Khanh N. Nguyen

Hanoi, 100000, Viet Nam

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 16 publications

Genotype-phenotype spectrum and clinical outcomes of glycogen storage disease type I: A 15-year experience at Vietnam National Children's Hospital.

Genotype-phenotype spectrum and clinical outcomes of glycogen storage disease type I: A 15-year experience at Vietnam National Children's Hospital.

Journal: Molecular genetics and metabolism reports

Published: April 01, 2026

Diagnostic Value of Circulating Long Non-Coding RNAs HOTAIR, NEAT1, and CCAT1 for Colorectal Cancer: A Vietnamese Case-Control Study.

Diagnostic Value of Circulating Long Non-Coding RNAs HOTAIR, NEAT1, and CCAT1 for Colorectal Cancer: A Vietnamese Case-Control Study.

Journal: Current issues in molecular biology

Published: March 25, 2026

Growth Assessment and Nutritional Status in Children with Congenital Adrenal Hyperplasia-A Cross-Sectional Study from a Vietnamese Tertiary Pediatric Center.

Growth Assessment and Nutritional Status in Children with Congenital Adrenal Hyperplasia-A Cross-Sectional Study from a Vietnamese Tertiary Pediatric Center.

Journal: Diagnostics (Basel, Switzerland)

Published: May 09, 2025

Phenotypes and Genotypes of Children with Vitamin D-Dependent Rickets Type 1A: A Single Tertiary Pediatric Center in Vietnam.

Phenotypes and Genotypes of Children with Vitamin D-Dependent Rickets Type 1A: A Single Tertiary Pediatric Center in Vietnam.

Journal: Diagnostics (Basel, Switzerland)

Published: February 25, 2025

Identification of POU1F1 Variants in Vietnamese Patients with Combined Pituitary Hormone Deficiency.

Identification of POU1F1 Variants in Vietnamese Patients with Combined Pituitary Hormone Deficiency.

Journal: International journal of molecular sciences

Published: January 24, 2025

Mitochondrial HMG-CoA Synthase Deficiency in Vietnamese Patients.

Mitochondrial HMG-CoA Synthase Deficiency in Vietnamese Patients.

Journal: International journal of molecular sciences

Published: January 19, 2025

Family hypercholesterolemia due to LDLR gene in Vietnamese children: characteristics of phenotype and genotype.

Family hypercholesterolemia due to LDLR gene in Vietnamese children: characteristics of phenotype and genotype.

Journal: Molecular genetics and metabolism reports

Published: December 08, 2024

Phenotypes, Genotypes, Treatment, and Outcomes of 14 Children with Sitosterolemia at Vietnam National Children's Hospital.

Phenotypes, Genotypes, Treatment, and Outcomes of 14 Children with Sitosterolemia at Vietnam National Children's Hospital.

Journal: Journal of clinical medicine

Published: December 03, 2024

Clinical and molecular characteristics of simple virilizing congenital adrenal hyperplasia due to 21-hydroxylase deficiency: insight from a tertiary pediatric center in Vietnam.

Clinical and molecular characteristics of simple virilizing congenital adrenal hyperplasia due to 21-hydroxylase deficiency: insight from a tertiary pediatric center in Vietnam.

Journal: Annals of pediatric endocrinology & metabolism

Published: November 13, 2024

Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome in Vietnamese Patients.

Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome in Vietnamese Patients.

Journal: Medicina (Kaunas, Lithuania)

Published: October 17, 2024

Histopathological Alterations in the Livers of Chronic Hepatitis Patients Exposed to Agent Orange/Dioxin in Vietnam.

Histopathological Alterations in the Livers of Chronic Hepatitis Patients Exposed to Agent Orange/Dioxin in Vietnam.

Journal: Toxics

Published: April 19, 2022

Molecular Analysis of Vietnamese Patients with Mucopolysaccharidosis Type I.

Molecular Analysis of Vietnamese Patients with Mucopolysaccharidosis Type I.

Journal: Life (Basel, Switzerland)

Published: August 31, 2021

Showing 1-12 of 16

Last Updated: 09/26/2026