Disease: Congenital craniosynostosis maternal hyperthyroiditis
- Congenital hyperthyroidism
- Congenital hyperthyroidism: autopsy report
- Diagnosis and therapy of fetal thyroid gland dysfunction in primary maternal disease
- Fetal and neonatal hyperthyroidism
- Foetal and neonatal thyroid disorders
- Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene
- Prescribing in pregnancy. Thyroid disease
- Squamosal Suture Craniosynostosis Due to Hyperthyroidism Caused by an Activating Thyrotropin Receptor Mutation (T632I)
- Transient neonatal hyperthyroidism caused by transplacental transport of pituitary TSH receptor antibodies