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15. NGHIÊN CỨU VỀ TÌNH TRẠNG SUY DINH DƯỠNG THẤP CÒI Ở HỌC SINH TIỂU HỌC THUỘC VÙNG VEN BIỂN HUYỆN PHÚ VANG, TỈNH THỪA THIÊN HUẾ

Tạp chí Y học Cộng đồng, 2024-03, Vol.65 (2)

2024

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2,6-Trisubstituted 1-benzimidazole derivatives as a new scaffold of antimicrobial and anticancer agents: design, synthesis, evaluation, and studies

RSC advances, 2022-12, Vol.13 (1), p.399-42

2022

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AB014. Beta-ketothiolase deficiency: phenotype, genotype and outcome of 48 Vietnamese patients

Annals of translational medicine, 2017-09, Vol.5 (S2), p.AB014-AB014

2017

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AB020. What is advance in molecular diagnosis for 46,XY and 46,XX testicular disorder of sex development?

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB031. Spectrum of IEMs in Vietnamese patients: data from 10 years of selected screening and diagnosis

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB067. X-linked adrenoleukodystrophy: Phenotype and genotype in Vietnamese patients

Annals of translational medicine, 2017-09, Vol.5 (S2), p.AB067-AB067

2017

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AB069. Effect of osteogenesis imperfecta on children and their families

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB070. Mutations of SRD5A2 in Vietnamese patients: phenotype and genotype

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB071. Mutations of AR gene in Vietnamese patients: genotype and phenotype

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB072. Novel mutation in the hepatocyte nuclear factor 1b/maturity-onset diabetes of the young type 5 gene—unreported Vietnamese case

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB073. Mutations in the type II 3β-hydroxysteroid dehydrogenase gene caused primary adrenal insufficiency & 46,XY disorders of sex development

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB074. Registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam during 15 years

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB076. Congenital hyperinsulinism due to mutation of HNF4A: a case report

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB077. Clinical symptoms, molecular genetics, genotype and phenotype correlations of children with congenital hyperinsulinism

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB078. Novel mutation of ABCC8 and KCNJ11 of children with congenital hyperinsulinism

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB099. Beta ketothiolase deficiency: phenotype and genotype in Vietnam population

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB100. Phenotypes of primary hyperlipidemia in a Vietnamese referral center

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB101. Neonatal form of Isovaleric acidemia in Vietnamese patients: clinical history and outcomes

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB102. Vietnamese patient with Tyrosinemia type 1: a case report

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB103. Phenotype and genotype of urea cycle defect in a Vietnamese referral center

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB111. Prenatal treatment and fertility of female patients with congenital adrenal hyperplasia

Annals of translational medicine, 2017-09, Vol.5 (S2), p.AB111-AB111

2017

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AB112. Spectrum of mucopolysaccharidoses in Vietnam

Annals of translational medicine, 2017-09, Vol.5 (S2), p.AB112-AB112

2017

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AB124. Mucolipidosis type II: clinical features and laboratories

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB125. Neonatal diabetes mellitus due to insulin gene mutation

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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AB128. Neonatal diabetes mellitus: genotype, phenotype and outcome

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

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15. NGHIÊN CỨU VỀ TÌNH TRẠNG SUY DINH DƯỠNG THẤP CÒI Ở HỌC SINH TIỂU HỌC THUỘC VÙNG VEN BIỂN HUYỆN PHÚ VANG, TỈNH THỪA THIÊN HUẾ

2,6-Trisubstituted 1-benzimidazole derivatives as a new scaffold of antimicrobial and anticancer agents: design, synthesis, evaluation, and studies

AB014. Beta-ketothiolase deficiency: phenotype, genotype and outcome of 48 Vietnamese patients

AB020. What is advance in molecular diagnosis for 46,XY and 46,XX testicular disorder of sex development?

AB031. Spectrum of IEMs in Vietnamese patients: data from 10 years of selected screening and diagnosis

AB067. X-linked adrenoleukodystrophy: Phenotype and genotype in Vietnamese patients

AB069. Effect of osteogenesis imperfecta on children and their families

AB070. Mutations of SRD5A2 in Vietnamese patients: phenotype and genotype

AB071. Mutations of AR gene in Vietnamese patients: genotype and phenotype

AB072. Novel mutation in the hepatocyte nuclear factor 1b/maturity-onset diabetes of the young type 5 gene—unreported Vietnamese case

AB073. Mutations in the type II 3β-hydroxysteroid dehydrogenase gene caused primary adrenal insufficiency & 46,XY disorders of sex development

AB074. Registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam during 15 years

AB076. Congenital hyperinsulinism due to mutation of HNF4A: a case report

AB077. Clinical symptoms, molecular genetics, genotype and phenotype correlations of children with congenital hyperinsulinism

AB078. Novel mutation of ABCC8 and KCNJ11 of children with congenital hyperinsulinism

AB099. Beta ketothiolase deficiency: phenotype and genotype in Vietnam population

AB100. Phenotypes of primary hyperlipidemia in a Vietnamese referral center

AB101. Neonatal form of Isovaleric acidemia in Vietnamese patients: clinical history and outcomes

AB102. Vietnamese patient with Tyrosinemia type 1: a case report

AB103. Phenotype and genotype of urea cycle defect in a Vietnamese referral center

AB111. Prenatal treatment and fertility of female patients with congenital adrenal hyperplasia

AB112. Spectrum of mucopolysaccharidoses in Vietnam

AB124. Mucolipidosis type II: clinical features and laboratories

AB125. Neonatal diabetes mellitus due to insulin gene mutation

AB128. Neonatal diabetes mellitus: genotype, phenotype and outcome

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