Role of reticulocyte haemoglobin content in diagnosis of iron deficiency anaemia by Badr, Mohamed, Elashkar, Shaimaa, Ismail, Weaam, Abozid, Asmaa, Hanna, Dianna

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Association of vitamin D receptor gene FokI polymorphism and susceptibility to CAP in Egyptian children: a multicenter study by Abouzeid, Heba, Abdelaal, NourEldin M., Abdou, Mohammed A., Mosabah, Amira A. A., Zakaria, Mervat T., Soliman, Mohammed M., Sherif, Ashraf M., Hamed, Mohammed E., Soliman, Attia A., Noah, Maha A., Khalil, Atef M., Hegab, Mohamed S., Abdel-Aziz, Alsayed, Elashkar, Shaimaa S. A., Nabil, Rehab M., Abdou, Adel M., Al-Akad, Ghada M., Elbasyouni, Hany A. A.

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Ficolin‐1 gene (FCN1) −144 C/A polymorphism is associated with adverse outcome of severe pneumonia in the under‐five Egyptian children: A multicenter study by Elkoumi, Mohamed A., Abdellatif, Sawsan H., Mohamed, Faisal Y., Sherif, Ahmed H., Elashkar, Shaimaa S. A., Saleh, Rabab M., Boraey, Naglaa F., Abdelaal, NourEldin M., Akeel, Nagwa E., Elhewala, Ahmed A., Mosbah, Amira A., Zakaria, Mervat T., Soliman, Mohammed M., Salah, Ahmed, Sedky, Yasser M., Sobieh, Alaa A., Mashali, Mohamed H., Waked, Nevin M., Elshreif, Anas M., Hafez, Sahbaa F., Hashem, Mustafa I. A., Shehab, Mohamed M., Soliman, Attia A., Emam, Ahmed A., Ahmed, Abdelrahman A. A., Fahim, Mohamed S., Elshehawy, Naglaa A., Abdel‐Aziz, Marwa M., Abdou, Adel M., El‐Shehawy, Ahmed A., Youssef, Manal A. A., Fahmy, Dalia S., Malek, Mai M., Osman, Sherif F., Ibrahim, Mohamed A. M., Alanwar, Mohamed I., Zeidan, Nancy M. S.

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Angiotensin‐converting enzyme insertion/deletion gene polymorphism in Egyptian children with CAP: A case‐control study by Abouzeid, Heba, Alkholy, Usama M., Abdou, Mohammed A., Morsy, Saeed M., Abdelrahman, Hind M., Sherif, Ashraf M., Abdalmonem, Nermin, Hamed, Mohammed E., Allah, Mayy A.N., Al Morshedy, Salah, Elashkar, Shaimaa S.A., Noah, Maha A., Hegab, Mohamed S., Akeel, Nagwa E., Hashem, Mustafa I.A., Gawish, Heba H., Fattah, Lobna Abdel

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Interleukin‐4 ‐590C/T gene polymorphism in Egyptian children with acute lower respiratory infection: A multicenter study by Emam, Ahmed A., Shehab, Mohamed M. M., Allah, Mayy A. N., Elkoumi, Mohamed A., Abdelaal, NourEldin M., Mosabah, Amira A. A., Zakaria, Mervat T., Sherif, Ashraf M., Soliman, Mohammed M., El‐Kaffas, Rania M. H., Abouzeid, Heba, Abdou, Mohammed A., Abdalmonem, Nermin, Abdelbaset, Heba R., Mohamed, Soma A., Soliman, Attia A., Elashkar, Shaimaa S. A., Hegab, Mohamed S., Khalil, Atef M., Abdel‐Aziz, Alsayed, Anany, Heba G., Salah, Hossam E., Abdou, Adel M., Elshehawy, Naglaa A., Elbasyouni, Hany A. A., Hafez, Sahbaa F. M., Abo‐Alella, Doaa A., Fawzi, Maggie M., Morsi, Samar S.

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Interleukin-1β and interleukin-1receptor antagonist polymorphisms in Egyptian children with febrile seizures: A case-control study by Al Morshedy, Salah, Elsaadany, Hosam F., Ibrahim, Hany E., Sherif, Ashraf M., Farghaly, Mohsen A.A., Allah, Mayy A.N., Abouzeid, Heba, Elashkar, Shaimaa S.A., Hamed, Mohammed E., Fathy, Manar M., Khalil, Atef M., Noah, Maha A., Hegab, Mohamed S., Ahmed, Ahmed R., Hashem, Mustafa I.A., Emam, Ahmed A., Anany, Heba G., Ibrahim, Boshra R., Gawish, Heba H., Nabil, Rehab M., Fattah, Lobna Abdel, Alsayed, Salah F.

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Association of IL-10 gene polymorphisms and susceptibility to Juvenile Idiopathic Arthritis in Egyptian children and adolescents: a case-control study by Fathy, Manar M, Elsaadany, Hosam F, Ali, Yasser F, Farghaly, Mohsen A A, Hamed, Mohammed E, Ibrahim, Hany E, Noah, Maha A, Allah, Mayy A N, Elashkar, Shaimaa S A, Abdelsalam, Nasser I, Abdelrahman, Hind M, Ahmed, Ahmed R, Anany, Heba G, Ismail, Sanaa M, Ibrahim, Boshra R, Al Azizi, Nashwa M, Gawish, Heba H, Al-Akad, Ghada M, Nabil, Rehab M, Fahmy, Dalia S, Alsayed, Salah F

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