Paediatric neurology service in Sudan: Current situation and future challenges

Por Elseed, Maha A., Mohammed, Inaam N., Hamed, Ahlam A.
Publicado no Sudan J Paediatr (2015)

Clinical profile of pediatric neurological disorders as seen in outpatient clinic in Khartoum, Sudan

Por Mohammed, Inaam N., Elseed, Maha A., Hamed, Ahlam A.
Publicado no Sudan J Paediatr (2015)

Epidemiology of epilepsy among school children in Khartoum State-2014

Por Hamed, Ahlam A., Elseed, Maha A., Mohammed, Inaam N.
Publicado no Sudan J Paediatr (2015)

Apert Syndrome: Late presentation and treatment challenges

Por Kheir, Abdelmoneim E M, Hamed, Ahlam A, Maki, Wala M, Hasan, Lina H M
Publicado no Sudan J Paediatr (2014)

Brain tuberculoma, an unusual cause of stroke in a child with trisomy 21: a case report

Por Kheir, Abdelmoneim E. M., Ibrahim, Salah A., Hamed, Ahlam A., Yousif, Badreldin M., Hamid, Farouk A.
Publicado no J Med Case Rep (2017)

Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family

Por 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
Publicado no BMC Med Genet (2018)

Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan

Por Elsayed, Liena E O, Mohammed, Inaam N, Hamed, Ahlam A A, Elseed, Maha A, Johnson, Adam, Mairey, Mathilde, Mohamed, Hassab Elrasoul S A, Idris, Mohamed N, Salih, Mustafa A M, El-sadig, Sarah M, Koko, Mahmoud E, Mohamed, Ashraf Y O, Raymond, Laure, Coutelier, Marie, Darios, Frédéric, Siddig, Rayan A, Ahmed, Ahmed K M A, Babai, Arwa M A, Malik, Hiba M O, Omer, Zulfa M B M, Mohamed, Eman O E, Eltahir, Hanan B, Magboul, Nasr Aldin A, Bushara, Elfatih E, Elnour, Abdelrahman, Rahim, Salah M Abdel, Alattaya, Abdelmoneim, Elbashir, Mustafa I, Ibrahim, Muntaser E, Durr, Alexandra, Audhya, Anjon, Brice, Alexis, Ahmed, Ammar E, Stevanin, Giovanni
Publicado no Eur J Hum Genet (2017)