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	1.	Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family. [electronic resource] by Saadi, Abdelkrim Borck, Guntram Boddaert, Nathalie Chekkour, Mohamed Chahine Imessaoudene, Belaïd Munnich, Arnold Colleaux, Laurence Chaouch, Malika Producer: 20091102 In: European journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Multicenter transversal two-phase study to determine a national prevalence of epilepsy in Algeria. [electronic resource] by Moualek, Dalila Pacha, Lamia Ali Abrouk, Samira Kediha, Mohamed Islam Nouioua, Sonia Aissa, Leila Ait Bellatache, Mounia Belarbi, Soreya Slimani, Saddek Khennouf, Houria Fellahi, Lynda El Amine Hamimed, Mohamed Benali, Nadia Chekkour, Mohamed Chahine Maamoun, Ramdane Dameche, Rachida Assami, Salima Tazir, Meriem Producer: 20130222 In: Neuroepidemiology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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