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ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS AS A CAUSE OF BRONCHIAL ASTHMA IN CHILDREN
Faculty
Medicine
Year:
2012
Type of Publication:
ZU Hosted
Pages:
Authors:
Manal Mohamed Djerbi Younis
Staff Zu Site
Abstract In Staff Site
Journal:
The Egyptian Journal Of Pediatric allergy and immunology EGYPT
Volume:
Keywords :
ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS , , CAUSE OF BRONCHIAL ASTHMA
Abstract:
Allergic pulmonary aspergillosis (ABPA) occurs in patients with asthma and cystic fibrosis " when aspergillus fumigatus spores are inhaled they grow in bronchial mucous as hyphae. It occur in immunocompromised and belong to hyprsesitivity
Author Related Publications
Manal Mohamed Djerbi Younis, "evaluation of analytical performance of hcv core antigen for hcv screening in blood donors", EGYPT, 2012
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Manal Mohamed Djerbi Younis, "Helicobacter pylori infection and its response to treatment in diabetic patients versus non diabetics", EGYPT, 2013
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Manal Mohamed Djerbi Younis, "Splenic Irradiation in the Treatment of Hypersplenism from Congestive Splenomegaly", britain, 2012
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Manal Mohamed Djerbi Younis, "Hepatitis C Virus Reactivation in Patients with Heamatological Malignancies, Single Egyptian Center Study", EGYPT, 2013
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Manal Mohamed Djerbi Younis, "FRAILTY: IDENTIFICATION AND MARKERS", Britain, 2012
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Rania Ahmed Khalil Ghonem, "Oxidative Stress Levels in Relation to Vitiligo Severity and Activity مستويات الإجهاد التاكسدى بالنسبة لشدة ونشاط البهاق", Acta Scientific MEDICAL SCIENCES, 2022
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Hanan Samer Ahmed Mouhamd, "Genetic polymorphism of methylenetetrahydrofolate reductase is associated with insulin resistance in Egyptian women with polycystic ovary syndrome", John Wiley & Sons, Ltd., 2019
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Mage Munir Hussein Fawzi, "A Comparative Study of MALDI-TOF MS and VITEK2 for Identification of Aerobic Gram Positive and Yeast Strains Isolated in Clinical Microbiology Laboratory", Egyptian Society of Medical Microbiology, 2019
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Mei Mahmoud Samy Ibraheem, "The Expression Level of Long Non-Coding RNA PVT1 as a Diagnostic Marker for Advanced Stages in Patients with Nonalcoholic Fatty Liver Disease", The Egyptian Journal of Hospital Medicine, 2022
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Doaa Metwally Abdelmoniem, "Relation between mutations in the 5′ UTR of ANKRD26 gene and inherited thrombocytopenia with predisposition to myeloid malignancies. An Egyptian study العلاقة بين طفرات جين ANKRD26 و نقص الصفائح الدموية الوراثي مع قابلية حدوث سرطانات الدم الميلودية: دراسـة مصريــة", Platelets, 2021
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