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Survival and lung function decline in patients with definite, probable and possible idiopathic pulmonary fibrosis treated with pirfenidone

PloS one, 2022-09, Vol.17 (9), p.e0273854-e0273854

2022

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The European MultiPartner IPF registry (EMPIRE): validating long-term prognostic factors in idiopathic pulmonary fibrosis

Respiratory research, 2020-01, Vol.21 (1), p.11-11, Article 11

2020

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Could Heart Rate Variability Serve as a Prognostic Factor in Patients with Pulmonary Hypertension? A Single-center Pilot Study

Türk Kardiyoloji Derneği arşivi, 2023-10, p.454-463

Musayev, Ogtay

2023

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Efficacy and safety of sildenafil added to pirfenidone in patients with advanced idiopathic pulmonary fibrosis and risk of pulmonary hypertension: a double-blind, randomised, placebo-controlled, phase 2b trial

The lancet respiratory medicine, 2021-01, Vol.9 (1), p.85-95

2021

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A rare tumor of the lung: Pulmonary sclerosing hemangioma (pneumocytoma)

Respiratory medicine, 2013-03, Vol.107 (3), p.448-450

2013

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Comorbidity burden and survival in patients with idiopathic pulmonary fibrosis: the EMPIRE registry study

Respiratory research, 2022-05, Vol.23 (1), p.135-135, Article 135

2022

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Intercostal Artery - Pulmonary Artery Arterio-Arteriolar Fistula: A Case Report

Chest, 2016-10, Vol.150 (4), p.1205A-1205A

2016

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Assessment of right ventricular function in patients with pulmonary arterial hypertension-congenital heart disease and repaired and unrepaired defects: Correlation among speckle tracking, conventional echocardiography, and clinical parameters

Anatolian journal of cardiology, 2020-04, Vol.23 (5), p.277-287

2020

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The DIAMORFOSIS (DIAgnosis and Management Of lung canceR and FibrOSIS) survey: international survey and call for consensus

ERJ open research, 2021-01, Vol.7 (1), p.529-2020

2021

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Interpolation-split: a data-centric deep learning approach with big interpolated data to boost airway segmentation performance

Journal of big data, 2024-12, Vol.11 (1), p.104-30, Article 104

2024

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Pulmonary Hypertension in Interstitial Lung Disease: Ege University Experience

Chest, 2016-10, Vol.150 (4), p.1178A-1178A

2016

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Effects of cardiopulmonary rehabilitation on pulmonary arterial hypertension: A prospective, randomized study

Türkiye fiziksel tip ve rehabilitasyon dergisi, 2019-09, Vol.65 (3), p.278

2019

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Differences in Baseline Characteristics and Access to Treatment of Newly Diagnosed Patients With IPF in the EMPIRE Countries

Frontiers in medicine, 2021-12, Vol.8, p.729203-729203

2021

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Pleuroparenchymal fibroelastosis in idiopathic pulmonary fibrosis: Survival analysis using visual and computer-based computed tomography assessment

EClinicalMedicine, 2021-08, Vol.38, p.101009-101009, Article 101009

2021

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Pulmonary Function in Idiopathic Pulmonary Fibrosis and Referral for Lung Transplantation

American journal of respiratory and critical care medicine, 2001-07, Vol.164 (1), p.103-108

2001

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High dose rate endobronchial brachytherapy in the management of lung cancer: Response and toxicity evaluation in 158 patients

Lung cancer (Amsterdam, Netherlands), 2008-12, Vol.62 (3), p.326-333

2008

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Comparison of echocardiographic markers of right ventricular function in determining prognosis in chronic pulmonary disease

Journal of the American Society of Echocardiography, 2002-06, Vol.15 (6), p.633-639

2002

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Pulmonary arterial hypertension and pregnancy

Journal of research in medical sciences, 2013-01, Vol.18 (1), p.73-76

2013

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Riociguat for idiopathic interstitial pneumonia-associated pulmonary hypertension (RISE-IIP): a randomised, placebo-controlled phase 2b study

The lancet respiratory medicine, 2019-09, Vol.7 (9), p.780-790

2019

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Hypersensitivity pneumonia in a schoolchild admitted to the hospital's asthma clinic

Turkish journal of pediatrics, 2015-09, Vol.57 (5), p.529-532

2015

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Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis

American journal of respiratory and critical care medicine, 2019-07, Vol.200 (2), p.199-208

2019

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Sarcoidosis Presenting with Membranous Nephropathy in a Patient with Hypertensive Nephropathy: Case Report

Turk nefroloji dializ ve transplantasyon dergisi, 2015-01, Vol.24 (3)

2015

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Survival and lung function decline in patients with definite, probable and possible idiopathic pulmonary fibrosis treated with pirfenidone

The European MultiPartner IPF registry (EMPIRE): validating long-term prognostic factors in idiopathic pulmonary fibrosis

Could Heart Rate Variability Serve as a Prognostic Factor in Patients with Pulmonary Hypertension? A Single-center Pilot Study

Efficacy and safety of sildenafil added to pirfenidone in patients with advanced idiopathic pulmonary fibrosis and risk of pulmonary hypertension: a double-blind, randomised, placebo-controlled, phase 2b trial

A rare tumor of the lung: Pulmonary sclerosing hemangioma (pneumocytoma)

Comorbidity burden and survival in patients with idiopathic pulmonary fibrosis: the EMPIRE registry study

Intercostal Artery - Pulmonary Artery Arterio-Arteriolar Fistula: A Case Report

Assessment of right ventricular function in patients with pulmonary arterial hypertension-congenital heart disease and repaired and unrepaired defects: Correlation among speckle tracking, conventional echocardiography, and clinical parameters

The DIAMORFOSIS (DIAgnosis and Management Of lung canceR and FibrOSIS) survey: international survey and call for consensus

Interpolation-split: a data-centric deep learning approach with big interpolated data to boost airway segmentation performance

Diagnosis and Treatment Patterns of Chronic Thromboembolic Pulmonary Hypertension in Russia, Kazakhstan, Turkey, Lebanon, and Saudi Arabia: A Registry Study

Pulmonary Hypertension in Interstitial Lung Disease: Ege University Experience

Effects of cardiopulmonary rehabilitation on pulmonary arterial hypertension: A prospective, randomized study

Differences in Baseline Characteristics and Access to Treatment of Newly Diagnosed Patients With IPF in the EMPIRE Countries

Delineating associations of progressive pleuroparenchymal fibroelastosis in patients with pulmonary fibrosis

Pleuroparenchymal fibroelastosis in idiopathic pulmonary fibrosis: Survival analysis using visual and computer-based computed tomography assessment

Pulmonary Function in Idiopathic Pulmonary Fibrosis and Referral for Lung Transplantation

Mortality in combined pulmonary fibrosis and emphysema patients is determined by the sum of pulmonary fibrosis and emphysema

High dose rate endobronchial brachytherapy in the management of lung cancer: Response and toxicity evaluation in 158 patients

Comparison of echocardiographic markers of right ventricular function in determining prognosis in chronic pulmonary disease

Pulmonary arterial hypertension and pregnancy

Riociguat for idiopathic interstitial pneumonia-associated pulmonary hypertension (RISE-IIP): a randomised, placebo-controlled phase 2b study

Hypersensitivity pneumonia in a schoolchild admitted to the hospital's asthma clinic

Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis

Sarcoidosis Presenting with Membranous Nephropathy in a Patient with Hypertensive Nephropathy: Case Report

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