Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive Overview von Elsayed, Liena E O, Eltazi, Isra Zuhair, Ahmed, Ammar E, Stevanin, Giovanni

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Reference Jitter Values for Concentric Needle Electrode of Orbicularis Oculi and Frontalis Muscles Using Voluntary Activation Method in Sudanese Population von Musa, Afraa M. M., Ahmed, Ammar E. M.

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Genetic heterogeneity in familial forms of genetic generalized epilepsy: from mono- to oligogenism von Dahawi, Maha, de Sainte Agathe, Jean-Madeleine, Elmagzoub, Mohamed S, Ahmed, Elhami A, Buratti, Julien, Courtin, Thomas, Noé, Eric, Bogoin, Julie, Copin, Bruno, Elmugadam, Fatima A, Abdelgadir, Wasma A, Ahmed, Ahmed K M A, Daldoum, Mohamed A, Altayeb, Rayan Mamoon Ibrahim, Bashir, Mohamed, Khalid, Leena Mohamed, Gamil, Sahar, Baldassari, Sara, Elsayed, Liena, Keren, Boris, Nuel, Gregory, Ahmed, Ammar E, Leguern, Eric

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Involvement of ADGRV1 Gene in Familial Forms of Genetic Generalized Epilepsy von 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

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A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report von Yahia, Ashraf, Chen, Zhefan Stephen, Ahmed, Ammar E, Emad, Sara, Adil, Rawaa, Abubaker, Rayan, Taha, Shaimaa Omer M A, Salih, Mustafa A, Elsayed, Liena, Chan, Ho Yin Edwin, Stevanin, Giovanni

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A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability von Amin, Mutaz, Vignal, Cedric, Eltaraifee, Esraa, Mohammed, Inaam N, Hamed, Ahlam A. A, Elseed, Maha A, Babai, Arwa, Elbadi, Iman, Mustafa, Doua, Abubaker, Rayan, Mustafa, Mohamed, Drunat, Severine, Elsayed, Liena E. O, Ahmed, Ammar E, Boespflug-Tanguy, Odile, Dorboz, Imen

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Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia von 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

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Novel variants causing megalencephalic leukodystrophy in Sudanese families von Amin, Mutaz, Vignal, Cedric, Hamed, Ahlam A A, Mohammed, Inaam N, Elseed, Maha A, Drunat, Severine, Babai, Arwa, Eltaraifee, Esraa, Elbadi, Iman, Abubaker, Rayan, Mustafa, Doaa, Yahia, Ashraf, Koko, Mahmoud, Osman, Melka, Bakhit, Yousuf, Elshafea, Azza, Alsiddig, Mohamed, Haroun, Sahwah, Lelay, Gurvan, Elsayed, Liena E O, Ahmed, Ammar E, Boespflug-Tanguy, Odile, Dorboz, Imen

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In transition: current health challenges and priorities in Sudan von Charani, Esmita, Cunnington, Aubrey J, Yousif, AlaEldin H A, Seed Ahmed, Mohammed, Ahmed, Ammar E M, Babiker, Souad, Badri, Shahinaz, Buytaert, Wouter, Crawford, Michael A, Elbashir, Mustafa I, Elhag, Kamal, Elsiddig, Kamal E, Hakim, Nadey, Johnson, Mark R, Miras, Alexander D, Swar, Mohamed O, Templeton, Michael R, Taylor-Robinson, Simon David

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Novel Homozygous Missense Mutation in the ARG1 Gene in a Large Sudanese Family von Elsayed, Liena E. O., Mohammed, Inaam N., Hamed, Ahlam A. A., Elseed, Maha A., Salih, Mustafa A. M., Yahia, Ashraf, Abubaker, Rayan, Koko, Mahmoud, Abd Allah, Amal S. I., Elbashir, Mustafa I., Ibrahim, Muntaser E., Brice, Alexis, Ahmed, Ammar E., Stevanin, Giovanni

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Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family von Elsayed, Liena E O, Mohammed, Inaam N, Hamed, Ahlam A A, Elseed, Maha A, Salih, Mustafa A M, Yahia, Ashraf, Siddig, Rayan A, Amin, Mutaz, Koko, Mahmoud, Elbashir, Mustafa I, Ibrahim, Muntaser E, Brice, Alexis, Ahmed, Ammar E, Stevanin, Giovanni

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Enhancing the detection of metamorphic malware using call graphs von Elhadi, Ammar Ahmed E., Maarof, Mohd Aizaini, Barry, Bazara I.A., Hamza, Hentabli

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Malware Detection Based on Hybrid Signature Behaviour Application Programming Interface Call Graph von Elhadi, Ammar Ahmed E, Maarof, Mohd Aizaini, Osman, Ahmed Hamza

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Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing von Yahia, Ashraf, Ayed, Ikhlas Ben, Hamed, Ahlam A., Mohammed, Inaam N., Elseed, Maha A., Bakhiet, Aisha M., Guillot‐Noel, Lena, Abozar, Fatima, Adil, Rawaa, Emad, Sara, Abubaker, Rayan, Musallam, Mhammed Alhassan, Eltazi, Isra Z. M., Omer, Zulfa, Maaroof, Omer M., Soussi, Amal, Bouzid, Amal, Kmiha, Sana, Kamoun, Hassen, Salih, Mustafa A., Ahmed, Ammar E., Elsayed, Liena, Masmoudi, Saber, Stevanin, Giovanni

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An identical‐by‐descent novel splice‐donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families von Koko, Mahmoud, Yahia, Ashraf, Elsayed, Liena E., Hamed, Ahlam A., Mohammed, Inaam N., Elseed, Maha A., Hamad, Muddathir H. A., Babai, Arwa M., Siddig, Rayan A., Abd Allah, Amal S. I., Mohamed, Mayada, EL‐Amin, Melka, Esteves, Typhaine, Altmüller, Janine, Toliat, Mohammad Reza, Thiele, Holger, Nürnberg, Peter, Salih, Mustafa A., Ahmed, Ammar E., Lerche, Holger, Stevanin, Giovanni

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Case Report: A New Family With Pontocerebellar Hypoplasia 10 From Sudan von Amin, Mutaz, Vignal, Cedric, Hamed, Ahlam A. A., Mohammed, Inaam N., Elseed, Maha A., Abubaker, Rayan, Bakhit, Yousuf, Babai, Arwa, Elbadi, Eman, Eltaraifee, Esraa, Mustafa, Doua, Yahia, Ashraf, Osman, Melka, Koko, Mahmoud, Mustafa, Mohamed, Alsiddig, Mohamed, Haroun, Sahwah, Elshafea, Azza, Drunat, Severine, Elsayed, Liena E. O., Ahmed, Ammar E., Boespflug-Tanguy, Odile, Dorboz, Imen

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Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations von 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

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Pattern of presentation and prognosis of GBS using clinical and electrophysiological parameters in Khartoum state March – September 2020 von Daoud, Mahmoud H.S., M.A., Khalid, Saeed, Mohammed K., Ahmed, Ammar E., Ibrahim, Eetedal A., Aladil, Omer, Elsayed, Muaz A.M., Abdalmagid, Abdalrahman, Ragab, Esraa Ahmed, Dafallah, Mumen Abdalazim

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Features Reweighting and Similarity Coefficient Based Method for Email Spam Filtering von Ali Elsiddig, Ahmed Osman, Elhadi, Ammar Ahmed E., Ahmed, Ali

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Possible predisposing factors for thrombotic cerebrovascular accidents in Sudanese patients von ELAGIB, Abdelgadir H, AHMED, Ammar E, HUSSEIN, Abbashar, MUSA, Ahmed M, KHALIL, Eltahir A, EL-HASSAN, Ahmed M

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