Luong LH - Search Results

1

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: luong lh. 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

2

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: luong lh. 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.

3

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: luong lh. 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.

4

Variation of Mitochondrial DNA HV1 AND HV2 of the Vietnamese Population.

Tran TTH, Nguyen DH, Tran VK, Nguyen QL, Trinh HA, Luong LH, Tran VA, Pham LAT, Nguyen TT, Nguyen VB, Tran TH, Van Ta T. Tran TTH, et al. Among authors: luong lh. Adv Exp Med Biol. 2020;1292:37-63. doi: 10.1007/5584_2018_301. Adv Exp Med Biol. 2020. PMID: 30838542

5

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

6

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: luong lh. 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.

7

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: luong lh. 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.

8

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

9

Diagnosis and Management of a Patient With Primary Hypertrophic Osteoarthropathy With SCLO2A1 Pathogenic Variants in Vietnam.

Tran TH, Luu BT, Pham AD, Luong LH, Nguyen LTN, Nguyen BN, Van Nguyen H, Bui TH, Ta VT, Van Tran K. Tran TH, et al. Among authors: luong lh. J Clin Rheumatol. 2021 Dec 1;27(8S):S739-S740. doi: 10.1097/RHU.0000000000001524. J Clin Rheumatol. 2021. PMID: 32833909 No abstract available.

10

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: luong lh. 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.

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