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Synergistic Effects of Korean Red Ginseng Extract and the Conventional Systemic Therapeutics of Atopic Dermatitis in a Murine Model

Nutrients, 2021-12, Vol.14 (1), p.133

2021

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Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode with m.3243A>G variant involving the cerebellum and basal ganglia

Journal of genetic medicine, 2024-06, Vol.21 (1), p.36-40

2024

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Growth Responses During 3 Years of Growth Hormone Treatment in Children and Adolescents With Growth Hormone Deficiency: Comparison Between Idiopathic, Organic and Isolated Growth Hormone Deficiency, and Multiple Pituitary Hormone Deficiency

Journal of Korean Medical Science, 2022, 37(11), , pp.1-13

2022

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Response of children with Turner syndrome with different types of karyotype abnormalities to growth hormone treatment

Annals of Pediatric Endocrinology & Metabolism, 2024, 29(5), , pp.308-315

2024

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Thyroid imaging study in children with suspected thyroid dysgenesis

Annals of Pediatric Endocrinology & Metabolism, 2021, 26(1), , pp.53-59

2021

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Basal serum luteinizing hormone value as the screening biomarker in female central precocious puberty

Annals of Pediatric Endocrinology & Metabolism, 2019, 24(3), , pp.164-171

2019

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A Novel Nonsense Variant in the BCL11A Gene in a Male Patient with Intellectual Disability and Epilepsy

Annals of child neurology, 2023-01, Vol.31 (1), p.82-85

2023

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Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene

Annals of Pediatric Endocrinology & Metabolism, 2019, 24(3), , pp.199-202

2019

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Endocrine disorders and the neurologic manifestations

Annals of Pediatric Endocrinology & Metabolism, 2014, 19(4), , pp.184-190

Yu, Jeesuk

2014

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Orolingual Tremor on Smiling

Annals of child neurology, 2020-01, Vol.28 (1), p.37-38

2020

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Korean Environmental Health Survey in Children and Adolescents (KorEHS-C): Survey design and pilot study results on selected exposure biomarkers

International journal of hygiene and environmental health, 2014-03, Vol.217 (2-3), p.260-270

2014

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1710-P: A Case with Monogenic Diabetes Caused by RFX6 Mutation in a 14-Year-Old-Girl

Diabetes (New York, N.Y.), 2019-06, Vol.68 (Supplement_1)

2019

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Epidemics of enterovirus infection in Chungnam Korea, 2008 and 2009

Virology journal, 2011-06, Vol.8 (1), p.297-297, Article 297

2011

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Clinical features of childhood diabetes mellitus focusing on latent autoimmune diabetes

Annals of Pediatric Endocrinology & Metabolism, 2016, 21(4), , pp.212-218

2016

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High allele frequency of the p.Q258X mutation and identification of a novel mis-splicing mutation in the STAR gene in Korean patients with congenital lipoid adrenal hyperplasia

European journal of endocrinology, 2011-11, Vol.165 (5), p.771-778

2011

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Effect of a combination of Korean red ginseng extract and probiotics on the prevention of atopic dermatitis in a murine model

Journal of ethnopharmacology, 2022-01, Vol.283, p.114687-114687, Article 114687

2022

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Risk factors of vitamin D deficiency in children with epilepsy taking anticonvulsants at initial and during follow-up

Annals of Pediatric Endocrinology & Metabolism, 2015, 20(4), , pp.198-205

2015

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MON-077 A Case of Growth Hormone Deficiency in Sturge-Weber Syndrome

Journal of the Endocrine Society, 2020-05, Vol.4 (Supplement_1)

2020

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A case of monogenic diabetes mellitus caused by a novel heterozygous RFX6 nonsense mutation in a 14-year-old girl

Journal of Pediatric Endocrinology and Metabolism, 2021-12, Vol.34 (12), p.1619-1622

2021

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PSUN340 Two cases of diffuse form of diazoxide-responsive congenital hyperinsulinism confirmed by 18F-DOPA PET-CT

Journal of the Endocrine Society, 2022-11, Vol.6 (Supplement_1), p.A415-A416

2022

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8656 A Case of Wolfram Syndrome Accompanied by Growth Hormone Deficiency

Journal of the Endocrine Society, 2024-10, Vol.8 (Supplement_1)

2024

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Clinical usefulness of the measurement of serum fructosamine in childhood diabetes mellitus

Annals of Pediatric Endocrinology & Metabolism, 2015, 20(1), , pp.21-26

2015

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FRI454 The Effect Of Growth Hormone Treatment According To Karyotype Classification In Turner Syndrome Patients

Journal of the Endocrine Society, 2023-10, Vol.7 (Supplement_1)

2023

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Clinical Features and Remission Rate of Pediatric Graves’ Hyperthyroidism Treated With Antithyroid Drug

Journal of the Endocrine Society, 2021-05, Vol.5 (Supplement_1), p.A710-A711

2021

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Retinal nerve fibre layer defect associated with MELAS syndrome

Canadian journal of ophthalmology, 2015-10, Vol.50 (5), p.e85-e88

2015

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Synergistic Effects of Korean Red Ginseng Extract and the Conventional Systemic Therapeutics of Atopic Dermatitis in a Murine Model

Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode with m.3243A>G variant involving the cerebellum and basal ganglia

Growth Responses During 3 Years of Growth Hormone Treatment in Children and Adolescents With Growth Hormone Deficiency: Comparison Between Idiopathic, Organic and Isolated Growth Hormone Deficiency, and Multiple Pituitary Hormone Deficiency

Response of children with Turner syndrome with different types of karyotype abnormalities to growth hormone treatment

Thyroid imaging study in children with suspected thyroid dysgenesis

Basal serum luteinizing hormone value as the screening biomarker in female central precocious puberty

A Novel Nonsense Variant in the BCL11A Gene in a Male Patient with Intellectual Disability and Epilepsy

Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene

Endocrine disorders and the neurologic manifestations

Orolingual Tremor on Smiling

Korean Environmental Health Survey in Children and Adolescents (KorEHS-C): Survey design and pilot study results on selected exposure biomarkers

1710-P: A Case with Monogenic Diabetes Caused by RFX6 Mutation in a 14-Year-Old-Girl

Epidemics of enterovirus infection in Chungnam Korea, 2008 and 2009

Clinical features of childhood diabetes mellitus focusing on latent autoimmune diabetes

High allele frequency of the p.Q258X mutation and identification of a novel mis-splicing mutation in the STAR gene in Korean patients with congenital lipoid adrenal hyperplasia

Effect of a combination of Korean red ginseng extract and probiotics on the prevention of atopic dermatitis in a murine model

Risk factors of vitamin D deficiency in children with epilepsy taking anticonvulsants at initial and during follow-up

MON-077 A Case of Growth Hormone Deficiency in Sturge-Weber Syndrome

A case of monogenic diabetes mellitus caused by a novel heterozygous RFX6 nonsense mutation in a 14-year-old girl

PSUN340 Two cases of diffuse form of diazoxide-responsive congenital hyperinsulinism confirmed by 18F-DOPA PET-CT

8656 A Case of Wolfram Syndrome Accompanied by Growth Hormone Deficiency

Clinical usefulness of the measurement of serum fructosamine in childhood diabetes mellitus

FRI454 The Effect Of Growth Hormone Treatment According To Karyotype Classification In Turner Syndrome Patients

Clinical Features and Remission Rate of Pediatric Graves’ Hyperthyroidism Treated With Antithyroid Drug

Retinal nerve fibre layer defect associated with MELAS syndrome

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