Search Results - Laila M. Sherief
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1
Case Report: Dubin-Johnson Syndrome Presenting With Infantile Cholestasis: An Overlooked Diagnosis in an Extended Family by Naglaa M. Kamal, Omar Saadah, Hamdan Alghamdi, Ali Algarni, Mortada H. F. El-Shabrawi, Laila M. Sherief, Salma A. S. Abosabie
Published 2022Call Number: Loading…Connect to this object online.
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2
Novel homozygous mutation of PNLIP gene in congenital pancreatic lipase deficiency: an extended family study by Naglaa M. Kamal, Omar I. Saadah, Shahad S. Alheraiti, Ruwayd Attar, Asmaa D. Alsufyani, Moratda H.F. El-Shabrawi, Laila M. Sherief
Published 2022Call Number: Loading…Connect to this object online.
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3
CMV, B and C hepatitis among multi-transfused hereditary hemolytic Anemia children: an updated Egyptian experience by Laila M. Sherief, Seham M. Ragab, Mohamed A. Helwa, Naglaa M. Kamal, Mona R. Afify, Rasha T. S. Mohammed, Ghada Abd Elmoniem Mokhtar, Hanan S. Sherbiny
Published 2021Call Number: Loading…Connect to this object online.
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4
Factor VIII inhibitor development in Egyptian hemophilia patients: does intron 22 inversion mutation play a role? by Laila M. Sherief, Osama A. Gaber, Hala Mosaad Youssef, Hanan S. Sherbiny, Wesam a Mokhtar, Asmaa A. A. Ali, Naglaa M. Kamal, Yehia H. Abdel Maksoud
Published 2020Call Number: Loading…Connect to this object online.
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5
Persistent Hypertransaminasemia Uncovered Occult Limb-Girdle-Muscle Dystrophy-Type-2C in a Saudi Child by Naglaa M. Kamal, Hamed A. Alghamdi, Abdulrahman Halabi, Abdullah O. Alharbi, Muhammad Rafique, Kamel Abidi, Mortada H.H. El-Shabrawi, Ayman E. Eskander, Hala Mansour, Laila M. Sherief
Published 2018Call Number: Loading…Connect to this object online.
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6
Validity of serum and urinary hepcidin as biomarkers for late-onset sepsis in premature infants by Hanan Sakr Sherbiny, Hanaa Abdel-el Fattah Mostafa, Laila M. Sherief, Naglaa M. Kamal, Amal Saeed El-Shal, Mahmoud Mohamed Abdel-el Halm, Hekmat Yaqoub Khan, Al Shaymaa Ahmed Ali
Published 2022Call Number: Loading…Connect to this object online.
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7
Serum endocan and endothelial dysfunction in childhood acute lymphoblastic leukemia survivors: a tertiary center experience by Laila M. Sherief, Elhamy R. Abd El-khalek, Ibrahim A. Libda, Osama A. Gaber, Naglaa M. Kamal, Basma K. Soliman, Wesam A. Mokhtar, Ghada A. Mokhtar, Hosam E. Salah, Gehad M. Kamar, Marwa Zakaria
Published 2021Call Number: Loading…Connect to this object online.
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8
Egyptian Pediatric Guidelines for the Management of Children with Isolated Thrombocytopenia Using the Adapted ADAPTE Methodology-A Limited-Resource Country Perspective by Galila Mokhtar, Ashraf Abdelbaky, Amira Adly, Dina Ezzat, Gehan Abdel Hakeem, Hoda Hassab, Ilham Youssry, Iman Ragab, Laila M. Sherief, Marwa Zakaria, Mervat Hesham, Niveen Salama, Nouran Salah, Rasha A. A. Afifi, Rasha El-Ashry, Sara Makkeyah, Sonia Adolf, Yasser S. Amer, Tarek E. I. Omar, James Bussel, Eman Abd El Raouf, Mervat Atfy, Mohamed Ellaboudy, Ivan Florez
Published 2024Call Number: Loading…Connect to this object online.
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9
Prevalence of iron deficiency anemia and beta thalassemia carriers among relatives of beta thalassemia patients in Nile Delta region, Egypt: a multicenter study by Mohamed R. El-Shanshory, Laila M. Sherief, Hoda M. Hassab, Seham M. Ragab, Sohier Yahia, Ahmed K. Mansour, Adel S. Ahmed, Said H. Abdou, Amal M. Helmy, Mona M. Watany, Ahmed M. Gad ALllah, Myriam A. Guindy, Zeinab I. Mourad, Mohamed A. Soliman, Reham M. El-Farahaty, Faeza El-Dahtory, Ahmad Darwish, Suzy Abd Elmabood, Ibrahim A. Kabbash, Shimaa M. Saied
Published 2021Call Number: Loading…Connect to this object online.
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