Vuong Tran Nguyen

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Prader-Willi syndrome (PWS) is a congenital neurodevelopmental disorder caused by loss of function of paternally expressed genes on chromosome 15 due to paternal deletion of 15q11–q13, maternal uniparental disomy for chromosome 15, or an imprinting mutation. We previously developed a DNA methylation-based PCR assay to identify each of these three genetic(More)
Human plasma-derived α1-antitrypsin (AAT) delivered by intravenous infusion is used as augmentation therapy in patients with emphysema who have a genetic mutation resulting in deficiency of AAT. Inhalation is an alternative route of administration that can potentially increase the efficacy and convenience of treatment. This study was conducted to determine(More)
Strokes are a major health problem in Vietnam, but to date, there has been no epidemiology survey reporting data in this country. We collected epidemiology data on strokes using a door-to-door survey in 1994-1995 in three different regions of southern Vietnam (one site in a Hô Chi Minh City and two rural areas in the Tiên Giang and Kiên Giang provinces).(More)
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