Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nesrin Mogulkoc"'
Autor:
Aysu Sinem Koc, Imren Nesil, Canan Gunduz, Selen Bayraktaroglu, Yasemin Kabasakal, Nesrin Mogulkoc, Zehra Erdemir, Feza Bacakoglu, Pervin Korkmaz Ekren
Publikováno v:
1.5 Diffuse Parenchymal Lung Disease.
Introduction: Our aim was to document the range of collagen vascular disease (CVD)-ILD seen at our department and the impact on survival. Results: Of 620 patients with ILD, 144 were found to have CVD-ILD after multidisciplinary team review (27 male,
Autor:
Selen Bayraktaroglu, Aysu Sinem Koc, Ahmet Uysal, Yasemin Kabasakal, Nesrin Mogulkoc, Ali Veral, Pervin Korkmaz Ekren, Feza Bacakoglu, Imren Nesil
Publikováno v:
1.5 Diffuse Parenchymal Lung Disease.
There is a recognised increased risk but few publications document the frequency of neoplasia in patients with idiopathic pulmonary fibrosis (IPF). We aimed to examine the frequency, nature and outcome of malignant neoplasms in a group of patients wi
Autor:
Biray Ertürk, Nesrin Mogulkoc, Hüseyin Onay, Sanem Nalbantgil, Meral Kayıkçıoğlu, Hakan Kültürsay, Zeynep Mutlu, Ozcan Vuran, Zuhal Eroglu, Hatice Kemal
Publikováno v:
Anatolian Journal of Cardiology
WOS: 000384426300007
PubMed ID: 26645265
Objective: Germline mutations in the bone morphogenetic protein receptor type-2 (BMPR2) gene are considered to be a major risk factor for pulmonary arterial hypertension (PAH). BMPR2 mutations have b
PubMed ID: 26645265
Objective: Germline mutations in the bone morphogenetic protein receptor type-2 (BMPR2) gene are considered to be a major risk factor for pulmonary arterial hypertension (PAH). BMPR2 mutations have b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dc408aa56d433ded0e92eaf01a0f162
https://hdl.handle.net/11454/52560
https://hdl.handle.net/11454/52560
Autor:
Paul N. Bishop, Malcolm I. Burgess, Nesrin Mogulkoc, Rowland J. Bright-Thomas, Simon Ray, Jim J. Egan
Publikováno v:
Journal of the American Society of Echocardiography. 15:633-639
Right ventricular (RV) dysfunction determines prognosis in patients with chronic pulmonary disease. We examined the relative prognostic potential of measures of systolic, diastolic, and global RV function in 87 patients with chronic pulmonary disease
Autor:
Paul W. Bishop, Ali Veral, Jim J. Egan, C. Anthony C. Pickering, Nesrin Mogulkoc, Uülkuü Bayindir
Publikováno v:
Chest. 115:1452-1455
We describe two patients with histologically proven pulmonary Langerhans' cell histiocytosis in whom radiologic improvement occurred following smoking cessation. The patients had 23- and 25-pack-year smoking histories, respectively. High-resolution C
Publikováno v:
Respiratory medicine. 107(3)
WOS: 000316163200016
PubMed ID: 23290153
A 67-year-old woman was referred to our department for further evaluation of her abnormal, chest radiogram. Thorax computed tomography revealed a well-circumscribed, round mass in the middle lobe of
PubMed ID: 23290153
A 67-year-old woman was referred to our department for further evaluation of her abnormal, chest radiogram. Thorax computed tomography revealed a well-circumscribed, round mass in the middle lobe of
Publikováno v:
Journal of clinical rheumatology : practical reports on rheumaticmusculoskeletal diseases. 12(2)
We report a case of anti-Jo-1 syndrome (a rare autoimmune condition that may manifest with various forms of interstitial lung disease), which in our case presented unusually with multiple pulmonary nodules, mimicking carcinoma. She subsequently devel