A Canine Model for the Ehlers Danlos Syndrome
A cohort of patients with generalized Fibromuscular Dysplasia and features of Ehlers-Danlos Syndrome
Caring for the Child With Ehlers-Danlos Syndrome
Characterization of the structural aberrations and mutations of the RCCX module in patients with ...
Clinical & Genetic Features of Ehlers-Danlos Syndrome Type IV, The Vascular Type
COL5A1 haploinsufficiency is a common molecular mechanism underlying the classical form of EDS
Deletions of Tenascin-X are associated with joint hypermobility and features of EDS...
Do abnormalities of extracellular matrix elements lead to autoimmune disorders?
GeneTests: EDS, Kyphoscoliotic Form
GeneTests: EDS, Classical Type
GeneTests: EDS, Hypermobility Type
GeneTests: EDS, Vascular Type
Genetic and congenital defect conditions that mimic child abuse
Genotype/Phenotype Correlations in Vascular Ehlers-Danlos Syndrome
High throughput analysis of extracellular matrix gene expression in connective tissue disorders
FAQ: Is genetic counseling recommended for those diagnosed with EDS?
FAQ: What does Mosaic or Mosaicism mean?
FAQ: What genes are related to Ehlers-Danlos syndrome, Vascular Type?
Largest Review of Loeys-Dietz Syndrome to Date
Metabolic and Genetic Arthropathies
Patients with Ehlers Danlos syndrome and CRPS: a possible association?
Phenotypic Variability of Vascular Ehlers-Danlos Syndrome in a Pedigree with a COL3A1 Mutation
Signs in Ehlers-Danlos Syndromes: The role of skin findings in determining the clinical diagnosis
Syndrome of occipitoatlantoaxial hypermobility, cranial settling, and chiari malformation type I in patients with hereditary disorders of connective tissue
Structural studies of arteries by quantitative MRI in vascular Ehlers-Danlos Syndrome (EDS type IV):
Tenascins: regulation & putative functions during pathological stress
The Spine and the Craniocervical Junction in Ehlers-Danlos Syndrome
Three arginine to cysteine substitutions in the pro-alpha (I)-collagen chain cause Ehlers-Danlos syndrome with a propensity to arterial rupture in early adulthood.
Total absence of the alpha2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problems