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손, 영배(Sohn, Young Bae)
Currently indexed
[School of Medicine / Graduate School of Medicine] - [Medical Genetics]
Author IDs
ORCID
-
ISNI
000000047379557X
WOS
-
SCOPUS
-
Research areas
유전질환
염색체이상
유전성 암
Co-Researcher
Articles
(80)
Thesis
(0)
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(0)
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(0)
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(0)
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(0)
Showing results 1 to 20 of 80
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Pub Year
Title
Author(s)
2024
Biomarkers of Glycosaminoglycans (GAG) accumulation in patients with mucopolysaccharidosis type VI—LeukoGAG, Corneal Opacification (COM) and Carotid Intima Media Thickening (CIMT)
손영배
2023
Using low-dose octreotide with diazoxide-resistant congenital hyperinsulinism resulting from com-pound heterozygous mutations in the ABCC8 gene
손영배
,
이해상
,
황진순
2023
Aperiodic alternating nystagmus in adult-onset Alexander disease with a novel mutation
손영배
,
이성준
,
이진수
,
홍지만
2022
RNA analysis of the GALNS transcript reveals novel pathogenic mechanisms associated with Morquio syndrome A
손영배
2022
Timing is everything: Clinical courses of Hunter syndrome associated with age at initiation of therapy in a sibling pair
손영배
2022
Genetic obesity: an update with emerging therapeutic approaches
손영배
2022
Updates on Paget’s Disease of Bone
손영배
,
정윤석
,
최용준
2022
The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure
손영배
2021
Somatic uniparental disomy mitigates the most damaging EFL1 allele combination in Shwachman-Diamond syndrome
손영배
2021
Genetic Analysis Using a Next Generation Sequencing-Based Gene Panel in Patients With Skeletal Dysplasia: A Single-Center Experience
김정택
,
손영배
,
조재호
2020
The GBA p.G85E mutation in Korean patients with non-neuronopathic Gaucher disease: founder and neuroprotective effects
손영배
2020
Ataxia Associated with CADASIL: a Pathology-Confirmed Case Report and Literature Review
박동규
,
손성향
,
손영배
,
윤정한
2019
Effects of recombinant human growth hormone treatment on growth, body composition, and safety in infants or toddlers with Prader-Willi syndrome: a randomized, active-controlled trial
손영배
2019
Deletion of exons 16-17b of CFTR is frequently identified in Korean patients with cystic fibrosis
손영배
,
장주영
2019
Correction to: Neuronopathic Gaucher disease presenting with microcytic hypochromic anemia
손영배
2019
Neuronopathic Gaucher disease presenting with microcytic hypochromic anemia
손영배
2018
The efficacy of intracerebroventricular idursulfase-beta enzyme replacement therapy in mucopolysaccharidosis II murine model: heparan sulfate in cerebrospinal fluid as a clinical biomarker of neuropathology
손영배
2018
Successful switching from insulin to sulfonylurea in a 3-month-old infant with diabetes due to p.G53D mutation in KCNJ11
박규정
,
손영배
,
이해상
,
황진순
2017
Familial Glycogen Storage Disease Type IXa Diagnosed by Targeted Exome Sequencing
손영배
,
이다근
,
장주영
2017
Rare presentation of Rothmund-Thomson syndrome with predominantly cutaneous findings
손영배
,
이은소
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아주대학교 의학문헌정보센터