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List of works by Can Thi Bich Ngoc

A case report of neonatal adrenocortical carcinoma

scientific article published on 28 April 2015

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

scientific article published in September 2015

AB069. Effect of osteogenesis imperfecta on children and their families.

scientific article published in September 2015

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

scientific article published in September 2015

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

scientific article

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

scientific article published in September 2015

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

scientific article

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

scientific article

AB082. Phenotype and genotype of Vietnamese patients with mucopolysaccharidosis II: first case series report.

scientific article published in September 2015

AB156. Clinical and laboratory characteristics of Prader-Willi syndrome.

scientific article published in September 2015

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

scientific article published on 30 June 2017

Congenital adrenal hyperplasia with cholestatic jaundice: a case report

scientific article published on 28 April 2015

Eye and renal complication in pediatric patients with diabetes mellitus type 1.

scientific article published on 28 April 2015

Genotype and phenotype of Vietnamese patients with androgen insensitivity syndrome.

scientific article published on 3 October 2013

Hearing loss in osteogenesis imperfecta patients

scientific article published on 28 April 2015

Hematopoietic Stem Cell Transplantation for Patients with Mucopolysaccharidosis II.

scientific article

Hypopituitarism due to central nervous system germinoma: a case report

scientific article published on 28 April 2015

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

scientific article published on 28 April 2015

Molecular genetics, correlation between genotype and phenotype of 65 Vietnames patients with congenital hyperinsulinism

scientific article published on 28 April 2015

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

scientific article published on 28 April 2015

Neonatal diabetes in Wolcott–Rallison syndrome: a case report

scientific article published on 3 October 2013

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

scientific article published on 28 April 2015

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

scientific article published on 28 April 2015

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

scientific article

Phenotype of patients with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

scientific article published on 28 April 2015

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

scientific article published on 28 April 2015

Primary hyperlipidemia in children: clinical, biochemistry characteristics and outcome

scientific article published on 28 April 2015

Pseudoaldosteronism due to mutation of SCNN1A gene: a case report

scientific article published on 28 April 2015

The pattern of disorders of sex development in Vietnamese children

scientific article published on 28 April 2015

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

scientific article published on 28 April 2015

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