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Mostrando ítems 61-70 de 272
Hipotiroidismo congénito, un tema vigente: ¿Qué pasa con prematuros y gemelares?
(Sociedad Uruguaya de Pediatría, 2013)
A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: Evidence for phenotypic variability in mother and child
(Endocrine Soc, 2001-08-01)
Congenital hypothyroidism associated with thyroid hypoplasia can be caused by several genetic defects, including mutations in the TSH beta -subunit, the TSH receptor, the G(A)alpha -subunit, and the transcription factor ...
Avaliação ultrassonográfica de crianças com hipotireoidismo congênito
(Colégio Brasileiro de Radiologia e Diagnóstico por Imagem, 2015)
To establish benchmarks and study some sonographic characteristics of the thyroid gland in a group of euthyroid children aged up to 5 years as compared with age-matched children with congenital hypothyroidism. Thirty-six ...
Aspectos genéticos do hipotireoidismo congênito
(Sociedade Brasileira de Endocrinologia e Metabologia, 2014)
Congenital Secondary Hypothyroidism Evidences in a Dog
(Universidade Federal do Rio Grande do Sul, 2017)
Deiodinase-mediated thyroid hormone inactivation minimizes thyroid hormone signaling in the early development of fetal skeleton
(ELSEVIER SCIENCE INC, 2008)
Thyroid hormone (TH) plays a key role on post-natal bone development and metabolism, while its relevance during fetal bone development is uncertain. To Study this, pregnant once were made hypothyroid and fetuses harvested ...
Evolution and Innovations of the National Neonatal and High Risk Screening Program in Costa Rica
(Universidad de Costa Rica, 2004)