Your search returned 6 results.

Results
	1.	Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25. [electronic resource] by Jen, Joanna Coulin, C J Bosley, T M Salih, M A M Sabatti, C Nelson, S F Baloh, R W Producer: 20020903 In: Neurology vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Expression profiling of Sudanese visceral leishmaniasis patients pre- and post-treatment with sodium stibogluconate. [electronic resource] by Salih, M A M Fakiola, M Lyons, P A Younis, B M Musa, A M Elhassan, A M Anderson, D Syn, G Ibrahim, M E Blackwell, J M Mohamed, H S Producer: 20171019 In: Parasite immunology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Refinement of the clinical phenotype in musk-related congenital myasthenic syndromes. [electronic resource] by Mihaylova, V Salih, M A M Mukhtar, M M Abuzeid, H A El-Sadig, S M von der Hagen, M Huebner, A Nürnberg, G Abicht, A Müller, J S Lochmüller, H Guergueltcheva, V Producer: 20091222 In: Neurology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3. [electronic resource] by Bosley, T M Salih, M A M Jen, J C Lin, D D M Oystreck, D Abu-Amero, K K MacDonald, D B al Zayed, Z al Dhalaan, H Kansu, T Stigsby, B Baloh, R W Producer: 20060210 In: Neurology vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs. [electronic resource] by Shaheen, R Al-Dirbashi, O Y Al-Hassnan, Z N Al-Owain, M Makhsheed, N Basheeri, F Seidahmed, M Z Salih, M A M Faqih, E Zaidan, H Al-Sayed, M Rahbeeni, Z Al-Sheddi, T Hashem, M Kurdi, W Shimozawa, N Alkuraya, F S Producer: 20110321 In: Clinical genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort. [electronic resource] by Davidson, G L Murphy, S M Polke, J M Laura, M Salih, M A M Muntoni, F Blake, J Brandner, S Davies, N Horvath, R Price, S Donaghy, M Roberts, M Foulds, N Ramdharry, G Soler, D Lunn, M P Manji, H Davis, M B Houlden, H Reilly, M M Producer: 20130604 In: Journal of neurology vol. 259 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)