Nong Van Hai
Overview
Explore the profile of Nong Van Hai including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
24
Citations
160
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Dinh T, Phuong Anh N, Thao D, Duy L, Bac N, Quyet P, et al.
Medicine (Baltimore)
. 2024 Sep;
103(39):e39839.
PMID: 39331878
Male infertility is a multifactorial disease due to spermatogenesis impairment, with etiology remaining unknown for roughly one-third of infertile cases. Several studies have demonstrated that genetic variants are male infertility...
2.
Thao D, Dinh T, Mitsunaga S, Duy L, Phuong N, Phuong Anh N, et al.
PLoS One
. 2024 Jun;
19(6):e0304964.
PMID: 38885215
Austronesian (AN) is the second-largest language family in the world, particularly widespread in Island Southeast Asia (ISEA) and Oceania. In Mainland Southeast Asia (MSEA), groups speaking these languages are concentrated...
3.
Hai N, Nhung V, Tam N, Ngoc T, Thuong M, Dai H, et al.
Hum Immunol
. 2024 Apr;
85(3):110796.
PMID: 38580537
The diversity of clinical manifestations in COVID-19 has been observed not only among individuals but also among various populations in globally. HLA molecules play a central role in physiology, protective...
4.
Thu Trang D, Phu N, Hung D, Nhung V, Ha N, Thuong M, et al.
Mol Vis
. 2023 Apr;
28:480-491.
PMID: 37089697
Background: Familial exudative vitreoretinopathy (FEVR) is a rare inherited disorder marked by incomplete retinal vascularization associated with exudation, neovascularization, and tractional retinal detachment. FEVR is genetically heterogeneous and is caused...
5.
Nhung V, Ton N, Ngoc T, Thuong M, Hai N, Oanh K, et al.
Genes (Basel)
. 2022 Oct;
13(10).
PMID: 36292769
Since the emergence and rapid transmission of SARS-CoV-2, numerous scientific reports have searched for the association of host genetic variants with COVID-19, but the data are mostly acquired from Europe....
6.
Thuong M, Lan Anh L, Nhung V, Ngoc T, Lan H, Phuong D, et al.
J Clin Lab Anal
. 2022 Jul;
36(9):e24625.
PMID: 35870188
Background: Oculocutaneous 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...
7.
Duong N, Dinh T, Mohl B, Hintze S, Quynh D, Ha D, et al.
Aging (Albany NY)
. 2022 Jun;
14(13):5299-5310.
PMID: 35748794
Cockayne syndrome (CS) is a rare progeroid disorder characterized by growth failure, microcephaly, photosensitivity, and premature aging, mainly arising from biallelic (CS-A) or (CS-B) variants. In this study we describe...
8.
Whole-exome sequencing revealed a novel ERCC6 variant in a Vietnamese patient with Cockayne syndrome
Duong N, Phuong Anh N, Bac N, Quang L, Miyake N, Hai N, et al.
Hum Genome Var
. 2022 Jun;
9(1):21.
PMID: 35668072
We describe a case of Cockayne syndrome without photosensitivity in a Vietnamese family. This lack of photosensitivity prevented the establishment of a confirmed medical clinical diagnosis for 16 years. Whole-exome...
9.
Duong N, Lan Anh L, Sau N, Anh N, Miyake N, Hai N, et al.
Hum Genome Var
. 2022 Jun;
9(1):22.
PMID: 35668061
No abstract available.
10.
Duong N, Lan Anh L, Sau N, Anh N, Miyake N, Hai N, et al.
Hum Genome Var
. 2022 May;
9(1):13.
PMID: 35581191
We present a homozygous missense mutation in the COL7A1 gene (NM_000094.4: c.6262G>A, p.G2088R) in a case of inversa recessive dystrophic epidermolysis bullosa (RDEB-I) from a nonconsanguineous Vietnamese family. Although a...