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Results: 1-12 |
Results: 12
The safety of human blood: experimental TSE/prion infectivity studies
Authors: Cervenakova, L
Citation: L. Cervenakova, The safety of human blood: experimental TSE/prion infectivity studies, TRANSF CL B, 8(3), 2001, pp. 260-260
Blood infectivity and the prospects for a diagnostic screening test in Creutzfeldt-Jakob disease
Authors: Brown, P Cervenakova, L Diringer, H
Citation: P. Brown et al., Blood infectivity and the prospects for a diagnostic screening test in Creutzfeldt-Jakob disease, J LA CL MED, 137(1), 2001, pp. 5-13
Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype
Authors: Lee, HS Brown, P Cervenakova, L Garruto, RM Alpers, MP Gajdusek, DC Goldfarb, LG
Citation: Hs. Lee et al., Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype, J INFEC DIS, 183(2), 2001, pp. 192-196
Infectivity of buffy coat in variant CJD - Reply
Authors: Brown, P Cervenakova, L
Citation: P. Brown et L. Cervenakova, Infectivity of buffy coat in variant CJD - Reply, TRANSFUSION, 40(6), 2000, pp. 755-755
Iatrogenic Creutzfeldt-Jakob disease at the millennium
Authors: Brown, P Preece, M Brandel, JP Sato, T McShane, L Zerr, I Fletcher, A Will, RG Pocchiari, M Cashman, NR d'Aignaux, JH Cervenakova, L Fradkin, J Schonberger, LB Collins, SJ
Citation: P. Brown et al., Iatrogenic Creutzfeldt-Jakob disease at the millennium, NEUROLOGY, 55(8), 2000, pp. 1075-1081
Inherited prion encephalopathy associated with the novel PRNP H187R mutation - A clinical study
Authors: Butefisch, CM Gambetti, P Cervenakova, L Park, KY Hallett, M Goldfarb, LG
Citation: Cm. Butefisch et al., Inherited prion encephalopathy associated with the novel PRNP H187R mutation - A clinical study, NEUROLOGY, 55(4), 2000, pp. 517-522
Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS)
Authors: Cervenakova, L Protas, II Hirano, A Votiakov, VI Nedzved, MK Kolomiets, ND Taller, I Park, KY Sambuughin, N Gajdusek, DC Brown, P Goldfarb, LG
Citation: L. Cervenakova et al., Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS), J NEUR SCI, 177(2), 2000, pp. 124-130
A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Straussler-Scheinker phenotype but no alterations in the PRNP gene
Authors: Liberski, PP Bratosiewicz, J Barcikowska, M Cervenakova, L Marczewska, M Brown, P Gajdusek, DC
Citation: Pp. Liberski et al., A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Straussler-Scheinker phenotype but no alterations in the PRNP gene, ACT NEUROP, 100(2), 2000, pp. 233-234
Safety of blood products: Are transmissible spongiform encephalopathies (prion diseases) a risk?
Authors: Drohan, WN Cervenakova, L
Citation: Wn. Drohan et L. Cervenakova, Safety of blood products: Are transmissible spongiform encephalopathies (prion diseases) a risk?, THROMB HAEM, 82(2), 1999, pp. 486-493
Novel PRNP sequence variant associated with familial encephalopathy
Authors: Cervenakova, L Buetefisch, C Lee, HS Taller, I Stone, G Gibbs, CJ Brown, P Hallett, M Goldfarb, LG
Citation: L. Cervenakova et al., Novel PRNP sequence variant associated with familial encephalopathy, AM J MED G, 88(6), 1999, pp. 653-656
Further studies of blood infectivity in an experimental model of transmissible spongiform encephalopathy, with an explanation of why blood componentsdo not transmit Creutzfeldt-Jakob disease in humans
Authors: Brown, P Cervenakova, L McShane, LM Barber, P Rubenstein, R Drohan, WN
Citation: P. Brown et al., Further studies of blood infectivity in an experimental model of transmissible spongiform encephalopathy, with an explanation of why blood componentsdo not transmit Creutzfeldt-Jakob disease in humans, TRANSFUSION, 39(11-12), 1999, pp. 1169-1178
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease
Authors: Lee, HS Sambuughin, N Cervenakova, L Chapman, J Pocchiari, M Litvak, S Qi, HY Budka, H del Ser, T Furukawa, H Brown, P Gajdusek, DC Long, JC Korczyn, AD Goldfarb, LG
Citation: Hs. Lee et al., Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease, AM J HU GEN, 64(4), 1999, pp. 1063-1070
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