Ngoc CTB - Search Results

1

Identification of three novel mutations in PCNT in vietnamese patients with microcephalic osteodysplastic primordial dwarfism type II.

Nguyen TH, Nguyen NL, Vu CD, Ngoc CTB, Nguyen NK, Nguyen HH. Nguyen TH, et al. Among authors: ngoc ctb. Genes Genomics. 2021 Feb;43(2):115-121. doi: 10.1007/s13258-020-01032-5. Epub 2021 Jan 18. Genes Genomics. 2021. PMID: 33460028

2

De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome.

Thanh DC, Ngoc CTB, Nguyen NL, Vu CD, Tung NV, Nguyen HH. Thanh DC, et al. Among authors: ngoc ctb. Medicina (Kaunas). 2020 Feb 14;56(2):76. doi: 10.3390/medicina56020076. Medicina (Kaunas). 2020. PMID: 32074972 Free PMC article.

3

Whole Exome Sequencing as a Diagnostic Tool for Unidentified Muscular Dystrophy in a Vietnamese Family.

Nguyen NL, Ngoc CTB, Vu CD, Nguyen TTH, Nguyen HH. Nguyen NL, et al. Among authors: ngoc ctb. Diagnostics (Basel). 2020 Sep 24;10(10):741. doi: 10.3390/diagnostics10100741. Diagnostics (Basel). 2020. PMID: 32987775 Free PMC article.

4

Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations.

Ngoc CTB, Dung VC, De Franco E, Lan NN, Thao BP, Khanh NN, Flanagan SE, Craig ME, Hoang NH, Dien TM. Ngoc CTB, et al. Front Endocrinol (Lausanne). 2022 Apr 19;13:866573. doi: 10.3389/fendo.2022.866573. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35518939 Free PMC article.

5

Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of K_ATP-Channel Neonatal Diabetes Mellitus in Vietnam National Children's Hospital.

Ngoc CTB, Dien TM, De Franco E, Ellard S, Houghton JAL, Lan NN, Thao BP, Khanh NN, Flanagan SE, Craig ME, Dung VC. Ngoc CTB, et al. Front Endocrinol (Lausanne). 2021 Sep 9;12:727083. doi: 10.3389/fendo.2021.727083. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34566892 Free PMC article.

6

An ABCC8 Nonsense Mutation Causing Neonatal Diabetes Through Altered Transcript Expression.

Flanagan SE, Dũng VC, Houghton JAL, De Franco E, Ngoc CTB, Damhuis A, Ashcroft FM, Harries LW, Ellard S. Flanagan SE, et al. Among authors: ngoc ctb. J Clin Res Pediatr Endocrinol. 2017 Sep 1;9(3):260-264. doi: 10.4274/jcrpe.4624. Epub 2017 Jun 30. J Clin Res Pediatr Endocrinol. 2017. PMID: 28663158 Free PMC article.

7

Hematopoietic Stem Cell Transplantation for Patients with Mucopolysaccharidosis II.

Kubaski F, Yabe H, Suzuki Y, Seto T, Hamazaki T, Mason RW, Xie L, Onsten TGH, Leistner-Segal S, Giugliani R, Dũng VC, Ngoc CTB, Yamaguchi S, Montaño AM, Orii KE, Fukao T, Shintaku H, Orii T, Tomatsu S. Kubaski F, et al. Among authors: ngoc ctb. Biol Blood Marrow Transplant. 2017 Oct;23(10):1795-1803. doi: 10.1016/j.bbmt.2017.06.020. Epub 2017 Jul 1. Biol Blood Marrow Transplant. 2017. PMID: 28673849 Free PMC article.

8

Glycosaminoglycan levels in dried blood spots of patients with mucopolysaccharidoses and mucolipidoses.

Kubaski F, Suzuki Y, Orii K, Giugliani R, Church HJ, Mason RW, Dũng VC, Ngoc CT, Yamaguchi S, Kobayashi H, Girisha KM, Fukao T, Orii T, Tomatsu S. Kubaski F, et al. Mol Genet Metab. 2017 Mar;120(3):247-254. doi: 10.1016/j.ymgme.2016.12.010. Epub 2016 Dec 22. Mol Genet Metab. 2017. PMID: 28065440 Free PMC article.

9

The clinical features of osteogenesis imperfecta in Vietnam.

Binh HD, Maasalu K, Dung VC, Ngoc CT, Hung TT, Nam TV, Nhan LN, Prans E, Reimann E, Zhytnik L, Kõks S, Märtson A. Binh HD, et al. Int Orthop. 2017 Jan;41(1):21-29. doi: 10.1007/s00264-016-3315-z. Epub 2016 Nov 2. Int Orthop. 2017. PMID: 27807717

10

Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-up.

Boonen SE, Mackay DJ, Hahnemann JM, Docherty L, Grønskov K, Lehmann A, Larsen LG, Haemers AP, Kockaerts Y, Dooms L, Vu DC, Ngoc CT, Nguyen PB, Kordonouri O, Sundberg F, Dayanikli P, Puthi V, Acerini C, Massoud AF, Tümer Z, Temple IK. Boonen SE, et al. Diabetes Care. 2013 Mar;36(3):505-12. doi: 10.2337/dc12-0700. Epub 2012 Nov 12. Diabetes Care. 2013. PMID: 23150280 Free PMC article.

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