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3. Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome

6. Inherited Ventricular Arrhythmia in Zebrafish: Genetic Models and Phenotyping Tools

9. Genetic association analysis of 77,539 genomes reveals rare disease etiologies

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

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

16. Loeys-Dietz Syndrome

17. Meester-Loeys Syndrome

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

22. Phenotypic spectrum of the first Belgian MYBPC3 founder: a large multi-exon deletion with a varying phenotype

25. Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients

26. Bicuspid Aortic Valve

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.

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

39. Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling

41. Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing

43. AVIATOR: An open international registry to evaluate medical and surgical outcomes of aortic valve insufficiency and ascending aorta aneurysm

45. Aortic Valve Surgery in Nonelderly Patients: Insights Gained From AVIATOR

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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