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	1.	Reduced body mass index in essential tremor: a study of 382 cases and 392 matched controls. [electronic resource] by Louis, E D Michalec, M Producer: 20151103 In: European journal of neurology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Prevalence and correlates of rest tremor in essential tremor: cross-sectional survey of 831 patients across four distinct cohorts. [electronic resource] by Louis, E D Hernandez, N Michalec, M Producer: 20151222 In: European journal of neurology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[Diagnostic pitfalls of pseudo-foster kennedy syndrome - a case report]. [electronic resource] by Michalec, M Vlková, E Matušková, V Vysloužilová, D Michalcová, L Producer: 20151027 In: Ceska a slovenska oftalmologie : casopis Ceske oftalmologicke spolecnosti a Slovenske oftalmologicke spolecnosti vol. 70 Availability: No items available. Save to lists Add to cart (remove)
	4.	Two 3' polymorphisms in DLX5: g126427delTATC and g126249T-->C. [electronic resource] by Hart, P S Michalec, M D Wright, J T Hart, T C Producer: 20001121 In: Human mutation vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature. [electronic resource] by Hart, P S Michalec, M D Seow, W K Hart, T C Wright, J T Producer: 20031007 In: Archives of oral biology vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta. [electronic resource] by Hart, P S Hart, T C Michalec, M D Ryu, O H Simmons, D Hong, S Wright, J T Producer: 20041221 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome. [electronic resource] by Hart, T C Hart, P S Bowden, D W Michalec, M D Callison, S A Walker, S J Zhang, Y Firatli, E Producer: 20000107 In: Journal of medical genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	8.	Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation. [electronic resource] by Hart, T C Hart, P S Michalec, M D Zhang, Y Marazita, M L Cooper, M Yassin, O M Nusier, M Walker, S Producer: 20000306 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects. [electronic resource] by Hart, T C Hart, P S Gorry, M C Michalec, M D Ryu, O H Uygur, C Ozdemir, D Firatli, S Aren, G Firatli, E Producer: 20040223 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C. [electronic resource] by Hart, T C Hart, P S Michalec, M D Zhang, Y Firatli, E Van Dyke, T E Stabholz, A Zlotogorski, A Shapira, L Soskolne, W A Zlorogorski, A Producer: 20000306 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Identification of cathepsin C mutations in ethnically diverse papillon-Lefèvre syndrome patients. [electronic resource] by Hart, P S Zhang, Y Firatli, E Uygur, C Lotfazar, M Michalec, M D Marks, J J Lu, X Coates, B J Seow, W K Marshall, R Williams, D Reed, J B Wright, J T Hart, T C Producer: 20010125 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)