Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Guiomar Pinheiro"'
Publikováno v:
European Journal of Case Reports in Internal Medicine (2020)
Pulmonary hypoplasia or agenesis is a rare congenital disorder that results in lung underdevelopment. This disease is usually found in children but rarely encountered in adults. We describe the case of an 84-year-old woman diagnosed with a unilateral
Externí odkaz:
https://doaj.org/article/42b54829e7034a78a1cc7a90c87e82af
Publikováno v:
European Journal of Case Reports in Internal Medicine (2020)
Fasciitis with eosinophilia (FE) is a rare connective tissue disease. Due to its rarity, large-scale studies are lacking, which makes its treatment challenging. Systemic corticosteroids (SCSs) are the cornerstone of treatment; however, additional imm
Externí odkaz:
https://doaj.org/article/fefb76cfaaa24715ae9c5843c94130cc
Publikováno v:
Journal of Medical Cases
A 29-year-old woman presented to the emergency department with red eyes and hypoacusia since the previous weeks associated with a sudden right facial palsy. Ophthalmologic examination revealed bilateral uveitis and lumbar puncture was compatible with
Autor:
Miguel Saraiva, Sofia Ribeiro, Carvalho André, Cruz Ana Rita, Freitas Cláudia, Guiomar Pinheiro, Costa Ana Rita, Garça Magda
Publikováno v:
Endocrine Abstracts.
Autor:
Guiomar Pinheiro, Júlio R. Oliveira, Ernestina Reis, João A. Gonçalves, Ana Rute Costa, Ana Vigário
Publikováno v:
Porto Biomedical Journal
Background: The emergence of carbapenemase-producing Enterobacterales (CPE) represents a major public health threat. Our purpose was to evaluate a surveillance and cohorting program implemented in patients infected or carriers of CPE. Methods: A pros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8691aef3f23c2a6916f9bc6b049df86b
https://hdl.handle.net/10400.16/2696
https://hdl.handle.net/10400.16/2696
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
European Journal of Case Reports in Internal Medicine
European Journal of Case Reports in Internal Medicine (2020)
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
European Journal of Case Reports in Internal Medicine
European Journal of Case Reports in Internal Medicine (2020)
Pulmonary hypoplasia or agenesis is a rare congenital disorder that results in lung underdevelopment. This disease is usually found in children but rarely encountered in adults. We describe the case of an 84-year-old woman diagnosed with a unilateral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::042f3d748b4603d33c5e5a2bf9aeff6c
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
European Journal of Case Reports in Internal Medicine (2020)
European Journal of Case Reports in Internal Medicine
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
European Journal of Case Reports in Internal Medicine (2020)
European Journal of Case Reports in Internal Medicine
Fasciitis with eosinophilia (FE) is a rare connective tissue disease. Due to its rarity, large-scale studies are lacking, which makes its treatment challenging. Systemic corticosteroids (SCSs) are the cornerstone of treatment; however, additional imm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::105b8c052f9918aeca474612891bb927
https://hdl.handle.net/10400.16/2598
https://hdl.handle.net/10400.16/2598
Publikováno v:
BMJ Case Rep
A 76-year-old-man with a medical history of hypertension presented in the emergency department with a 3-month history of lumbar pain, associated with the appearance of a mass in the left lumbar region. He also described a 2-week history of progressiv
Publikováno v:
BMJ Case Rep
Systemic lupus erythematosus (SLE) is a multisystemic autoimmune disorder. Neuromyelitis optica (NMO) is an infrequent neuroinflammatory disorder, whose association with SLE remains rare. The authors report the case of an 18-year-old woman, with SLE