- Pulsatile Compression of StentGraft by Re-pressurizing Aneurysmal Sac With Type III Endoleak After Endovascular Aneurysm Repair: A Case Report
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Oh PC, Jang AY, Kang WC
- KMID: 2530457
- Korean Circ J.
- 2022 Jun;52(6):478-480.
- doi: 10.4070/kcj.2021.0333
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- Echocardiographic Screening Methods for Pulmonary Hypertension: A Practical Review
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Jang AY, Shin MS
- KMID: 2468374
- J Cardiovasc Imaging.
- 2020 Jan;28(1):1-9.
- doi: 10.4250/jcvi.2019.0104
Pulmonary hypertension (PH) is a debilitating condition defined as mean pulmonary arterial pressure (mPAP) ≥ 25 mmHg. The importance of impaired right ventricular (RV) hemodynamics is increasingly being recognized in... -
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- Pulmonary arterial hypertension due to antiphospholipid syndrome initially mimicking chronic thromboembolic pulmonary hypertension
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Yeo J, Shin N, Ahn KJ, Seo M, Jang AY, Kim M, Chung WJ
- KMID: 2527998
- Clin Hypertens.
- 2022;28(1):10.
- doi: 10.1186/s40885-021-00191-1
Pulmonary arterial hypertension (PAH) is the second most common lung complication in antiphospholipid syndrome (APS) patients. However, the concurrent development of APS-related nonthrombotic PAH is rarely reported. Lack of awareness... -
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- Pulmonary Hypertension in Heart Failure
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Jang AY, Park SJ, Chung WJ
- KMID: 2532570
- Int J Heart Fail.
- 2021 Jul;3(3):147-159.
- doi: 10.36628/ijhf.2020.0053
Pulmonary hypertension (PH) is traditionally defined as a mean pulmonary arterial pressure (mPAP) ≥25 mmHg. Although various factors cause PH, the most common etiology is PH due to left heart... -
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- Current status of pulmonary arterial hypertension in Korea
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Jang AY, Chung WJ
- KMID: 2457302
- Korean J Intern Med.
- 2019 Jul;34(4):696-707.
- doi: 10.3904/kjim.2019.185
Pulmonary arterial hypertension (PAH) is characterized by remodeling of the distal pulmonary arteries resulting in high pulmonary vascular resistance and, eventually, right ventricular heart failure. Although current advances in PAH... -
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- Stem Cell and Exosome Therapy in Pulmonary Hypertension
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Oh S, Jung JH, Ahn KJ, Jang AY, Byun K, Yang PC, Chung WJ
- KMID: 2525450
- Korean Circ J.
- 2022 Feb;52(2):110-122.
- doi: 10.4070/kcj.2021.0191
Pulmonary hypertension is a rare and progressive illness with a devastating prognosis. Promising research efforts have advanced the understanding and recognition of the pathobiology of pulmonary hypertension. Despite remarkable achievements... -
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- Association between Smoking and Periodontal Disease in Korean Adults: The Fifth Korea National Health and Nutrition Examination Survey (2010 and 2012)
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Jang AY, Lee JK, Shin JY, Lee HY
- KMID: 2160985
- Korean J Fam Med.
- 2016 Mar;37(2):117-122.
- doi: 10.4082/kjfm.2016.37.2.117
BACKGROUND: This study aimed to evaluate an association between smoking, smoking cessation, and periodontal disease in Korean adults. METHODS: The data were collected from 8,336 participants, aged between 20 and 64... -
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- Binding of the Streptococcus gordonii Surface Glycoprotein Hsa to alpha(2-3) Linked Sialic Acid Residues on Fibronectin
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Jang AY, Lin S, Lim S, Kim DH, Seo HS
- KMID: 1737320
- J Bacteriol Virol.
- 2014 Dec;44(4):317-325.
- doi: 10.4167/jbv.2014.44.4.317
The binding of microorganisms to platelets is a critical step in the development of infective endocarditis. In Streptococcus gordonii, this binding is mediated in part by serine-rich repeat proteins, which... -
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- Valsartan Dosage on Ventriculo-Vascular Coupling Index Dose-Dependency in Heart Failure Patients
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Ahn KJ, Yu J, Jang AY, Kim DH, Kwan J, Chung WJ
- KMID: 2515236
- Yonsei Med J.
- 2021 May;62(5):391-399.
- doi: 10.3349/ymj.2021.62.5.391
Purpose: Heart failure (HF) poses significant morbidity and mortality. Recently, the ventriculo-vascular coupling index (VVI) was introduced as an independent prognostic factor reflective of the overall cardiovascular performance index in... -
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- Cardiac Structural or Functional Changes Associated with CHAâ‚‚DSâ‚‚-VASc Scores in Nonvalvular Atrial Fibrillation: A Cross-Sectional Study Using Echocardiography
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Jang AY, Yu J, Park YM, Shin MS, Chung WJ, Moon J
- KMID: 2429854
- J Cardiovasc Imaging.
- 2018 Sep;26(3):135-143.
- doi: 10.4250/jcvi.2018.26.e17
BACKGROUND: CHA2DS2-VASc is the most widely accepted scoring system for atrial fibrillation (AF) to assess stroke risk, although little has been revealed regarding the accompanying cardiac functional/structural changes. This echocardiography... -
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- Epidemiology of PAH in Korea: An Analysis of the National Health Insurance Data, 2002–2018
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Jang AY, Lee HH, Lee H, Kim HC, Chung WJ
- KMID: 2542301
- Korean Circ J.
- 2023 May;53(5):313-327.
- doi: 10.4070/kcj.2022.0231
Background and Objectives: Pulmonary arterial hypertension (PAH) is a rare but fatal disease. Recent advances in PAH-specific drugs have improved its outcomes, although the healthcare burden of novel therapeutics may... -
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- 15 years journey of idiopathic pulmonary arterial hypertension with BMPR2 mutation
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Ahn KJ, Jang AY, Park SJ, Chung WJ
- KMID: 2468628
- Clin Hypertens.
- 2019 ;25(1):22.
- doi: 10.1186/s40885-019-0127-7
Pulmonary arterial hypertension (PAH) is known as one of diseases with the worst prognosis. Recently, targeted PAH drugs have been developed and approved for use; therefore, the treatment strategy and... -
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- Feasibility and Applicability of Wireless Handheld Ultrasound Measurement of Carotid Intima-Media Thickness in Patients with Cardiac Symptoms
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Jang AY, Ryu J, Oh PC, Moon J, Chung WJ
- KMID: 2468487
- Yonsei Med J.
- 2020 Feb;61(2):129-136.
- doi: 10.3349/ymj.2020.61.2.129
PURPOSE: Routine screening for carotid intima-media thickness (CIMT) and cardiovascular (CV) disease in asymptomatic patients has been criticized for the high costs and large number of patients required for detecting... -
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- A Nationwide multicenter registry and biobank program for deep phenotyping of idiopathic and hereditary pulmonary arterial hypertension in Korea: the PAH platform for deep phenotyping in Korean subjects (PHOENIKS) cohort
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Jang AY, Kim S, Park SJ, Choi H, Oh PC, Oh S, Kim KH, Kim KH, Byun K, Chung WJ, for the PHOENIKS Investigators
- KMID: 2468627
- Clin Hypertens.
- 2019 ;25(1):21.
- doi: 10.1186/s40885-019-0126-8
BACKGROUND: Pulmonary arterial hypertension (PAH) is a progressive, chronic disease without curative treatment. Large registry data of these patient populations have been published, although, phenotypic variants within each subtype of... -
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