Results 61 to 70 of about 275,003 (237)

MRI of the lung (3/3)-current applications and future perspectives [PDF]

, 2011
BACKGROUND: MRI of the lung is recommended in a number of clinical indications. Having a non-radiation alternative is particularly attractive in children and young subjects, or pregnant women.
A Hebestreit, A Kluge, A Kluge, A Kluge, AA Bankier, AC Henderson, AS Brody, BJ Pichler, BJ Pichler, C Fink, C Hintze, C Hintze, C Rieger, CA Yi, CA Yi, CP Heussel, DM Mannino, F Molinari, F Risse, F Santamaria, G Antoch, G Antoch, G Bauman, G Bauman, G Lutterbey, G Lutterbey, G Sergiacomi, H Hatabu, H Zaidi, HF Wehrl, HK Song, HK Song, IL Theissen, J Biederer, J Biederer, J Biederer, J Biederer, J Biederer, J Biederer, J Biederer, J Ley-Zaporozhan, J Ley-Zaporozhan, JC Hogg, K Cederlund, K Sandek, K Suga, K Suga, LP Qi, M Bhalla, M Decramer, M Eichinger, M Gaeta, M Oudkerk, M Puderbach, M Puderbach, M Puderbach, M Puderbach, M Stern, M Wagner, MD Cohen, ND Abolmaali, NJ Morrison, NL Müller, O Ratib, PA Jong de, PA Jong de, PD Stein, PD Stein, R Eibel, R Failo, RE Jacob, RG McFadden, RJ Theilmann, RL Gibson, S Akata, S Montella, S Pauls, SK Alford, T Amundsen, T Iwasawa, T Iwasawa, T Iwasawa, T Mori, T Rupprecht, TA Kuder, TH Helbich, US Euler, V Peltola, W Hirsch, W Lin, Y Berthezène, Y Ohba, Y Ohno, Y Ohno, Y Ohno, Y Ohno, Y Shao   +96 more
core   +1 more source

Senescence of bone marrow-derived mesenchymal stem cells from patients with idiopathic pulmonary fibrosis

Stem Cell Research & Therapy, 2018
Background Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease for which age is the most important risk factor. Different mechanisms associated with aging, including stem cell dysfunction, have been described to participate in the ...
Nayra Cárdenes, Diana Álvarez, Jacobo Sellarés, Yating Peng, Catherine Corey, Sophie Wecht, Seyed Mehdi Nouraie, Swaroop Shanker, John Sembrat, Marta Bueno, Sruti Shiva, Ana L. Mora, Mauricio Rojas   +12 more
doaj   +1 more source

Familial Interstitial Lung Disease in Two Young Korean Sisters [PDF]

, 2005
Most of the interstitial lung diseases are rare, chronic, progressive and fatal disorders, especially in familial form. The etiology of the majority of interstitial lung disease is still unknown. Host susceptibility, genetic and environmental factors may
American Thoracic Society and European Respiratory Society, Amin, Balasubramanyan, Bitterman, Chernick, Chung, Desmarquest, Fan, Hodgson, Hyo-Bin Kim, Ja-Hyung Kim, Jooryung Huh, Ju-Young Jang, Lee, Nogee, Seong-Jong Park, Shulenin, So-Yeon Lee, Solliday, Soo-Jong Hong, Stern, Thomas, Verleden, Whitsett   +23 more
core   +2 more sources

Multidisciplinary-derived clinical score for accurate prediction of long-term mortality in fibrotic lung disease patients

European Journal of Medical Research
Background Idiopathic pulmonary fibrosis (IPF) stands out as one of the most aggressive forms of interstitial lung diseases (ILDs), currently without a definitive cure.
Yu-Wan Liao, Yi-Ming Chen, Ming-Cheng Liu, Yu-Cheng Wu, Chiann-Yi Hsu, Pin-Kuei Fu, Wen-Nan Huang, Yi-Hsing Chen   +7 more
doaj   +1 more source

Performance of pulmonary artery dimensions measured on high-resolution computed tomography scan for identifying pulmonary hypertension

ERJ Open Research, 2020
Background On high-resolution computed tomography (HRCT), pulmonary artery (PA) dimensions may hint at the presence of pulmonary hypertension. We aimed to determine how accurately various measures of the PA, as viewed on HRCT, predict right heart ...
Pailin Ratanawatkul, Andrea Oh, J. Caleb Richards, Jeffrey J. Swigris   +3 more
doaj   +1 more source

Multi-source Transfer Learning with Convolutional Neural Networks for Lung Pattern Analysis [PDF]

, 2016
Early diagnosis of interstitial lung diseases is crucial for their treatment, but even experienced physicians find it difficult, as their clinical manifestations are similar. In order to assist with the diagnosis, computer-aided diagnosis (CAD) systems have been developed. These commonly rely on a fixed scale classifier that scans CT images, recognizes
arxiv   +1 more source

Semantic Segmentation of Pathological Lung Tissue with Dilated Fully Convolutional Networks [PDF]

, 2018
Early and accurate diagnosis of interstitial lung diseases (ILDs) is crucial for making treatment decisions, but can be challenging even for experienced radiologists. The diagnostic procedure is based on the detection and recognition of the different ILD pathologies in thoracic CT scans, yet their manifestation often appears similar.
arxiv   +1 more source

Different features of lung involvement in Niemann-Pick disease and Gaucher disease [PDF]

, 2012
SummaryBackgroundNiemann-Pick disease (NPD) and Gaucher disease (GD) are well-known lysosomal storage diseases. Respiratory system involvement is an important cause of morbidity and mortality in patients with NPD and GD.ObjectivesWe tried to assess the ...
Cinel, Güzin, Ersöz, Deniz Doğru, Gülhan, Bora, Gürakan, Figen, Güçer, Şafak, Kale, Gülsev, Kiper, Nural, Orhan, Diclehan, Yalçın, Ebru, Yüce, Aysel, Özçelik, Uğur   +10 more
core   +1 more source

Desquamative interstitial pneumonia: a systematic review of its features and outcomes

European Respiratory Review, 2020
Background Desquamative Interstitial Pneumonia (DIP) is a rare form of idiopathic interstitial pneumonia (IIP). Data on clinical features, aetiology, prognosis and effect of treatment strategies are limited.
Merel E. Hellemons, Catharina C. Moor, Jan von der Thüsen, Mariska Rossius, Arlette Odink, Laila Haugen Thorgersen, Johny Verschakelen, Wim Wuyts, Marlies S. Wijsenbeek, Elisabeth Bendstrup   +9 more
doaj   +1 more source

Acute Interstitial Pneumonia (Hamman-Rich Syndrome) as a Cause of Idiopathic Acute Respiratory Distress Syndrome [PDF]

, 2011
Hamman-Rich syndrome, also known as acute interstitial pneumonia, is a rare and fulminant form of idiopathic interstitial lung disease. It should be considered as a cause of idiopathic acute respiratory distress syndrome.
Bruminhent, Jackrapong, Pippim, James, Yassir, Shahla   +2 more
core   +3 more sources