Results 11 to 20 of about 6,913,935 (243)

Three Novel Pathogenic Variants in Unrelated Vietnamese Patients with Cardiomyopathy. [PDF]

Diagnostics (Basel)
Background: Cardiomyopathy, including dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM), is a major cause of heart failure (HF) and a leading indication for heart transplantation. Of these patients, 20–50% have a genetic cause, so understanding the genetic basis of cardiomyopathy will provide knowledge about the pathogenesis of the ...
Tran DD, Lien NTK, Tung NV, Huu NC, Nguyen PT, Tien DA, Thu DTH, Huy BQ, Oanh TTK, Lien NTP, Hien NT, Lan NN, Thanh LT, Duc NM, Hoang NH.   +14 more
europepmc   +5 more sources

‘Vietnamese Londoners: Transnational Identities Through Community Networks’ [PDF]

This research examines Vietnamese in London, focusing on identity formation and community networks through transnational activities. I argue that ‘the transnational’ is a ‘subset’ of migrant categories, and that Vietnamese transnational identities ...
James, Stephen
core   +8 more sources

BRAF and RAS mutations in Vietnamese patients with ameloblastoma. [PDF]

BMC Oral Health
Abstract Background Ameloblastoma is a benign but locally aggressive odontogenic tumor. Genetic mutations in the mitogen-activated protein kinase (MAPK) signaling pathway, particularly those in BRAF and RAS , have been ...
Hoang KA, Nguyen CTK, Ho CQ, Duong TB, Luu TTT, Bui TTT, Huynh NCN, Vu HA, Vo TD.   +8 more
europepmc   +2 more sources

Syntax of Vietnamese Aspect [PDF]

, 2013
The aim of this thesis is two-fold: to develop an articulated Vietnamese clause structure in two syntactic domains: VP-external and VP-internal in the spirit of generative grammar, and to see how this functional architecture is supported empirically from
Phan, Trang
core   +6 more sources

Molecular Analysis of Vietnamese Patients with Mucopolysaccharidosis Type I [PDF]

Life, 2021
Mucopolysaccharidosis type I (MPS I) is a rare autosomal recessive disorder caused by deleterious mutations in the α-L-iduronidase (IDUA) gene. Until now, MPS I in Vietnamese has been poorly addressed. Five MPS I patients were studied with direct DNA sequencing using Illumina technology confirming pathogenic variants in the IDUA gene.
Ngoc Thi Bich Can, Dien Minh Tran, Thao Phuong Bui, Khanh Ngoc Nguyen, Hoang Huy Nguyen, Tung Van Nguyen, Wuh-Liang Hwu, Shunji Tomatsu, Dung Chi Vu   +8 more
openaire   +3 more sources

Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome in Vietnamese Patients. [PDF]

Medicina (Kaunas)
October 17, 2024 Dear Prof. Dr. Rizzo and Dr. Oshiro, Prof. Dr. Rizzo: Editor-in-Chief of the Endocrinology section. Dr. Oshiro: Guest Editor of the “Advances in Clinical Diabetes, Obesity, and Metabolic Diseases” special Issue. I would like to submitt the manuscript entitled “Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome in Vietnamese ...
Nguyen KN, Tran VK, Nguyen NL, Can TBN, Dang TKG, Nguyen TH, Do TTM, Phuong LT, Tran TH, Ta TV, Tu NH, Vu CD.   +11 more
europepmc   +4 more sources

Prevalence of CYLD mutations in Vietnamese patients with polycythemia vera [PDF]

Advances in Clinical and Experimental Medicine, 2022
Antecedentes. La policitemia vera (PV) se caracteriza por una mayor proliferación y acumulación de células eritroides y mieloides maduras y megacariocitos en la médula ósea y la sangre periférica. La mutación JAK2V617F está presente en la mayoría de los pacientes con PV.
Do Van Trang, Nguyen Duc Giang, Bui Kieu Trang, Nguyen Thy Ngoc, Giang Nguyen, Nguyen Xuan Canh, Nguyen Lam Vuong, Nguyễn Thị Xuân   +7 more
openaire   +2 more sources

Discussing Depression with Vietnamese American Patients [PDF]

Journal of Immigrant and Minority Health, 2009
Asian patients preferentially seek mental health care from their primary care providers but are unlikely to receive it. Primary care providers need culturally-informed strategies for addressing stigmatizing illnesses.11 Vietnamese American community members participated in semi-structured interviews. Interviews were audio-taped and transcribed.
Fancher, Tonya L., Ton, Hendry, Meyer, Oanh, Ho, Thuan, Paterniti, Debora A.   +4 more
openaire   +4 more sources

Genetic analyses of Vietnamese patients with oculocutaneous albinism

Journal of Clinical Laboratory Analysis, 2022
AbstractBackgroundOculocutaneous albinism (OCA) is an autosomal recessive disease with hypopigmentation in skin, hair, and eyes, causing by the complete absence or reduction of melanin in melanocytes. Many types of OCA were observed based on the mutation in different causing genes relating to albinism. OCA can occur in non‐syndromic and syndromic forms,
Ma Thi Huyen Thuong, Luong Thi Lan Anh, Vu Phuong Nhung, Tran Thi Bich Ngoc, Hoang Thu Lan, Doan Kim Phuong, Nguyen Hai Ha, Nong Van Hai, Nguyen Dang Ton   +8 more
openaire   +2 more sources

Health disparities in chronic liver disease

Hepatology, EarlyView., 2022
Abstract The syndemic of hazardous alcohol consumption, opioid use, and obesity has led to important changes in liver disease epidemiology that have exacerbated health disparities. Health disparities occur when plausibly avoidable health differences are experienced by socially disadvantaged populations.
Ani Kardashian, Marina Serper, Norah Terrault, Lauren D. Nephew   +3 more
wiley   +1 more source