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Results: 1-12 |
Results: 12
Nebulin expression in patients with nemaline myopathy
Authors: Gurgel-Giannetti, J Reed, U Bang, ML Pelin, K Donner, K Marie, SK Carvalho, M Fireman, MAT Zanoteli, E Oliveira, ASB Zatz, M Wallgren-Pettersson, C Labeit, S Vainzof, M
Citation: J. Gurgel-giannetti et al., Nebulin expression in patients with nemaline myopathy, NEUROMUSC D, 11(2), 2001, pp. 154-162
In search of the visual pigment template
Authors: Govardovskii, VI Fyhrquist, N Reuter, T Kuzmin, DG Donner, K
Citation: Vi. Govardovskii et al., In search of the visual pigment template, VIS NEUROSC, 17(4), 2000, pp. 509-528
Flicker sensitivity as a function of target area with and without temporalnoise
Authors: Rovamo, J Donner, K Nasanen, R Raninen, A
Citation: J. Rovamo et al., Flicker sensitivity as a function of target area with and without temporalnoise, VISION RES, 40(28), 2000, pp. 3841-3851
Measurement of thermal contribution to photoreceptor sensitivity
Authors: Koskelainen, A Ala-Laurila, P Fyhrquist, N Donner, K
Citation: A. Koskelainen et al., Measurement of thermal contribution to photoreceptor sensitivity, NATURE, 403(6766), 2000, pp. 220-223
Wave-front reconstruction with a Shack-Hartmann sensor with an iterative spline fitting method
Authors: Groening, S Sick, B Donner, K Pfund, J Lindlein, N Schwider, J
Citation: S. Groening et al., Wave-front reconstruction with a Shack-Hartmann sensor with an iterative spline fitting method, APPL OPTICS, 39(4), 2000, pp. 561-567
Robust motion estimation for calibrated cameras from monocular image sequences
Authors: Wagner, R Liu, FY Donner, K
Citation: R. Wagner et al., Robust motion estimation for calibrated cameras from monocular image sequences, COMP VIS IM, 73(2), 1999, pp. 258-268
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy
Authors: Nowak, KJ Wattanasirichaigoon, D Goebel, HH Wilce, M Pelin, K Donner, K Jacob, RL Hubner, C Oexle, K Anderson, JR Verity, CM North, KN Iannaccone, ST Muller, CR Nurnberg, P Muntoni, F Sewry, C Hughes, I Sutphen, R Lacson, AG Swoboda, KJ Vigneron, J Wallgren-Pettersson, C Beggs, AH Laing, NG
Citation: Kj. Nowak et al., Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy, NAT GENET, 23(2), 1999, pp. 208-212
Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy
Authors: Wallgren-Pettersson, C Pelin, K Hilpela, P Donner, K Porfirio, B Graziano, C Swoboda, KJ Fardeau, M Urtizberea, JA Muntoni, F Sewry, C Dubowitz, V Iannaccone, S Minetti, C Pedemonte, M Seri, M Cusano, R Lammens, M Castagna-Sloane, A Beggs, AH Laing, NG de la Chapelle, A
Citation: C. Wallgren-pettersson et al., Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy, NEUROMUSC D, 9(8), 1999, pp. 564-572
Special issue: Progress and paradigm shifts in vision research over the 20years of ECVP - Guest editorial
Authors: Donner, K
Citation: K. Donner, Special issue: Progress and paradigm shifts in vision research over the 20years of ECVP - Guest editorial, PERCEPTION, 28(12), 1999, pp. 1433-1434
Gender and risk of autoimmune diseases: Possible role of estrogenic compounds
Authors: Ahmed, SA Hissong, BD Verthelyi, D Donner, K Becker, K Karpuzoglu-Sahin, E
Citation: Sa. Ahmed et al., Gender and risk of autoimmune diseases: Possible role of estrogenic compounds, ENVIR H PER, 107, 1999, pp. 681-686
The effects of temporal noise and retinal illuminance on foveal flicker sensitivity
Authors: Rovamo, J Raninen, A Donner, K
Citation: J. Rovamo et al., The effects of temporal noise and retinal illuminance on foveal flicker sensitivity, VISION RES, 39(3), 1999, pp. 533-550
Mutations in the nebulin gene associated with autosomal recessive nemalinemyopathy
Authors: Pelin, K Hilpela, P Donner, K Sewry, C Akkari, PA Wilton, SD Wattanasirichaigoon, D Bang, ML Centner, T Hanefeld, F Odent, S Fardeau, M Urtizberea, JA Muntoni, F Dubowitz, V Beggs, AH Laing, NG Labeit, S de la Chapelle, A Wallgren-Pettersson, C
Citation: K. Pelin et al., Mutations in the nebulin gene associated with autosomal recessive nemalinemyopathy, P NAS US, 96(5), 1999, pp. 2305-2310
Risultati: 1-12 |