Zobrazeno 1 - 10
of 6 655
pro vyhledávání: '"Steroid Therapy"'
Publikováno v:
Muller Journal of Medical Sciences and Research, Vol 15, Iss 1, Pp 1-4 (2024)
Objective: The objective of the study was to determine the clinical features, treatment received, and outcomes of severely ill children with multisystem inflammatory syndrome in children (MIS-C). Methods: The study was a retrospective observation car
Externí odkaz:
https://doaj.org/article/00e04f9658ac4be285817c3490b33d5e
Publikováno v:
Nigerian Journal of Paediatrics, Vol 42, Iss 2, Pp 154-157 (2024)
In this report, we described the case of a 14-year-old boy with steroid-sensitive nephrotic syndrome who developed hyperglycaemia and ultimately, diabetic ketoacidosis, following high-dose steroid therapy for a primary renal disease. The nephrotic sy
Externí odkaz:
https://doaj.org/article/78a0c8ffc99a48759e24f462391a873d
Autor:
Petrović Dušan, Dimić Saša, Tabaković Dejan, Božović Aleksandar, Jakšić Maša, Janković Miljan
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 152, Iss 5-6, Pp 264-269 (2024)
Introduction/Objective. Adhesive capsulitis (AC) is a condition characterized by pain and significant reduction in active and passive movements in the glenohumeral joint, especially in external rotation. It is one of the most common and challenging c
Externí odkaz:
https://doaj.org/article/3454adcf8b6c4eb8a4dcd7e954f3e37e
Autor:
Sichao Liang, Yunshuo Li, Zhenping Guo, Manlin Lu, Xin Li, Jia Xu, Wenjing Chen, Juanjuan Gao, Haijin Yi
Publikováno v:
Journal of Otology, Vol 19, Iss 1, Pp 19-23 (2024)
Background: Sudden sensorineural hearing loss (SSNHL) is a prevalent emergency in ear, nose, and throat practice. Previous studies have demonstrated that intratympanic steroid therapy (IST) can serve as a salvage treatment for SSNHL after the failure
Externí odkaz:
https://doaj.org/article/0dc32fbe5baf4876be1c77beb83450ca
Autor:
E. R. Buklis, N. I. Kokina, E. L. Bueverova, M. V. Feldsherov, V. S. Komarova, V. T. Ivashkin
Publikováno v:
Российский журнал гастроэнтерологии, гепатологии, колопроктологии, Vol 33, Iss 5, Pp 105-113 (2023)
Aim: to present a clinical case of post-COVID bronchiolitis in an adult.Key points. A 54-year-old female patient with a long history of smoking was hospitalized in the pulmonology department of the Clinic with a leading complaint of progressive short
Externí odkaz:
https://doaj.org/article/8642381b6f9b48569aeac85a9abd2112
Autor:
Özlem Sarıtaş Nakip, Selman Kesici, Ayşe Ünal Yüksekgönül, Yelda Bilginer, Seza Özen, Benan Bayrakcı
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 10, Iss 3, Pp 216-220 (2023)
Kawasaki disease shock syndrome (KDSS) is a rare disease characterized by cardiovascular collapse that requires aggressive supportive and immunomodulatory therapy. The purpose of this report is to highlight our management strategies in KSSS patients.
Externí odkaz:
https://doaj.org/article/54dc51cbeff742a9b2ab68c4838b22e1
Autor:
Francesco Signorelli, Omar Ktari, Ludovico Agostini, Giorgio Ducoli, Fabio Zeoli, Massimiliano Visocchi
Publikováno v:
Brain Sciences, Vol 14, Iss 11, p 1143 (2024)
Background: Spontaneous intracranial hypotension (SIH) is a rare and frequently misdiagnosed disorder characterized by a low volume of cerebrospinal fluid (CSF) caused by the leakage of CSF through the spinal dural membrane. Patients with Marfan Synd
Externí odkaz:
https://doaj.org/article/e887acc55be3443c9b139c099acad6c4
Publikováno v:
GAIMS Journal of Medical Sciences, Vol 4, Iss 1, Pp 45-49 (2023)
Background: Mucor mycosis is an emerging dreadful opportunistic angio-invasive fungal infection occurring predominantly in immunocompromised individuals. Popularly known as “Black fungus”, it gained popularity due to its association with SARS-CO
Externí odkaz:
https://doaj.org/article/7cb117aab5f1408ab99c5fcb47fe5942
Publikováno v:
Journal of Medical and Scientific Research, Vol 11, Iss 2, Pp 81-85 (2023)
Introduction: SARS-COV-2 infection (COVID-19) may be associated with wide range of bacterial and fungal infections. Mucormycosis is a common and potentially life threatening opportunistic fungal infection responsible for morbidity and mortality. Many
Externí odkaz:
https://doaj.org/article/b190c301b23d4e4faf635f84fc084130
Autor:
Kalezić T, Vuković I, Stojković M, Stanojlović S, Karanović J, Brajušković G, Savić-Pavićević D
Publikováno v:
Balkan Journal of Medical Genetics, Vol 25, Iss 1, Pp 79-84 (2023)
Keratitis-ichthyosis-deafness (KID) syndrome is a rare congenital ectodermal dysplastic syndrome presenting with keratitis, ichthyosis and sensorineural hearing loss. The most common causes of KID syndrome are heterozygous missense mutations in the G
Externí odkaz:
https://doaj.org/article/d29aebd0a3e14c93a30b86b60a9158fb