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Results: 1-19 |
Results: 19

Authors: Reiss, J Razzouk, AJ Kiev, J Bansal, R Bailey, LL
Citation: J. Reiss et al., Concomitant traumatic coronary artery and tricuspid valve injury: A heterogeneous presentation, J TRAUMA, 50(5), 2001, pp. 942-944

Authors: Alberdi, E Becher, JC Gilhooly, K Hunter, J Logie, R Lyon, A McIntosh, N Reiss, J
Citation: E. Alberdi et al., Expertise and the interpretation of computerized physiological data: implications for the design of computerized monitoring in neonatal intensive care, INT J HUM-C, 55(3), 2001, pp. 191-216

Authors: Menzer, G Muller-Thomsen, T Meins, W Alberici, A Binetti, G Hock, C Nitsch, RM Stoppe, G Reiss, J Finckh, U
Citation: G. Menzer et al., Non-replication of association between cathepsin D genotype and late onsetAlzheimer disease, AM J MED G, 105(2), 2001, pp. 179-182

Authors: Uysal, E Trainer, FH Reiss, J
Citation: E. Uysal et al., Revisiting mean-variance optimization, J PORTFOLIO, 27(4), 2001, pp. 71

Authors: Reiss, J Gross-Hardt, S Christensen, E Schmidt, P Mendel, RR Schwarz, G
Citation: J. Reiss et al., A mutation in the gene for the neurotransmitter receptor-clustering protein gephyrin causes a novel form of molybdenum cofactor deficiency, AM J HU GEN, 68(1), 2001, pp. 208-213

Authors: Alberdi, E Gilhooly, K Hunter, J Logie, R Lyon, A McIntosh, N Reiss, J
Citation: E. Alberdi et al., Computerisation and decision making in neonatal intensive care: A cognitive engineering investigation, J CLIN M C, 16(2), 2000, pp. 85-94

Authors: Reiss, J
Citation: J. Reiss, Genetics of molybdenum cofactor deficiency, HUM GENET, 106(2), 2000, pp. 157-163

Authors: Shalata, A Mandel, H Dorche, C Zabot, MT Shalev, S Hugeirat, Y Arieh, D Ronit, Z Reiss, J Anbinder, Y Cohen, N
Citation: A. Shalata et al., Prenatal diagnosis and carrier detection for molybdenum cofactor deficiency type A in Northern Israel using polymorphic DNA markers, PRENAT DIAG, 20(1), 2000, pp. 7-11

Authors: Finckh, U von der Kammer, H Velden, J Michel, T Andresen, B Deng, A Zhang, J Muller-Thomsen, T Zuchowski, K Menzer, G Mann, U Papassotiropoulos, A Heun, R Zurdel, J Holst, F Benussi, L Stoppe, G Reiss, J Miserez, AR Staehelin, HB Rebeck, GW Hyman, BT Binetti, G Hock, C Growdon, JH Nitsch, RM
Citation: U. Finckh et al., Genetic association of a cystatin C gene polymorphism with late-onset Alzheimer disease, ARCH NEUROL, 57(11), 2000, pp. 1579-1583

Authors: Reiss, J Christensen, E Dorche, C
Citation: J. Reiss et al., Molybdenum cofactor deficiency: First prenatal genetic analysis, PRENAT DIAG, 19(4), 1999, pp. 386-388

Authors: Popovic, T Kim, C Reiss, J Reeves, M Nakao, H Golaz, A
Citation: T. Popovic et al., Use of molecular subtyping to document long-term persistence of Corynebacterium diphtheriae in South Dakota, J CLIN MICR, 37(4), 1999, pp. 1092-1099

Authors: Mischaikow, K Mrozek, M Reiss, J Szymczak, A
Citation: K. Mischaikow et al., Construction of symbolic dynamics from experimental time series, PHYS REV L, 82(6), 1999, pp. 1144-1147

Authors: von Hayek, D Huttl, V Reiss, J Schweiger, HD Fuessl, HS
Citation: D. Von Hayek et al., Hyperglycaemia and ketoacidosis on olanzapine, NERVENARZT, 70(9), 1999, pp. 836-837

Authors: Stallmeyer, B Schwarz, G Schulze, J Nerlich, A Reiss, J Kirsch, J Mendel, RR
Citation: B. Stallmeyer et al., The neurotransmitter receptor-anchoring protein gephyrin reconstitutes molybdenum cofactor biosynthesis in bacteria, plants, and mammalian cells, P NAS US, 96(4), 1999, pp. 1333-1338

Authors: Reiss, J
Citation: J. Reiss, 'Apple Face', COLL ENGL, 61(5), 1999, pp. 604-604

Authors: Stallmeyer, B Drugeon, G Reiss, J Haenni, AL Mendel, RR
Citation: B. Stallmeyer et al., Human molybdopterin synthase gene: Identification of a bicistronic transcript with overlapping reading frames, AM J HU GEN, 64(3), 1999, pp. 698-705

Authors: Reiss, J Dorche, C Stallmeyer, B Mendel, RR Cohen, N Zabot, MT
Citation: J. Reiss et al., Human molybdopterin synthase gene: genomic structure and mutations in molybdenum cofactor deficiency type B, AM J HU GEN, 64(3), 1999, pp. 706-711

Authors: Reiss, J Christensen, E Kurlemann, G Zabot, MT Dorche, C
Citation: J. Reiss et al., Genomic structure and mutational spectrum of the bicistronic MOCS1 gene defective in molybdenum cofactor deficiency type A, HUM GENET, 103(6), 1998, pp. 639-644

Authors: Strobel, G Reiss, J Friedmann, B Bartsch, P
Citation: G. Strobel et al., Effect of repeated bouts of short-term exercise on plasma free and sulphoconjugated catecholamines in humans, EUR J A PHY, 79(1), 1998, pp. 82-87
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