Hyposialylated thyroglobulin in a patient with congenital goiter and hypothyroidism (1992)
- Autores:
- Autores USP: WAJCHENBERG, BERNARDO LEO - FM ; MEDEIROS NETO, GERALDO ANTONIO DE - FM
- Unidade: FM
- DOI: 10.1210/jcem.74.1.1727828
- Assunto: ENDOCRINOLOGIA
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Journal of Clinical Endocrinology and Metabolism
- Volume/Número/Paginação/Ano: v.74, n.1 , p.43-8, jan. 1992
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
GROLLMAN, E F et al. Hyposialylated thyroglobulin in a patient with congenital goiter and hypothyroidism. Journal of Clinical Endocrinology and Metabolism, v. 74, n. ja 1992, p. 43-8, 1992Tradução . . Disponível em: https://doi.org/10.1210/jcem.74.1.1727828. Acesso em: 20 abr. 2024. -
APA
Grollman, E. F., Doi, S. Q., Weiss, P., Ashwell, G., Wajchenberg, B. L., & Medeiros Neto, G. A. (1992). Hyposialylated thyroglobulin in a patient with congenital goiter and hypothyroidism. Journal of Clinical Endocrinology and Metabolism, 74( ja 1992), 43-8. doi:10.1210/jcem.74.1.1727828 -
NLM
Grollman EF, Doi SQ, Weiss P, Ashwell G, Wajchenberg BL, Medeiros Neto GA. Hyposialylated thyroglobulin in a patient with congenital goiter and hypothyroidism [Internet]. Journal of Clinical Endocrinology and Metabolism. 1992 ;74( ja 1992): 43-8.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1210/jcem.74.1.1727828 -
Vancouver
Grollman EF, Doi SQ, Weiss P, Ashwell G, Wajchenberg BL, Medeiros Neto GA. Hyposialylated thyroglobulin in a patient with congenital goiter and hypothyroidism [Internet]. Journal of Clinical Endocrinology and Metabolism. 1992 ;74( ja 1992): 43-8.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1210/jcem.74.1.1727828 - Effect of hypocaloric diet with and without d-fenfluramine treatment on growth hormone release after growth hormone-releasing factor stimulation in patients with android obesity
- Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin
- Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism
- 138- nucleotid deletion in the thyroglobulin ribunocleic acid messenger in a congenital goiter with defective thyroglobulin synthesis
- Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger
- Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis
- Human thyroid tissue do not express thyroalbumin
- Genetic linkage studies of thyroid peroxidase (tpo) gene in families with tpo deficiency
- Defective organification of iodice causing hereditary goitrous hypothyroidism
- Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism
Informações sobre o DOI: 10.1210/jcem.74.1.1727828 (Fonte: oaDOI API)
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