Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Laura Gruñeiro-Papendieck"'
Autor:
Rachel Reynaud, Maria Virginia Méndez, Debora Braslavsky, Nicolas Jullien, Ana Chiesa, Ana Keselman, Thierry Brue, Laura Gruñeiro-Papendieck, Laura Prieto, Alexandru Savenau, Rosa Enacan, Ignacio Bergadá
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Background/Aim: Congenital hypothyroidism (CH) is a heterogeneous entity. Neonatal screening programs based on thyrotropin (TSH) determination allow primary CH diagnosis but miss central CH (CCH). CCH causes morbidity, alerts to other pituitary defic
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Thyroglossal duct cysts are the most common thyroid developmental anomalies accounting for 75% of midline neck tumors in children. Carcinomas arising fromthis remnant are very rare in adults and even scarcer in pediatrics. Preoperative diagnosis is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bdabeba9a15a0f75aada01fcdca2efb
https://www.oatext.com/primary-thyroglossal-duct-carcinoma-with-lateral-neck-metastasis-in-an-adolescent-girl.php
https://www.oatext.com/primary-thyroglossal-duct-carcinoma-with-lateral-neck-metastasis-in-an-adolescent-girl.php
Autor:
Héctor M. Targovnik, Rosa Enacan, Maria Eugenia Masnata, Ana Chiesa, Patricia Papendieck, Laura Gruñeiro-Papendieck, Sofia Siffo, Fiorella Sabrina Belforte, María Cecilia Olcese, Carina M. Rivolta
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Congenital hypothyroidism affects 1:2000-3000 newborns detected by neonatal screening programs. Dual oxidases, DUOX1 and 2, generate hydrogen peroxide needed for the thyroid hormone synthesis. Mutations in the DUOX2 gene have been described in transi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd79556f3516c6785f69a86c24f386b5
https://www.sap.org.ar/docs/publicaciones/archivosarg/2017/v115n3a19.pdf
https://www.sap.org.ar/docs/publicaciones/archivosarg/2017/v115n3a19.pdf
Autor:
Rosa E, Enacán, María E, Masnata, Fiorella, Belforte, Patricia, Papendieck, María C, Olcese, Sofía, Siffo, Laura, Gruñeiro-Papendieck, Héctor, Targovnik, Carina M, Rivolta, Ana E, Chiesa
Publikováno v:
Archivos argentinos de pediatria. 115(3)
Congenital hypothyroidism affects 1:2000-3000 newborns detected by neonatal screening programs. Dual oxidases, DUOX1 and 2, generate hydrogen peroxide needed for the thyroid hormone synthesis. Hipotiroidismo congénito transitorio por defectos bialé
Autor:
Ana Chiesa, Laura Prieto, Laura Gruñeiro-Papendieck, Patricia Papendieck, María de Luján Calcagno, Virginia Mendez
Publikováno v:
Hormone Research in Paediatrics. 80:185-192
Introduction: We retrospectively assessed the incidence of congenital hypothyroidism (CH) detected through our neonatal screening program between 1997 and 2010. We describe the diagnostic characteristics of the detected population and verify the impa
Autor:
Carina M. Rivolta, María Cecilia Olcese, Rogelio González-Sarmiento, Mirta Miras, Graciela Testa, Liliana Muñoz, Héctor M. Targovnik, Gabriela Sobrero, Laura Gruñeiro-Papendieck, Fiorella Sabrina Belforte, Ana Chiesa
Publikováno v:
Clinical Endocrinology. 76:568-576
Summary Background Iodide organification defect (IOD) is characterized by a reduced ability of the thyroid gland to retain iodide resulting in hypothyroidism. Mutations in thyroid peroxidase (TPO) gene appear to be the most common cause of IOD and ar
Autor:
Ana, Chiesa, Maria Cecilia, Olcese, Patricia, Papendieck, Alicia, Martinez, Ana, Vieites, Sonia, Bengolea, Héctor Manuel, Targovnik, Carina Marcela, Rivolta, Carina Maria, Rivolta, Laura, Gruñeiro-Papendieck
Publikováno v:
Endocrine. 41:130-137
Resistance to thyroid hormone (RTH) is characterized by elevated levels of thyroid hormones, normal or slightly increased TSH levels respondent to TRH, resistance to thyroid hormone administration, and variable clinical expression. To describe the di
Autor:
Héctor M. Targovnik, Rogelio González-Sarmiento, Alicia Gauna, Laura Gruñeiro-Papendieck, Fiorella Sabrina Belforte, Sonia Iorcansky, María Cecilia Olcese, V Herzovich, Ana Chiesa, Fernando Cassorla, Carina M. Rivolta
Publikováno v:
Molecular and Cellular Probes. 23:148-153
Thyroid Hormone Receptor β (THRB) defects, typically transmitted as autosomal dominant traits, cause Resistance to Thyroid Hormone (RTH). We analyzed the THRB gene in thirteen South American patients with clinical evidence RTH from eleven unrelated
Autor:
Ana Chiesa, Viviana J. Gutnisky, Carina M. Rivolta, Laura Gruñeiro-Papendieck, Héctor M. Targovnik, Mariela Caputo, Geraldo Medeiros-Neto, Rogelio González-Sarmiento
Publikováno v:
Journal of Endocrinology. 195:167-177
Thyroglobulin (TG) functions as the matrix for thyroid hormone synthesis. Thirty-five different loss-of-function mutations in the TG gene have been reported. These mutations are transmitted in an autosomal recessive mode. The objective of this study
Autor:
Mariela Caputo, Carina M. Rivolta, Héctor M. Targovnik, Rogelio González-Sarmiento, Claudia Gabriela Pellizas, Sebastián A. Esperante, Laura Gruñeiro-Papendieck, Ana Chiesa
Publikováno v:
Clinical Endocrinology. 67:351-357
Summary Context Thyroid dyshormonogenesis is associated with mutations in the thyroglobulin (TG) gene and characterized by normal organification of iodide and low serum TG. These mutations give rise to congenital goitrous hypothyroidism, transmitted