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Identification of a novel PML-RARG fusion in acute promyelocytic leukemia

Leukemia, 2017-09, Vol.31 (9), p.1992-1995

2017

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Pantothenate kinase-associated neurodegeneration in Korea: recurrent R440P mutation in PANK2 and outcome of deep brain stimulation

European journal of neurology, 2012-04, Vol.19 (4), p.556-561

2012

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Frequency of FMR1 premutation carriers and rate of expansion to full mutation in a retrospective diagnostic FMR1 Korean sample

Clinical genetics, 2014-05, Vol.85 (5), p.441-445

2014

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Dual mode gelation behavior of silk fibroin microgel embedded poly(ethylene glycol) hydrogels

Journal of materials chemistry. B, Materials for biology and medicine, 2016-01, Vol.4 (26), p.4574-4584

2016

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A novel ACAD8 mutation in asymptomatic patients with isobutyryl-CoA dehydrogenase deficiency and a review of the ACAD8 mutation spectrum

Clinical genetics, 2015-02, Vol.87 (2), p.196-198

2015

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Liquid culture enhances diagnosis of patients with milder forms of non-tuberculous mycobacterial lung disease

The international journal of tuberculosis and lung disease, 2017-03, Vol.21 (3), p.345-350

2017

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Effect of ethanol treatment on physical property of photopolymerized hyaluronic acid/silk fibroin hybrid hydrogel

Polymer (Guilford), 2020-08, Vol.202, p.122733, Article 122733

2020

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Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation

European journal of neurology, 2012-01, Vol.19 (1), p.e7-e8

2012

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Radiological Findings of Two Sisters with Aceruloplasminemia Presenting with Chorea

Clinical neuroradiology (Munich), 2017-09, Vol.27 (3), p.385-388

2017

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Frequency of DMPK mutation carriers in Korean women of childbearing age

Clinical genetics, 2014-10, Vol.86 (4), p.398-399

2014

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Effect of silk fibroin molecular weight on physical property of silk hydrogel

Polymer (Guilford), 2016-05, Vol.90, p.26-33

2016

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Epstein–Barr virus reactivation in extranodal natural killer/T-cell lymphoma patients: a previously unrecognized serious adverse event in a pilot study with romidepsin

Annals of oncology, 2016-03, Vol.27 (3), p.508-513

2016

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Clinical characterization and molecular classification of 12 Korean patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism

Experimental and clinical endocrinology & diabetes, 2013-10, Vol.121 (9), p.539-545

2013

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Identification of 11 novel mutations in 49 Korean patients with mucopolysaccharidosis type II

Clinical genetics, 2012-02, Vol.81 (2), p.185-190

2012

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Characterization of silk hydrogel formed with hydrolyzed silk fibroin-methacrylate via photopolymerization

Polymer (Guilford), 2018-09, Vol.153, p.232-240

2018

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Clinical and genetic analysis of Korean patients with Marfan syndrome: possible ethnic differences in clinical manifestation

Clinical genetics, 2010-02, Vol.77 (2), p.177-182

2010

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Late-onset vanishing white matter disease with compound heterozygous EIF2B5 gene mutations

European journal of neurology, 2009-03, Vol.16 (3), p.e42-e43

2009

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The Ala53Thr mutation in the α-synuclein gene in a Korean family with Parkinson disease

Clinical genetics, 2007-05, Vol.71 (5), p.471-473

2007

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Characterization of gelatin nanofiber prepared from gelatin–formic acid solution

Polymer (Guilford), 2005-06, Vol.46 (14), p.5094-5102

2005

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Molecular characterization of enteroviruses isolated from patients with aseptic meningitis in Korea, 2005

Archives of virology, 2007-05, Vol.152 (5), p.963-970

2007

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Carrier frequency of the R778L, A874V, and N1270S mutations in the ATP7B gene in a Korean population

Clinical genetics, 2009-04, Vol.75 (4), p.405-407

2009

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Mutational spectrum in eight Korean patients with 3-methylcrotonyl-CoA carboxylase deficiency

Clinical genetics, 2012-01, Vol.81 (1), p.96-98

2012

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Effects of warm acupuncture on breast cancer-related chronic lymphedema: a randomized controlled trial

Current oncology (Toronto), 2016-02, Vol.23 (1), p.e27-34

2016

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A novel locus for X-linked recessive CMT with deafness and optic neuropathy maps to Xq21.32-q24

Neurology, 2005-06, Vol.64 (11), p.1964-1967

2005

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Electrospun silk fibroin scaffolds with macropores for bone regeneration: an in vitro and in vivo study

Tissue engineering. Part A, 2010-04, Vol.16 (4), p.1271-1279

2010

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Identification of a novel PML-RARG fusion in acute promyelocytic leukemia

Pantothenate kinase-associated neurodegeneration in Korea: recurrent R440P mutation in PANK2 and outcome of deep brain stimulation

Frequency of FMR1 premutation carriers and rate of expansion to full mutation in a retrospective diagnostic FMR1 Korean sample

Dual mode gelation behavior of silk fibroin microgel embedded poly(ethylene glycol) hydrogels

A novel ACAD8 mutation in asymptomatic patients with isobutyryl-CoA dehydrogenase deficiency and a review of the ACAD8 mutation spectrum

Liquid culture enhances diagnosis of patients with milder forms of non-tuberculous mycobacterial lung disease

Effect of ethanol treatment on physical property of photopolymerized hyaluronic acid/silk fibroin hybrid hydrogel

Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation

Radiological Findings of Two Sisters with Aceruloplasminemia Presenting with Chorea

Frequency of DMPK mutation carriers in Korean women of childbearing age

Effect of silk fibroin molecular weight on physical property of silk hydrogel

Epstein–Barr virus reactivation in extranodal natural killer/T-cell lymphoma patients: a previously unrecognized serious adverse event in a pilot study with romidepsin

Clinical characterization and molecular classification of 12 Korean patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism

Identification of 11 novel mutations in 49 Korean patients with mucopolysaccharidosis type II

Characterization of silk hydrogel formed with hydrolyzed silk fibroin-methacrylate via photopolymerization

Clinical and genetic analysis of Korean patients with Marfan syndrome: possible ethnic differences in clinical manifestation

Late-onset vanishing white matter disease with compound heterozygous EIF2B5 gene mutations

The Ala53Thr mutation in the α-synuclein gene in a Korean family with Parkinson disease

Characterization of gelatin nanofiber prepared from gelatin–formic acid solution

Molecular characterization of enteroviruses isolated from patients with aseptic meningitis in Korea, 2005

Carrier frequency of the R778L, A874V, and N1270S mutations in the ATP7B gene in a Korean population

Mutational spectrum in eight Korean patients with 3-methylcrotonyl-CoA carboxylase deficiency

Effects of warm acupuncture on breast cancer-related chronic lymphedema: a randomized controlled trial

A novel locus for X-linked recessive CMT with deafness and optic neuropathy maps to Xq21.32-q24

Electrospun silk fibroin scaffolds with macropores for bone regeneration: an in vitro and in vivo study

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