Involvement of ADGRV1 Gene in Familial Forms of Genetic Generalized Epilepsy
Dahawi, Maha, Elmagzoub, Mohamed S., A. Ahmed, Elhami, Baldassari, Sara, Achaz, Guillaume, Elmugadam, Fatima A., Abdelgadir, Wasma A., Baulac, Stéphanie, Buratti, Julien, Abdalla, Omer, Gamil, Sahar, Alzubeir, Maha, Abubaker, Rayan, Noé, Eric, Elsayed, Liena, Ahmed, Ammar E., Leguern, Eric
Published in Frontiers in neurology (21.10.2021)
Published in Frontiers in neurology (21.10.2021)
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Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
Koko, Mahmoud, Elseed, Maha A, Mohammed, Inaam N, Hamed, Ahlam A, Abd Allah, Amal S I, Yahia, Ashraf, Siddig, Rayan A, Altmüller, Janine, Toliat, Mohammad Reza, Elmahdi, Esra O, Amin, Mutaz, Ahmed, Elhami A, Eltazi, Isra Z M, Elmugadam, Fatima A, Abdelgadir, Wasma A, Eltaraifee, Esraa, Ibrahim, Mohamed O M, Ali, Nabila M H, Malik, Hiba M, Babai, Arwa M, Bakhit, Yousuf H, Nürnberg, Peter, Ibrahim, Muntaser E, Salih, Mustafa A, Schubert, Julian, Elsayed, Liena E O, Lerche, Holger
Published in European journal of human genetics : EJHG (05.02.2024)
Published in European journal of human genetics : EJHG (05.02.2024)
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Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations
Yahia, Ashraf, Hamed, Ahlam A A, Mohamed, Inaam N, Elseed, Maha A, Salih, Mustafa A, El-Sadig, Sarah M, Siddig, Hassab Elrasoul, Nasreldien, Ali Elsir Musa, Abdullah, Mohamed Ahmed, Elzubair, Maha, Omer, Farouk Yassen, Bakhiet, Aisha Motwakil, Abubaker, Rayan, Abozar, Fatima, Adil, Rawaa, Emad, Sara, Musallam, Mhammed Alhassan, Eltazi, Isra Z M, Omer, Zulfa, Malik, Hiba, Mohamed, Mayada O E, Elhassan, Ali A, Mohamed, Eman O E, Ahmed, Ahmed K M A, Ahmed, Elhami A A, Eltaraifee, Esraa, Hussein, Bidour K, Abd Allah, Amal S I, Salah, Lina, Nimir, Mohamed, Tag Elseed, Omnia M, Elhassan, Tasneem E A, Elbashier, Abubakr, Alfadul, Esraa S A, Fadul, Moneeb, Ali, Khalil F, Taha, Shaimaa Omer M A, Bushara, Elfatih E, Amin, Mutaz, Koko, Mahmoud, Ibrahim, Muntaser E, Ahmed, Ammar E, Elsayed, Liena E O, Stevanin, Giovanni
Published in European journal of human genetics : EJHG (03.04.2023)
Published in European journal of human genetics : EJHG (03.04.2023)
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Awareness of consanguineous marriage burden and willingness towards premarital genetic testing in Sudan: a national cross-sectional study
Elmugadam, Fatima M., Ahmed, Haythem, KARAMELGHANI, MOHAMMED, Ali, Almigdad, Ali, Israa, Ahmed, Almegdad, Salman, Mohammed, Mohamed, Wadah, Ahmed, Elhami A., Abbasher Hussien Mohamed Ahmed, Khabab, Mustafa Ahmed, Ghassan E., Elsayed, Liena, Musa, Ahmed
Published in Annals of medicine and surgery (01.07.2024)
Published in Annals of medicine and surgery (01.07.2024)
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Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia
Yahia, Ashraf, Elsayed, Liena E. O., Valter, Remi, Hamed, Ahlam A. A., Mohammed, Inaam N., Elseed, Maha A., Salih, Mustafa A., Esteves, Typhaine, Auger, Nicolas, Abubaker, Rayan, Koko, Mahmoud, Abozar, Fatima, Malik, Hiba, Adil, Rawaa, Emad, Sara, Musallam, Mhammed Alhassan, Idris, Razaz, Eltazi, Isra Z. M., Babai, Arwa, Ahmed, Elhami A. A., Abd Allah, Amal S. I., Mairey, Mathilde, Ahmed, Ahmed K. M. A., Elbashir, Mustafa I., Brice, Alexis, Ibrahim, Muntaser E., Ahmed, Ammar E., Lamari, Foudil, Stevanin, Giovanni
Published in Frontiers in neurology (20.08.2021)
Published in Frontiers in neurology (20.08.2021)
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