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Progressive Familial Intrahepatic Cholestasis Type 3: a Novel Mutation in a Saudi Child
Faculty
Medicine
Year:
2013
Type of Publication:
ZU Hosted
Pages:
Authors:
Laila Metwally Ibrahim Sharif
Staff Zu Site
Abstract In Staff Site
Journal:
Journal of gastroentrology and Hepatology research W
Volume:
Keywords :
Progressive Familial Intrahepatic Cholestasis Type , , Novel Mutation
Abstract:
Progressive familial intrahepatic cholestasis type 3 (PFIC3) is caused by defects in ABCB4 gene. Liver histology although important, but is nonspecific, and molecular genetic testing is essential for diagnosis. To report PFIC3 in a Saudi
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Laila Metwally Ibrahim Sharif, "18. Factors associated with delayed cancer diagnosis in egyptian children.", Clin Med Insights Pediatr, 2015
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Laila Metwally Ibrahim Sharif, "serum trace elements in obese Egyptian children: a case -control study", BioMed Centr, 2014
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Laila Metwally Ibrahim Sharif, "Biomarkers and early detection of late onset anthracycline-induced cardiotoxicity in children", W.S.&son Ltd 2012, 2012
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Laila Metwally Ibrahim Sharif, "Diarrhea in neutropenic children with cancer: An Egyptian center experience, with emphasis on neutropenic enterocolitis", w, 2012
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Department Related Publications
Ashgan Abdallah Abdelaal, "HAEMORATHROTHRO PATHY SCORE IN HAEMOPHILIA", لايوجد, 1900
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Doaa Youssef Mohamed, "Out come of children treated with Hemodialysis for chronic kidney disease in nephrology unit Zagazig University, Egypt, 9 year single center experience NULL NULL NULL", لايوجد, 1900
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Tarek Abdelrahman Mohamed Attia, "الانيما ونقل كرات الدم الحمراء بؤحدة العناية المركزة بالطفال", لايوجد, 1900
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Laila Raslan AbdulAziz, "تقييم سمية الصفراء كريات الدم الحمراء وانعكاساتها على معالجة الصفراء الوليدية", لايوجد, 1900
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Laila Raslan AbdulAziz, "دراسة عن الموت المبرمج للخلايا والفاس المذاب ومستقبل انترلوكين -2 فى الاطفال المصابين بالاورام الليمفاوية الغير هودجكن ", لايوجد, 1900
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