Results 191 to 200 of about 182,666 (399)

Chronic extrinsic allergic alveolitis in a family with idiopathic pulmonary fibrosis: the importance of histological diagnosis [PDF]

, 1992
PL van Valenberg, JW Lammers, HA van den Hout, Johan Molema, CL van Herwaarden   +4 more
openalex   +1 more source

Proceedings: Regenerative Medicine for Lung Diseases: A CIRM Workshop Report. [PDF]

, 2017
The mission of the California Institute of Regenerative Medicine (CIRM) is to accelerate treatments to patients with unmet medical needs. In September 2016, CIRM sponsored a workshop held at the University of California, Los Angeles, to discuss ...
DeWitt, Natalie D, Gomperts, Brigitte, Kadyk, Lisa C   +2 more
core   +1 more source

Familial Interstitial Pulmonary Fibrosis: A Large Family with Atypical Clinical Features

Canadian Respiratory Journal, 2010
A large kindred of familial pulmonary fibrosis is reported. Six members from the first two generations of this particular kindred were described more than 40 years previously; six more individuals from the third and fourth generations have also been ...
Ranji Chibbar, John A Gjevre, Francis Shih, Heather Neufeld, Edmond G Lemire, Derek A Fladeland, Donald W Cockcroft   +6 more
doaj   +1 more source

CIResDiff: A Clinically-Informed Residual Diffusion Model for Predicting Idiopathic Pulmonary Fibrosis Progression [PDF]

arXiv
The progression of Idiopathic Pulmonary Fibrosis (IPF) significantly correlates with higher patient mortality rates. Early detection of IPF progression is critical for initiating timely treatment, which can effectively slow down the advancement of the disease. However, the current clinical criteria define disease progression requiring two CT scans with
arxiv  

4D VQ-GAN: Synthesising Medical Scans at Any Time Point for Personalised Disease Progression Modelling of Idiopathic Pulmonary Fibrosis [PDF]

arXiv
Understanding the progression trajectories of diseases is crucial for early diagnosis and effective treatment planning. This is especially vital for life-threatening conditions such as Idiopathic Pulmonary Fibrosis (IPF), a chronic, progressive lung disease with a prognosis comparable to many cancers.
arxiv  

Idiopathic Pulmonary Hilar Fibrosis: An Unusual Cause of Pulmonary Hypertension [PDF]

, 1993
Raúl E. Espinosa, William D. Edwards, Edward C. Rosenow, Hartzell V. Schaff   +3 more
openalex   +1 more source

Bronchiolitis obliterans. [PDF]

, 1989
Bronchiolitis obliterans in the adult patient is a relatively uncommon and vexing clinical entity. This confusion results because this pathologic finding occurs in a variety of diverse clinical settings.
King, TE
core  

Familial restrictive cardiomyopathy with novel missense variant of uncertain significance in the FLNC gene

ESC Heart Failure, EarlyView.
Ryo Nakayama, Toshikazu D. Tanaka, Shunsuke Inoue, Jun Yoshida, Jun Hasegawa, Tomohisa Nagoshi, Seitaro Nomura, Hiroyuki Morita, Michihiro Yoshimura   +8 more
wiley   +1 more source

Regulation of the terminal complement cascade in adipose tissue for control of its volume, cellularity, and fibrosis

Obesity, EarlyView.
Abstract White adipose tissue (WAT) is a reservoir for various pathogens and their products, such as lipopolysaccharides. Therefore, it must be equipped with a defense mechanism connected with the activation of innate immunity. This explains the phenomenon that adipocytes express components of the classical and alternative complement pathways, which ...
Ilja L. Kruglikov, Philipp E. Scherer
wiley   +1 more source

Effect of lung T lymphocytes on fibroblasts in idiopathic pulmonary fibrosis and extrinsic allergic alveolitis. [PDF]

, 1990
Moisés Selman, Georgina González-Ávila, María Gabriela Espinoza Bravo, J Sullivan-Lopez, Carlos Ramos, Martha Montaño, Nora Barquín, Felipe Vadillo‐Ortega   +7 more
openalex   +1 more source