort
22. Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies
23. Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy
24. Informing relatives at risk of inherited cardiac conditions: experiences and attitudes of healthcare professionals and counselees
25. UNRAVEL: big data analytics research data platform to improve care of patients with cardiomyopathies using routine electronic health records and standardised biobanking
26. Artificially Ambiguous Genetic Code Confers Growth Yield Advantage
27. QI-452785-2 INDIVIDUALIZED FAMILY SCREENING FOR ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY
28. Influence of stressful life events and personality traits on PLN cardiomyopathy severity: an exploratory study.
29. Mechanisms of calcification in Fahr disease and exposure of potential therapeutic targets
30. Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome
31. Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants
32. Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants
33. Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants
34. The genetic basis of apparently idiopathic ventricular fibrillation:A retrospective overview
35. Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity:an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers
36. The Genetic Basis of Apparently Idiopathic Ventricular Fibrillation - a Retrospective Overview
37. Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy
38. Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers
39. Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants
40. Penetrance and Prognosis of MYH7Variant-Associated Cardiomyopathies
41. Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population
42. Meta‐analysis of individual‐patient data from EVAR‐1, DREAM, OVER and ACE trials comparing outcomes of endovascular or open repair for abdominal aortic aneurysm over 5 years
43. Abdominal Aortic Aneurysm
44. Statin therapy is associated with improved survival after endovascular and open aneurysm repair
45. Evaluation of gene panels for inherited cardiac disease—is less more?
46. Long-term survival and secondary procedures after open or endovascular repair of abdominal aortic aneurysms
47. Programs of the european commission on organic materials for the electronics industry
48. Phenylalanine biosynthesis and its relationship to accumulation of capsaicinoids during Capsicum chinense fruit development
49. Blood‐based biomarkers for the prediction of hypertrophic cardiomyopathy prognosis: a systematic review and meta‐analysis
50. Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN)
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