Jeesuk Yu
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View article: SAT-197 Clinical and genetic investigation in children with short stature and comparison of effectiveness of growth hormone therapy
SAT-197 Clinical and genetic investigation in children with short stature and comparison of effectiveness of growth hormone therapy Open
Disclosure: G. Kim: None. J. Yu: None. Objective: Growth hormone stimulation tests (GHST) have been performed to identify growth hormone deficiency (GHD) as a cause of short stature (SS). With the advancement of genetic testing techniques,…
View article: Impact of COVID-19 on growth hormone therapy efficacy in pediatric patients with short stature
Impact of COVID-19 on growth hormone therapy efficacy in pediatric patients with short stature Open
The coronavirus disease (COVID-19) pandemic has affected global healthcare and raised concerns about growth hormone (GH) therapy outcomes in pediatric patients with short stature. This study compared GH therapy efficacy and outcomes before…
View article: Pituitary abnormalities in patients with pediatric growth hormone deficiency in a single tertiary center
Pituitary abnormalities in patients with pediatric growth hormone deficiency in a single tertiary center Open
Purpose: There is controversy as to whether brain magnetic resonance imaging (MRI) should be performed on all children with growth hormone deficiency (GHD) including those judged to have mild GHD. This study was aimed to determine the freq…
View article: Response of children with Turner syndrome with different types of karyotype abnormalities to growth hormone treatment
Response of children with Turner syndrome with different types of karyotype abnormalities to growth hormone treatment Open
Purpose: Short stature is the main characteristic of Turner syndrome (TS) patients and growth hormone (GH) therapy has been essential for achieving the final adult height (Ht). In the present study, the response of TS patients with differe…
View article: 8656 A Case of Wolfram Syndrome Accompanied by Growth Hormone Deficiency
8656 A Case of Wolfram Syndrome Accompanied by Growth Hormone Deficiency Open
Disclosure: H. Jung: None. G. Kim: None. Y. Park: None. J. Yu: None. Background: This case report explores the presentation, diagnosis, and multidisciplinary management of an 11-year-old female patient with Wolfram syndrome, a rare and pro…
View article: Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode with m.3243A>G variant involving the cerebellum and basal ganglia
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode with m.3243A>G variant involving the cerebellum and basal ganglia Open
Other SectionsAbstractINTRODUCTIONCASEDISCUSSIONACKNOWLEDGEMENTSFUNDINGAUTHORS' CONTRIBUTIONSFigureReference
View article: FRI454 The Effect Of Growth Hormone Treatment According To Karyotype Classification In Turner Syndrome Patients
FRI454 The Effect Of Growth Hormone Treatment According To Karyotype Classification In Turner Syndrome Patients Open
Disclosure: J. Choi: None. J. Yu: None. H. Kim: None. OBJECTIVES Short stature is the main characteristics for Turner syndrome (TS) patients, and growth hormone (GH) therapy has been used as an essential treatment for developing final adul…
View article: A Novel Nonsense Variant in the BCL11A Gene in a Male Patient with Intellectual Disability and Epilepsy
A Novel Nonsense Variant in the BCL11A Gene in a Male Patient with Intellectual Disability and Epilepsy Open
View article: PSUN340 Two cases of diffuse form of diazoxide-responsive congenital hyperinsulinism confirmed by 18F-DOPA PET-CT
PSUN340 Two cases of diffuse form of diazoxide-responsive congenital hyperinsulinism confirmed by 18F-DOPA PET-CT Open
Introduction Congenital hyperinsulinism is one of the most common causes of severe hypoglycemia in infants. Brain can be more damaged in the situation of hypoketotic hypoglycemia because there are no sufficient ketones for brain metabolism…
View article: Allergic Sensitization Pattern in the Korean Dermatologic Patients
Allergic Sensitization Pattern in the Korean Dermatologic Patients Open
The common allergens have changed over time. Based on the findings of this study, physicians and patients should consider changing their strategies for disease prevention and management.
View article: 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
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 Open
ClinicalTrials.gov Identifier: NCT01604395.
View article: Synergistic Effects of Korean Red Ginseng Extract and the Conventional Systemic Therapeutics of Atopic Dermatitis in a Murine Model
Synergistic Effects of Korean Red Ginseng Extract and the Conventional Systemic Therapeutics of Atopic Dermatitis in a Murine Model Open
The synergistic effects of Korean Red ginseng (KRG, Panax ginseng C.A. Mey.) on conventional systemic therapeutics of atopic dermatitis (AD) have not been studied yet. To analyze the synergistic effects of KRG extract and the conventional …
View article: Clinical Features and Remission Rate of Pediatric Graves’ Hyperthyroidism Treated With Antithyroid Drug
Clinical Features and Remission Rate of Pediatric Graves’ Hyperthyroidism Treated With Antithyroid Drug Open
Introduction: Pediatric Graves’ hyperthyroidism needs long-term therapy and there is no specific guideline. Antithyroid medication is used as the first line of treatment, among antithyroid medication, radioiodine therapy, and surgery. The …
View article: Thyroid imaging study in children with suspected thyroid dysgenesis
Thyroid imaging study in children with suspected thyroid dysgenesis Open
This study showed that thyroid ultrasonography is useful as the first-line imaging study to detect normal-sized eutopic thyroid gland. Thyroid scan should be performed to investigate the presence of ectopia if hypoplasia or aplasia is susp…
View article: Maternal Nutritional Status and the Development of Gestational Diabetes Using Common Data Model
Maternal Nutritional Status and the Development of Gestational Diabetes Using Common Data Model Open
View article: MON-077 A Case of Growth Hormone Deficiency in Sturge-Weber Syndrome
MON-077 A Case of Growth Hormone Deficiency in Sturge-Weber Syndrome Open
Introduction: Sturge-Weber syndrome (SWS) is a congenital neurocutaneous disorder characterized by a port wine stain on the skin in the distribution of the ophthalmic branch of the trigeminal nerve (vascular malformation of skin), glaucoma…
View article: Orolingual Tremor on Smiling
Orolingual Tremor on Smiling Open
Orolingual tremor is a rhythmic, involuntary movement of the jaw, tongue, pharynx, or lower face [1].It is often described in Parkinson's disease and can be seen in patients with severe essential tremor.Some medications, especially neurole…
View article: Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene
Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene Open
Congenital hypothyroidism (CH) is the most common endocrine disorder in neonates and infants with an incidence of one in 2,000 to one in 4,000 newborns. Primary CH can be caused by thyroid dysgenesis and thyroid dyshormonogenesis. CH due t…
View article: Basal serum luteinizing hormone value as the screening biomarker in female central precocious puberty
Basal serum luteinizing hormone value as the screening biomarker in female central precocious puberty Open
Basal serum LH level is a useful screening parameter for diagnosing CPP and EP in girls. Peak LH levels were lower with increasing BMI z-score, although older BA eliminated this effect.
View article: MON-270 Diagnostic Exome Sequencing in Children with Permanent Congenital Hypothyroidism
MON-270 Diagnostic Exome Sequencing in Children with Permanent Congenital Hypothyroidism Open
Introduction: Congenital hypothyroidism can be caused by aplasia or hypoplasia of the thyroid gland, ectopic thyroid, or dyshormonogenesis. Thyroid function test, thyroid ultrasonography, and thyroid scintigraphy may be helpful in diagnosi…
View article: Factors Associated with the Presence and Severity of Diabetic Ketoacidosis at Diagnosis of Type 1 Diabetes in Korean Children and Adolescents
Factors Associated with the Presence and Severity of Diabetic Ketoacidosis at Diagnosis of Type 1 Diabetes in Korean Children and Adolescents Open
The aim of this study was to identify the risk factors for presence and severity of diabetic ketoacidosis (DKA) at the onset of type 1 diabetes mellitus (T1DM) in Korean children and adolescents. A retrospective chart review of children an…
View article: A Case of Diffuse Neonatal Hemangiomatosis Successfully Treated with Propranolol
A Case of Diffuse Neonatal Hemangiomatosis Successfully Treated with Propranolol Open
We present a case of a 41-day-old girl with diffuse hemangiomatosis on her chin, right thigh, occipital area, and liver. She also had hepatomegaly, heart failure, and hypothyroidism. Hemangiomatosis did not respond to 2 weeks of oral admin…
View article: Representative levels of blood lead, mercury, and urinary cadmium in youth: Korean Environmental Health Survey in Children and Adolescents (KorEHS-C), 2012–2014
Representative levels of blood lead, mercury, and urinary cadmium in youth: Korean Environmental Health Survey in Children and Adolescents (KorEHS-C), 2012–2014 Open
View article: Clinical features of childhood diabetes mellitus focusing on latent autoimmune diabetes
Clinical features of childhood diabetes mellitus focusing on latent autoimmune diabetes Open
Initial autoantibody evaluation is useful for classification and management. Close monitoring of the patients with LAD is important due to the expected need for intensive insulin treatment within several years.
View article: 1p36 deletion syndrome confirmed by fluorescence<i>in situ</i>hybridization and array-comparative genomic hybridization analysis
1p36 deletion syndrome confirmed by fluorescence<i>in situ</i>hybridization and array-comparative genomic hybridization analysis Open
Pediatric epilepsy can be caused by various conditions, including specific syndromes. 1p36 deletion syndrome is reported in 1 in 5,000-10,000 newborns, and its characteristic clinical features include developmental delay, mental retardatio…
View article: Analysis of Dermatologic Diseases in Neurosurgical In-Patients: A Retrospective Study of 463 Cases
Analysis of Dermatologic Diseases in Neurosurgical In-Patients: A Retrospective Study of 463 Cases Open
This study characterizes the distribution of skin disorders in patients admitted to the neurosurgery service based on the consultations that have been made for dermatologic evaluation. Collaboration between the neurosurgeons and dermatolog…
View article: Retinal nerve fibre layer defect associated with MELAS syndrome
Retinal nerve fibre layer defect associated with MELAS syndrome Open
View article: Risk factors of vitamin D deficiency in children with epilepsy taking anticonvulsants at initial and during follow-up
Risk factors of vitamin D deficiency in children with epilepsy taking anticonvulsants at initial and during follow-up Open
Vitamin D deficiency is common in children with epilepsy taking anticonvulsants, especially in adolescents more than 12 years of age. This study emphasizes the regular monitoring of vitamin D level, especially in the presence of longer dur…
View article: Clinical usefulness of the measurement of serum fructosamine in childhood diabetes mellitus
Clinical usefulness of the measurement of serum fructosamine in childhood diabetes mellitus Open
The measurement of both fructosamine and HbA1c was useful in managing childhood diabetes mellitus, especially when there was discrepancy between the clinical information and the HbA1c level.
View article: Assessment of Bone Age in Prepubertal Healthy Korean Children: Comparison among the Korean Standard Bone Age Chart, Greulich-Pyle Method, and Tanner-Whitehouse Method
Assessment of Bone Age in Prepubertal Healthy Korean Children: Comparison among the Korean Standard Bone Age Chart, Greulich-Pyle Method, and Tanner-Whitehouse Method Open
The KS, GP, and TW3 methods show good reliability in the evaluation of bone age of prepubertal healthy Korean children without significant difference between them. Any are useful for evaluation of bone age in prepubertal healthy Korean chi…