Assessment of endothelial dysfunction in idiopathic pulmonary fibrosis / Noha Hassan Okasha ; Supervised Mostafa Ibrahim Elshazly , Hossam Hosny Masoad , Abir Zakaria Mohamed
Material type:![Text](/opac-tmpl/lib/famfamfam/BK.png)
- تقييم الاختلال الوظيفى فى الغشاء المبطن للأوعية الدموية فى مرض التليف الرئوي غير معلوم السبب [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Date due | Barcode | |
---|---|---|---|---|---|---|---|---|
![]() |
قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.06.M.Sc.2012.No.A (Browse shelf(Opens below)) | Not for loan | 01010110059225000 | |||
![]() |
مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.06.M.Sc.2012.No.A (Browse shelf(Opens below)) | 59225.CD | Not for loan | 01020110059225000 |
Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Chest Diseases and Tuberculosis
IPF 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
Issued also as CD
There are no comments on this title.