- Surgical Simulation and Training
- Anatomy and Medical Technology
- Cancer, Hypoxia, and Metabolism
- Glutathione Transferases and Polymorphisms
- Macrophage Migration Inhibitory Factor
- Urological Disorders and Treatments
- Neonatal and fetal brain pathology
- Nuclear Receptors and Signaling
- Fetal and Pediatric Neurological Disorders
- Intestinal Malrotation and Obstruction Disorders
- Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Augmented Reality Applications
- Autoimmune Neurological Disorders and Treatments
- Histiocytic Disorders and Treatments
- Peripheral Neuropathies and Disorders
- Cancer-related Molecular Pathways
- Dam Engineering and Safety
- Pectus Deformity Diagnosis and Treatment
- Biomedical and Engineering Education
- Ovarian function and disorders
- Legionella and Acanthamoeba research
- Bacteriophages and microbial interactions
- Salivary Gland Tumors Diagnosis and Treatment
- Groundwater flow and contamination studies
- Growth Hormone and Insulin-like Growth Factors
Hunan Children's Hospital
2002-2023
Children's Hospital of Chongqing Medical University
2023
Chongqing Medical University
2023
University of South China
2021
Capital Medical University
2017
Beijing Tongren Hospital
2017
UPMC Hillman Cancer Center
2014
Carnegie Mellon University
2011
Mycobacteriophages are viruses that infect mycobacterial hosts such as Mycobacterium smegmatis and tuberculosis. All mycobacteriophages characterized to date dsDNA tailed phages, have either siphoviral or myoviral morphotypes. However, their genetic diversity is considerable, although sixty-two genomes been sequenced comparatively analyzed, these likely represent only a small portion of the mycobacteriophage population at large. Here we report isolation, sequencing comparative genomic...
This study sought to assess, using subjective (self-assessment) and objective (MCQ) methods, the efficacy of heart models with ventricular septal defect lesions produced three-dimensional printing technology in a congenital disease curriculum for medical students. Three computed tomography datasets three subtypes defects (perimembranous, subarterial muscular, one each) were obtained processed building into out 3D models. Then total 63 students class randomly allocated two groups (32...
Abstract Neonatal subpial hemorrhage is a poorly understood type of intracranial hemorrhage. Herein, we reported on 34 neonates with hemorrhages, focusing the imaging features, clinical factors, and outcomes this This retrospective case series enrolled hemorrhages. We analyzed their magnetic resonance (MR) images, manifestations, prognoses. categorized, for first time, MR images patients hemorrhages into three patterns; moreover, basis yin-yang sign, added sandwich attaining an image feature...
Background: Congenital pyriform sinus fistula (CPSF) is a rare branchial cleft deformity. The characteristics and management of CPSF in neonates are different from those children or adults, comprehensive understanding the imaging features neonatal can facilitate its preoperative diagnosis. Thus, aim this study was to summarize ultrasonography (US) CT findings neonates. Methods: Forty-five full-term with CPSF, confirmed by pathology after surgical resection January 2012 October 2020, were...
Abstract Background The 3D printing technology in congenital cardiac surgery has been widely utilized to improve patients’ understanding of their disease. However, there no randomized controlled study on its usefulness surgical consent for heart disease repair. Methods A was performed during process which guardians candidates ventricular septal defect repair were given detailed explanation the anatomy, indication and potential complication risks using print model (n = 20) versus a...
Background Myelin oligodendrocyte glycoprotein antibody disease (MOGAD) is a newly defined autoimmune inflammatory demyelinating central nervous system (CNS) characterized by antibodies against MOG. Leptomeningeal enhancement (LME) on contrast-enhanced fluid-attenuated inversion recovery (CE-FLAIR) images has been reported in patients with other diseases and interpreted as biomarker of inflammation. This study retrospectively analyzed the prevalence distribution LME CE-FLAIR children MOG...
Abstract Objective Conservative treatment with a vacuum bell (VB) for pectus excavatum (PE) has now been gradually popularized as an alternative to surgery. We describe our initial experience novel three dimensional (3D) printed VB device. Methods Prospectively collected data of all patients who started using 3D in 2018 at institution were analyzed. Linear and logistic regressions used identify factors associated effectiveness device usage. Results In total, forty-two median age 3.6 years...
Short stature, onychodysplasia, facial dysmorphism and hypotrichosis (SOFT) syndrome is a rare autosomal recessive disease caused by POC1 centriolar protein A (<em>POC1A</em>) pathogenic variants. However, knowledge of genotypic phenotypic features SOFT remain limited as few families have been examined; therefore, the clinical identification remains challenge. The aim present case report was to investigate genetic cause this in patient with short unusual appearance, skeletal dysplasia sparse...
Fractured porous reservoirs are of great importance in the exploration and production gas reservoirs. Generally, active aquifer fractured can provide energy for fluid flow. However, water usually invades formation, affecting reservoir increasing threshold pressure When formation is lower than pressure, will be blocked, these gases difficult to capture. Therefore, objective this study understand mechanism invasion discuss influence factors on depth In study, we established an ideal model...
He, Siping MD; Falk, Kerac Kannan, Akshaya BA; Kelley, Robert S. DO, MBA Author Information
Abstract Chronic granulomatous disease (CGD) is a rare inborn error of immunity (IEI) characterized by defective respiratory burst phagocytes and clearance phagocytosed microorganisms; these phenomena, caused defect in NADPH oxidase, result severe life-threatening infections affected children. The genetically heterogeneous X-linked recessive (XL-CGD) form GCD mutations the CYBB gene, whereas autosomal (AR-CGD) CYBA , NCF1 NCF2 NCF4 or CYBC1 genes. Mutations gene account for small number CGD...
Objective:At different times and cultural background,people have definition of beauty.With the improvement economic level culture quality,people are becoming more recognition nasal appearance function equally important.Even importance is higher than shape nose. Concurrent rhinoplasty (nasal dorsum lateral wall reduction) functional sinus surgery septum reconstructory, middle turbinate,inferior turbinate even extended to cavity expansion tecunhnique, sinusitis surgery) with endoscopic...