Clinical and neuropsychological outcomes for children with phenylketonuria in Upper Egypt; a single-center study over 5 years

por Sadek, Abdelrahim A, Hassan, Mohammed H, Mohammed, Nesreen A
Publicado 2018

Role of umbilical cord C-peptide levels in early prediction of hypoglycemia in infants of diabetic mothers

por Saber, Ahlam M., Mohamed, Magdy A., Sadek, Abdelrahim A., Mahmoud, Ramadan A.
Publicado 2021

Propionic and Methylmalonic Acidemias: Initial Clinical and Biochemical Presentation

por Mobarak, Amira, Dawoud, Heba, Mokhtar, Wesam A., Sadek, Abdelrahim A., Bebars, Gihan Mohamed, Othman, Amr Ahmed, Magdy, Rofaida M., Nofal, Hanaa, Zoair, Amr
Publicado 2020

Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction

por Akizu, Naiara, Cantagrel, Vincent, Zaki, Maha S., Al-Gazali, Lihadh, Wang, Xin, Rosti, Rasim Ozgur, Dikoglu, Esra, Gelot, Antoinette Bernabe, Rosti, Basak, Vaux, Keith K., Scott, Eric M., Silhavy, Jennifer L., Schroth, Jana, Copeland, Brett, Schaffer, Ashleigh E., Gordts, Philip, Esko, Jeffrey D., Buschman, Matthew D., Fields, Seth J., Napolitano, Gennaro, Ozgul, R. Koksal, Sagiroglu, Mahmut Samil, Azam, Matloob, Ismail, Samira, Aglan, Mona, Selim, Laila, Gamal, Iman, Hadi, Sawsan Abdel, El Badawy, Amera, Sadek, Abdelrahim A., Mojahedi, Faezeh, Kayserili, Hulya, Masri, Amira, Bastaki, Laila, Temtamy, Samia, Müller, Ulrich, Desguerre, Isabelle, Casanova, Jean-Laurent, Dursun, Ali, Gunel, Murat, Gabriel, Stacey B., de Lonlay, Pascale, Gleeson, Joseph G.
Publicado 2015