Results 131 to 140 of about 250,188 (305)
Background: Skeletal muscle atrophy is one of the main side effects of high-dose or continuous use of glucocorticoids (such as dexamethasone). However, there are limited studies on dexamethasone-induced skeletal muscle atrophy in zebrafish and even fewer
Chen-Chen Sun +8 more
doaj +1 more source
Efeitos da suplementação com óleo de peixe sobre alterações no metabolismo da glicose e dos lipídios induzidas por glicocorticoide em ratos [PDF]
Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Programa de Pós-Graduação em Nutrição, Florianópolis, 2014.A dexametasona (Dex) é um glicocorticoide sintético usado como potente anti-inflamatório na prática ...
Barbosa, Amanda Marreiro
core
Non-traumatic intracerebral hemorrhage (ICH) is the most common type of hemorrhagic stroke. The therapeutic effects of dexamethasone in ICH patients remain unclear.
Yuexin Lu +5 more
doaj +1 more source
High-dose dexamethasone induced LPS-stimulated rat alveolar macrophages apoptosis
Si Zeng,1,* Hui Qiao,2,* Xue-wen Lv,1 Dan Fan,1 Tong Liu,1 Dongli Xie1 1Department of Anesthesiology, Sichuan Academy of Medical Sciences & Sichuan Provincial People’s Hospital, Chengdu, 2Department of Anesthesiology, The Eye and ENT Hospital ...
Lv XW +5 more
core
Our meta‐analysis showed significant improvement of PFS with lenalidomide, proteasome inhibitors, and CD38‐based therapies. A significant OS benefit was noted only with lenalidomide in transplant‐eligible (TE) patients, while CD38‐directed therapy showed a trend toward improved OS.
Heinz Ludwig +25 more
wiley +1 more source
Background Intravenous dexamethasone has been used clinically to reduce surgical pain. Our study aims to investigate the analgesic efficacy, optimal dosage, mechanisms, and effects on surgical wound healing of dexamethasone in an animal postoperative ...
Yan-Ting Cheung, Stanley Sau Ching Wong
doaj +1 more source
ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi +6 more
wiley +1 more source
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu +23 more
wiley +1 more source

