Glenda J. Sobey
Sheffield, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 31 publications
Spontaneous coronary artery dissection and vascular Ehlers-Danlos syndrome: a systematic review and case series.
Journal: European journal of human genetics : EJHG
Published: July 23, 2025
Vascular Ehlers-Danlos syndrome: a heritable condition with potentially fatal consequences.
Journal: The Lancet. Rheumatology
Published: March 17, 2025
The Natural History of Dermatosparaxis Ehlers Danlos Syndrome: An Adult Case Series.
Journal: American journal of medical genetics. Part A
Published: September 12, 2024
Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome.
Journal: European journal of human genetics : EJHG
Published: April 19, 2024
Non-oral manifestations in adults with a clinical and molecularly confirmed diagnosis of periodontal Ehlers-Danlos syndrome.
Journal: Frontiers in genetics
Published: January 02, 2023
Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield.
Journal: European journal of human genetics : EJHG
Published: October 24, 2022
An exemplary model of genetic counselling for highly specialised services.
Journal: Journal of community genetics
Published: June 23, 2022
Oral characteristics in adult individuals with periodontal Ehlers-Danlos syndrome.
Journal: Journal of clinical periodontology
Published: January 28, 2022
Rough endoplasmic reticulum expansion: a consistent finding in a patient cohort with vascular Ehlers-Danlos Syndrome and Osteogenesis Imperfecta.
Journal: Ultrastructural pathology
Published: September 20, 2021
Amniotic band sequence in vascular Ehlers-Danlos Syndrome (EDS): Experience of the EDS National Diagnostic Services in the UK.
Journal: European journal of medical genetics
Published: August 01, 2021
Clinical and molecular features of 66 patients with musculocontractural Ehlers-Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14).
Journal: Journal of medical genetics
Published: November 29, 2020
Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia.
Journal: Circulation
Published: September 08, 2020
Last Updated: 09/26/2026