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	1.	[Study of the duplication of 17p11.2-12 chromosome region in the patients with hereditary motor and sensory neuropathy type 1A]. [electronic resource] by Hryshchenko, N V Bychkova, A M Pichkur, N A Skyban, H V Dmytrenko, V V Livshyts', L A Producer: 20040621 In: TSitologiia i genetika vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Immunologic aspects of embryonal nerve tissue transplantation]. [electronic resource] by Tsymbaliuk, V I Pichkur, L D Rudenko, V A Lisianyĭ, N I Pichkur, N A Gordienko, O V Producer: 20020412 In: Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko no. 3 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Syndrome Leigh caused by mutations in the SURF1 gene: clinical and molecular-genetic characteristics]. [electronic resource] by Tsygankova, P G Mikhaĭlova, S V Zakharova, E Iu Pichkur, N A Il'ina, E S Nikolaeva, E A Rudenskaia, G E Dadali, E L Kolpakchi, L M Fedoniuk, I D Matiushchenko, G N Producer: 20100715 In: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova vol. 110 Availability: No items available. Save to lists Add to cart (remove)
	4.	[Open, non-comparative phase III clinical study to evaluate the efficacy and safety of sapropterin in patients with phenylketonuria and hyperphenylalaninemia]. [electronic resource] by Bushueva, T V Kuzenkova, L M Borovik, T É Nazarenko, L P Seitova, G N Filimonova, M N Pichkur, N A Samonenko, N V Shkurko, T A Akhmadeeva, É N Mardanova, A K Garifullina, É R Kovtun, O P Bazhenova, Iu L Alimova, I L Kostiakova, E A Minaĭcheva, L I Saliukova, O A Sivokha, V M Rozenson, O L Producer: 20150223 In: Vestnik Rossiiskoi akademii meditsinskikh nauk no. 7-8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)