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Coevolutionary augmented Lagrangian methods for constrained optimization

IEEE transactions on evolutionary computation, 2000-07, Vol.4 (2), p.114-124

2000

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Attitude Controller Design and Test of Korea Space Launch Vehicle-I Upper Stage

International journal of aeronautical and space sciences, 2010-12, Vol.11 (4), p.303-312

2010

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Practical Dual-Control Guidance Using Adaptive Intermittent Maneuver Strategy

Journal of guidance, control, and dynamics, 2001-09, Vol.24 (5), p.1009-1015

2001

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Control design of spinning rockets based on co-evolutionary optimization

Control engineering practice, 2001-02, Vol.9 (2), p.149-157

2001

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Controller reduction using a new invariant set

International journal of control, 1998-01, Vol.70 (3), p.447-467

1998

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Attitude Controller Design and Test of Korea Space Launch Vehicle-I Upper Stage

International journal of aeronautical and space sciences, 2010, Vol.11 (4), p.303-312

2010

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Modeling and simulation of a launch vehicle thrust vector control system

2012 12th International Conference on Control, Automation and Systems, 2012, p.2088-2092

2012

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Payload fairing separation analysis using constraint force equation

ICCAS 2010, 2010, p.1134-1138

2010

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Missile guidance using neural networks

Control engineering practice, 1997-06, Vol.5 (6), p.753-762

1997

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Sloshing analysis using ground experimental apparatus

2008 International Conference on Control, Automation and Systems, 2008, p.2203-2207

2008

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Hardware in the loop tests for upper stage control systems of Korean space launch vehicle

2007 International Conference on Control, Automation and Systems, 2007, p.2313-2318

2007

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Tofacitinib relieves symptoms of stimulator of interferon genes (STING)–associated vasculopathy with onset in infancy caused by 2 de novo variants in TMEM173

Journal of allergy and clinical immunology, 2017-04, Vol.139 (4), p.1396-1399.e12

2017

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Corrigendum: Incidence of Guillain-Barré syndrome in South Korea during the early COVID-19 pandemic

Frontiers in neurology, 2023-04, Vol.14, p.1184177-1184177

2023

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Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis

Scientific reports, 2018-06, Vol.8 (1), p.8678-7, Article 8678

2018

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Surgical outcome and predictive factors of epilepsy surgery in pediatric isolated focal cortical dysplasia

Epilepsy research, 2018-01, Vol.139, p.54-59

2018

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Expanding the clinical phenotype and genetic spectrum of PURA-related neurodevelopmental disorders

Brain & development (Tokyo. 1979), 2021-10, Vol.43 (9), p.912-918

2021

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Effect of platelet-rich plasma on the degenerative rotator cuff tendinopathy according to the compositions

Journal of orthopaedic surgery and research, 2019-12, Vol.14 (1), p.408-408, Article 408

2019

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Genetic diagnosis of Duchenne and Becker muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform

Journal of medical genetics, 2011-11, Vol.48 (11), p.731-736

2011

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Early-onset autosomal dominant GTP-cyclohydrolase I deficiency: Diagnostic delay and residual motor signs

Brain & development (Tokyo. 1979), 2021-08, Vol.43 (7), p.759-767

2021

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Change of centrotemporal spikes from onset to remission in self-limited epilepsy with centrotemporal spikes (SLECTS)

Brain & development (Tokyo. 1979), 2020-03, Vol.42 (3), p.270-276

2020

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The Korean undiagnosed diseases program: lessons from a one-year pilot project

Orphanet journal of rare diseases, 2019-03, Vol.14 (1), p.68-68, Article 68

2019

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Development of a common platform for the noninvasive prenatal diagnosis of X‐linked diseases

Prenatal diagnosis, 2018-10, Vol.38 (11), p.835-840

2018

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Robust control design for spinning rocket

Proceedings of the 35th SICE Annual Conference. International Session Papers, 1996, p.1325-1330

1996

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Large-scale structural alteration of brain in epileptic children with SCN1A mutation

NeuroImage clinical, 2017-01, Vol.15, p.594-600

2017

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Novel HEXA variants in Korean children with Tay–Sachs disease with regression of neurodevelopment from infancy

Molecular genetics & genomic medicine, 2021-06, Vol.9 (6), p.e1677-n/a

2021

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Coevolutionary augmented Lagrangian methods for constrained optimization

Attitude Controller Design and Test of Korea Space Launch Vehicle-I Upper Stage

Practical Dual-Control Guidance Using Adaptive Intermittent Maneuver Strategy

Control design of spinning rockets based on co-evolutionary optimization

Controller reduction using a new invariant set

Attitude Controller Design and Test of Korea Space Launch Vehicle-I Upper Stage

Modeling and simulation of a launch vehicle thrust vector control system

Payload fairing separation analysis using constraint force equation

Missile guidance using neural networks

Sloshing analysis using ground experimental apparatus

Hardware in the loop tests for upper stage control systems of Korean space launch vehicle

Tofacitinib relieves symptoms of stimulator of interferon genes (STING)–associated vasculopathy with onset in infancy caused by 2 de novo variants in TMEM173

Corrigendum: Incidence of Guillain-Barré syndrome in South Korea during the early COVID-19 pandemic

Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis

Surgical outcome and predictive factors of epilepsy surgery in pediatric isolated focal cortical dysplasia

Expanding the clinical phenotype and genetic spectrum of PURA-related neurodevelopmental disorders

Effect of platelet-rich plasma on the degenerative rotator cuff tendinopathy according to the compositions

Genetic diagnosis of Duchenne and Becker muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform

Early-onset autosomal dominant GTP-cyclohydrolase I deficiency: Diagnostic delay and residual motor signs

Change of centrotemporal spikes from onset to remission in self-limited epilepsy with centrotemporal spikes (SLECTS)

The Korean undiagnosed diseases program: lessons from a one-year pilot project

Development of a common platform for the noninvasive prenatal diagnosis of X‐linked diseases

Robust control design for spinning rocket

Large-scale structural alteration of brain in epileptic children with SCN1A mutation

Novel HEXA variants in Korean children with Tay–Sachs disease with regression of neurodevelopment from infancy

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