Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Maria Inês Alexandre"'
Publikováno v:
Acta Médica Portuguesa, Vol 35, Iss 9 (2022)
N/a.
Externí odkaz:
https://doaj.org/article/6b993779bdb14cf389fd9419a6ddb2d2
Publikováno v:
Diagnostics, Vol 13, Iss 2, p 281 (2023)
Functioning metastases from differentiated thyroid carcinoma are rare and present a great therapeutic challenge. Here, we present an unusual case of a patient with metastatic thyroid carcinoma who developed a hyperthyroid state a few years after the
Externí odkaz:
https://doaj.org/article/653788b31e26488d819f1a05dd230a4a
Autor:
Maria Inês Alexandre, Ana Raquel Henriques, Daniela Cavaco, Luís Rodrigues, Sara Costa, Brígida Robalo, Carla Pereira, Maria de Lurdes Sampaio
Publikováno v:
Acta Médica Portuguesa, Vol 34, Iss 9 (2021)
N/a.
Externí odkaz:
https://doaj.org/article/21c9572f59614674a0917dc88f2620ca
Autor:
Carolina Peixe, Maria Inês Alexandre, Ana Raquel Gomes, Ema Nobre, Ana Luísa Silva, Tiago Oliveira, Dolores López-Presa, Cláudia C. Faria, José Miguens, Maria João Bugalho, Pedro Marques
Purpose: Trouillas’ clinicopathological classification is a five-tiered grading system designed to predict recurrence/progression in patients with pituitary adenomas (PAs). We aimed to study its usefulness in predicting PAs that will have a challen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e7ed0b7417b027204cb227bacd4eecb
https://doi.org/10.21203/rs.3.rs-2725892/v1
https://doi.org/10.21203/rs.3.rs-2725892/v1
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a70f51faa0e69daf17e9ed05dd488d8d
https://doi.org/10.1210/jcemcr/luac014.025
https://doi.org/10.1210/jcemcr/luac014.025
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism.
Objectives Pituitary gigantism is a rare condition and it often has an identifiable genetic cause. In this article we report a case of a young girl with pituitary gigantism and two genetic changes. Case presentation A 15-year-old girl with primary am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82fe00349ceba9c6f77344a33958d5db
https://doi.org/10.1515/jpem-2022-0488
https://doi.org/10.1515/jpem-2022-0488
Autor:
Maria Inês Alexandre, Ana Gomes
Publikováno v:
Medicina Clínica.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20cba19fbd55c0d6e17c9c1b97d21045
https://doi.org/10.1016/j.medcli.2022.12.001
https://doi.org/10.1016/j.medcli.2022.12.001
Autor:
Ana Raquel Henriques, Maria Inês Alexandre, Luís Monteiro Rodrigues, Carla Pereira, Brígida Robalo, Daniela Cavaco, Maria de Lurdes Sampaio, Sara T. Costa
Publikováno v:
Acta Médica Portuguesa, Vol 34, Iss 9, Pp 642-643 (2021)
N/a.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95cf6b7900c85ad0fc05777c7759d9ca
https://doi.org/10.20344/amp.16412
https://doi.org/10.20344/amp.16412
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
© 2020 Wiley Periodicals LLC.
Bullous pemphigoid (BP) is the most common autoimmune blistering disease. High potency topical and/or systemic corticosteroids as well as immunosuppressants are the current mainstay of treatment. However, long-term
Bullous pemphigoid (BP) is the most common autoimmune blistering disease. High potency topical and/or systemic corticosteroids as well as immunosuppressants are the current mainstay of treatment. However, long-term
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::713a1cdc326d2478c8bbcd51ed57f5d1
https://doi.org/10.1111/dth.14160
https://doi.org/10.1111/dth.14160
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a285d5b493092c4a4abcc8c11699a86
http://europepmc.org/articles/PMC7208473
http://europepmc.org/articles/PMC7208473