Han W. Yoo

Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 14 publications

A Randomized, Double-Blind, 2-Treatment, 2-Period, Crossover Phase 1 Study to Compare the Pharmacokinetics, Safety and Tolerability of 60 IU/Kg of Abcertin and Cerezyme in Healthy Volunteers Following a Single Intravenous Administration.

A Randomized, Double-Blind, 2-Treatment, 2-Period, Crossover Phase 1 Study to Compare the Pharmacokinetics, Safety and Tolerability of 60 IU/Kg of Abcertin and Cerezyme in Healthy Volunteers Following a Single Intravenous Administration.

Journal: Molecular genetics & genomic medicine

Published: December 11, 2024

Trajectories in glycated hemoglobin and body mass index in children and adolescents with diabetes using the common data model.

Trajectories in glycated hemoglobin and body mass index in children and adolescents with diabetes using the common data model.

Journal: Scientific reports

Published: January 26, 2021

Genotype-Phenotype Correlation of SMN1 and NAIP Deletions in Korean Patients with Spinal Muscular Atrophy.

Genotype-Phenotype Correlation of SMN1 and NAIP Deletions in Korean Patients with Spinal Muscular Atrophy.

Journal: Journal of clinical neurology (Seoul, Korea)

Published: April 14, 2016

Erratum to: Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome.

Erratum to: Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome.

Journal: Journal of clinical neurology (Seoul, Korea)

Published: April 14, 2016

Compound heterozygous mutations of ACADS gene in newborn with short chain acyl-CoA dehydrogenase deficiency: case report and literatures review.

Compound heterozygous mutations of ACADS gene in newborn with short chain acyl-CoA dehydrogenase deficiency: case report and literatures review.

Journal: Korean journal of pediatrics

Published: September 14, 2015

Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome.

Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome.

Journal: Journal of clinical neurology (Seoul, Korea)

Published: March 27, 2015

The first Korean case of HDR syndrome confirmed by clinical and molecular investigation.

The first Korean case of HDR syndrome confirmed by clinical and molecular investigation.

Journal: Yonsei medical journal

Published: December 17, 2014

Phenotypic variability of a terminal 7q deletion/8q duplication in Korean siblings.

Phenotypic variability of a terminal 7q deletion/8q duplication in Korean siblings.

Journal: Annals of laboratory medicine

Published: October 09, 2014

The PRSS1 c.623G>C (p.G208A) mutation is the most common PRSS1 mutation in Korean children with hereditary pancreatitis.

The PRSS1 c.623G>C (p.G208A) mutation is the most common PRSS1 mutation in Korean children with hereditary pancreatitis.

Journal: Gut

Published: May 01, 2014

Clinical features of congenital adrenal insufficiency including growth patterns and significance of ACTH stimulation test.

Clinical features of congenital adrenal insufficiency including growth patterns and significance of ACTH stimulation test.

Journal: Journal of Korean medical science

Published: July 31, 2013

A Korean boy with atypical X-linked adrenoleukodystrophy confirmed by an unpublished mutation of ABCD1.

A Korean boy with atypical X-linked adrenoleukodystrophy confirmed by an unpublished mutation of ABCD1.

Journal: Korean journal of pediatrics

Published: July 11, 2013

Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome.

Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome.

Journal: Annals of pediatric endocrinology & metabolism

Published: May 29, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026