Zobrazeno 1 - 9
of 9
pro vyhledávání: '"APS - antiphospholipid antibody syndrome"'
Autor:
Stanley Niznik, Micha J. Rapoport, Orly Avnery, Aharon Lubetsky, Ronen Shavit, Martin H. Ellis, Nancy Agmon-Levin
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Introduction: Primary obstetric antiphospholipid syndrome (OAPS) is defined by specific morbidities and/or losses of pregnancy in the presence of persistent antiphospholipid antibodies (aPL). This variant of APS is usually treated during pregnancy an
Externí odkaz:
https://doaj.org/article/aab57b5660084552b3a619e15f4fe6f1
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Antiphospholipid syndrome (APS) is a rare condition in childhood, but even more in the neonatal age. Most neonatal cases are considered a passively acquired autoimmune disease, due to a transplacental passage of maternal antiphospholipid antibodies (
Externí odkaz:
https://doaj.org/article/b438e8a1e6e14915a2bd02909cc9fbc3
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 1, Iss 3, Pp 297-300 (2019)
JACC: Case Reports, Vol 1, Iss 3, Pp 297-300 (2019)
Libman-Sacks endocarditis (LSE), a cardiac complication of systemic lupus erythematosus, is commonly treated with anticoagulation for stroke prevention. We describe a patient with multifocal strokes secondary to LSE, treated with aspirin, without fur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::438aeec519445759ddee473604ec89a8
http://europepmc.org/articles/PMC8288987
http://europepmc.org/articles/PMC8288987
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
International Journal of Surgery Case Reports
Highlights • Acute adrenal insufficiency, although rare, is the most frequently reported endocrine manifestation of the APS. • Major surgery has been identified as a precipitating factor for this potentially fatal condition. • Effective treatme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ccf0a14af129ae88f39bf6711104163
https://doi.org/10.1016/j.ijscr.2018.07.034
https://doi.org/10.1016/j.ijscr.2018.07.034
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Kniha
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Mengeot L; Department of Dermatology, Cliniques universitaires Saint-Luc, Université catholique de Louvain (UCLouvain), Brussels, Belgium., Marot L; Department of Anatomopathology, Cliniques universitaires Saint-Luc, Université catholique de Louvain (UCLouvain), Brussels, Belgium., Baeck M; Department of Dermatology, Cliniques universitaires Saint-Luc, Université catholique de Louvain (UCLouvain), Brussels, Belgium.
Publikováno v:
JAAD case reports [JAAD Case Rep] 2022 Sep 21; Vol. 28, pp. 149-151. Date of Electronic Publication: 2022 Sep 21 (Print Publication: 2022).
Autor:
Krawczyk M; Department of Clinical Neurological Sciences, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada., Budhram A; Department of Clinical Neurological Sciences, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada., Sposato LA; Department of Clinical Neurological Sciences, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.; Stroke, Brain, and Heart Disease Laboratory, Western University, London, Ontario, Canada.
Publikováno v:
JACC. Case reports [JACC Case Rep] 2019 Sep 11; Vol. 1 (3), pp. 297-300. Date of Electronic Publication: 2019 Sep 11 (Print Publication: 2019).