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Results: 1-18 |
Results: 18

Authors: Andersen, PM Spitsyn, VA Makarov, SV Nilsson, L Kravchuk, OI Bychkovskaya, LS Marklund, SL
Citation: Pm. Andersen et al., The geographical and ethnic distribution of the D90A CuZn-SOD mutation in the Russian Federation, AMYOTROPH L, 2(2), 2001, pp. 63-69

Authors: Andersen, PM
Citation: Pm. Andersen, Genetics of sporadic ALS, AMYOTROPH L, 2, 2001, pp. S37-S41

Authors: Lund, A Udd, B Juvonen, V Andersen, PM Cederquist, K Davis, M Gellera, C Kolmel, C Ronnevi, LO Sperfeld, AD Sorensen, SA Tranebjaerg, L Van Maldergem, L Watanabe, M Weber, M Yeung, L Savontaus, ML
Citation: A. Lund et al., Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world, EUR J HUM G, 9(6), 2001, pp. 431-436

Authors: Parton, MJ Andersen, PM Broom, WJ Shaw, CE
Citation: Mj. Parton et al., Compound heterozygosity and variable penetrance in SOD1 amyotrophic lateral sclerosis pedigrees, ANN NEUROL, 50(4), 2001, pp. 553-554

Authors: Russ, C Lovestone, S Baker, M Pickering-Brown, SM Andersen, PM Furlong, R Mann, D Powell, JF
Citation: C. Russ et al., The extended haplotype of the microtubule associated protein tau gene is not associated with Pick's disease, NEUROSCI L, 299(1-2), 2001, pp. 156-158

Authors: Weber, M Eisen, A Stewart, HG Andersen, PM Hirota, N
Citation: M. Weber et al., The physiological basis of conduction slowing in ALS patients homozygous for the D90A CuZn-SOD mutation, MUSCLE NERV, 24(1), 2001, pp. 89-97

Authors: Andersen, PM
Citation: Pm. Andersen, Genetics of amyotrophic lateral sclerosis, ZH NEVR PS, 101(3), 2001, pp. 54-63

Authors: Andersen, PM Gronberg, H Franzen, L Funegard, U
Citation: Pm. Andersen et al., External radiation of the parotid glands significantly reduces drooling inpatients with motor neurone disease with bulbar paresis, J NEUR SCI, 191(1-2), 2001, pp. 111-114

Authors: Jacobsson, J Jonsson, PA Andersen, PM Forsgren, L Marklund, SL
Citation: J. Jacobsson et al., Superoxide dismutase in CSF from amyotrophic lateral sclerosis patients with and without CuZn-superoxide dismutase mutations, BRAIN, 124, 2001, pp. 1461-1466

Authors: Andersen, PM
Citation: Pm. Andersen, Genetic factors in the early diagnosis of ALS, AMYOTROPH L, 1, 2000, pp. S31-S42

Authors: Lund, A Udd, B Juvonen, V Andersen, PM Cederquist, K Ronnevi, LO Sistonen, P Sorensen, SA Tranebjaerg, L Wallgren-Pettersson, C Savontaus, ML
Citation: A. Lund et al., Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia, EUR J HUM G, 8(8), 2000, pp. 631-636

Authors: De Farias, AX Robbs, CF Bittencourt, AM Andersen, PM Correa, TBS
Citation: Ax. De Farias et al., Endogenous Aspergillus spp. contamination of postharvest corn in Parana State, Brazil, PESQ AGROP, 35(3), 2000, pp. 617-621

Authors: Andersen, PM Fagerlund, M
Citation: Pm. Andersen et M. Fagerlund, Vertebrogenic dysphagia and gait disturbance mimicking motor neuron disease, J NE NE PSY, 69(4), 2000, pp. 560-561

Authors: Weber, M Eisen, A Stewart, HG Andersen, PM
Citation: M. Weber et al., Preserved slow conducting corticomotoneuronal projections in amyotrophic lateral sclerosis with autosomal recessive D90A CuZn-superoxide dismutase mutation, BRAIN, 123, 2000, pp. 1505-1515

Authors: Van Landeghem, GF Tabatabaie, P Beckman, G Beckman, L Andersen, PM
Citation: Gf. Van Landeghem et al., Manganese-containing superoxide dismutase signal sequence polymorphism associated with sporadic motor neuron disease, EUR J NEUR, 6(6), 1999, pp. 639-644

Authors: Al-Chalabi, A Andersen, PM Nilsson, P Chioza, B Andersson, JL Russ, C Shaw, CE Powell, JF Leigh, PN
Citation: A. Al-chalabi et al., Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis, HUM MOL GEN, 8(2), 1999, pp. 157-164

Authors: Mezei, M Andersen, PM Stewart, H Weber, M Eisen, A
Citation: M. Mezei et al., Motor system abnormalities in heterozygous relatives of a D90A homozygous CuZn-SOD ALS patient of Finnish extraction, J NEUR SCI, 169(1-2), 1999, pp. 49-55

Authors: Al-Chalabi, A Andersen, PM Chioza, B Shaw, C Sham, PC Robberecht, W Matthijs, G Camu, V Marklund, SL Forsgren, L Rouleau, G Laing, NG Hurse, PV Siddique, T Leigh, PN Powell, JF
Citation: A. Al-chalabi et al., Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor, HUM MOL GEN, 7(13), 1998, pp. 2045-2050
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