Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mireia Tirado"'
Autor:
Laura Català, Judit Casas, Sean Yeh, Maria Josa-Eritja, Mireia Tirado-Capistros, Elisenda Moliner, Gemma Carreras
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Congenital hypothyroidism (CH) is the most common cause of endocrinopathy in the newborn Its incidence lies between 1 in 3,000 and 1 in 2,000, However, congenital goiter is a rare form of presentation. Hypothyroidism secondary to autoimmune etiology
Externí odkaz:
https://doaj.org/article/6d6f0e81beb54de7b5c66a6048305a4d
Autor:
Eulàlia Urgell, Mireia Tondo, Mireia Tirado, Rosa Corcoy, Francisco Blanco-Vaca, Madalina Nicoleta Nan, Susana Martínez, Anna Aulinas, Gemma Carreras, Juan José Espinós, Jose Rives, Susan M. Webb, Rosa Roig
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 1183, p 1183 (2021)
Journal of Clinical Medicine
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Volume 10
Issue 6
Journal of Clinical Medicine
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Volume 10
Issue 6
The most common form of congenital adrenal hyperplasia (CAH) results from a deficiency of the 21-hydroxylase enzyme (21-OHD), presenting with a broad spectrum of clinical phenotypes according to the CYP21A2 gene mutations. Of the 59 patients with sus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff00fafca65e69e048d39011bc7e7beb
https://www.mdpi.com/2077-0383/10/6/1183
https://www.mdpi.com/2077-0383/10/6/1183
Autor:
Madalina Nicoleta, Nan, Rosa, Roig, Susana, Martínez, Jose, Rives, Eulàlia, Urgell, Juan José, Espinós, Mireia, Tirado, Gemma, Carreras, Anna, Aulinas, Susan M, Webb, Rosa, Corcoy, Francisco, Blanco-Vaca, Mireia, Tondo
Publikováno v:
Journal of Clinical Medicine
The most common form of congenital adrenal hyperplasia (CAH) results from a deficiency of the 21-hydroxylase enzyme (21-OHD), presenting with a broad spectrum of clinical phenotypes according to the CYP21A2 gene mutations. Of the 59 patients with sus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5d87c0f0f3aeb29327d7608b2aadd012
https://pubmed.ncbi.nlm.nih.gov/33809035
https://pubmed.ncbi.nlm.nih.gov/33809035