1,088 results on '"Loeys, Bart"'
Search Results
2. Variants in structural cardiac genes in patients with cancer therapy-related cardiac dysfunction after anthracycline chemotherapy: a case control study
3. Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome
4. An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome
5. Circulating MicroRNA as Biomarkers of Anthracycline-Induced Cardiotoxicity: JACC: CardioOncology State-of-the-Art Review
6. Inherited Ventricular Arrhythmia in Zebrafish: Genetic Models and Phenotyping Tools
7. Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population
8. Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotyping
9. Genetic association analysis of 77,539 genomes reveals rare disease etiologies
10. Toward reporting standards for the pathogenicity of variant combinations involved in multilocus/oligogenic diseases
11. HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD). A statement from the HTAD working group of VASCERN
12. Phenotype of COL3A1/COL5A2 deletion patients
13. Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN)
14. Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort
15. Regional Vascular Changes and Aortic Dilatation in Pediatric Patients With Bicuspid Aortic Valve
16. Loeys-Dietz Syndrome
17. Meester-Loeys Syndrome
18. Structural genomic variants in thoracic aortic disease
19. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
20. Luminescent Human iPSC-Derived Neurospheroids Enable Modeling of Neurotoxicity After Oxygen–glucose Deprivation
21. SMAD6-deficiency in human genetic disorders
22. Phenotypic spectrum of the first Belgian MYBPC3 founder: a large multi-exon deletion with a varying phenotype
23. An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome
24. Genetic testing in patients with unexplained coronary aneurysms or dilation
25. Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients
26. Bicuspid Aortic Valve
27. Pathophysiology and Principles of Management of Hereditary Aneurysmal Aortopathies
28. Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death
29. Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients
30. Vascular Ehlers-Danlos Syndrome:A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients
31. Arterial aneurysm and dissection: toward the evolving phenotype of Tatton- Brown- Rahman syndrome.
32. Genetics of Marfan Syndrome and Loeys-Dietz Syndrome
33. Clinical Aspects of Heritable Connective Tissue Disorders
34. Chondrodysplasias and Aneurysmal Thoracic Aortopathy: An Emerging Tale of Molecular Intersection
35. Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome
36. HomozygousSMAD6variants in two unrelated patients with craniosynostosis and radioulnar synostosis
37. The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunction
38. Update on the molecular landscape of thoracic aortic aneurysmal disease
39. Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
40. Marfan Syndrome and Related Disorders
41. Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing
42. Inherited Ventricular Arrhythmia in Zebrafish: Genetic Models and Phenotyping Tools
43. AVIATOR: An open international registry to evaluate medical and surgical outcomes of aortic valve insufficiency and ascending aorta aneurysm
44. Aortic aneurysm/dissection and osteogenesis imperfecta: Four new families and review of the literature
45. Aortic Valve Surgery in Nonelderly Patients: Insights Gained From AVIATOR
46. Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and Epigenomics
47. Health-Related Quality of Life in Children and Young Adults with Marfan Syndrome
48. Correction to: Luminescent Human iPSC-Derived Neurospheroids Enable Modeling of Neurotoxicity After Oxygen–glucose Deprivation
49. Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome.
50. Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis.
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