Keyphrases
Abnormal Pattern
33%
Age at Diagnosis
33%
At Birth
66%
Biochemical Characterization
33%
Biochemical Phenotype
33%
Clinical Characterization
33%
Clinical Entities
33%
Clinical Features
33%
Clinical Spectrum
33%
Cognitive Delay
33%
Cognitive Development
33%
Collagen
66%
Connective Tissue Disease
33%
Developmental Delay
33%
Disease Frequency
33%
Disease Severity
66%
Ehlers-Danlos Syndrome
100%
Electron Microscopy
33%
First Year of Life
33%
Genotype-phenotype Association
33%
Gross Motor Development
33%
Hyperelasticity
33%
Hypotonia
66%
Joint Hypermobility
33%
Kyphoscoliosis
66%
Lysyl Hydroxylase
33%
Molecular Background
33%
Molecular Characterization
33%
Molecular Investigation
33%
Newly Diagnosed
33%
Phenotypic Variation
100%
PLOD1
33%
Pyridinoline
33%
Pyridinoline Crosslinks
33%
Rare Type
33%
Vascular Events
33%
Vascular Rupture
33%
Biochemistry, Genetics and Molecular Biology
Cognitive Development
25%
Cross-Link
25%
Electron Microscopy
25%
Energy-Dispersive X-Ray Spectroscopy
100%
Genotyping
25%
Lysyl Hydroxylase
25%
Morbidity
25%
Motor Development
25%
Pyridinoline
50%