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Results: 1-18 |
Results: 18

Authors: Horvath, R Magura, T Szinetar, C
Citation: R. Horvath et al., Effects of immission load on spiders living on black pine, BIODIVERS C, 10(9), 2001, pp. 1531-1542

Authors: Horvath, R Kerekgyarto, T Csucs, G Gaspar, S Illyes, P Ronto, G Papp, E
Citation: R. Horvath et al., The effect of UV irradiation on uracil thin layer measured by optical waveguide lightmode spectroscopy, BIOSENS BIO, 16(1-2), 2001, pp. 17-21

Authors: Horvath, R Voros, J Graf, R Fricsovszky, G Textor, M Lindvold, LR Spencer, ND Papp, E
Citation: R. Horvath et al., Effect of patterns and inhomogeneities on the surface of waveguides used for optical waveguide lightmode spectroscopy applications, APP PHYS B, 72(4), 2001, pp. 441-447

Authors: Horvath, R
Citation: R. Horvath, Some integral properties of the heat equation, COMPUT MATH, 42(8-9), 2001, pp. 1135-1141

Authors: Zielinski, JM Carvill, BT Gardner, SA Kimak, MF Horvath, R Rovira, JE
Citation: Jm. Zielinski et al., Polymer/solvent equilibrium measurements via vapor-phase infrared spectroscopy, IND ENG RES, 40(14), 2001, pp. 2990-2994

Authors: Jaksch, M Horvath, R Horn, N Auer, DP Macmillan, C Peters, J Gerbitz, KD Kraegeloh-Mann, I Muntau, A Karcagi, V Kalmanchey, R Lochmuller, H Shoubridge, EA Freisinger, P
Citation: M. Jaksch et al., Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathy, NEUROLOGY, 57(8), 2001, pp. 1440-1446

Authors: Jaksch, M Lochmuller, H Schmitt, F Volpel, B Obermaier-Kusser, B Horvath, R
Citation: M. Jaksch et al., A mutation in mt tRNALeu ((UUR)) causing a neuropsychiatric syndrome with depression and cataract, NEUROLOGY, 57(10), 2001, pp. 1930-1931

Authors: Klivenyi, P Karg, E Rozsa, C Horvath, R Komoly, S Nemeth, I Turi, S Vecsei, L
Citation: P. Klivenyi et al., alpha-Tocopherol/lipid ratio in blood is decreased in patients with Leber's hereditary optic neuropathy and asymptomatic carriers of the 11778 mtDNA mutation, J NE NE PSY, 70(3), 2001, pp. 359-362

Authors: Jaksch, M Kleinle, S Scharfe, C Klopstock, T Pongratz, D Muller-Hocker, J Gerbitz, KD Liechti-Gallati, S Lochmuller, H Horvath, R
Citation: M. Jaksch et al., Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies, J MED GENET, 38(10), 2001, pp. 665-673

Authors: Horvath, R Cerny, J Benedik, J Hokl, J Jelinkova, I Benedik, J
Citation: R. Horvath et al., The possible role of human cytomegalovirus (HCMV) in the origin of atherosclerosis, J CLIN VIRO, 16(1), 2000, pp. 17-24

Authors: Gulyas, L Deak, G Keki, S Horvath, R Zsuga, M
Citation: L. Gulyas et al., A high-yielding synthesis and kinetics of glycine formation from monochloroacetic acid and NH3 in the presence of hexamethylenetetramine, ACH-MODEL C, 137(4), 2000, pp. 503-509

Authors: Horvath, R Magura, T Peter, G Bayar, K
Citation: R. Horvath et al., Edge effect on weevil and spider communities at the Bukk National Park in Hungary, ACT ZOOL H, 46(4), 2000, pp. 275-290

Authors: Horvath, R Abicht, A Shoubridge, EA Karcagi, V Rozsa, C Komoly, S Lochmuller, H
Citation: R. Horvath et al., Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNS, J NEUROL, 247(1), 2000, pp. 65-67

Authors: Horvath, R Lochmuller, H Stucka, R Yao, JB Shoubridge, EA Kim, SH Gerbitz, KD Jaksch, M
Citation: R. Horvath et al., Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency, BIOC BIOP R, 276(2), 2000, pp. 530-533

Authors: Farago, I Horvath, R
Citation: I. Farago et R. Horvath, An optimal mesh choice in the numerical solution of the heat equation, COMPUT MATH, 38(9-10), 1999, pp. 79-85

Authors: Michalek, J Horvath, R Benedik, J Hrstkova, H
Citation: J. Michalek et al., Human herpesvirus-6 infection in children with cancer, PED HEM ONC, 16(5), 1999, pp. 423-430

Authors: Horvath, R
Citation: R. Horvath, Maximum norm contractivity in the numerical solution of the one-dimensional heat equation, APPL NUM M, 31(4), 1999, pp. 451-462

Authors: Abicht, A Stucka, R Karcagi, V Herczegfalvi, A Horvath, R Mortier, W Schara, U Ramaekers, V Jost, W Brunner, J Janssen, G Seidel, U Schlotter, B Muller-Felber, W Pongratz, D Rudel, R Lochmuller, H
Citation: A. Abicht et al., A common mutation (epsilon 1267delG) in congenital myasthenic patients of Gypsy ethnic origin, NEUROLOGY, 53(7), 1999, pp. 1564-1569
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