- COVID-19 Pandemic Impacts
- Pituitary Gland Disorders and Treatments
- Growth Hormone and Insulin-like Growth Factors
- CRISPR and Genetic Engineering
- Inflammatory mediators and NSAID effects
- Healthcare professionals’ stress and burnout
- Eicosanoids and Hypertension Pharmacology
- Magnesium in Health and Disease
- RNA Interference and Gene Delivery
- Birth, Development, and Health
- Parathyroid Disorders and Treatments
- Public Health and Nutrition
- Cancer, Hypoxia, and Metabolism
- Analytic and geometric function theory
- Genetic Syndromes and Imprinting
- COVID-19 and Mental Health
- Finite Group Theory Research
- RNA Research and Splicing
- Child Nutrition and Water Access
- Peroxisome Proliferator-Activated Receptors
- graph theory and CDMA systems
- Viral Infections and Outbreaks Research
- SARS-CoV-2 and COVID-19 Research
- COVID-19 epidemiological studies
Hanoi Medical University
2025
National Hospital of Pediatrics
2017-2025
Children's Hospital 1
2025
National Institute of Nutrition
2024
Yonsei University
2023
Foreign Trade University
2023
108 Military Central Hospital
2020
Kyoto University
2004
Abstract Objective: SEANUTS II Vietnam aims to obtain an in-depth understanding of the nutritional status and nutrient intake children between 0.5-11.9 years old Design: Cross-sectional survey Setting: A multistage cluster systematic random sampling method was implemented in different regions Vietnam: North Mountainous, Central Highlands, Red River Delta, Coastal Area, Southeast Mekong Delta. Participants: 4001 6 months 11.9 age Results: Prevalence stunting underweight higher rural than...
Background/Objectives: Hypopituitarism is a condition characterized by the deficiency of several hormones produced pituitary gland. Genetic factors play an important role. Variants in POU1F1 gene are associated with combined hormone deficiency-1 (CPHD1), which manifests as deficiencies growth (GH), thyroid-stimulating (TSH), and prolactin (PRL). This study aimed to analyze phenotype, genotype, treatment, outcomes Vietnamese patients deficiency. Methods: Six from five unrelated families,...
Hypopituitarism is a condition characterized by the deficiency of several hormones produced pituitary gland. Genetic factors play an important role. Variants in POU1F1 gene are associated with combined hormone 1 (CPHD1), which manifests as deficiencies growth (GH), thyroid-stimulating (TSH), and prolactin (PRL). This study aimed to analyze phenotype, genotype, treatment, outcomes Vietnamese patients deficiency. Six from five unrelated families, initially diagnosed hypopituitarism, were...
Abstract Vascular calcification is a serious complication of hyperphosphatemia that causes cardiovascular morbidity and mortality. Previous studies have reported plasmalemmal phosphate (Pi) transporters, such as PiT-1/2, mediate depolarization, Ca 2+ influx, oxidative stress, calcific changes in vascular smooth muscle cells (VSMCs). However, the pathogenic mechanism mitochondrial Pi uptake associated with has not been elucidated. We demonstrated carrier (PiC) dominant transporter responsible...
Objective: To estimate the incubation period of Vietnamese confirmed COVID−19 cases. Methods: Only cases who are and locally infected with available data on date symptom onset clearly defined window possible SARS−CoV−2 exposure were included. We used three parametric forms Hamiltonian Monte Carlo method for Bayesian Inference to Leave-one-out Information Criterion was assess performance models. Results: A total 19 identified from 23 Jan 2020 13 April included in our analysis. Average periods...
BACKGROUND: In 2022, many universities transitioned from virtual learning back to in-person teaching. Significant changes in working conditions, along with COVID-19-related anxiety during the pandemic, might impact well-being of lecturers. OBJECTIVE: This study aims assess perceived stress, self-rated physical and occupational health Vietnamese lecturers 2022 compared pre-pandemic levels, identify their associating factors. METHOD: is a cross-sectional conducted May–June through an online...
Background: X-linked adrenoleukodystrophy (X-ALD) is caused by a defect in the gene ABCD1, which maps to Xq28 and codes for peroxisomal membrane protein that member of ATP-binding cassette transporter superfamily. This disease characterized progressive neurologic dysfunction, occasionally associated with adrenal insufficiency. Objective identify phenotype genotype Vietnamese patients X-ALD. Methods: Genomic DNA from 20 18 unrelated families was extracted using standard procedures peripheral...
COVID-19 temporarily hindered the development of physical stores, nevertheless, triggered outbreak online business. Consequently, there should be growing demands for purchasing over internet-based platform. In order to investigate purchase intention and shopping behaviour, this study developed a research framework basing on analysis 05 different variables, namely: subjective norm, attitude, behavioural control, trust, perceived risk. A sample 307 Vietnamese customers have been surveyed,...