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Clinical benefit of AI-assisted lung ultrasound in a resource-limited intensive care unit

Critical care (London, England), 2023-07, Vol.27 (1), p.257-257, Article 257

2023

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Characterization and outcome of 41 patients with beta-ketothiolase deficiency: 10 years’ experience of a medical center in northern Vietnam

Journal of inherited metabolic disease, 2017-05, Vol.40 (3), p.395-401

2017

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A simple method for in vitro growth stimulation of tomato plantlets (Solanum lycopersicum) through supplementation of Rhizophagusirregularis MUCL43194 spores in the MS culture medium

Plant cell, tissue and organ culture, 2023-06, Vol.153 (3), p.577-586

2023

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A simple method for in vitro growth stimulation of tomato plantlets (Solanum lycopersicum) through supplementation of Rhizophagus irregularis MUCL43194 spores in the MS culture medium

Plant cell, tissue and organ culture, 2023-06, Vol.153 (3), p.577-586

2023

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Starch-assisted sol-gel synthesis of Cr-doped Al2O3 as new light lilac pigments with NIR reflective ability for cool coating

Emergent materials (Online), 2024-06, Vol.7 (3), p.1139-1149

2024

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Phenotype and genotype of patients with disorder of sex development due to 5α-reductase deficiency

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P112-P112, Article P112

2015

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Primary hyperlipidemia in children: clinical, biochemistry characteristics and outcome

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P124-P124, Article P124

2015

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Hypopituitarism due to central nervous system germinoma: a case report

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P118-P118, Article P118

2015

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Hearing loss in osteogenesis imperfecta patients

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P68-P68, Article P68

2015

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Novel mutation in the hepatocyte nuclear factor 1B/maturity – onset diabetes of the young type 5 gene – unreported Vietnamese case

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P25-P25, Article P25

2015

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Pseudoaldosteronism due to mutation of SCNN1A gene: a case report

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P127-P127, Article P127

2015

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Multiple endocrine glands insufficiency due to langerhans cell histiocytosis (LCH): a case report

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P119-P119, Article P119

2015

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Congenital adrenal hyperplasia with cholestatic jaundice: a case report

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P55-P55, Article P55

2015

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Evaluation of parental knowledge after establishing CAH clubs in Vietnam & Indonesia

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P53-P53, Article P53

2015

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Phenotype & genotype of congenital adrenal hyperplasia due to mutation in the type ii 3β-hydroxysteroid dehydrogenase gene: a report of two Vietnamese families

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P50-P50, Article P50

2015

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Phenotype, genotype of neonatal diabetes mellitus due to insulin gene mutation

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P12-P12, Article P12

2015

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The pattern of disorders of sex development in Vietnamese children

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P115-P115, Article P115

2015

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Updated registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P49-P49, Article P49

2015

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Mixed embryonal carcinoma – teratoma cause early puberty: a case report

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P93-P93, Article P93

2015

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Study relationship between the value of 17-OHP and the value of testosterone in monitoring for congenital adrenal hyperplasia

International journal of pediatric endocrinology, 2013-10, Vol.2013 (S1), p.P124-P124, Article P124

2013

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Clinical and laboratory characteristics of Prader-Willi syndrome

International journal of pediatric endocrinology, 2013-10, Vol.2013 (S1), p.P60-P60, Article P60

2013

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Factors affecting on the mental development in children with Congenital Hypothyroidism

International journal of pediatric endocrinology, 2013-10, Vol.2013 (S1), p.P147-P147, Article P147

2013

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Effect of osteogenesis imperfecta on children and their families

International journal of pediatric endocrinology, 2013-10, Vol.2013 (S1), p.P169-P169, Article P169

2013

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Treatment outcome and some affecting factors of congenital adrenalhyperplasia

International journal of pediatric endocrinology, 2013-10, Vol.2013 (S1), p.P120-P120, Article P120

2013

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Adrenal cortex tumors: clinical features and laboratory finding

International journal of pediatric endocrinology, 2013-10, Vol.2013 (S1), p.P110-P110, Article P110

2013

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Clinical benefit of AI-assisted lung ultrasound in a resource-limited intensive care unit

Characterization and outcome of 41 patients with beta-ketothiolase deficiency: 10 years’ experience of a medical center in northern Vietnam

A simple method for in vitro growth stimulation of tomato plantlets (Solanum lycopersicum) through supplementation of Rhizophagusirregularis MUCL43194 spores in the MS culture medium

A simple method for in vitro growth stimulation of tomato plantlets (Solanum lycopersicum) through supplementation of Rhizophagus irregularis MUCL43194 spores in the MS culture medium

Starch-assisted sol-gel synthesis of Cr-doped Al2O3 as new light lilac pigments with NIR reflective ability for cool coating

Phenotype and genotype of patients with disorder of sex development due to 5α-reductase deficiency

Primary hyperlipidemia in children: clinical, biochemistry characteristics and outcome

Hypopituitarism due to central nervous system germinoma: a case report

Hearing loss in osteogenesis imperfecta patients

Novel mutation in the hepatocyte nuclear factor 1B/maturity – onset diabetes of the young type 5 gene – unreported Vietnamese case

Pseudoaldosteronism due to mutation of SCNN1A gene: a case report

Multiple endocrine glands insufficiency due to langerhans cell histiocytosis (LCH): a case report

Congenital adrenal hyperplasia with cholestatic jaundice: a case report

Evaluation of parental knowledge after establishing CAH clubs in Vietnam & Indonesia

Phenotype & genotype of congenital adrenal hyperplasia due to mutation in the type ii 3β-hydroxysteroid dehydrogenase gene: a report of two Vietnamese families

Phenotype, genotype of neonatal diabetes mellitus due to insulin gene mutation

The pattern of disorders of sex development in Vietnamese children

Updated registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam

Mixed embryonal carcinoma – teratoma cause early puberty: a case report

Study relationship between the value of 17-OHP and the value of testosterone in monitoring for congenital adrenal hyperplasia

Clinical and laboratory characteristics of Prader-Willi syndrome

Factors affecting on the mental development in children with Congenital Hypothyroidism

Effect of osteogenesis imperfecta on children and their families

Treatment outcome and some affecting factors of congenital adrenalhyperplasia

Adrenal cortex tumors: clinical features and laboratory finding

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