Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

213 results
Display

Speckle Tracking Imaging in Patients with Pulmonary Hypertension

Prieto O, Cianciulli TF, Stewart-Harris A, Rodriguez A, Saccheri MC, Lax JA, Kazelián LR, Argento LV, Marambio GM, Gagliardi JA

BACKGROUND: Right ventricular (RV) systolic dysfunction is a strong predictor of mortality in pulmonary hypertension (PH). The goal of this study was to investigate whether right atrium (RA) and RV...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pulmonary hypertension in patients with Philadelphia-negative myeloproliferative neoplasms: a single-center retrospective analysis of 225 patients

Lee MW, Ryu H, Choi YS, Song IC, Lee HJ, Yun HJ, Sun BJ, Jeong JO, Jo DY

Background The prevalence of pulmonary hypertension (PH) in myeloproliferative neoplasms (MPNs) varies among studies. We analyzed the prevalence of PH in Korean patients with Philadelphia-negative (Ph-) MPNs. Methods Medical records of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinical Status of Inhaled Nitric Oxide Treatment in Infants with Persistent Pulmonary Hypertension of the Newborn in Korea: Post-Marketing Surveillance Results

Ha J, Lee EH, Park HK, Choi BM

Purpose: Inhaled nitric oxide (iNO) is a potent selective pulmonary vasodilator and an important treatment for newborn infants with hypoxic respiratory failure due to persistent pulmonary hypertension of the newborn...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Coronary Stent Fracture in a Patient with an Atrial Septal Defect and Severe Pulmonary Hypertension

Leong MC, Darshinee J

A 38-year-old female with an atrial septal defect and severe pulmonary hypertension presented with angina. Coronary angiogram revealed compression of the proximal left main stem coronary artery. A coronary stent...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Fatal progressive right heart failure in a pancreatic cancer patient

Byoun JT, Cho JY

Pulmonary tumor thrombotic microangiopathy (PTTM) is a rare but fatal complication of cancer and causes pulmonary hypertension and acute/subacute right heart failure. PTTM is most commonly associated with gastric cancer...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Natural courses and prognostic factors of pulmonary underdevelopment except for congenital diaphragmatic hernia

Kim MS, Choi YJ, Lee Sh, Kim WS, Suh DI, Kim MJ

Purpose: Pulmonary underdevelopment is one of the pulmonary causes of neonatal mortality, which is categorized into pulmonary agenesis, pulmonary aplasia, and pulmonary hypoplasia. Congenital diaphragmatic hernia is a well-known cause...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Echocardiographic Screening Methods for Pulmonary Hypertension: A Practical Review

Jang AY, Shin MS

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Emergency Pulmonary Artery–to-Systemic Artery Shunt to Break the Positive Feedback Loop of a Pulmonary Hypertensive Crisis after Neonatal Coarctation Repair

Shin YR, Yang YH, Park YH, Park HK

A 2.5-kg neonate with coarctation of the aorta and a small left ventricle experienced a severe pulmonary hypertensive crisis. An emergency pulmonary artery-to-systemic artery shunt was placed to break the...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pulmonary Hypertension in Newborn Infants with Vein of Galen Malformation

Song WS, Oh MY, Cho JY, Kim CY, Suh DC, Jung E, Kim EA, Kim KS, Lee BS

OBJECTIVE: Vein of Galen malformation (VGM) is a rare cerebrovascular malformation. Children with VGM presenting in newborn period demonstrate various clinical courses from normal development to severe neurologic impairment or...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Central extracorporeal membrane oxygenation and early rehabilitation for persistent severe pulmonary hypertension following pulmonary endarterectomy

Seong GM, Hong SB, Huh JW, Lim CM, Koh Y, Lee JW, Jung SH, Park DW, Lee JS

Chronic thromboembolic pulmonary hypertension is potentially curable with a pulmonary endarterectomy. However, approximately 20% of patients have persistent pulmonary hypertension after pulmonary endarterectomy, which is a major risk factor for...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Sudden Death due to Rupture of Pulmonary Trunk Aneurysm in a Patient with Eisenmenger Syndrome

Kim SZ, Lee S

Proximal pulmonary artery aneurysms and dissection are rare and life-threatening conditions, which are usually detected only during autopsy examination in cases of sudden death. These pathological entities often occur as...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Involvement of immune responses in pulmonary arterial hypertension; lessons from rodent models

Kim K, Choi JH

Pulmonary hypertension (PH) is a pathological state with sustained elevation of pulmonary artery (PA) pressure. Since the pathogenesis of PH is mostly irreversible, the disease often comes up with poor...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Improvement of Left Ventricular Ejection Fraction and Pulmonary Hypertension Are Significant Prognostic Factors in Heart Failure with Reduced Ejection Fraction Patients

Kwon HJ, Park JH, Park JJ, Lee JH, Seong IW

BACKGROUND: We evaluated long-term prognosis according to improvement of pulmonary hypertension (PH) and left ventricular ejection fraction (LVEF) in patients with heart failure with reduced ejection fraction (HFrEF) and PH. METHODS:...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Reversibility of Pulmonary Hypertension Following Surgical Atrial Septal Defect Closure in Children with Down Syndrome

Lee JS, Cha SG, Kim GB, Lee SY, Song MK, Kwon HW, Bae EJ, Kwak JG, Kim WH, Lee JR

BACKGROUND: Many Down syndrome (DS) patients have an atrial septal defect (ASD) and associated pulmonary hypertension (PH) from early childhood. ASD closure in DS patients with PH is often controversial...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Hemodynamic and Histopathologic Benefits of Early Treatment with Macitentan in a Rat Model of Pulmonary Arterial Hypertension

Kim KH, Kim HK, Chan SY, Kim YJ, Sohn DW

BACKGROUND AND OBJECTIVES: Macitentan (MAC) reduces morbidity and mortality among advanced-stage pulmonary arterial hypertension (PAH) patients. However, data regarding the histopathologic and hemodynamic benefits of MAC treatment at an early...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinical Characteristics, Presentation, and Outcomes of Bronchopulmonary Dysplasia-Associated Pulmonary Hypertension

Kim DH, Kim HS

Bronchopulmonary dysplasia-associated pulmonary hypertension (BPD-PH) is increasingly being recognized as a cause of morbidity and mortality in preterm infants. Recently, BPD-PH has also been shown to have additional long-term negative...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pulmonary Hypertension in Connective Tissue Disease is Associated with the New York Heart Association Functional Class and Forced Vital Capacity, But Not with Interstitial Lung Disease

Jung JY, Lee CH, Kim HA, Choi ST, Lee JH, Yoon BY, Kang DR, Suh CH

OBJECTIVE: Pulmonary hypertension (PH) develops frequently in connective tissue diseases (CTD) and is an important prognostic factor. The aim of this study was to assess the prevalence of PH in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Angiotensin-(1-9) ameliorates pulmonary arterial hypertension via angiotensin type II receptor

Cha SA, Park BM, Kim SH

Angiotensin-(1-9) [Ang-(1-9)], generated from Ang I by Ang II converting enzyme 2, has been reported to have protective effects on cardiac and vascular remodeling. However, there is no report about...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinical Presentation with High Penetrance in a Korean Family with Pulmonary Arterial Hypertension Associated with a BMPR2 Intron 3 Splice Site Pathogenic Variant

Kim MJ, Lee S, Jekarl DW, Chae H, Kim M, Jung HO, Jeon DS

Pathogenic variants of bone morphogenic protein receptor type 2 gene (BMPR2) are related to the majority of cases of heritable pulmonary arterial hypertension (PAH). Over 400 pathogenic variants have been...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Anesthetic Management for Elective Total Hip Replacement Arthoroplasty in a Patient with Eisenmenger's Syndrome

Chung J, Park J, Seo Y, Gong H

Eisenmenger's syndrome describes the elevation of pulmonary arterial pressure to the systemic level caused by an increased pulmonary vascular resistance with reversed or bi-directional shunt through an intracardiac or aortopulmonary...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2021 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr