Next‐generation sequencing in identification of pathogenic variants in primary hyperoxaluria among 21 Egyptian families: Identification of two novel AGXT gene mutations

por Ahmed, Hoda A., Fadel, Fatina I., Abdel Mawla, Mohamed A., Salah, Doaa M., Fathallah, Mohamed Gamal, Amr, Khalda
Publicado 2022

Risk Factors of Intractable Epilepsy in Children with Cerebral Palsy

por ABDEL MAKSOUD, Yehia Hamed, SULIMAN, Hany Abdelaziz, ElSAYED ABDULSAMEA, Sameh, MOHAMED KAMAL, Naglaa, AL-SHOKRAY, Ashraf Hamed, IBRAHIM, Asmaa Obada, ELSHORBAGY, Hatem Hamed, FATHALLAH, Mohamed Gamal El Din, ATTIA, Ahmed Mahmoud, ELSADEK, Akram Elshafey
Publicado 2021

A Comparative Study of Levetiracetam and Phenobarbital for Neonatal Seizures as a First Line Treatment

por Akeel, Nagwa Elsayed, Suliman, Hany Abdelaziz, Al-Shokary, Ashraf Hamed, Ibrahim, Asmaa Obada, Kamal, Naglaa M., Abdelgalil, Abobakr Abosree, Elmala, Moustafa Kotb, Elshorbagy, Hatem Hamed, Nasef, Khaled Amin, Attia, Ahmed Mahmoud, Fathallah, Mohamed Gamal El Din
Publicado 2022