Hee Joon Yu

ORCID: 0000-0003-2022-2332
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About
Contact & Profiles
Research Areas
  • Nail Diseases and Treatments
  • Herpesvirus Infections and Treatments
  • Acne and Rosacea Treatments and Effects
  • Genomics and Rare Diseases
  • Cancer and Skin Lesions
  • Fungal Infections and Studies
  • Autoimmune Bullous Skin Diseases
  • Skin and Cellular Biology Research
  • Autoimmune and Inflammatory Disorders
  • Cutaneous lymphoproliferative disorders research
  • Nonmelanoma Skin Cancer Studies
  • Plant Pathogens and Fungal Diseases
  • Tumors and Oncological Cases
  • Genetics and Neurodevelopmental Disorders
  • Health, Environment, Cognitive Aging
  • Soft tissue tumor case studies
  • Machine Learning in Healthcare
  • Oral Health Pathology and Treatment
  • Dermatological and Skeletal Disorders
  • Genomic variations and chromosomal abnormalities
  • Inflammatory Myopathies and Dermatomyositis
  • Dermatology and Skin Diseases
  • Skin Diseases and Diabetes
  • Syphilis Diagnosis and Treatment
  • Cardiac tumors and thrombi

Chonnam National University Hwasun Hospital
2024

Jeonnam Bioindustry Foundation
2024

Hallym University
2022

Hallym University Sacred Heart Hospital
2016-2022

Hallym University Medical Center
2022

Hallym University Dongtan Sacred Heart Hospital
2020

Gangnam Severance Hospital
2018-2019

Yonsei University
2018-2019

Hanyang University
2007-2017

Samsung Medical Center
1970-2016

Stroke risk in atrial fibrillation (AF) is often assessed at initial presentation, and stratification performed as a 'one off'. In validation studies of prediction, baseline values are used to 'predict' events that occur many years later. Many clinical variables have 'dynamic' changes over time, the patient followed up. These dynamic factors may increase CHA2DS2-VASc score, stroke category absolute ischaemic rate. This article evaluates its effect on prediction risk. From Korea National...

10.1055/s-0038-1651482 article EN Thrombosis and Haemostasis 2018-05-03

Ketogenic diet (KD) is known to be effective in intractable epilepsy. However, the role of KD refractory status epilepticus (RSE) has not been well described. The aim this study explore patients with RSE. We retrospectively reviewed medical records four children and one adult RSE between October 2006 August 2010. All presented (SE) that was presumed associated viral encephalitis. After we failed control seizures standard measures for SE, tried KD. overall seizure frequency decreased <50%...

10.1111/j.1528-1167.2011.03289.x article EN Epilepsia 2011-10-17

Tinea incognito (TI) is a dermatophytic infection which has lost its typical clinical appearance because of improper use steroids or calcineurin inhibitors.The incidence TI increasing nowadays.We conducted retrospective review on 283 patients with from 25 dermatology training hospitals in Korea 2002-2010 to investigate the demographical, clinical, and mycological characteristics TI, determine associated risk factors.More than half (59.3%) were previously treated by non-dermatologists...

10.3346/jkms.2013.28.1.145 article EN cc-by-nc Journal of Korean Medical Science 2013-01-01

Electronic cigarettes are novel tobacco products that frequently used these days. The cartridge contains liquid nicotine and accidental poisoning, even with a small oral dose, endangers children. We present here mortality case of 15-month-old child who ingested mistaking it for cold medicine. When the emergency medical technicians arrived, she was found to have pulseless electrical activity. Spontaneous circulation restored after approximately 40 minutes cardiopulmonary resuscitation....

10.3345/kjp.2016.59.12.490 article EN cc-by-nc-nd Korean Journal of Pediatrics 2016-01-01

We used cardiovascular magnetic resonance (CMR) to investigate the association between epicardial adipose tissue (EAT) thickness and silent myocardial ischemia, as well coronary artery stenosis, in asymptomatic type 2 diabetic patients. The study included 100 subjects (51 male 49 female; mean age: 56 ± 7 years). Silent determined by CMR, was defined evidence of inducible ischemia or infarction. Signal reduction stenosis ≥ 50% vessel diameter criteria for significant on (MR) angiography. EAT...

10.1186/1475-2840-11-83 article EN cc-by Cardiovascular Diabetology 2012-01-01

There have been no prior nationwide reports on the prevalence of hypertrophic cardiomyopathy (HCM) among patients suffering from atrial fibrillation (AF). It is also unclear how much stroke risk attributable to HCM compared with other risks in AF. This study assessed non-valvular AF (NVAF) and assess magnitude increase NVAF HCM, those without HCM. From Korean National Health Insurance Service database January 1, 2005 December 31, 2016, we analysed 979,784 prevalent aged 18 years or older....

10.1055/s-0038-1676818 article EN Thrombosis and Haemostasis 2019-01-02

Most developmental screening tools in Korea are adopted from foreign tests. To ensure efficient of infants and children Korea, a nationwide tool with high reliability validity is needed.This study aimed to independently develop, standardize, validate the Korean Developmental Screening Test for Infants Children (K-DST) neurodevelopmental disorders Korea.The standardization validation conducted 2012-2014 3,284 subjects (4-71 months age) resulted first edition K-DST. The restandardization...

10.3345/cep.2020.00640 article EN cc-by-nc Clinical and Experimental Pediatrics 2020-05-14

The diagnostic yield of whole-exome sequencing (WES) varies from 30%-50% among patients with mild to severe neurodevelopmental delay (NDD)/intellectual disability (ID). Routine retrospective reanalysis undiagnosed has increased the total by 10-15%. Here, we performed proband-only WES 1065 NDD/ID and applied a prospective, daily automated pipeline without clinically significant variants facilitate diagnoses.The study included consecutive 1056 nonconsanguineous unrelated families 10...

10.1186/s10020-022-00464-x article EN cc-by Molecular Medicine 2022-03-26

Hashimoto encephalopathy is a steroid-responsive associated with elevated titers of antithyroid antibodies. Clinical symptoms are characterized by behavioral and cognitive changes, speech disturbance, seizures, myoclonus, psychosis, hallucination, involuntary movements, cerebellar signs, coma. The standard treatment the use corticosteroids along any concurrent dysthyroidism. Other options immunoglobulins plasmapheresis. We described outcomes on 3 teenage girls encephalopathy. Presenting were...

10.1177/0883073813499823 article EN Journal of Child Neurology 2013-09-20

Summary. We report four cases of occupational asthma caused by chromium salts, three whom showed dual and one isolated early asthmatic responses on specific bronchoprovocation test (BPT). All them were ex–smokers. Two positive skin–prick tests to 10mg/ml Cr 2 (SO 4 ) 3 , but negative results patch testing. The remaining two testing with . Three had airway hyperresponsiveness methacholine initial examination. Although challenge a result in the patient, developed transiently 24 h after an...

10.1111/j.1365-2222.1994.tb00972.x article EN Clinical & Experimental Allergy 1994-07-01

Myopericytoma is a benign neoplasm consisting of cells that appear to have distinct differentiation towards presumed perivascular myoid cells. Amongst myopericytoma, an intravascular variant appears been reported only rarely. A 67‐year‐old man presented with 15‐year history painful, slow growing 3 × 3.5 cm sized mass in the subcutis his right lateral thigh. Histopathological studies showed subcutaneous entirely within lumen vein. The tumor was composed spindle‐shaped myoid‐appearing...

10.1111/j.1440-1827.2010.02628.x article EN Pathology International 2011-01-05

Hyperekplexia is a rare inherited neurologic disorder that characterized by hypertonia and an exaggerated startle response to sudden external stimuli. Until now, 5 genes are known be associated with hyperekplexia: GLRA1, SLC6A5, GLRB, GPHN, ARHGEF9. In this report, we performed clinical genetic analysis of 4 Korean children hyperekplexia. Two patients had typical manifestations hyperekplexia initially were misdiagnosed as epilepsy. Direct sequencing the GLRB GLRA1 revealed 2 novel mutations,...

10.1177/0883073812441058 article EN Journal of Child Neurology 2012-04-24

Many factors affect the cure rate (CR), duration required for complete (DC) and recurrence (RR) of onychomycosis. The aim this study was to evaluate CR, DC RR in onychomycosis according various clinical factors. We retrospectively reviewed medical records 637 Korean patients with between December 2000 2006. examined six effects on RR: age, sex, type, treatment pattern, presence diabetes mellitus (DM) extent nail involvement. On view appearance potassium hydroxide (KOH) preparation, we...

10.1111/j.1439-0507.2010.01928.x article EN Mycoses 2010-07-19

Objectives: The objective of this study was to compare neonatal morbidity and neurologic outcome at 2 years between groups treated with antibiotics regimens consisting clarithromycin erythromycin in preterm premature rupture the membranes (pPROM) patients delivered before 32 weeks gestation.Methods: This a retrospective comparing as primary measures neurological secondary outcome.Results: A total 166 women were included: 80 86 clarithromycin. median gestational age delivery greater group (p...

10.1080/14767058.2016.1243097 article EN The Journal of Maternal-Fetal & Neonatal Medicine 2016-09-30

Pigmented Bowen's disease is characterized by increased melanin pigment in the epidermis or papillary dermis, addition to typical findings of disease.This disorder has been infrequently reported and it represents less than 2% all cases disease.Thus far, there only 1 case pigmented on umbilicus medical literature, no such Korea.Pigmented develops sun-exposed areas face neck, as well sun-unexposed like trunk, extremities, perianal area umbilcus.A 36-year-old man presented with a 9-month...

10.5021/ad.2009.21.2.197 article EN Annals of Dermatology 2009-01-01

Background and Purpose: Rufinamide (RUF) is a novel antiepileptic drug (AED) its efficacy has been proven in Lennox-Gastaut syndrome (LGS).However, there lack of data regarding the pediatric intractable epilepsies other than LGS.The purpose study was to explore tolerability RUF patients with as well LGS.Methods: This retrospective observation conducted Samsung medical center from August 2010 September 2011.Thirty seven (27 males, 10 females, aged between 1.8 18.4 years), refractory or LGS...

10.14581/jer.12009 article EN cc-by-nc Journal of Epilepsy Research 1970-01-01

The purpose of this study is to evaluate the efficacy Q-switched ruby laser in treatment nevus Ota, a pigmented lesion on face. has been shown remove tattoos without scarring. With mind, Ota with cells dermis could be effectively treated laser. Eighty patients (19 men, and 61 women) face were enlisted tested evaluating efficiency therapy. age ranged from 1 62 years. energy fluence used varied 6 8.5 J/cm2. Treatment intervals 4 16 weeks, number sessions between 9 visits. During 2-year...

10.3346/jkms.1996.11.2.165 article EN Journal of Korean Medical Science 1996-01-01

This study was carried out to determine whether slow nail growth is a predisposing factor for onychomycosis or if results in growth. Forty-nine patients with unilateral of the great toenail were enrolled and classified two groups according size affected area, i.e. more than half less toenail. The rates unaffected toenails all measured. Before normal appearance reached, toenails, when area occupied total plate, slower that toenails. After achieved, there no differences between Therefore, this...

10.1111/j.1365-2230.2004.01543.x article EN Clinical and Experimental Dermatology 2004-07-01

Mal de Meleda (MDM), also known as keratoderma palmoplantaris transgrediens, is a rare inherited form of palmoplantar keratoderma.It characterized by erythema and hyperkeratosis the palms soles, extending to dorsal aspects hands feet.A 15-year-old Korean female presented with sharply demarcated hyperkeratotic plaques on which extended surfaces feet, in "glove-and-socks" distribution.The histopathologic study showed marked hyperkeratosis, acanthosis, normogranulosis, without epidermolysis.Her...

10.5021/ad.2011.23.3.396 article EN Annals of Dermatology 2011-01-01

Dowling-Degos disease (DDD) is an autosomal dominant genodermatosis and this a genetically determined disturbance of epidermal proliferation.It characterized by acquired, slowly progressive pigmented lesions that primarily involve the great skin folds flexural areas such as axilla, neck, limb flexures, inframammary area inguinal folds.The vulva unusual location for DDD.A 41-year-old woman presented with 10-year history multiple, small, reticulated brownish macules distributed symmetrically...

10.5021/ad.2011.23.2.205 article EN cc-by-nc Annals of Dermatology 2011-01-01
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