The type of variants at the COL3A1 gene associates with the phenotype and severity of vascular Ehlers-Danlos syndrome

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5. Nonsyndromic arteriopathy and aortopathy and vascular Ehlers–Danlos syndrome causing COL3A1 variants
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6. Cervical artery dissections and type A aortic dissection in a family with a novel missense COL3A1 mutation of vascular type Ehlers–Danlos syndrome
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9. Bowel Perforation in Vascular Ehlers–Danlos Syndrome: Case Report and Comprehensive Review
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11. Vascular Ehlers-Danlos syndrome in children: evaluating the importance of diagnosis and follow-up during childhood
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12. Spontaneous Dissection of the Renal Artery in Vascular Ehlers-Danlos Syndrome
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13. The Current Status of Genes and Genetic Testing in Emergency Medicine: A Narrative Review.
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14. Surgical management of vascular Ehlers-Danlos syndrome and its challenges: a case report
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15. Deciphering disease signatures and molecular targets in vascular Ehlers-Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts
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16. Vascular Ehlers-Danlos Syndrome With a Novel Missense COL3A1 Mutation Present With Pulmonary Complications and Iliac Arterial Dissection
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20. Diagnosis and treatment of cardiovascular disease in patients with heritable connective tissue disorders or heritable thoracic aortic diseases
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21. Generation of two iPSC lines from vascular Ehlers-Danlos Syndrome (vEDS) patients carrying a missense mutation in COL3A1 gene
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22. Genetic diagnosis of the Ehlers-Danlos syndromes
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24. Vascular Ehlers-Danlos Syndrome: Pathological Variants, Recent Discoveries, and Theoretical Approaches
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25. Vascular Genetics: Presentations, Testing, and Prognostics
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26. Heritable Thoracic Aortic Diseases: Syndromal and Isolated (F)TAAD
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27. Longitudinal echocardiography in pediatric patients with hypermobile Ehlers‐Danlos syndrome
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28. Uncommon association between vascular Ehlers–Danlos syndrome and ocular complications
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29. Rough endoplasmic reticulum expansion: a consistent finding in a patient cohort with vascular Ehlers-Danlos Syndrome and Osteogenesis Imperfecta
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30. Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological Pathways
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31. COL3A1 Variants in Spontaneous Coronary Artery Dissection
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32. Communication of genetic information to at‐risk relatives during the multidisciplinary monitoring of vascular Ehlers–Danlos syndrome in a French referral clinic
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34. Two novel presentations of KCNMA1‐related pathology––Expanding the clinical phenotype of a rare channelopathy
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35. Identification of a missense mutation of COL3A1 in a Chinese family with atypical Ehlers-Danlos syndrome using targeted next-generation sequencing
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37. Case report and discussion: Pre-implantation genetic diagnosis with surrogacy in vascular Ehlers–Danlos syndrome
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38. Identification of two novel COL3A1 variants in patients with vascular Ehlers‐Danlos syndrome
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39. Contributions of Germline and Somatic Mosaic Genetics to Thoracic Aortic Aneurysms in Nonsyndromic Individuals
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41. Case report: A novel COL3A1 variant in a Colombian patient with isolated cerebrovascular involvement in vascular Ehlers–Danlos syndrome
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42. Heritable Thoracic Aortic Disorders
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44. Carriers of COL3A1 pathogenic variants in Denmark: Interfamilial variability in severity and outcome of elective surgical procedures
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45. Case report: Mild phenotype of a patient with vascular Ehlers–Danlos syndrome and COL3A1 duplication mutation without alteration in the [Gly-X-Y] repeat sequence
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46. Percutaneous transjugular approach without arterial monitoring for the treatment of a direct carotid-cavernous fistula with vascular Ehlers–Danlos syndrome: illustrative case
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47. Stretched beyond the limit : Well-being and functioning in patients with Ehlers-Danlos syndrome and other hypermobility syndromes
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48. Genetic Disorders of the Vasculature
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49. Association Between Cardiac Size, Systolic Function, and Complications in Vascular Ehlers-Danlos Syndrome
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50. Early diagnosis of vascular Ehlers-Danlos syndrome through AI-powered facial analysis: Results from the Montalcino Aortic Consortium
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52. Prevalence and outcomes of select rare vascular conditions in females: A descriptive review
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53. Comparative and Prognosis Study of Peripheral Arterial Dissections
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54. Identification and Structural Characterization of a Novel COL3A1 Gene Duplication in a Family With Vascular Ehlers–Danlos Syndrome
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55. Non-atherosclerotic coronary artery disease in molecular autopsy: a literature review
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56. Spontaneous perforation of small intestine followed by rupture of the cystic artery: the natural history of Vascular Ehlers-Danlos Syndrome
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57. Classification, nosology and diagnostics of Ehlers-Danlos syndrome
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58. Vascular Ehlers-Danlos syndrome, an often unrecognized clinical entity: a case report of a novel mutation in the COL3A1 gene
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59. Pearls & Oy-sters: Vascular EDS presenting with acute proptosis
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60. Vascular Ehlers–Danlos syndrome patient with a novel COL3A1 gene deletion mutation without alteration in the triple sequence of (Gly‐X‐Y) repeat
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63. Multi-OMICs analysis on tridimensional fibroblast spheroids to model vascular Ehlers-Danlos syndrome pathogenesis
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