Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Manuel dos S. Faria"'
Autor:
Lucio Vilar, Julio Abucham, José Luciano Albuquerque, Luiz Antônio Araujo, Monalisa F. Azevedo, Cesar Luiz Boguszewski, Luiz Augusto Casulari, Malebranche B. C. Cunha Neto, Mauro A. Czepielewski, Felipe H. G. Duarte, Manuel dos S. Faria, Monica R. Gadelha, Heraldo M. Garmes, Andrea Glezer, Maria Helane Gurgel, Raquel S. Jallad, Manoel Martins, Paulo A. C. Miranda, Renan M. Montenegro, Nina R. C. Musolino, Luciana A. Naves, Antônio Ribeiro-Oliveira Júnior, Cíntia M. S. Silva, Camila Viecceli, Marcello D. Bronstein
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 62, Iss 2, Pp 236-263
ABSTRACT Prolactinomas are the most common pituitary adenomas (approximately 40% of cases), and they represent an important cause of hypogonadism and infertility in both sexes. The magnitude of prolactin (PRL) elevation can be useful in determining t
Externí odkaz:
https://doaj.org/article/ea921cd49a65412cbf3b05be01822578
Autor:
Renata C. Campelo, Maria L. M. da Silva, Gilvan C. Nascimento, Rossana S. S. Azulay, Viviane C. C. Rocha, Sabrina S. P. Damianse, Marcelo Magalhães, Manuel dos S. Faria, Vandilson P. Rodrigues
Publikováno v:
Oral Diseases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a773b3ba0ab32d0ff461c7637ecf2fb
https://doi.org/10.1111/odi.14511
https://doi.org/10.1111/odi.14511
Autor:
Sabrina S.P. Damianse, Gilvan C. Nascimento, Viviane C.C. Rocha, Ana Gisélia P.A. C. Nascimento, Nadja C. Gaido, Rossana S.S. Azulay, Wellyandra C. dos Santos, Vandilson P. Rodrigues, Ana Rosa P. Quidute, Marcelo Magalhães, Manuel dos S. Faria
Publikováno v:
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists. 28(5)
Multiple endocrine neoplasia type 1 (MEN1) is a rare genetic syndrome characterized by parathyroid, anterior pituitary, and/or duodenopancreatic neuroendocrine tumors. Studies have indicated that investigating primary hyperparathyroidism (pHPT) with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22898f04ecd23de4789798ea7ba45879
https://pubmed.ncbi.nlm.nih.gov/35247589
https://pubmed.ncbi.nlm.nih.gov/35247589
Autor:
Leonardo, Vieira Neto, Julio, Abucham, Luiz Antônio de, Araujo, Cesar L, Boguszewski, Marcello D, Bronstein, Mauro, Czepielewski, Raquel S, Jallad, Nina R de C, Musolino, Luciana A, Naves, Antônio, Ribeiro-Oliveira Júnior, Lucio, Vilar, Manuel Dos S, Faria, Mônica R, Gadelha
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 55(9)
Acromegaly is a disease associated with increased morbidity and reduced life expectancy. Because of its insidious character and its non-recognition, the diagnosis is often made with delay, which, along with the complications related to GH/IGF-I exces
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8fbf4ae568b4ada438c8f4af66ddade3
https://pubmed.ncbi.nlm.nih.gov/22231978
https://pubmed.ncbi.nlm.nih.gov/22231978