Zobrazeno 1 - 10
of 1 001
pro vyhledávání: '"Idiopathic hypereosinophilic syndrome"'
Autor:
Michael Cieza-Terrones, José C. De La Flor, Christian Requejo, Daniel Villa, Jacqueline Apaza, Pablo Rodríguez-Doyágüez, Rocío Zamora, Carmen Asato-Higa, David Rivera-Estrella, Antonio Carrasco-Yalán
Publikováno v:
Medicines, Vol 11, Iss 6, p 13 (2024)
Background: Idiopathic hypereosinophilic syndrome (IHES) is a disorder characterized by abnormal and persistent peripheral blood hypereosinophilia (eosinophil count ≥ 1.5 × 109/L and ≥10% eosinophils) with duration ≥ 6 months, associated organ
Externí odkaz:
https://doaj.org/article/ecc5fc55e2bb4b729039f16202860108
Publikováno v:
Journal of Asthma and Allergy, Vol Volume 15, Pp 1763-1771 (2022)
Hyo In Rhyou,1 Seung Eun Lee,2 Mi-Yeong Kim,3 Chan Sun Park,4 Eun-Jung Jo,5 Gil Soon Choi,6 Young Hee Nam7 1Department of Internal Medicine, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Republic of Korea; 2Departme
Externí odkaz:
https://doaj.org/article/43c1e3c62a5c44d3b309f2515647bcbf
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
Idiopathic hypereosinophilic syndrome (IHES) is a rare disease characterized by causeless persistent hypereosinophilia and eosinophilia-associated end-organ damage. Current treatment modalities don’t meet the needs due to adverse events of steroids
Externí odkaz:
https://doaj.org/article/328872470223477c835da03639b66ab8
Akademický článek
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Publikováno v:
Journal of Inflammation Research, Vol Volume 15, Pp 1899-1906 (2022)
Junshuai Xue,* Jianjun Jiang,* Yang Liu Department of General Surgery, Vascular Surgery, Shandong University Qilu Hospital, Jinan City, Shandong Province, People’s Republic of China*These authors contributed equally to this workCorrespo
Externí odkaz:
https://doaj.org/article/eaf03fc2d6904d05bc6339d67ffd5ec0
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Idiopathic hypereosinophilic syndrome (IHES) is a rare but life-threatening disease related to a group of myeloproliferative disorders characterized by prolonged eosinophilia of unknown cause and inflammatory damage to multiple organs. Here, we prese
Externí odkaz:
https://doaj.org/article/2faa78d95f3f41d286c45c4b39c78fe1
Publikováno v:
Case Reports in Oncology, Vol 14, Iss 1, Pp 249-255 (2021)
Idiopathic hypereosinophilic syndrome is a rare disease which is diagnosed after excluding other conditions. The syndrome is characterized by multiple organ involvement including the heart, nervous system, lungs, and gastrointestinal tract. The disea
Externí odkaz:
https://doaj.org/article/602c8ffcc6dd476488c5f1711b5b9f79
Autor:
Kristine Appel Uldall Pallesen, Troels Herlin, Mette Holm, Christian Høst, Mette Christiansen, Mette Ramsing, Mads Kirchheiner Rasmussen, Mette Sommerlund
Publikováno v:
Clinical Case Reports, Vol 8, Iss 10, Pp 2013-2016 (2020)
Abstract Idiopathic hypereosinophilic syndrome (IHES) is one of numerous hypereosinophilic syndromes. The incidence of IHES among children is unknown, but it is considered a rare disease. We report a pediatric case of IHES and the challenges to findi
Externí odkaz:
https://doaj.org/article/4ea275b29ca94fc5a80213f1562cb254
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-5 (2020)
Abstract Background Idiopathic hypereosinophilic syndrome (IHES) is associated with various organ system dysfunctions. Neurologic abnormalities have been previously noted in this syndrome. Cerebral infarction secondary to occlusion of large cerebral
Externí odkaz:
https://doaj.org/article/c44a727be97c4d2a9b818ae3a9ad2435
Publikováno v:
BMC Gastroenterology, Vol 20, Iss 1, Pp 1-4 (2020)
Abstract Background Hypereosinophilic syndrome (HES) is a very rare disease and usually treated with corticosteroids. Gastrointestinal (GI) cytomegalovirus (CMV) infection is also rare but frequent in patients with immunocompromised status. These two
Externí odkaz:
https://doaj.org/article/8e93960f986a42aeb36a5f65499684ae