Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Patrícia Afonso Mendes"'
Autor:
Andreia Carvalho de Matos, Cristiane Pais Macedo, Patrícia Afonso Mendes, Maria Augusta Cipriano, Artur Paiva, Adélia Simão
Publikováno v:
GE: Portuguese Journal of Gastroenterology, Pp 1-7 (2021)
Antibiotics are known to cause adverse reactions, but multiple organ involvement associated with nonspecific symptoms can lead to a delay in diagnosis. A definitive correlation between each toxin and its effects is difficult to establish due to conco
Externí odkaz:
https://doaj.org/article/e7302738f25a46f3aab930f8c6de7802
Publikováno v:
GE: Portuguese Journal of Gastroenterology, Pp 1-2 (2021)
Externí odkaz:
https://doaj.org/article/3bcf3e340eab4d86b4168e3e245fdd1c
Publikováno v:
European Journal of Case Reports in Internal Medicine, Vol 5, Iss 4 (2018)
The association between mesenteric panniculitis and Sjögren's syndrome, although rare, is starting to be recognized. Usually, mesenteric panniculitis is symptomatic, presenting with either general or gastrointestinal symptoms. Sjögren's syndrome is
Externí odkaz:
https://doaj.org/article/1dea39c8869f4a8dadca9da19db33748
Publikováno v:
European Journal of Case Reports in Internal Medicine (2017)
Chlorpyrifos is an organophosphate compound recognized as causing acute toxicity. However, organophosphate-induced delayed polyneuropathy (OPIDP), although rare, has also been described. We describe an unusual presentation of OPIDP with flaccid quadr
Externí odkaz:
https://doaj.org/article/1a291d02ebb84315bf480eeec06282e9
Publikováno v:
European Journal of Case Reports in Internal Medicine, Vol 4, Iss 1 (2017)
Creutzfeldt-Jakob disease (CJD) is a rare, incurable and fatal condition that can only be confirmed through neuropathological investigation, such as brain biopsy or post-mortem study. However, a probable diagnosis can be made using clinical criteria.
Externí odkaz:
https://doaj.org/article/c11d2f51acd64d0185dff5b160a840a4
Autor:
Diana Marques Ferreira, Patrícia Afonso Mendes, António Aragão, Manuel Teixeira Veríssimo, Armando Carvalho
Publikováno v:
European Journal of Case Reports in Internal Medicine, Vol 2, Iss 7 (2015)
Anti-signal recognition particle (SRP) myopathy is a rare idiopathic inflammatory myositis that usually affects middle-age women, and is characterized by rapidly progressive proximal and symmetrical muscle weakness, elevated creatine kinase levels, s
Externí odkaz:
https://doaj.org/article/bf9e7202b0c64c7ca01795ef7246c8ee
Autor:
Maria Augusta Cipriano, Patrícia Afonso Mendes, Cristiane Macedo, Adélia Simão, Andreia Carvalho de Matos, Artur Paiva
Publikováno v:
GE: Portuguese Journal of Gastroenterology, Pp 1-7 (2021)
Antibiotics are known to cause adverse reactions, but multiple organ involvement associated with nonspecific symptoms can lead to a delay in diagnosis. A definitive correlation between each toxin and its effects is difficult to establish due to conco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f903ae665c500a3a6c820ca5f6441adc
https://www.karger.com/Article/FullText/516940
https://www.karger.com/Article/FullText/516940
Autor:
Jorge Miguel Bastos Mendes, João Filipe Gomes, Lurdes Rovisco Branquinho, Patrícia Afonso Mendes, João Madaleno, Catarina Oliveira Carvalho
Publikováno v:
European Journal of Case Reports in Internal Medicine (2020)
CIÊNCIAVITAE
Eur J Case Rep Intern Med
CIÊNCIAVITAE
Eur J Case Rep Intern Med
Introduction Chest pain is a very frequent reason for seeking medical care. When there is no obvious cause, patients are sometimes subjected to tests and treatments that may be unnecessary and potentially harmful. Mondor's disease is a rare but usual
Publikováno v:
European Journal of Case Reports in Internal Medicine
European Journal of Case Reports in Internal Medicine (2017)
European Journal of Case Reports in Internal Medicine (2017)
Chlorpyrifos is an organophosphate compound recognized as causing acute toxicity. However, organophosphate-induced delayed polyneuropathy (OPIDP), although rare, has also been described. We describe an unusual presentation of OPIDP with flaccid quadr
Publikováno v:
European Journal of Case Reports in Internal Medicine, Vol 4, Iss 1 (2017)
European Journal of Case Reports in Internal Medicine
European Journal of Case Reports in Internal Medicine
Creutzfeldt-Jakob disease (CJD) is a rare, incurable and fatal condition that can only be confirmed through neuropathological investigation, such as brain biopsy or post-mortem study. However, a probable diagnosis can be made using clinical criteria.