• "Cryptothyroidism", the major cause of sporadic "athyreotic" cretinism
• Athyreotic congenital hypothyroidism in two sisters
• Athyreotic cretinism
• Athyreotic cretinism associated with thymic hypoplasia and amyloidosis of lymphoid tissue
• Athyreotic cretinism in two sisters
• Autoimmune thyroid disease
• Comparison of radioisotopic and ultrasonic scanning in the evaluation of neonatal hypothyroidism
• Congenital athyreotic hypothyroidism. Late diagnosis
• Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site
• Congenital hypothyroidism in one of monozygotic twins: comparison of their long-term psychosomatic development
• Familial athyreotic cretinism: report of 3 cases
• Foetal and neonatal thyroid disorders
• HLA antigens and congenital hypothyroidism
• Increased incidence of non-tasters of phenylthiocarbamide among congenital athyreotic cretins
• Influence of thyroid morphology on psychomotor development in patients with congenital hypothyroidism during 8 year follow-up
• Insulin-like growth factor binding protein-3 proteolysis and growth of athyreotic infants in the first weeks of life
• Low-dose radioisotope scanning and quantitative analysis in the diagnosis of congenital hypothyroidism
• Measurement of thyroglobulin in newborn screening specimens from normal and hypothyroid infants
• Monomeric calcitonin secretion in infants with congenital hypothyroidism
• Prevalence and etiology of congenital hypothyroidism detected through an argentine neonatal screening program (1997-2010)
• Psychomotor development in congenital hypothyroidism. The Greek screening programme
• Results of national evaluation tests (primary schools) of CE2 and 6th classes of 73 students with congenital hypothyroidism screened at birth
• Role of genetic factor in the development of congenital athyreotic myxedema
• Seasonal variations in TSH serum levels in athyreotic patients under L-thyroxine replacement monotherapy
• Serum thyroglobulin determinations in the differential diagnosis of congenital hypothyroidism
• Sporadic goitrous cretinism
• The different requirement of L-T4 therapy in congenital athyreosis compared with adult-acquired hypothyroidism suggests a persisting thyroid hormone resistance at the hypothalamic-pituitary level
• The ratio of serum free triiodothyronine to free thyroxine in children: a retrospective database survey of healthy short individuals and patients with severe thyroid hypoplasia or central hypothyroidism
• THYROID REFRACTORINESS IN AN ATHYREOTIC CRETIN FED SOYBEAN FORMULA
• Thyroid screening in congenital hypothyroidism: a review of 41 cases
• Thyroxine and treatment of hypothyroidism: seven decades of experience
• Transient neonatal 'athyreosis' resulting from thyrotropin-binding inhibitory immunoglobulins
• Twenty years later: a reevaluation of the contribution of plasma thyroglobulin to the diagnosis of thyroid dysgenesis in infants with congenital hypothyroidism
• Two children with cerebral gigantism and congenital primary hypothyroidism
• Very low birth weight newborns do not need repeat screening for congenital hypothyroidism