Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Katarzyna Piotrowicz-Wójcik"'
Publikováno v:
Children, Vol 11, Iss 2, p 237 (2024)
Hereditary angioedema (HAE) is a rare genetic disease. It is characterized by recurrent attacks of angioedema. Evidence to what extent it affects patient functioning is limited in the pediatric population. We aimed to determine the clinical character
Externí odkaz:
https://doaj.org/article/74696041227d45fd9cb5136fca6cf72c
Publikováno v:
Pharmacy, Vol 7, Iss 1, p 12 (2019)
Paracetamol is a popular and easily available drug which is used world-wide as analgesic, antipyretic agent. Hypersensitivity reactions to this drug involve a wide range of symptoms of various importance for patient management. The EudraVigilance (EV
Externí odkaz:
https://doaj.org/article/7f74d9f9e1bd4d21a77358e0d4e8e5c2
Autor:
Robert Pawłowicz, Aldona Juchacz, Katarzyna Piotrowicz-Wójcik, Jacek Gocki, Joanna Jamróz-Brzeska, Krzysztof Kuziemski, Małgorzata Bulanda, Grzegorz Porebski
Publikováno v:
Journal of Clinical Medicine; Volume 10; Issue 23; Pages: 5609
Journal of Clinical Medicine, Vol 10, Iss 5609, p 5609 (2021)
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 10, Iss 5609, p 5609 (2021)
Journal of Clinical Medicine
Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency is a rare disease characterized by recurrent swellings. This study aims to determine (i) the clinical characteristics of the HAE patient population from Poland, and (ii) real-life pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c3e340cac972a780683d4b8f0e7df3c
Publikováno v:
Journal of immunological methods. 495
In patients with drug hypersensitivity reactions, confirmation of causality frequently facilitates decision on a continuation or withdrawal of a given treatment. Unfortunately, identification of the culprit drug often proves difficult. In vivo method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7c0fc762f55ea27017629c10b7452c0
https://pubmed.ncbi.nlm.nih.gov/33940020
https://pubmed.ncbi.nlm.nih.gov/33940020
Publikováno v:
Otolaryngologia polska = The Polish otolaryngology. 74(2)
Background: Hereditary angioedema due to C1-inhibitor deficiency (HAE-C1INH) is a rare genetic disease that runs in the family. As a result of the disease, acute swellings of the subcutaneous tissue and mucous membranes of the digestive and respirato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdabe682b78bd703824677f9d719899f
https://pubmed.ncbi.nlm.nih.gov/32308206
https://pubmed.ncbi.nlm.nih.gov/32308206
Publikováno v:
Przeglad lekarski. 70(12)
Drug hypersensitivity can occur with almost any drug and may range widely in clinical severity from mild pruritus, acute urticaria or angioedema to life-threatening anaphylaxis. Affected patients usually avoid the suspected drug in the future, but in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::92f42360749df2190ac1d6b02326df98
https://pubmed.ncbi.nlm.nih.gov/24720117
https://pubmed.ncbi.nlm.nih.gov/24720117