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	1.	Apert Syndrome: Late presentation and treatment challenges. [electronic resource] by Kheir, Abdelmoneim E M Hamed, Ahlam A Maki, Wala M Hasan, Lina H M Producer: 20160805 In: Sudanese journal of paediatrics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Brain tuberculoma, an unusual cause of stroke in a child with trisomy 21: a case report. [electronic resource] by Kheir, Abdelmoneim E M Ibrahim, Salah A Hamed, Ahlam A Yousif, Badreldin M Hamid, Farouk A Producer: 20180221 In: Journal of medical case reports vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Intelligence quotient (IQ) among children with epilepsy: National epidemiological study - Sudan. [electronic resource] by Mohamed, Inaam N Osman, Abdelgadir H Mohamed, Somia Hamid, Emtinan K Hamed, Ahlam A Alsir, Ali Gerais, Yasmin A Bakhiet, Aisha M Elsadig, Sarah M Elseed, Maha A Producer: 20201104 In: Epilepsy & behavior : E&B vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Classification and management of epilepsy and epileptic syndromes in a cohort of 202 school children- a 2 year follow up study- Sudan. [electronic resource] by Mohamed, Inaam N Elseed, Maha A Mohamed, Somia Alsir, Ali Hamid, Emtinan K Omer, Ilham M Elsadig, Sara M Gerais, Yasmin M Osman, Abdelgadir H Bakhiet, Aisha M Hamed, Ahlam A Producer: 20200127 In: BMC neurology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Prevalence of epilepsy in 74,949 school children in Khartoum State, Sudan. [electronic resource] by Mohamed, Inaam N Elseed, Maha A Hamed, Ahlam A Abdel-Rahman, Manar E El-Sadig, Sarah M Omer, Ilham M Osman, Abdelgadir H Ahmed, Ammar E Karrar, Zein A Salih, Mustafa A Producer: 20180308 In: Paediatrics and international child health vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family. [electronic resource] by 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 Producer: 20190225 In: BMC medical genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan. [electronic resource] by Saha, Madhurima Reddy, Hemakumar M Salih, Mustafa A Estrella, Elicia Jones, Michael D Mitsuhashi, Satomi Cho, Kyung-Ah Suzuki-Hatano, Silveli Rizzo, Skylar A Hamad, Muddathir H Mukhtar, Maowia M Hamed, Ahlam A Elseed, Maha A Lek, Monkol Valkanas, Elise MacArthur, Daniel G Kunkel, Louis M Pacak, Christina A Draper, Isabelle Kang, Peter B Producer: 20190917 In: Physiological genomics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan. [electronic resource] by 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 Producer: 20170726 In: European journal of human genetics : EJHG vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Expanding the phenome and variome of skeletal dysplasia. [electronic resource] by Maddirevula, Sateesh Alsahli, Saud Alhabeeb, Lamees Patel, Nisha Alzahrani, Fatema Shamseldin, Hanan E Anazi, Shams Ewida, Nour Alsaif, Hessa S Mohamed, Jawahir Y Alazami, Anas M Ibrahim, Niema Abdulwahab, Firdous Hashem, Mais Abouelhoda, Mohamed Monies, Dorota Al Tassan, Nada Alshammari, Muneera Alsagheir, Afaf Seidahmed, Mohammed Zain Sogati, Samira Aglan, Mona S Hamad, Muddathir H Salih, Mustafa A Hamed, Ahlam A Alhashmi, Nadia Nabil, Amira Alfadli, Fatima Abdel-Salam, Ghada M H Alkuraya, Hisham Peitee, Winnie Ong Keng, W T Qasem, Abdullah Mushiba, Aziza M Zaki, Maha S Fassad, Mahmoud R Alfadhel, Majid Alexander, Saji Sabr, Yasser Temtamy, Samia Ekbote, Alka V Ismail, Samira Hosny, Gamal Ahmed Otaify, Ghada A Amr, Khalda Al Tala, Saeed Khan, Arif O Rizk, Tamer Alaqeel, Aida Alsiddiky, Abdulmonem Singh, Ankur Kapoor, Seema Alhashem, Amal Faqeih, Eissa Shaheen, Ranad Alkuraya, Fowzan S Producer: 20190514 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)