Latest papers

Screening of parents and siblings of patients with thyroid dysgenesis by thyroid function tests and ultrasound.

Papillary carcinoma of a thyroglossal duct cyst in a patient with thyroid hemiagenesis: effectiveness of conservative surgical treatment.

Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis.

Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis.

Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis.

Clinical evaluation of isolated nonvisualized fetal gallbladder.

Random variability in congenital hypothyroidism from thyroid dysgenesis over 16 years in Québec.

High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis.

Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.

The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning.

FOXE1 polymorphisms: a new piece in the puzzle of thyroid dysgenesis.

[Thyroid hemiagenesis associated with Flajani's disease and papillary carcinoma. A case report].

Thyroid imaging in children.

Familial forms of thyroid dysgenesis.

Possible non-Mendelian mechanisms of thyroid dysgenesis.

Murine models for the study of thyroid gland development.

[Tc]-99m thyroid scintigraphy in congenital hypothyroidism screening program.

[Thyroid dysgenesis]

Congenital hypothyroidism: from paracelsus to molecular diagnosis.

Analysis of physical and mental development of children with aplasia, hypoplasia and ectopy of the thyroid gland.