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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 1 |
2021 | 1 |
2022 | 1 |
2023 | 2 |
2024 | 0 |
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Page 1
The first Vietnamese patient who presented late onset of pantothenate kinase-associated neurodegeneration diagnosed by whole exome sequencing: A case report.
Medicine (Baltimore). 2023 Oct 27;102(43):e34853. doi: 10.1097/MD.0000000000034853.
Medicine (Baltimore). 2023.
PMID: 37904482
Free PMC article.
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: tran ht.
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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BRCA1/2 Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome.
Le TN, Tran VK, Nguyen TT, Vo NS, Hoang TH, Vo HL, Nguyen TT, Nguyen PD, Nguyen VT, Ta TV, Tran HT.
Le TN, et al. Among authors: tran ht.
Genes (Basel). 2022 Jan 29;13(2):268. doi: 10.3390/genes13020268.
Genes (Basel). 2022.
PMID: 35205313
Free PMC article.
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Oro-Dental Health and Primary Nephrotic Syndrome among Vietnamese Children.
Luong HM, Nguyen TT, Tran HT, Tran PT, Nguyen PN, Nguyen HT, Nguyen DM, Duc HTT, Tong SM.
Luong HM, et al. Among authors: tran ht.
Children (Basel). 2021 Jun 10;8(6):494. doi: 10.3390/children8060494.
Children (Basel). 2021.
PMID: 34200617
Free PMC article.
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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.
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.
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