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Results: 1-11 |
Results: 11
Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation
Authors: Tuominen, S Juvonen, V Amberla, K Jolma, T Rinne, JO Tuisku, S Kurki, T Marttila, R Poyhonen, M Savontaus, ML Viitanen, M Kalimo, H
Citation: S. Tuominen et al., Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation, STROKE, 32(8), 2001, pp. 1767-1774
Mutations in the tyrosine phosphatase CD45 gene in a child with severe combined immunodeficiency disease
Authors: Kung, C Pingel, JT Heikinheimo, M Klemola, T Varkila, K Yoo, LI Vuopala, K Poyhonen, M Uhari, M Rogers, M Speck, SH Chatila, T Thomas, ML
Citation: C. Kung et al., Mutations in the tyrosine phosphatase CD45 gene in a child with severe combined immunodeficiency disease, NAT MED, 6(3), 2000, pp. 343-345
POLSSS: surveying stakeholders about acceptability of risks and system changes
Authors: Poyhonen, M
Citation: M. Poyhonen, POLSSS: surveying stakeholders about acceptability of risks and system changes, SAF SCI, 35(1-3), 2000, pp. 123-137
Conduction defects after coronary artery bypass grafting - A disappearing problem?
Authors: Mustonen, P Poyhonen, M Rehnberg, S Kouri, J Jaakkola, P Berg, E Loponen, P Hippelainen, M
Citation: P. Mustonen et al., Conduction defects after coronary artery bypass grafting - A disappearing problem?, ANN CHIR GY, 89(1), 2000, pp. 33-39
There is hope in attribute weighting
Authors: Poyhonen, M Hamalainen, RP
Citation: M. Poyhonen et Rp. Hamalainen, There is hope in attribute weighting, INFOR, 38(3), 2000, pp. 272-282
Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1
Authors: Lin, AE Birch, PH Korf, BR Tenconi, B Niimura, M Poyhonen, M Uhas, KA Sigorini, M Virdis, R Romano, C Bonioli, E Wolkenstein, P Pivnick, EK Lawrence, M Friedman, JM
Citation: Ae. Lin et al., Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1, AM J MED G, 95(2), 2000, pp. 108-117
Epidemiology of neurofibromatosis type 1 (NF1) in northern Finland
Authors: Poyhonen, M Kytola, S Leisti, J
Citation: M. Poyhonen et al., Epidemiology of neurofibromatosis type 1 (NF1) in northern Finland, J MED GENET, 37(8), 2000, pp. 632-636
New function for NF1 tumor suppressor
Authors: Koivunen, J Yla-Outinen, H Korkiamaki, T Karvonen, SL Poyhonen, M Laato, M Karvonen, J Peltonen, S Peltonen, J
Citation: J. Koivunen et al., New function for NF1 tumor suppressor, J INVES DER, 114(3), 2000, pp. 473-479
Occult neurofibroma and increased S100 protein in the skin of patients with neurofibromatosis type 1 - New insight to the etiopathomechanism of neurofibromas
Authors: Karvonen, SL Kallioinen, M Yla-Outinen, H Poyhonen, M Oikarinen, A Peltonen, J
Citation: Sl. Karvonen et al., Occult neurofibroma and increased S100 protein in the skin of patients with neurofibromatosis type 1 - New insight to the etiopathomechanism of neurofibromas, ARCH DERMAT, 136(10), 2000, pp. 1207-1209
A prospective, randomized study of goal-oriented hemodynamic therapy in cardiac surgical patients
Authors: Polonen, P Ruokonen, E Hippelainen, M Poyhonen, M Takala, J
Citation: P. Polonen et al., A prospective, randomized study of goal-oriented hemodynamic therapy in cardiac surgical patients, ANESTH ANAL, 90(5), 2000, pp. 1052-1059
CADASIL: hereditary disease of arteries causing brain infarcts and dementia
Authors: Kalimo, H Viitanen, M Amberla, K Juvonen, V Marttila, R Poyhonen, M Rinne, JO Savontaus, ML Tuisku, S Winblad, B
Citation: H. Kalimo et al., CADASIL: hereditary disease of arteries causing brain infarcts and dementia, NEUROP AP N, 25(4), 1999, pp. 257-265
Risultati: 1-11 |