K Demopoulos

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Idiopathic pulmonary fibrosis (IPF) is a specific form of chronic interstitial pneumonia limited to the lung and characterized by a fibroproliferative response with only minor signs of inflammation, which almost always causes rapid fibrotic destruction of the lung. In this study, we investigated genomic instability in IPF, using microsatellite DNA analysis,(More)
Pulmonary sarcoidosis shares certain features with immune disease and neoplasia, and microsatellite DNA alterations are detectable in sputum specimens of pulmonary sarcoidosis patients. The biological basis and significance of these findings remain obscure, while information regarding the genetic basis of the disease is limited. Using multiplex PCR-based(More)
In the present study seven children, aged 5-16 years, who were admitted to the paediatric unit for nephorlithiasis had the 24 hour urinary calcium (UCa), Phosphorus (UP) and magnesium (UMg) excretions 8.2±2.5, 40.9±16.7 and 3.8±2.14 mg/kg, respectively. The UCa to urinary creatinine (UCr) concentration ratio (UCa/UCr), the UP/UCr and the UMg/UCr were 0.30(More)
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