Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Ana Coelho Gomes"'
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2017)
Hypogonadotropic hypogonadism (HH) is common and occurs prematurely in HIV-infected men. However, HH with very low testosterone has not been described. Three men with normal pubertal development and HIV1 diagnosis at the ages of 22, 34 and 35 years.
Externí odkaz:
https://doaj.org/article/4eaad2c4644f46d58ce69e7c41339129
Autor:
Sónia do Vale, Lenka Selinger, João Martin Martins, Ana Coelho Gomes, Manuel Bicho, Isabel do Carmo, Carles Escera
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e104869 (2014)
Dehydroepiandrosterone (DHEA) and dehydroepiandrosterone-sulphate (DHEAS) have been reported to have memory enhancement effects in humans. A neuro-stimulatory action and an anti-cortisol mechanism of action may contribute to that relation. In order t
Externí odkaz:
https://doaj.org/article/6533791f4acc4251b9812dfeae67717a
Autor:
Marta Vaz Lopes, Jose Vicente Rocha, Carolina Peixe, Grine Severino Mariana de, Ana Coelho Gomes, Maria Joao Bugalho
Publikováno v:
Endocrine Abstracts.
Publikováno v:
JCEM Case Reports. 1
Introduction Type 1 diabetes mellitus (T1DM) is a chronic inflammatory disease that courses with high serum glucose levels as a result of pancreatic beta cell destruction and subsequent insulinopenia. LADA is a type of autoimmune diabetes where damag
Autor:
Ines Cosme, Catarina Silvestre, Alexandre Maria Ines, Maria Joao Bugalho, Luisa Pinto, Ana Coelho Gomes
Publikováno v:
Endocrine Abstracts.
Publikováno v:
Journal of the Endocrine Society
Background: Adrenal myelolipoma is a rare benign tumor of the adrenal gland, consisting of adipose tissue and hematopoetic elements. It has been reported to be associated with many chronic diseases such as haematological disorders. The majority of th
Autor:
Rita B. Domingues, Ana Luísa Silva, Jose Marcalo, Maria João Bugalho, Ana Coelho Gomes, Maria Inês Alexandre
Publikováno v:
Journal of the Endocrine Society. 5:A199-A199
Background: Hyperparathyroidism-jaw tumor syndrome (HPT-JT) is a rare autosomal dominant disease, caused by mutations in the CDC73 gene, characterized by parathyroid tumors in association with fibro-osseous lesions of the mandible or maxilla. The occ
Autor:
José Maria Aragüés, Joana P. Fernandes, Ana Coelho Gomes, Mário Rui Mascarenhas, Silvia Del Guerra
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2017)
Endocrinology, Diabetes & Metabolism Case Reports
Endocrinology, Diabetes & Metabolism Case Reports
Hypogonadotropic hypogonadism (HH) is common and occurs prematurely in HIV-infected men. However, HH with very low testosterone has not been described. Three men with normal pubertal development and HIV1 diagnosis at the ages of 22, 34 and 35 years.
Publikováno v:
Endocrine Abstracts.
Publikováno v:
Journal of the Endocrine Society
Introduction: Successful long-term management in Cushing’s disease (CD) is challenging. Transsphenoidal surgery (TS) is the treatment of choice. Recurrence rates vary from 15–66% within 5-10 years of initially successful surgery. Objective: To ev