Association of sodium voltage-gated channel genes polymorphisms with epilepsy risk and prognosis in the Saudi population by Alghamdi, Mansour A., AL-Eitan, Laith N., Asiri, Ashwag, Rababa'h, Doaa M., Alqahtani, Sultan A., Aldarami, Mohammed S., Alsaeedi, Manar A., Almuidh, Raghad S., Alzahrani, Abdulbari A., Sakah, Ahmad H., El Nashar, Eman Mohamad, Otaif, Mansour Y., Abdel Ghaffar, Nawal F.

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Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomalies by Accogli, Andrea, Zaki, Maha S, Al-Owain, Mohammed, Otaif, Mansour Y, Jackson, Adam, Argilli, Emanuela, Chandler, Kate E, De Goede, Christian G E L, Cora, Tülün, Alvi, Javeria Raza, Eslahi, Atieh, Asl Mohajeri, Mahsa Sadat, Ashtiani, Setareh, Au, P Y Billie, Scocchia, Alicia, Alakurtti, Kirsi, Pagnamenta, Alistair T, Toosi, Mehran Beiraghi, Karimiani, Ehsan Ghayoor, Mojarrad, Majid, Arab, Fatemeh, Duymuş, Fahrettin, Scantlebury, Morris H, Yeşil, Gözde, Rosenfeld, Jill Anne, Türkyılmaz, Ayberk, Sağer, Safiye Güneş, Sultan, Tipu, Ashrafzadeh, Farah, Zahra, Tatheer, Rahman, Fatima, Maqbool, Shazia, Abdel-Hamid, Mohamed S, Issa, Mahmoud Y, Efthymiou, Stephanie, Bauer, Peter, Zifarelli, Giovanni, Salpietro, Vincenzo, Al-Hassnan, Zuhair, Banka, Siddharth, Sherr, Elliot H, Gleeson, Joseph G, Striano, Pasquale, Houlden, Henry, Severino, Mariasavina, Maroofian, Reza

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Neonatal Kawasaki Disease: A Case Report by Huneif, Mohamed A., Shati, Ayed A., Abudiah, Abdu M., Aljaser, Abdullah M., Otaif, Mansour Y.

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