Results 171 to 180 of about 195,645 (350)
Idiopathic Pulmonary Hilar Fibrosis: An Unusual Cause of Pulmonary Hypertension [PDF]
, 1993 Raúl E. Espinosa +3 more
openalex +1 more source
Telomerase and idiopathic pulmonary fibrosis
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 2012 Idiopathic pulmonary fibrosis (IPF) is the most common manifestation of telomere-mediated disorders. Germline mutations in the essential telomerase genes, hTERT and hTR, are the causal genetic defect in up to one-sixth of pulmonary fibrosis families. The presence of telomerase mutations in this subset is significant for clinical decisions as affected ...
openaire +3 more sources
iLABMED, EarlyView.Extrachromosomal circular DNA (eccDNA) has quite recently turned out to be a cardinal component in cardiovascular diseases (CVD), governing the gene expression and mechanisms of disease causation. Studies indicated an upregulation of eccDNA in pulmonary arterial hypertension (PAH), which makes it strikingly potential as a sensitive and specific ...
Saim Mahmood Khan +6 more
wiley +1 more source
First report of multinodular pulmonary fibrosis associated with equine herpesvirus 5 in Belgium [PDF]
, 2010 A 20-year-old horse was evaluated for symptoms of weight loss, anorexia, fever and lethargy. Clinical examination revealed tachypnea, poor body condition and increased breath sounds on auscultation. Ultrasound showed multiple consolidations on the lungs.
Borchers, K +6 more
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Dyskeratosis Congenita Associated Non-Specific Interstitial Pneumonia [PDF]
Journal of Krishna Institute of Medical Sciences University, 2017 Dyskeratosis Congenita (DC) is a rare inherited disorder of ectodermal dysplasia. It consists of a classical mucocutaneous triad of abnormal skin pigmentation, nail dystrophy and leukoplakia. Pulmonary disease is seen in 10-15%.
Unnati D. Desai , Jyotsna M. Joshi
doaj
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 +6 more
doaj +1 more source
Idiopathic nonspecific interstitial pneumonia/fibrosis: comparison with idiopathic pulmonary fibrosis and BOOP [PDF]
, 1998 Shuntaro Nagai +5 more
openalex +1 more source
Journal of Magnetic Resonance Imaging, EarlyView.ABSTRACT The aging of the world population gave rise to an increased prevalence of many lung diseases, with chronic obstructive pulmonary disease now ranking as the third‐leading cause of death according to the World Health Organization. To diagnose lung disease, a thorough assessment of lung function is essential since it may reveal unique signatures ...
Agilo L. Kern +4 more
wiley +1 more source
Transcriptomic Features of Recurrence Rates in Idiopathic Subglottic Stenosis
The Laryngoscope, EarlyView.Idiopathic subglottic stenosis (iSGS) is a rare disease that can lead to potentially life‐threatening shortness of breath. For most patients, iSGS is a chronic, recurrent disease, and rates of recurrence can differ markedly between patients. Using RNA sequencing, we found that patients with high recurrence rates exhibited transcriptional markers of an ...
Shengjie Ying +20 more
wiley +1 more source