000 | 01708cam a2200325 a 4500 | ||
---|---|---|---|
003 | EG-GiCUC | ||
008 | 130112s2012 ua dh f m 000 0 eng d | ||
040 |
_aEG-GiCUC _beng _cEG-GiCUC |
||
041 | 0 | _aeng | |
049 | _aDeposite | ||
097 | _aM.Sc | ||
099 | _aCai01.11.06.M.Sc.2012.No.A | ||
100 | 0 | _aNoha Hassan Okasha | |
245 | 1 | 0 |
_aAssessment of endothelial dysfunction in idiopathic pulmonary fibrosis / _cNoha Hassan Okasha ; Supervised Mostafa Ibrahim Elshazly , Hossam Hosny Masoad , Abir Zakaria Mohamed |
246 | 1 | 5 | _aتقييم الاختلال الوظيفى فى الغشاء المبطن للأوعية الدموية فى مرض التليف الرئوي غير معلوم السبب |
260 |
_aCairo : _bNoha Hassan Okasha , _c2012 |
||
300 |
_a157 P. : _bcharts , facsimiles ; _c25cm |
||
502 | _aThesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Chest Diseases and Tuberculosis | ||
520 | _aIPF is defined as a specific form of chronic fibrosing interstitial pneurmonia limited to the lung, with the histopathology of UIP on surgical lung biopsy. Pulmonary hypertension (PH) is frequently seen in patients with IPF and is commonly include endothelial proliferation and medial hypertrophy that exceed those expected in the setting of hypoxia | ||
530 | _aIssued also as CD | ||
653 | 4 | _aBrachial artery flow mediated dilatation | |
653 | 4 | _aEstimated pulmonary artery systolic pressure | |
653 | 4 | _aIPF | |
700 | 0 |
_aAbir Zakaria Mohamed , _eSupervisor |
|
700 | 0 |
_aHossam Hosny Masoad , _eSupervisor |
|
700 | 0 |
_aMostafa Ibrahim Elshazly , _eSupervisor |
|
905 |
_aNazla _eRevisor |
||
905 |
_aSamia _eCataloger |
||
942 |
_2ddc _cTH |
||
999 |
_c41021 _d41021 |