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An observational study of the prevalence of classic metaphyseal fractures in children with osteogenesis imperfecta in the first two years of life.

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Diagnosis of metaphyseal fractures in infants and young children with suspected inflicted injury: a systematic review of cross-sectional imaging techniques.

Clinical radiology·2023

Parathyroid hormone changes in infants investigated for inflicted injury; an observational retrospective single centre cohort study.

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Frequent FBN2 variants in pectus excavatum highlight underlying phenotypic variability.

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Longest surviving patient with a homozygous splice-altering EGFR pathogenic variant presenting with skin autoinflammation and a Bartter-like salt-losing tubulopathy.

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Functional characterisation and pathological significance of variants of MEF2C promoter in tetralogy of Fallot.

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Healthcare professionals' perspectives and preferences regarding adolescent meningococcal disease vaccination in the United States.

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Cureus·2026

Homozygous familial hypercholesterolemia, experience with Evinacumab treatment in two Mexican pediatric patients: case report.

Frontiers in genetics·2026

Psychiatric and medical profiles of children receiving health protection measures in a tertiary care facility: A five-year analysis.

Dusunen adam : Bakirkoy Ruh ve Sinir Hastaliklari Hastanesi yayin organi·2026

Predictors of parental stress in families of children with neurodevelopmental disabilities.

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Related Experiment Videos

Sponastrime dysplasia: presentation in infancy

Related Concept Videos

Equity, diversity, and inclusion: variations in clinical and academic radiology.

Fracture detection using a low-dose computed tomography paediatric bone fracture phantom: A multi-reader study of radiographers.

An observational study of the prevalence of classic metaphyseal fractures in children with osteogenesis imperfecta in the first two years of life.

The impact of sedation on the quality of initial skeletal surveys performed for suspected physical abuse in children: a comparative two-centre audit.

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Frequent <i>FBN2</i> variants in pectus excavatum highlight underlying phenotypic variability.

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Sponastrime dysplasia: presentation in infancy

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