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Ngoc Thi Bich Can

Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants
2018 · Jennifer J. Johnston, Jasper J. van der Smagt, et al. · Genetics in Medicine · 236
Characterization and outcome of 41 patients with beta‐ketothiolase deficiency: 10 years’ experience of a medical center in northern Vietnam
2017 · Khanh Ngoc Nguyen, Elsayed Abdelkreem, et al. · Journal of Inherited Metabolic Disease · 32
A common mutation, R208X, identified in Vietnamese patients with mitochondrial acetoacetyl-CoA thiolase (T2) deficiency
2010 · Toshiyuki Fukao, Hoan Thi Nguyen, et al. · Molecular Genetics and Metabolism · 28
Molecular Analysis of Vietnamese Patients with Mucopolysaccharidosis Type I
2021 · Ngoc Thi Bich Can, Dien Minh Tran, et al. · Life · 6
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Incidence rate and characteristics of newly diagnosed type 1 diabetes in a Vietnamese tertiary pediatric center: challenges in early detection
2025 · Ngoc Can Thi Bich, Son Do Tien, et al. · Annals of Pediatric Endocrinology & Metabolism · 2
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AB112. Spectrum of mucopolysaccharidoses in Vietnam
2017 · Dung Chi Vu, Ngoc Bich Thi Can, et al. · Annals of Translational Medicine · 2
AB125. Neonatal diabetes mellitus due to insulin gene mutation.
2015 · Ngoc Thi Bich Can, Dũng Chí Vũ, et al. · PubMed Central · 2
Family hypercholesterolemia due to LDLR gene in Vietnamese children: characteristics of phenotype and genotype
2025 · Mai Thi Thanh Do, Dung Chi Vu, et al. · Molecular Genetics and Metabolism Reports · 1
AB128. Neonatal diabetes mellitus: genotype, phenotype and outcome
2015 · Ngoc Thi Bich Can, Dũng Chí Vũ, et al. · PubMed Central · 1
AB132. Neonatal diabetes in Wolcott-Rallison syndrome: a case report
2015 · Ngoc Thi Bich Can, Dũng Chí Vũ, et al. · PubMed Central · 1
The Result of Sulphonylureas Treatment in Patients with Neonatal Diabetes Mellitus due to kcnj11/abcc8 Gene Mutations in Vietnam
2014 · Ngoc Can Thi Bich, Dung Vu, et al. · 53rd ESPE Meeting · 1
Genotype–phenotype spectrum and clinical outcomes of glycogen storage disease type I: A 15-year experience at Vietnam National Children's Hospital
2026 · Hang Thi Nguyen, Dung Chi Vu, et al. · Molecular Genetics and Metabolism Reports
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Pseudohypoparathyroidism due to GNAS inactivation: a case report
2025 · Huyền Đặng, Dung Vu, et al. · Endocrine Abstracts
Clinical and molecular characteristics of simple virilizing congenital adrenal hyperplasia due to 21-hydroxylase deficiency: insight from a tertiary pediatric center in Vietnam
2025 · Khanh Ngoc Nguyen, Giang Thi Kim Dang, et al. · Annals of Pediatric Endocrinology & Metabolism
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P466: Bilateral pheochromocytomas in Von Hippel-Lindau disease
2025 · Ngoc Can, Dung Vu, et al. · Genetics in Medicine Open
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P162: Registry and gene replacement therapy for spinal muscular atrophy at referral center of pediatrics in Vietnam*
2025 · Dung Dung-Chi, Khanh Nguyen, et al. · Genetics in Medicine Open
P436: Hutchinson-Gilford progeria syndrome due to homozygous missense variant of LMNA gene
2025 · Ngoc Can, Dung Vu, et al. · Genetics in Medicine Open
P256: Mucolipidosis typs II: Data from northern referral pediatric center in Vietnam
2024 · Ngoc Can, Dung Vu, et al. · Genetics in Medicine Open
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P216: Phenotype and genotype of Vietnamese patients with X-linked adrenoleukodystrophy
2024 · Dung Vu, Khanh Nguyen, et al. · Genetics in Medicine Open
Treatment Outcome of Growth Hormone in Turner Syndrome Children
2019 · Bùi Phương Thảo, Vũ Chí Dũng, et al. · 58th Annual ESPE Meeting (ESPE 2019)
AB073. Classic infantile-onset Pompe disease: phenotypes and outcomes of 5 Vietnamese patients receiving enzyme replacement therapy
2017 · Khanh Ngoc Nguyen, Mai Thi Thanh Do, et al. · Annals of Translational Medicine
AB111. Prenatal treatment and fertility of female patients with congenital adrenal hyperplasia
2017 · Dung Chi Vu, Khanh Ngoc Nguyen, et al. · Annals of Translational Medicine
AB014. Beta-ketothiolase deficiency: phenotype, genotype and outcome of 48 Vietnamese patients
2017 · Khanh Ngoc Nguyen, Hoan Thi Nguyen, et al. · Annals of Translational Medicine
AB067. X-linked adrenoleukodystrophy: Phenotype and genotype in Vietnamese patients
2017 · Khanh Ngoc Nguyen, Ha Thu Nguyen, et al. · Annals of Translational Medicine
AB110. Genotype and phenotype of 107 patients with congenital hyperinsulinism
2017 · Dung Chi Vu, Ngoc T. B. Can, et al. · Annals of Translational Medicine
Works count: 40
Citation count: 312
H-index: 4
I10-index: 3
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