Bui TH - 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: bui th. 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

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: bui th. 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.

3

Genetic analysis of 55 northern Vietnamese patients with Wilson disease: seven novel mutations in ATP7B.

Tuan Pham LA, Nguyen TT, Nga Le HB, Tran DQ, Ho CT, Tran TH, Ta VT, Bui TH, Tran VK. Tuan Pham LA, et al. Among authors: bui th. J Genet. 2017 Dec;96(6):933-939. doi: 10.1007/s12041-017-0857-9. J Genet. 2017. PMID: 29321352 Free article.

4

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: bui th. 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.

5

Mosaicism in carrier of Duchenne muscular dystrophy mutation - Implication for prenatal diagnosis.

Dinh LT, Nguyen DH, Luong LH, Le PT, Le-Anh TP, Tran DQ, Tran TH, Bui TH, Van Ta T, Tran VK. Dinh LT, et al. Among authors: bui th. Taiwan J Obstet Gynecol. 2018 Dec;57(6):878-880. doi: 10.1016/j.tjog.2018.10.019. Taiwan J Obstet Gynecol. 2018. PMID: 30545545 Free article.

6

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: bui th. 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.

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: bui th, bui htt. 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: bui th. 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: bui th. 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

Assessment of 6 STR loci for prenatal diagnosis of Duchenne Muscular Dystrophy.

Dinh LT, Tran VK, Luong LH, Le PT, Nguyen AD, Thi Nguyen BS, Chi DV, Tran TH, Bui TH, Van Ta T, Nguyen DH. Dinh LT, et al. Among authors: bui th. Taiwan J Obstet Gynecol. 2019 Sep;58(5):645-649. doi: 10.1016/j.tjog.2019.07.011. Taiwan J Obstet Gynecol. 2019. PMID: 31542086 Free article.

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