Tran VK - Search Results

1

In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome.

Pham HM, Nguyen DP, Ta TD, Le TP, Phan PH, Trinh HA, Tran TV, Luong TLA, Nguyen HM, Bui TH, Tran TH, Ta TV, Tran VK. Pham HM, et al. Among authors: tran vk. Mol Genet Genomic Med. 2023 Dec;11(12):e2263. doi: 10.1002/mgg3.2263. Epub 2023 Aug 7. Mol Genet Genomic Med. 2023. PMID: 37547970 Free PMC article.

2

Novel variants of CYP21A2 in Vietnamese patients with congenital adrenal hyperplasia.

Chi DV, Tran TH, Nguyen DH, Luong LH, Le PT, Ta MH, Ngo HTT, Nguyen MP, Le-Anh TP, Nguyen DP, Bui TH, Ta VT, Tran VK. Chi DV, et al. Among authors: tran th, tran vk. Mol Genet Genomic Med. 2019 May;7(5):e623. doi: 10.1002/mgg3.623. Epub 2019 Feb 27. Mol Genet Genomic Med. 2019. PMID: 30816000 Free PMC article.

3

Association of the STAT4, CDKN1A, and IRF5 variants with risk of lupus nephritis and renal biopsy classification in patients in Vietnam.

Nghiem TD, Do GT, Luong LH, Nguyen QL, Dang HV, Viet AN, Nguyen TT, Tran VK, Ta TV, Tran TH. Nghiem TD, et al. Among authors: tran th, tran vk. Mol Genet Genomic Med. 2021 Apr;9(4):e1648. doi: 10.1002/mgg3.1648. Epub 2021 Mar 9. Mol Genet Genomic Med. 2021. PMID: 33687153 Free PMC article.

4

Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam.

Ngo TT, Tran TH, Ta TD, Le TP, Nguyen PD, Tran MA, Bui TH, Ta TV, Tran VK. Ngo TT, et al. Among authors: tran th, tran ma, tran vk. Anemia. 2022 Jul 5;2022:2653089. doi: 10.1155/2022/2653089. eCollection 2022. Anemia. 2022. PMID: 35845714 Free PMC article.

5

Mutation spectrum of retinoblastoma patients in Vietnam.

Linh DNH, Van Huy N, Nguyen PD, Le Thi P, Tuan HA, Van Nguyen T, Tran TH, Tran HA, Ta TD, Pham TLA, Bui TH, Tran TH, Van Ta T, Tran VK. Linh DNH, et al. Among authors: tran vk. Mol Genet Genomic Med. 2023 Nov;11(11):e2244. doi: 10.1002/mgg3.2244. Epub 2023 Aug 7. Mol Genet Genomic Med. 2023. PMID: 37548407 Free PMC article.

6

Rapid method for targeted prenatal diagnosis of Duchenne muscular dystrophy in Vietnam.

Ta MH, Tran TH, Do NH, Pham le AT, Bui TH, Ta VT, Tran VK. Ta MH, et al. Among authors: tran th, tran vk. Taiwan J Obstet Gynecol. 2013 Dec;52(4):534-9. doi: 10.1016/j.tjog.2013.10.014. Taiwan J Obstet Gynecol. 2013. PMID: 24411039 Free article.

7

Mutation characteristic of 103 haemophilia A patients in Vietnam: Identification of novel mutations.

Luu DV, Tran TH, Nguyen DH, Luong LH, Bui HTT, Nguyen MT, Ta MH, Tran VK, Bui TH, Ta TV. Luu DV, et al. Among authors: tran th, tran vk. Haemophilia. 2019 Jul;25(4):e274-e277. doi: 10.1111/hae.13738. Epub 2019 Mar 26. Haemophilia. 2019. PMID: 30913330 No abstract available.

8

Acromesomelic dysplasia Maroteaux-type in patients from Vietnam.

Tran TH, Cao MH, Luong LH, Le PT, Vu DC, Ta TD, Bui TH, Nguyen DH, Van Ta T, Tran VK. Tran TH, et al. Among authors: tran vk. Am J Med Genet A. 2019 Aug;179(8):1420-1422. doi: 10.1002/ajmg.a.61192. Epub 2019 May 11. Am J Med Genet A. 2019. PMID: 31077548

9

Primary congenital glaucoma in Vietnam: analysis and identification of novel CYP1B1 variants.

Tran HT, Tran HT, Luong LH, Nguyen TS, Nguyen HQ, Vu TT, Ta TD, Dao TMA, Bui TH, Ta TV, Tran VK. Tran HT, et al. Among authors: tran vk. Ophthalmic Genet. 2019 Jun;40(3):286-287. doi: 10.1080/13816810.2019.1616304. Epub 2019 May 31. Ophthalmic Genet. 2019. PMID: 31149863 No abstract available.

10

A case of self-improving collodion ichthyosis in Vietnam.

Diep QM, Luong LH, Tran TH, Dinh OTL, Nguyen HQ, Bui TH, Ta TV, Tran VK. Diep QM, et al. Among authors: tran th, tran vk. Pediatr Dermatol. 2020 May;37(3):574-575. doi: 10.1111/pde.14128. Epub 2020 Feb 27. Pediatr Dermatol. 2020. PMID: 32105361

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