Ta TV - Search Results

1

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: ta tv. Pediatr Dermatol. 2020 May;37(3):574-575. doi: 10.1111/pde.14128. Epub 2020 Feb 27. Pediatr Dermatol. 2020. PMID: 32105361

2

Prenatal diagnosis of a case with SEA-HPFH deletion thalassemia with whole HBB gene deletion.

Ly Thi Thanh H, Le Thi Thanh H, Hoang Luong L, Huy Tran T, Liu SC, Truong HN, Ta TV, Bui TH, Tran VK. Ly Thi Thanh H, et al. Among authors: ta tv. Taiwan J Obstet Gynecol. 2018 Jun;57(3):435-441. doi: 10.1016/j.tjog.2018.04.019. Taiwan J Obstet Gynecol. 2018. PMID: 29880180 Free article.

3

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: ta mh, ta tv. Haemophilia. 2019 Jul;25(4):e274-e277. doi: 10.1111/hae.13738. Epub 2019 Mar 26. Haemophilia. 2019. PMID: 30913330 No abstract available.

4

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: ta tv, ta td. 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.

5

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: ta tv. 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.

6

Whole exome sequencing analysis in a couple with three children who died prematurely due to carnitine-acylcarnitine translocase deficiency.

Tran VK, Diep QM, Qiu Z, Le TP, Do LD, Tran HA, Bui TH, Ta TV, Tran TH. Tran VK, et al. Among authors: ta tv. Taiwan J Obstet Gynecol. 2022 Jan;61(1):153-156. doi: 10.1016/j.tjog.2021.11.027. Taiwan J Obstet Gynecol. 2022. PMID: 35181030 Free article.

7

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: ta tv, ta td. Anemia. 2022 Jul 5;2022:2653089. doi: 10.1155/2022/2653089. eCollection 2022. Anemia. 2022. PMID: 35845714 Free PMC article.

8

Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia.

Vuong VVH, Tran TH, Nguyen PD, Thi NN, Le Thi P, Minh Nguyet DT, Nguyen MH, Bui TH, Ta TV, Tran VK. Vuong VVH, et al. Among authors: ta tv. PLoS One. 2022 Dec 7;17(12):e0278539. doi: 10.1371/journal.pone.0278539. eCollection 2022. PLoS One. 2022. PMID: 36476827 Free PMC article.

9

Targeted next-generation sequencing determined a novel SGCG variant that is associated with limb-girdle muscular dystrophy type 2C: A case report.

Tran NC, Nguyen TA, Ta TD, Tran TH, Nguyen PD, Vu CD, Nguyen VH, Bui TH, Ta TV, Tran VK. Tran NC, et al. Among authors: ta tv, ta td. Clin Case Rep. 2023 Mar 27;11(3):e7025. doi: 10.1002/ccr3.7025. eCollection 2023 Mar. Clin Case Rep. 2023. PMID: 36992678 Free PMC article.

10

Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients.

Tran VK, Nguyen NL, Tran LNT, Le PT, Tran AH, Pham TLA, Lien NTK, Xuan NT, Thanh LT, Ta TV, Tran TH, Nguyen HH. Tran VK, et al. Among authors: ta tv. Front Genet. 2023 Jun 14;14:1183663. doi: 10.3389/fgene.2023.1183663. eCollection 2023. Front Genet. 2023. PMID: 37388928 Free PMC article.

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