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Results: 1-10 |
Results: 10
European surveillance on Creutzfeldt-Jakob disease: a case-control study for medical risk factors
Authors: Zerr, I Brandel, JP Masullo, C Wientjens, D de Silva, R Zeidler, M Granieri, E Sampaolo, S van Duijn, C Delasnerie-Laupretre, N Will, R Poser, S
Citation: I. Zerr et al., European surveillance on Creutzfeldt-Jakob disease: a case-control study for medical risk factors, J CLIN EPID, 53(7), 2000, pp. 747-754
Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease
Authors: Haik, S Brandel, JP Sazdovitch, V Delasnerie-Laupretre, N Peoc'h, K Laplanche, JL Privat, N Duyckaerts, C Kemeny, JL Kopp, N Laquerriere, A Mohr, M Deslys, JP Dormont, D Hauw, JJ
Citation: S. Haik et al., Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease, NEUROLOGY, 55(9), 2000, pp. 1401-1404
Analysis of EEG and CSF 14-3-3 protein as aids to the diagnosis of Creutzfeldt-Jakob disease
Authors: Zerr, I Pocchiari, M Collins, S Brandel, JP Cuesta, JD Knight, RSG Bernheimer, H Cardone, F Delasnerie-Laupretre, N Corrales, NC Ladogana, A Bodemer, M Fletcher, A Awan, T Bremon, AR Budka, H Laplanche, JL Will, RG Poser, S
Citation: I. Zerr et al., Analysis of EEG and CSF 14-3-3 protein as aids to the diagnosis of Creutzfeldt-Jakob disease, NEUROLOGY, 55(6), 2000, pp. 811-815
Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene
Authors: Hauw, JJ Sazdovitch, V Laplanche, JL Peoc'h, K Kopp, N Kemeny, J Privat, N Delasnerie-Laupretre, N Brandel, JP Deslys, JP Dormont, D Alperovitch, A
Citation: Jj. Hauw et al., Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene, NEUROLOGY, 54(8), 2000, pp. 1641-1646
Diagnosis of Creutzfeldt-Jakob disease - Effect of clinical criteria on incidence estimates
Authors: Brandel, JP Delasnerie-Laupretre, N Laplanche, JL Hauw, JJ Alperovitch, A
Citation: Jp. Brandel et al., Diagnosis of Creutzfeldt-Jakob disease - Effect of clinical criteria on incidence estimates, NEUROLOGY, 54(5), 2000, pp. 1095-1099
Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7
Authors: d'Aignaux, JH Laplanche, JL Delasnerie-Laupretre, N Brandel, JP Peoc'h, K Salomon, D Hauw, JJ Alperovitch, A
Citation: Jh. D'Aignaux et al., Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7, J NE NE PSY, 68(6), 2000, pp. 787-789
14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
Authors: Beaudry, P Cohen, P Brandel, JP Delasnerie-Laupretre, N Richard, S Launay, JM Laplanche, JL
Citation: P. Beaudry et al., 14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease, DEMENT G C, 10(1), 1999, pp. 40-46
Creutzfeldt Jakob disease: diagnostic value of protein 14-3-3 and neuronalspecific enolase assay in cerebrospinal fluid.
Authors: Brandel, JP Beaudry, P Delasnerie-Laupretre, N Laplanche, JL
Citation: Jp. Brandel et al., Creutzfeldt Jakob disease: diagnostic value of protein 14-3-3 and neuronalspecific enolase assay in cerebrospinal fluid., REV NEUROL, 155(2), 1999, pp. 148-151
Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene
Authors: Laplanche, JL El Hachimi, KH Durieux, I Thuillet, P Defebvre, L Delasnerie-Laupretre, N Peoc'h, K Foncin, JF Destee, A
Citation: Jl. Laplanche et al., Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene, BRAIN, 122, 1999, pp. 2375-2386
Multiple sclerosis in North African migrants to France
Authors: Kurtzke, JF Delasnerie-Laupretre, N Wallin, MT
Citation: Jf. Kurtzke et al., Multiple sclerosis in North African migrants to France, ACT NEUR SC, 98(5), 1998, pp. 302-309
Risultati: 1-10 |