Congenital hypothyroidism and thyroid cancer.

Autor: Penna G; Department of Clinical Medicine, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.; Endocrinology Service of Institute Orizonti, Belo Horizonte, Minas Gerais, Brazil., Rubio IGS; Department of Biological Science, Molecular Thyroid Science Laboratory, Federal University of São Paulo, São Paulo, Brazil.; Biotechnology Post-graduation Program, Federal University of São Paulo, São Paulo, Brazil.; Estructural and Functional Biology Program, Federal University of São Paulo, São Paulo, Brazil., Brust ES; Department of Biological Science, Molecular Thyroid Science Laboratory, Federal University of São Paulo, São Paulo, Brazil.; Biotechnology Post-graduation Program, Federal University of São Paulo, São Paulo, Brazil., Cazarin J; Laboratory of Endocrine Physiology, Institute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil., Hecht F; Laboratory of Endocrine Physiology, Institute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil., Alkmim NR; Endocrinology Service of Institute Orizonti, Belo Horizonte, Minas Gerais, Brazil.; Post-Graduation Program Molecular Medicine, Faculty of Medicine, Federal University of Minas Gerais, Belo Horizonte, Brazil., Rajão KMAB; Endocrinology Service of Institute Orizonti, Belo Horizonte, Minas Gerais, Brazil.; Endocrinology Service of Hospital das Clínicas, Federal University of Minas Gerais, Belo Horizonte, Brazil., Ramos HE; Department of Bioregulation, Health & Science Institute, Thyroid Study Laboratory, Federal University of Bahia, Salvador, Brazil.; Post-Graduation Program Medicine and Health, Faculty of Medical Sciences, Federal University of Bahia, Salvador, Bahia, Brazil.; Post-Graduate Program in Interactive Processes of Organs and Systems, Health & Science Institute, Federal University of Bahia, Salvador, Bahia, Brazil.

Publikováno v: Endocrine-related cancer [Endocr Relat Cancer] 2021 Jul 22; Vol. 28 (9), pp. R217-R230. Date of Electronic Publication: 2021 Jul 22 (Print Publication: 2021).

Novel mutation in MCT8 gene in a Brazilian boy with thyroid hormone resistance and severe neurologic abnormalities.

Autor: Filho HC; Pediatric Endocrinology Unit, Instituto da Criança, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil. hamiltoncm@uol.com.br, Marui S, Manna TD, Brust ES, Radonsky V, Kuperman H, Dichtchekenian V, Setian N, Damiani D

Publikováno v: Arquivos brasileiros de endocrinologia e metabologia [Arq Bras Endocrinol Metabol] 2011 Feb; Vol. 55 (1), pp. 60-6.