A5048022496- Mitochondrial Function and Pathology
- Vascular Anomalies and Treatments
- Inflammatory Myopathies and Dermatomyositis
- Metabolism and Genetic Disorders
- Autoimmune and Inflammatory Disorders Research
- Inflammasome and immune disorders
- Sharing Economy and Platforms
- ECG Monitoring and Analysis
- Cerebral Venous Sinus Thrombosis
- ATP Synthase and ATPases Research
- Tuberculosis Research and Epidemiology
- Infectious Diseases and Tuberculosis
- Mycobacterium research and diagnosis
- Neurosurgical Procedures and Complications
- Congenital Ear and Nasal Anomalies
- Otitis Media and Relapsing Polychondritis
- Intracerebral and Subarachnoid Hemorrhage Research
- Spectroscopy and Chemometric Analyses
- Monoclonal and Polyclonal Antibodies Research
- Botulinum Toxin and Related Neurological Disorders
- Tracheal and airway disorders
- Systemic Lupus Erythematosus Research
- Neurological diseases and metabolism
- Fault Detection and Control Systems
- Pulmonary Hypertension Research and Treatments
Sir Run Run Shaw Hospital
2004-2024
Zhejiang University
2009-2024
The sensitivity and specificity of immunocytochemical staining mycobacterial antigens in the cytoplasm cerebrospinal fluid (CSF) macrophages for diagnosis tuberculous meningitis (TBM) was prospectively compared with Ahuja criteria from 393 consecutive CSF specimens. assay can play an important role TBM, 73.5% 90.7%.
This study was designed to investigate the role of nucleotide-binding-domain -and leucine-rich repeat -containing (NLR) family, pyrin-domain-containing 3 (NLRP3) inflammasome in pathogenesis polymyositis (PM).Immunochemistry performed analyze NLRP3, caspase-1 and interleukin-1 beta (IL-1β) expression muscle tissue PM patients. Rat model C2C12 cell were used potential NLRP3 PM.The percentage CD 68+ macrophages, levels IL-1β elevated 27 LPS/ATP treatment resulted activation secretion as well...
To assess the prevalence and related factors of benign paroxysmal positional vertigo (BPPV) in patients with spontaneous intracranial hypotension (SIH).We retrospectively reviewed 156 consecutive inpatients SIH, collected clinical radiological data. These were divided into BPPV group non-BPPV according to manifestation results Dix-Hallpike or supine roll tests during hospitalization period. We performed a univariate analysis further multiple logistic regression identify development SIH...
Abstract Background Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant inherited vascular disorder that can involve multiple organs, thus be associated with so many clinical departments proper screening and diagnosis of HHT are needed for providing better management both patients their family members. Case presentation: we present 58-year-old female patient recurrent paradoxical brain embolism due to HHT. Though ischemic stroke caused by HHT-induced disorders has been...
Abstract Backgrounds: This study was designed to investigate the role of nucleotide-binding-domain (NBD)-and leucine-rich repeat (LRR)-containing (NLR) family, pyrin-domain-containing 3 (NLRP3) inflammasome in pathogenesis polymyositis (PM). Results: We found that percentage CD68+ cells, and expression levels NLRP3, caspase-1 interleukin-1 beta (IL-1β) muscle tissue were elevated 27 PM patients. LPS/ATP treatment Raw 264.7 macrophages resulted activation NLRP3 secretion IL-1β as well...