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Eardrum-inspired soft viscoelastic diaphragms for CNN-based speech recognition with audio visualization images

Scientific reports, 2023-04, Vol.13 (1), p.6414-6414, Article 6414

2023

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Crack Monitoring in Rotating Shaft Using Rotational Speed Sensor-Based Torsional Stiffness Estimation with Adaptive Extended Kalman Filters

Sensors (Basel, Switzerland), 2023-02, Vol.23 (5), p.2437

2023

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Phenotype categorization of neurofibromatosis type I and correlation to NF1 mutation types

Journal of human genetics, 2020-01, Vol.65 (2), p.79-89

2020

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Phenotypes of atopic dermatitis identified by cluster analysis in early childhood

Journal of dermatology, 2019-02, Vol.46 (2), p.117-123

2019

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Predominance of the c.648G > T G6PC gene mutation and late complications in Korean patients with glycogen storage disease type Ia

Orphanet journal of rare diseases, 2020-02, Vol.15 (1), p.45-45, Article 45

2020

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PDDL Planning with Natural Language-Based Scene Understanding for UAV-UGV Cooperation

Applied sciences, 2019-09, Vol.9 (18), p.3789

2019

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Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort

Genes, 2021-04, Vol.12 (5), p.675

2021

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Spectrum of Mutations in Noonan Syndrome and Their Correlation with Phenotypes

The Journal of pediatrics, 2011-12, Vol.159 (6), p.1029-1035

2011

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Enhanced thrombospondin-1 causes dysfunction of vascular endothelial cells derived from Fabry disease-induced pluripotent stem cells

EBioMedicine, 2020-02, Vol.52, p.102633, Article 102633

2020

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Long-term enzyme replacement therapy for Fabry disease: efficacy and unmet needs in cardiac and renal outcomes

Journal of human genetics, 2016-11, Vol.61 (11), p.923-929

2016

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Characteristic dysmorphic features in congenital disorders of glycosylation type IIb

Journal of human genetics, 2018-03, Vol.63 (3), p.383-386

2018

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Biochemical and molecular characteristics of citrin deficiency in Korean children

Journal of human genetics, 2017-02, Vol.62 (2), p.305-307

2017

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Intelligent lead: a novel HRI sensor for guide robots

Sensors (Basel, Switzerland), 2012-06, Vol.12 (6), p.8301-8318

2012

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Regeneration of Normal Distributions Transform for Target Lattice Based on Fusion of Truncated Gaussian Components

IEEE robotics and automation letters, 2019-04, Vol.4 (2), p.684-691

2019

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Psychological characteristics of adult neurofibromatosis type 1 patients seeking elective surgery

Archives of Aesthetic Plastic Surgery, 2020, 26(4), , pp.150-156

2020

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Pose compensation framework with explicit loop closing for multiple robots

Electronics letters, 2014-10, Vol.50 (22), p.1581-1583

2014

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Impaired Osteogenesis of Disease-Specific Induced Pluripotent Stem Cells Derived from a CFC Syndrome Patient

International journal of molecular sciences, 2017-12, Vol.18 (12), p.2591

2017

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Deep learning image segmentation for the reliable porosity measurement of high-capacity Ni-based oxide cathode secondary particles

Journal of analytical science and technology, 2023-12, Vol.14 (1), p.47-11, Article 47

2023

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Setleis syndrome due to inheritance of the 1p36.22p36.21 duplication: evidence for lack of penetrance

Journal of human genetics, 2015-11, Vol.60 (11), p.717-722

2015

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Improved Feature Map Merging Using Virtual Supporting Lines for Multi-Robot Systems

Advanced robotics, 2011-01, Vol.25 (13-14), p.1675-1696

2011

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Argininemia Presenting With Progressive Spastic Diplegia

Pediatric neurology, 2011-03, Vol.44 (3), p.218-220

2011

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Familial Focal Segmental Glomerulosclerosis Associated With an ACTN4 Mutation and Paternal Germline Mosaicism

American journal of kidney diseases, 2008-05, Vol.51 (5), p.834-838

2008

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Quantitative analysis of methylation status at 11p15 and 7q21 for the genetic diagnosis of Beckwith-Wiedemann syndrome and Silver-Russell syndrome

Journal of human genetics, 2013-09, Vol.58 (9), p.604-610

2013

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Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay

Molecular medicine (Cambridge, Mass.), 2022-03, Vol.28 (1), p.38-38, Article 38

2022

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Clinical Genetic Testing in Children with Kidney Disease

Childhood Kidney Diseases, 2021, 25(1), , pp.14-21

2021

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Eardrum-inspired soft viscoelastic diaphragms for CNN-based speech recognition with audio visualization images

Crack Monitoring in Rotating Shaft Using Rotational Speed Sensor-Based Torsional Stiffness Estimation with Adaptive Extended Kalman Filters

Phenotype categorization of neurofibromatosis type I and correlation to NF1 mutation types

Phenotypes of atopic dermatitis identified by cluster analysis in early childhood

Predominance of the c.648G > T G6PC gene mutation and late complications in Korean patients with glycogen storage disease type Ia

PDDL Planning with Natural Language-Based Scene Understanding for UAV-UGV Cooperation

Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort

Spectrum of Mutations in Noonan Syndrome and Their Correlation with Phenotypes

Enhanced thrombospondin-1 causes dysfunction of vascular endothelial cells derived from Fabry disease-induced pluripotent stem cells

Long-term enzyme replacement therapy for Fabry disease: efficacy and unmet needs in cardiac and renal outcomes

Characteristic dysmorphic features in congenital disorders of glycosylation type IIb

Biochemical and molecular characteristics of citrin deficiency in Korean children

Intelligent lead: a novel HRI sensor for guide robots

Regeneration of Normal Distributions Transform for Target Lattice Based on Fusion of Truncated Gaussian Components

Psychological characteristics of adult neurofibromatosis type 1 patients seeking elective surgery

Pose compensation framework with explicit loop closing for multiple robots

Impaired Osteogenesis of Disease-Specific Induced Pluripotent Stem Cells Derived from a CFC Syndrome Patient

Deep learning image segmentation for the reliable porosity measurement of high-capacity Ni-based oxide cathode secondary particles

Setleis syndrome due to inheritance of the 1p36.22p36.21 duplication: evidence for lack of penetrance

Improved Feature Map Merging Using Virtual Supporting Lines for Multi-Robot Systems

Argininemia Presenting With Progressive Spastic Diplegia

Familial Focal Segmental Glomerulosclerosis Associated With an ACTN4 Mutation and Paternal Germline Mosaicism

Quantitative analysis of methylation status at 11p15 and 7q21 for the genetic diagnosis of Beckwith-Wiedemann syndrome and Silver-Russell syndrome

Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay

Clinical Genetic Testing in Children with Kidney Disease

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