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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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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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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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AB155. Clinical presentation and its relationship with chromosomal abnormalities in Turner syndrome

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

2015

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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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AB129. Osteogenesis imperfecta: clinical features and bisphosphonate treatment outcome

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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AB124. Mucolipidosis type II: clinical features and laboratories

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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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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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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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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AB156. Clinical and laboratory characteristics of Prader-Willi syndrome

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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AB130. Pseudoaldosteronism due to mutation of SCNN1A gene: a case report

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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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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AB128. Neonatal diabetes mellitus: genotype, phenotype and outcome

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

2015

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AB131. Genotype, phenotype of transient neonatal diabetes mellitus

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

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

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

AB155. Clinical presentation and its relationship with chromosomal abnormalities in Turner syndrome

AB112. Spectrum of mucopolysaccharidoses in Vietnam

AB129. Osteogenesis imperfecta: clinical features and bisphosphonate treatment outcome

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

AB124. Mucolipidosis type II: clinical features and laboratories

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

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

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

AB100. Phenotypes of primary hyperlipidemia in a Vietnamese referral center

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

AB156. Clinical and laboratory characteristics of Prader-Willi syndrome

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

AB130. Pseudoaldosteronism due to mutation of SCNN1A gene: a case report

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

AB069. Effect of osteogenesis imperfecta on children and their families

AB128. Neonatal diabetes mellitus: genotype, phenotype and outcome

AB131. Genotype, phenotype of transient neonatal diabetes mellitus

AB125. Neonatal diabetes mellitus due to insulin gene mutation

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

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

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

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

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