Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Antonio C. do Nascimento"'
Autor:
Dulce R. Guedes, Geraldo Medeiros-Neto, Cecília L. S. Santos, Ileana G.S. Rubio, Meyer Knobel, Antonio C. do Nascimento
Publikováno v:
Thyroid. 13:1145-1151
Mutations of the thyroperoxidase (TPO) gene have been reported as being the most severe and frequent abnormality in thyroid iodide organification defect (IOD) causing goitrous congenital hypothyroidism. The objective of this study was to screen and s
Autor:
Ileana G.S. Rubio, Cecília L. Santos, Antonio C. do Nascimento, Geraldo Medeiros-Neto, Meyer Knobel, Jussara V. Toniolo
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia. 46:391-401
Congenital hypothyroidism (CH), as seen in the neonatal period, is predominantly caused by defects in the organogenesis (athyreosis, ectopic thyroid, thyroid hypoplasia) or by specific defects in hormonogenesis (dyshormonogenesis). Central hypothyroi
Autor:
Cecília L. S. Santos, Hennie Bikker, Antonio C. do Nascimento, K. G. M. Rego, J. J. M. De Vijlder, Geraldo Medeiros-Neto, Marcos Antonio Tambascia
Publikováno v:
Clinical Endocrinology. 51:165-172
OBJECTIVE To screen and subsequently sequence the TPO gene for mutations in patients with congenital goitre, hypothyroidism and evidence for an organification defect (positive perchlorate discharge test). PATIENTS We have studied seven hypothyroid an