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	1.	[Specific learning and cognitive deficits in neurofibromatosis type 1]. [electronic resource] by Mahajnah, M Zimmerman, S Weitz, R Producer: 20010517 In: Harefuah vol. 140 Availability: No items available. Save to lists Add to cart (remove)
	2.	Cognition, psychosocial adjustment and coping in familial cases of velocardiofacial syndrome. [electronic resource] by Gothelf, D Aviram-Goldring, A Burg, M Steinberg, T Mahajnah, M Frisch, A Fennig, S Zalsman, G Weizman, A Producer: 20080311 In: Journal of neural transmission (Vienna, Austria : 1996) vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab-Israeli family. [electronic resource] by Abu-Rashid, M Mahajnah, M Jaber, L Kornreich, L Bar-On, E Basel-Vanagaite, L Soffer, D Koenig, M Straussberg, R Producer: 20140117 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures. [electronic resource] by Straussberg, R Basel-Vanagaite, L Kivity, S Dabby, R Cirak, S Nurnberg, P Voit, T Mahajnah, M Inbar, D Saifi, G M Lupski, J R Delague, V Megarbane, A Richter, A Leshinsky, E Berkovic, S F Producer: 20050927 In: Neurology vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)