Van Tung N - Search Results

1

A novel frameshift PHKA2 mutation in a family with glycogen storage disease type IXa: A first report in Vietnam and review of literature.

Nguyen NL, Thi Bich Ngoc C, Dung Vu C, Van Tung N, Hoang Nguyen H. Nguyen NL, et al. Among authors: van tung n. Clin Chim Acta. 2020 Sep;508:9-15. doi: 10.1016/j.cca.2020.05.010. Epub 2020 May 7. Clin Chim Acta. 2020. PMID: 32387637 Review.

2

Draft genome sequencing of halotolerant bacterium Salinicola sp. DM10 unravels plant growth-promoting potentials.

Nguyen NL, Van Dung V, Van Tung N, Nguyen TKL, Quan ND, Giang TTH, Ngan NTT, Hien NT, Nguyen HH. Nguyen NL, et al. Among authors: van tung n. 3 Biotech. 2023 Dec;13(12):416. doi: 10.1007/s13205-023-03833-3. Epub 2023 Nov 24. 3 Biotech. 2023. PMID: 38009164

3

The Role of p.Ser1105Ser (in NPHS1 Gene) and p.Arg548Leu (in PLCE1 Gene) with Disease Status of Vietnamese Patients with Congenital Nephrotic Syndrome: Benign or Pathogenic?

Thi Kim Lien N, Van Dem P, Thu Huong N, Minh Dien T, Thi Thu Thuy T, Van Tung N, Huy Hoang N, Thi Quynh Huong N. Thi Kim Lien N, et al. Among authors: van tung n. Medicina (Kaunas). 2019 Apr 12;55(4):102. doi: 10.3390/medicina55040102. Medicina (Kaunas). 2019. PMID: 31013750 Free PMC article.

4

Two novel CD40LG gene mutations causing X-linked hyper IgM syndrome in Vietnamese patients.

Lien NTK, Van Anh NT, Chi LQ, Le NNQ, Huyen TT, Mai NTP, Van Tung N, Hoang NH. Lien NTK, et al. Among authors: van tung n. Clin Exp Med. 2023 Feb;23(1):157-161. doi: 10.1007/s10238-021-00774-0. Epub 2021 Nov 29. Clin Exp Med. 2023. PMID: 34842998

5

The role of p.Val444Ala variant in the ABCB11 gene and susceptibility to biliary atresia in Vietnamese patients.

Van Tung N, Lien NTK, Lan NN, Mai NTP, Yen PTH, Hoa NPA, Hoang NH. Van Tung N, et al. Medicine (Baltimore). 2021 Nov 24;100(47):e28011. doi: 10.1097/MD.0000000000028011. Medicine (Baltimore). 2021. PMID: 34964797 Free PMC article.

6

Case Report: Novel rare mutation c.6353C > G in the ABCA12 gene causing harlequin ichthyosis identified by whole exome sequencing.

Tran VK, Diep QM, Zilong Q, Phuong LT, Tran HA, Van Tung N, Lien NTK, Xuan NT, Ha LT, Van Ta T, Tran TH, Hoang NH. Tran VK, et al. Among authors: van tung n. Front Pediatr. 2023 Feb 15;11:1128716. doi: 10.3389/fped.2023.1128716. eCollection 2023. Front Pediatr. 2023. PMID: 36873642 Free PMC article.

7

Novel mutations in the SGCA gene in unrelated Vietnamese patients with limb-girdle muscular dystrophies disease.

Chung Tran N, Lien NTK, Ta TD, Nguyen VH, Tran HT, Van Tung N, Xuan NT, Huy Hoang N, Tran VK. Chung Tran N, et al. Among authors: van tung n. Front Genet. 2023 Oct 13;14:1248338. doi: 10.3389/fgene.2023.1248338. eCollection 2023. Front Genet. 2023. PMID: 37900180 Free PMC article.

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