Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Virgilio, Melgar"'
Autor:
Guadalupe Vargas, Lourdes-Josefina Balcazar-Hernandez, Virgilio Melgar, Roser-Montserrat Magriña-Mercado, Baldomero Gonzalez, Javier Baquera, Moisés Mercado
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2017)
A 19-year-old woman with a history of isosexual precocious puberty and bilateral oophorectomy at age 10 years because of giant ovarian cysts, presents with headaches and mild symptoms and signs of hyperthyroidism. Hormonal evaluation revealed elevate
Externí odkaz:
https://doaj.org/article/8bc6ab0764ee4dab96e2792bf0558c06
Autor:
Moisés Mercado, Keiko Taniguchi-Ponciano, Aldo Ferreira-Hermosillo, Daniel Marrero-Rodríguez, Claudia Ramírez-Rentería, Virgilio Melgar-Manzanilla
Publikováno v:
Archives of Medical Research. 51:765-776
Although neuroendocrine neoplasms (NEN) were once thought to be rare and mostly "benign" diseases, they are now being redefined in light of recently discovered molecular information. NENs constitute a spectrum of variably differentiated neoplasms, ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::535cd39b9414f1aca94af075a507cd74
https://doi.org/10.1016/j.arcmed.2020.06.018
https://doi.org/10.1016/j.arcmed.2020.06.018
Autor:
Pattsy Etual Espinosa Cardenas, Nitzia López-Juárez, Moisés Mercado, Sergio Moreno-Jimenez, David Enrique Hernandez-Calderon, Lesly A Portocarrero-Ortiz, Irene Mora Irisson, Alejandra Albarrán-Sánchez, Virgilio Melgar-Manzanilla, Maura E. Noyola-García, Ernesto Sosa, Eduardo Almeida-Gutiérrez, Claudia Ramírez-Rentería
Publikováno v:
Journal of the Endocrine Society. 5:A90-A91
Background: paragangliomas (PGN) (including adrenal PGN or pheochromocytomas) are uncommon neuroendocrine neoplasias. Their ubiquity and lack of uniform nomenclature has resulted in systematic sub-registry and limited resources for patients and clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::207c90c5e634812b3f74dcda2256532d
https://doi.org/10.1210/jendso/bvab048.181
https://doi.org/10.1210/jendso/bvab048.181
Publikováno v:
Endocrinología, Diabetes y Nutrición. 64:384-395
Clinically non-functioning pituitary adenomas (NFPAs) are among the most common tumors in the sellar region. These lesions do not cause a hormonal hypersecretion syndrome, and are therefore found incidentally (particularly microadenomas) or diagnosed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7aba17887927a07cb6f449266785da09
https://doi.org/10.1016/j.endinu.2017.05.009
https://doi.org/10.1016/j.endinu.2017.05.009
Autor:
Moisés Mercado, Guadalupe Vargas, Baldomero González, Virgilio Melgar, Lourdes-Josefina Balcazar-Hernandez, Javier Baquera, Roser-Montserrat Magriña-Mercado
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2017)
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2017)
A 19-year-old woman with a history of isosexual precocious puberty and bilateral oophorectomy at age 10 years because of giant ovarian cysts, presents with headaches and mild symptoms and signs of hyperthyroidism. Hormonal evaluation revealed elevate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c9cd4786b1ccc08c97456b602b66247
http://europepmc.org/articles/PMC5510394
http://europepmc.org/articles/PMC5510394
Publikováno v:
Revista medica del Instituto Mexicano del Seguro Social. 55(2)
Autism spectrum disorder (ASD) was described for the first time in 1943 by Leo Kanner, and since 2004, 18 490 articles in the subject have been published, which in turn have been cited 48 416 times.1 Almost half of these publications come from the Un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::46031bed7ac725c886ce13e5222617e6
https://pubmed.ncbi.nlm.nih.gov/28296371
https://pubmed.ncbi.nlm.nih.gov/28296371
Autor:
Maricela Vidrio-Velázquez, Juan O Talavera, Alfredo Reza-Albarrán, Avril García-Dominguez, Aleida de Jesus Rivera-Hernandez, Daniel Cuevas-Ramos, Moisés Mercado, Ana María Uribe-Diaz, Virgilio Melgar, Alma Vergara-López, Lesly A Portocarrero-Ortiz, Carla Valentina Valencia-Méndez
Publikováno v:
The Journal of clinical endocrinology and metabolism. 101(11)
Context: Acromegaly is a systemic disorder caused by a GH-secreting pituitary adenoma. As with other rare diseases, acromegaly registries developed in various European countries have provided us with important information. Objective: The objective of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1466c221e4db9f68fbeddfddc4975cf
https://pubmed.ncbi.nlm.nih.gov/27428551
https://pubmed.ncbi.nlm.nih.gov/27428551
Autor:
Virgilio, Melgar, Etual, Espinosa, Ernesto, Sosa, María José, Rangel, Dalia, Cuenca, Claudia, Ramírez, Moisés, Mercado
Publikováno v:
Revista medica del Instituto Mexicano del Seguro Social. 54(1)
Hyperprolactinemia is a frequent neuroendocrinological condition that should be approached in an orderly and integral fashion, starting with a complete clinical history. Once physiological causes such as pregnancy, systemic disorders such as primary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9b311168d4cf7229f5b73df8455cd307
https://pubmed.ncbi.nlm.nih.gov/26820213
https://pubmed.ncbi.nlm.nih.gov/26820213
Autor:
Donato Iacovazzo, Karen Stals, Joachim Burger, Serban Radian, Ana Laura Espinosa-de-los-Monteros, Claudia Ramírez-Rentería, Márta Korbonits, Baldomero González, Virgilio Melgar, Laura C. Hernández-Ramírez, Mary Dang, Martina Unterländer, Sian Ellard, Federico Roncaroli, Sonal Kapur, Lesly A Portocarrero-Ortiz, Etual Espinosa, Plamena Gabrovska, Anne-Marie Bussell, Sergio Zúñiga, Guadalupe Vargas, Ernesto Sosa, Moisés Mercado
Publikováno v:
Endocrine. 53(2)
Although aryl hydrocarbon receptor-interacting protein (AIP) mutations are rare in sporadic acromegaly, their prevalence among young patients is nonnegligible. The objectives of this study were to evaluate the frequency of AIP mutations in a cohort o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d5565a7b4d542b020f149a6fffe7a60
https://pubmed.ncbi.nlm.nih.gov/27981517
https://pubmed.ncbi.nlm.nih.gov/27981517
Publikováno v:
Revista medica del Instituto Mexicano del Seguro Social. 53(1)
Acromegaly is a rare condition characterized by the excessive secretion of growth hormone (GH), usually by a pituitary adenoma. The clinical manifestations of acromegaly include enlarged hands, feet and face, headaches, arthralgias, fatigue and hyper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::705f23e7f9d41d938b450d658ce56cb9
https://pubmed.ncbi.nlm.nih.gov/25680646
https://pubmed.ncbi.nlm.nih.gov/25680646