Predictors of COVID-19 outcome in type 2 diabetes mellitus: a hospital-based study von Elsayed, Amira M., Elsayed, Mohamad S., Mansour, Ahmed E., Mahedy, Ahmed W., Araby, Eman M., Morsy, Maha H., Abd Elmoniem, Rasha O.

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Angiotensin‐converting enzyme insertion/deletion gene polymorphism in Egyptian children with CAP: A case‐control study von 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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Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications von Rosenhahn, Erik, O'Brien, Thomas J, Zaki, Maha S, Sorge, Ina, Wieczorek, Dagmar, Rostasy, Kevin, Vitobello, Antonio, Nambot, Sophie, Alkuraya, Fowzan S, Hashem, Mais O, Alhashem, Amal, Tabarki, Brahim, Alamri, Abdullah S, Al Safar, Ayat H, Bubshait, Dalal K, Alahmady, Nada F, Gleeson, Joseph G, Abdel-Hamid, Mohamed S, Lesko, Nicole, Ygberg, Sofia, Correia, Sandrina P, Wredenberg, Anna, Alavi, Shahryar, Seyedhassani, Seyed M, Nasab, Mahya Ebrahimi, Hussien, Haytham, Omar, Tarek E, Harzallah, Ines, Touraine, Renaud, Tajsharghi, Homa, Morsy, Heba, Houlden, Henry, Shahrooei, Mohammad, Ghavideldarestani, Maryam, Abdel-Salam, Ghada M.H, Torella, Annalaura, Zanobio, Mariateresa, Terrone, Gaetano, Brunetti-Pierri, Nicola, Omrani, Abdolmajid, Hentschel, Julia, Lemke, Johannes R, Sticht, Heinrich, Abou Jamra, Rami, Brown, Andre E.X, Maroofian, Reza, Platzer, Konrad

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The morbid genome of ciliopathies: an update von Shamseldin, Hanan E., Shaheen, Ranad, Ewida, Nour, Bubshait, Dalal K., Alkuraya, Hisham, Almardawi, Elham, Howaidi, Ali, Sabr, Yasser, Abdalla, Ebtesam M., Alfaifi, Abdullah Y., Mohammed Alghamdi, Jameel, Alsagheir, Afaf, Alfares, Ahmed, Morsy, Heba, Hussein, Maged H., Al-Muhaizea, Mohammad A., Shagrani, Mohammad, Al Sabban, Essam, Salih, Mustafa A., Meriki, Neama, Khan, Rubina, Almugbel, Maisoon, Qari, Alya, Tulba, Maha, Mahnashi, Mohammed, Alhazmi, Khalid, Alsalamah, Abrar K., Nowilaty, Sawsan R., Alhashem, Amal, Hashem, Mais, Abdulwahab, Firdous, Ibrahim, Niema, Alshidi, Tarfa, AlObeid, Eman, Alenazi, Mona M., Alzaidan, Hamad, Rahbeeni, Zuhair, Al-Owain, Mohammed, Sogaty, Sameera, Zain Seidahmed, Mohammed, Alkuraya, Fowzan S.

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Assessment of retinol-binding protein 4 in patients with alopecia areata and androgenetic alopecia von El Morsy, Eman H, Genedy, Rasha M, Younan, Doreen N, Abou Ghadega, Maha G

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