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	21.	[Suspected abscess formation in the inferior rectus muscle]. [electronic resource] by Schenke, T Lehmann, G Kunze, C Bauer, M Pazaitis, N Odparlik, A Krug, S Sperfeld, A-D Plontke, S K Glien, A Kisser, U Producer: 20201007 In: HNO vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation. [electronic resource] by Sperfeld, A D Collatz, M B Baier, H Palmbach, M Storch, A Schwarz, J Tatsch, K Reske, S Joosse, M Heutink, P Ludolph, A C Producer: 19991124 In: Annals of neurology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24. [electronic resource] by Schüle, R Bonin, M Dürr, A Forlani, S Sperfeld, A D Klimpe, S Mueller, J C Seibel, A van de Warrenburg, B P Bauer, P Schöls, L Producer: 20090714 In: Neurology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case. [electronic resource] by Funke, A D Esser, M Krüttgen, A Weis, J Mitne-Neto, M Lazar, M Nishimura, A L Sperfeld, A D Trillenberg, P Senderek, J Krasnianski, M Zatz, M Zierz, S Deschauer, M Producer: 20100706 In: Clinical genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia. [electronic resource] by Beetz, C Nygren, A O H Schickel, J Auer-Grumbach, M Bürk, K Heide, G Kassubek, J Klimpe, S Klopstock, T Kreuz, F Otto, S Schüle, R Schöls, L Sperfeld, A-D Witte, O W Deufel, T Producer: 20070108 In: Neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation. [electronic resource] by Baba, Y Baker, M C Le Ber, I Brice, A Maeck, L Kohlhase, J Yasuda, M Stoppe, G Bugiani, O Sperfeld, A D Tsuboi, Y Uitti, R J Farrer, M J Ghetti, B Hutton, M L Wszolek, Z K Producer: 20091123 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)
	27.	Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world. [electronic resource] by Lund, A Udd, B Juvonen, V Andersen, P M Cederquist, K Davis, M Gellera, C Kölmel, C Ronnevi, L O Sperfeld, A D Sörensen, S A Tranebjaerg, L Van Maldergem, L Watanabe, M Weber, M Yeung, L Savontaus, M L Producer: 20011011 In: European journal of human genetics : EJHG vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)