Vu C. Dung

Hanoi, Viet Nam

Last Updated: 09/26/2026

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Found 17 publications

Nuclear Enlargement as a Histological Hallmark of Skeletal Muscle Aging, Revealed by Deep Learning-Driven Analysis and Validated in Inflammatory Myopathies.

Nuclear Enlargement as a Histological Hallmark of Skeletal Muscle Aging, Revealed by Deep Learning-Driven Analysis and Validated in Inflammatory Myopathies.

Journal: Aging cell

Published: January 17, 2026

Sarcopenia and Muscle Aging: Updated Insights into Molecular Mechanisms and Translational Therapeutics.

Sarcopenia and Muscle Aging: Updated Insights into Molecular Mechanisms and Translational Therapeutics.

Journal: Endocrinology and metabolism (Seoul, Korea)

Published: September 11, 2025

Severe pediatric hypocalcemia in Vietnam: etiologic profile, clinical outcomes and risk factors in 246 cases.

Severe pediatric hypocalcemia in Vietnam: etiologic profile, clinical outcomes and risk factors in 246 cases.

Journal: Frontiers in endocrinology

Published: September 09, 2025

Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations.

Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations.

Journal: Frontiers in endocrinology

Published: January 31, 2022

Transformative effect of a Humanitarian Program for individuals affected by rare diseases: building support systems and creating local expertise.

Transformative effect of a Humanitarian Program for individuals affected by rare diseases: building support systems and creating local expertise.

Journal: Orphanet journal of rare diseases

Published: November 08, 2021

Cockayne syndrome without UV-sensitivity in Vietnamese siblings with novel ERCC8 variants.

Cockayne syndrome without UV-sensitivity in Vietnamese siblings with novel ERCC8 variants.

Journal: Aging

Published: September 24, 2021

De Novo Mutations in EIF2B1 Affecting eIF2 Signaling Cause Neonatal/Early-Onset Diabetes and Transient Hepatic Dysfunction.

De Novo Mutations in EIF2B1 Affecting eIF2 Signaling Cause Neonatal/Early-Onset Diabetes and Transient Hepatic Dysfunction.

Journal: Diabetes

Published: October 11, 2019

Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening.

Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening.

Journal: Molecular genetics and metabolism reports

Published: March 31, 2018

Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants.

Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 25, 2017

Hematopoietic Stem Cell Transplantation for Patients with Mucopolysaccharidosis II.

Hematopoietic Stem Cell Transplantation for Patients with Mucopolysaccharidosis II.

Journal: Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation

Published: April 11, 2017

Glycosaminoglycan levels in dried blood spots of patients with mucopolysaccharidoses and mucolipidoses.

Glycosaminoglycan levels in dried blood spots of patients with mucopolysaccharidoses and mucolipidoses.

Journal: Molecular genetics and metabolism

Published: November 15, 2016

Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort.

Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort.

Journal: Genome biology

Published: July 28, 2016

Showing 1-12 of 17

Last Updated: 09/26/2026