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Serum surfactant protein D as a prognostic factor idiopathic pulmonary fibrosis patients / Haidi Abdallah Abuhussein ; Supervised Dawlat Elmiligy , Laila Ahmed Rashed , Mohamed Wafai Zakaria

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Haidi Abdallah Abuhussein , 2011Description: 106 P. : charts , facsimiles ; 25cmOther title:
  • مصل بروتين (د) الخافض للتوتر السطحى كعامل تنبؤى لمرضى التليف الرئوى مجهول 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 Medical Biochemistry Summary: Pulmonary fibrosis (PF) is defined as aspecific form of chronic fibrosing interstitial pneumonia that is limited to the lung and associated with the histological appearance of UIP on a surgical lung biopsy . The diagnosis of IPF can only be made after the exclusion of other known causes of interstitial lung disease such as drug toxicities environmental exposures and collagen vascular diseases
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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 Cai01.11.03.M.Sc.2011.Ha.S (Browse shelf(Opens below)) Not for loan 01010110055513000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.03.M.Sc.2011.Ha.S (Browse shelf(Opens below)) 55513.CD Not for loan 01020110055513000

Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Medical Biochemistry

Pulmonary fibrosis (PF) is defined as aspecific form of chronic fibrosing interstitial pneumonia that is limited to the lung and associated with the histological appearance of UIP on a surgical lung biopsy . The diagnosis of IPF can only be made after the exclusion of other known causes of interstitial lung disease such as drug toxicities environmental exposures and collagen vascular diseases

Issued also as CD

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