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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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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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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Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy von 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

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Awareness of consanguineous marriage burden and willingness towards premarital genetic testing in Sudan: a national cross-sectional study von 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

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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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Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations von Yahia, Ashraf, Hamed, Ahlam AA, 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 ZM, Omer, Zulfa, Malik, Hiba, Mohamed, Mayada OE, Elhassan, Ali A, Mohamed, Eman OE, Ahmed, Ahmed KMA, Ahmed, Elhami AA, Eltaraifee, Esraa, Hussein, Bidour K, Abd Allah, Amal SI, Salah, Lina, Nimir, Mohamed, Tag Elseed, Omnia M, Elhassan, Tasneem EA, Elbashier, Abubakr, Alfadul, Esraa SA, Fadul, Moneeb, Ali, Khalil F, Taha, Shaimaa Omer MA, Bushara, Elfatih E, Amin, Mutaz, Koko, Mahmoud, Ibrahim, Muntaser E, Ahmed, Ammar E, Elsayed, Liena EO, Stevanin, Giovanni

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Gut Microbiota Dysbiosis: A Neglected Risk Factor for Male and Female Fertility von Beni, Faeze Ahmadi, Saffarfar, Hossein, Elhami, Anis, Kazemi, Mohammad

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Integrated evaluation of urban development suitability based on remote sensing and GIS techniques: contribution from the analytic hierarchy process von Youssef, Ahmed M., Pradhan, Biswajeet, Tarabees, Elhami

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Nanomedicine in the treatment of Alzheimer's disease: bypassing the blood-brain barrier with cutting-edge nanotechnology von Dong, Nana, Ali-Khiavi, Payam, Ghavamikia, Nima, Pakmehr, SeyedAbbas, Sotoudegan, Farzaneh, Hjazi, Ahmed, Gargari, Morad Kohandel, Gargari, Homa Kohandel, Behnamrad, Parisa, Rajabi, Mohammadreza, Elhami, Anis, Saffarfar, Hossein, Nourizadeh, Mehrdad

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Frequency Response and Modal Parameters of Sandwich Composite with Debonding Under Random Vibration Excitations von Ben Ameur, Sirine, Yaich, Ahmed, Elhami, Abdelkahalk, Beyaoui, Moez, Saouab, Abdelghani, Haddar, Mohamed

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