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Assessment of endothelial dysfunction in idiopathic pulmonary fibrosis / Noha Hassan Okasha ; Supervised Mostafa Ibrahim Elshazly , Hossam Hosny Masoad , Abir Zakaria Mohamed

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Noha Hassan Okasha , 2012Description: 157 P. : charts , facsimiles ; 25cmOther title:
  • تقييم الاختلال الوظيفى فى الغشاء المبطن للأوعية الدموية فى مرض التليف الرئوي غير معلوم السبب [Added title page title]
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  • Issued also as CD
Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Chest Diseases and Tuberculosis Summary: 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
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis 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
CD - Rom CD - Rom 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

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