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홍윤호 교수

Hong, Yoon-Ho

서울대학교 신경과학교실 · 의학

연구실 소개

홍윤호 교수의 연구실은 신경과학 분야에서 신경근육계 질환과 신경병증의 전기생리학적 평가 및 병태생리학 기전을 중심으로 연구를 진행하고 있습니다. 특히 모터 유닛 수 지수(MUNIX)를 활용한 신경퇴행성질환, 예를 들어 뇌경색성 암모티브 루프병증(ALS)과 혈관성 뇌병변의 전기생리학적 특성 분석에 초점을 맞추고 있으며, 신경계 질환의 유전적 기반과 면역학적 기전에 대해서도 깊이 있는 연구를 수행하고 있습니다. 최근에는 코로나19 백신과 관련된 신경질환, 특히 급성염증성해면성신경병증(GBS)의 임상적 특성에 대한 분석도 포함하고 있습니다.

신경근육질환전기생리학신경병증면역학적 기전신경퇴행성질환

연구 현황

논문 수
222
총 인용 수
3,118
최근 5년 논문
39
주요 분야
의학

연구 성과 추이

표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.

5개년 연도별 논문 게재 수
39총합
2021
2022
2023
2024
2025
5개년 연도별 피인용 수
268총합
20212022202320242025

주요 논문

15
1
논문|인용수 89·2010
Reproducibility of the motor unit number index (MUNIX) in normal controls and amyotrophic lateral sclerosis patients
Suk‐Won Ahn, Suhyun Kim, Jee‐Eun Kim, Sung‐Min Kim, Seung Hyun Kim, Kyung Seok Park, Jung‐Joon Sung, Kwang‐Woo Lee, Yoon‐Ho Hong
SJR Q1FWCI 3.1Muscle & Nerve

The motor unit number index (MUNIX) refers to an electrophysiologic technique that measures the approximate number of motor units using the surface electromyographic interference pattern (SIP) recorded during voluntary contraction. This study was done to assess the reproducibility of MUNIX performed on hypothenar muscles in 62 normal controls and 22 amyotrophic lateral sclerosis (ALS) patients. Inter- and intraoperator correlation coefficients for MUNIX were 0.74 and 0.86, respectively, in norma

NeurologyMedicine
2
논문|인용수 80·2004
Diffusion tensor MRI as a diagnostic tool of upper motor neuron involvement in amyotrophic lateral sclerosis
Yoon‐Ho Hong, Kwang‐Woo Lee, Jung‐Joon Sung, Kee‐Hyun Chang, In Chan Song
SJR Q1FWCI 6.5Journal of the Neurological Sciences
Radiology, Nuclear Medicine and ImagingMedicine
3
논문|인용수 70·2008
Prognosis of ocular myasthenia in Korea: A retrospective multicenter analysis of 202 patients
Yoon‐Ho Hong, Seok-Beom Kwon, Byung‐Jo Kim, Byoung Joon Kim, Seung Hyun Kim, Jong Kuk Kim, Kyung Seok Park, Ki‐Jong Park, Jung‐Joon Sung, Eun Hee Sohn, Yeong‐Bae Lee, Dushin Jeong
SJR Q1FWCI 1.0Journal of the Neurological SciencesOA
NeurologyMedicine
4
논문|인용수 60·1996
Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiency
Yoon‐Ho Hong
SJR Q1FWCI 1.6Human Molecular GeneticsOA

An infant girl with elevated blood lactate, pyruvate, and plasma branched-chain amino acids was diagnosed with dihydrolipoamide dehydrogenase (E3; dihydrolipoamide: NAD+ oxidoreductase, EC 1.8.1.4) deficiency. Activities of the pyruvate dehydrogenase complex and E3 from patient were 26 and 2% of controls in blood lymphocytes, and 11 and 14% in cultured skin fibroblasts, respectively. Western blot analysis demonstrated that the amount of E3 protein in fibroblasts from the patient and her father w

BiochemistryBiochemistry, Genetics and Molecular Biology
5
논문|인용수 49·2022
Guillain–Barré Syndrome and Variants Following COVID-19 Vaccination: Report of 13 Cases
Jee‐Eun Kim, Young Gi Min, Je-Young Shin, Young Nam Kwon, Jong Seok Bae, Jung‐Joon Sung, Yoon‐Ho Hong
SJR Q2FWCI 6.1Frontiers in NeurologyOA

Our observations suggest that COVID-19 vaccines may be associated with GBS of distinctive clinical features characterized by severe quadriplegia, disproportionately frequent bilateral facial palsy or atypical incomplete variants. Continuous surveillance and further studies using robust study designs are warranted to fully assess the significance of the association.

NeurologyMedicine
6
논문|인용수 44·2003
Clinical and electrophysiologic features of HNPP patients with 17p11.2 deletion
Yoon‐Ho Hong, Mi-Kyung Kim, Han‐Joon Kim, J.J. Sung, S. H. Kim, K.-W. Lee
SJR Q1FWCI 1.0Acta Neurologica Scandinavica

HNPP is characterized electrophysiologically by a generalized neuropathy, superimposed by focal entrapment neuropathies. The slowing of sensory conduction in nearly all nerves and the distal accentuation of motor conduction abnormalities are the main features of background polyneuropathy in HNPP. The distribution and severity of the background electrophysiologic abnormalities are closely related to the topography of common entrapment or compression sites, which suggests the possible pathogenetic

Cellular and Molecular NeuroscienceNeuroscience
7
논문|인용수 40·2002
Hemichorea as an initial manifestation of moyamoya disease: Reversible striatal hypoperfusion demonstrated on single photon emission computed tomography
Yoon‐Ho Hong, Tae‐Beom Ahn, Chang Wan Oh, Beom S. Jeon
SJR Q1FWCI 0.7Movement Disorders

We describe a case with unilateral moyamoya disease that showed progressive hemichorea as an initial manifestation. Single photon emission computed tomography showed perfusion defect in the contralateral basal ganglia although magnetic resonance imaging was unremarkable. Hemichorea improved along with normalization of perfusion after bypass surgery, suggestive of striatal hypoperfusion as the cause of hemichorea.

Endocrinology, Diabetes and MetabolismMedicine
8
논문|인용수 36·2018
Myasthenia gravis seronegative for acetylcholine receptor antibodies in South Korea: Autoantibody profiles and clinical features
Kee Hong Park, Patrick Waters, Mark Woodhall, Bethan Lang, Thomas B. Smith, Jung‐Joon Sung, Kwang‐Kuk Kim, Young‐Min Lim, Jee‐Eun Kim, Byung‐Jo Kim, Jin‐Sung Park, Jeong-Geon Lim
SJR Q1FWCI 2.5PLoS ONEOA

Acquired myasthenia gravis (MG) is a prototype autoimmune disease of the neuromuscular junction, caused in most patients by autoantibodies to the muscle nicotinic acetylcholine receptor (AChR). There seem to be ethnic and regional differences in the frequency and clinical features of MG seronegative for the AChR antibody. This study aimed to describe the autoantibody profiles and clinical features of Korean patients with generalized MG seronegative for the AChR antibody. A total of 62 patients w

NeurologyMedicine
9
논문|인용수 35·2011
Frontal Assessment Battery to Evaluate Frontal Lobe Dysfunction in ALS Patients
Suk‐Won Ahn, Suhyun Kim, Jee‐Eun Kim, Sung‐Min Kim, Seung Hyun Kim, Jung‐Joon Sung, Kwang‐Woo Lee, Yoon‐Ho Hong
SJR Q2FWCI 2.1Canadian Journal of Neurological Sciences / Journal Canadien des Sciences NeurologiquesOA

The FAB shows promise as a method of screening for frontal lobe dysfunction in ALS, as it is not only quick and easy, but also reliable. Additional studies should examine how FAB performance changes as ALS progresses.

NeurologyMedicine
10
논문|인용수 32·2008
Soy isoflavones supplementation alleviates disease severity in autoimmune-prone MRL-lpr/lpr mice
Yoon‐Ho Hong, Wang Tc, Huang Cj, W. M. Cheng, Bi‐Fong Lin
SJR Q2FWCI 0.6Lupus

Soy isoflavones supplements, which are phyto-oestrogens widely used as alternatives to alleviate menopausal syndromes or prevent chronic diseases, may exert oestrogenic and anti-oestrogenic activities. This study aimed to investigate the effects of soy isoflavones supplement on oestrogen-related autoimmune disease, such as systemic lupus erythematosus, using autoimmune-prone female MRL-lpr/lpr mice. Eighty mice of 8 weeks were divided into five groups: 0 (Control), 2 (Isf 2), 10 (Isf 10) and 20

Pathology and Forensic MedicineMedicine
11
논문|인용수 28·2023
Small RNA sequencing of circulating small extracellular vesicles microRNAs in patients with amyotrophic lateral sclerosis
Jinah Kim, Canaria Park, Jung‐Joon Sung, Do-Jin Seo, Seok Jin Choi, Yoon‐Ho Hong
SJR Q1FWCI 6.2Scientific ReportsOA

Dysregulation of microRNAs (miRNA) in small extracellular vesicles (sEV) such as exosomes have been implicated in the pathogenesis of amyotrophic lateral sclerosis (ALS). Although circulating cell-free miRNA have been extensively investigated in ALS, sEV-derived miRNAs have not been systemically explored yet. Here, we performed small RNA sequencing analysis of serum sEV and identified 5 differentially expressed miRNA in a discovery cohort of 12 patients and 11 age- and sex-matched healthy contro

NeurologyMedicine
12
논문|인용수 25·2014
Pattern difference of dissociated hand muscle atrophy in amyotrophic lateral sclerosis and variants
Jee‐Eun Kim, Yoon‐Ho Hong, Joon‐Hyung Lee, Suk‐Won Ahn, Sung‐Min Kim, Kyung‐Seok Park, Jung‐Joon Sung, Kwang‐Woo Lee, Seung‐Yong Seong
SJR Q1FWCI 1.9Muscle & Nerve

The absolute ADM/APB CMAP amplitude ratio was not specific for ALS; however, several findings from simple electrophysiological measurements may help predict prognosis in patients with motor neuron diseases and may be early diagnostic markers for ALS.

NeurologyMedicine
13
논문|인용수 22·2008
Diffusion Tensor Tractography‐based Analysis of the Pyramidal Tract in Patients with Amyotrophic Lateral Sclerosis
Yoon‐Ho Hong, Jung‐Joon Sung, Sung‐Min Kim, Kyung‐Seok Park, Kwang‐Woo Lee, Kee‐Hyun Chang, In Chan Song
SJR Q1FWCI 2.5Journal of Neuroimaging

These results suggest, compared with simple ROI analysis, that tract-specific analysis using DTI fiber-tracking is more reliable and sensitive for detecting upper motor neuron pathology in ALS.

Radiology, Nuclear Medicine and ImagingMedicine
14
논문|인용수 22·2014
Neuroprotective effects of JGK-263 in transgenic SOD1-G93A mice of amyotrophic lateral sclerosis
Suk-Won Ahn, Gye Sun Jeon, Myung-Jin Kim, Jee-Heun Shon, Jee‐Eun Kim, Je-Young Shin, Sung‐Min Kim, Seung Hyun Kim, In-Hae Ye, Kwang Woo Lee, Yoon‐Ho Hong, Jung‐Joon Sung
SJR Q1FWCI 1.9Journal of the Neurological Sciences
NeurologyMedicine
15
논문|인용수 21·2009
The ethyl acetate extract of alfalfa sprout ameliorates disease severity of autoimmune-prone MRL-lpr/lpr mice
Yoon‐Ho Hong, Huang Cj, SC Wang, Bi‐Fong Lin
SJR Q2FWCI 0.9Lupus

Previous study showed that soy isoflavone supplement alleviates disease severity in autoimmune-prone mice. As the ethyl acetate extract of alfalfa sprout (AS) has selective oestrogenic and anti-inflammatory activity, this study evaluated the effects of alfalfa sprout ethyl acetate extract (ASEA) on disease severity of systemic lupus erythematosus, using autoimmune-prone female MRL-lpr/lpr mice. In Experiment 1, five groups of 12-week-old female mice were per oral treated with vehicle (control),

ImmunologyImmunology and Microbiology

대표 연구 분야

NeurologyRadiology, Nuclear Medicine and ImagingPathology and Forensic MedicineCellular and Molecular NeurosciencePhysiologyEpidemiology

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