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Results: 1-25 | 26-30
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A signalling fuction for the prion protein
Authors: Chebassier, C Mouillet-Richard, S Laplanche, JL Kellermann, O Launay, JM
Citation: C. Chebassier et al., A signalling fuction for the prion protein, PATH BIOL, 49(3), 2001, pp. 191-193
14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients
Authors: Brandel, JP Peoc'h, K Beaudry, P Welaratne, A Bottos, C Agid, Y Laplanche, JL
Citation: Jp. Brandel et al., 14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients, ANN NEUROL, 49(2), 2001, pp. 257-260
Determination of 14-3-3 protein levels in cerebrospinal fluid from Creutzfeldt-Jakob patients by a highly sensitive capture assay
Authors: Peoc'h, K Schroder, HC Laplanche, JL Ramljak, S Muller, WEG
Citation: K. Peoc'H et al., Determination of 14-3-3 protein levels in cerebrospinal fluid from Creutzfeldt-Jakob patients by a highly sensitive capture assay, NEUROSCI L, 301(3), 2001, pp. 167-170
Serotonin transporter gene polymorphism and psychiatric disorders in NF1 patients
Authors: Bellivier, F Laplanche, JL Fournier, G Wolkenstein, P
Citation: F. Bellivier et al., Serotonin transporter gene polymorphism and psychiatric disorders in NF1 patients, AM J MED G, 105(8), 2001, pp. 758-760
This is really a case of new variant Creutzfeldt-Jakob - Response
Authors: Streichenberger, N Biacabe, AG Perret-Liaudet, A Deslys, JP Laplanche, JL Chazot, G Kopp, N
Citation: N. Streichenberger et al., This is really a case of new variant Creutzfeldt-Jakob - Response, ACT NEUROP, 102(6), 2001, pp. 647-648
PrP immunohistochemistry: Different protocols, including a procedure for long formalin fixation, and a proposed schematic classification for depositsin sporadic Creutzfeldt-Jakob disease
Authors: Privat, N Sazdovitch, V Seilhean, D Laplanche, JL Hauw, JJ
Citation: N. Privat et al., PrP immunohistochemistry: Different protocols, including a procedure for long formalin fixation, and a proposed schematic classification for depositsin sporadic Creutzfeldt-Jakob disease, MICROSC RES, 50(1), 2000, pp. 26-31
Biochemical mechanisms in the physiopathology of migraines.
Authors: Manivet, P Soliman, HR Callebert, J Laplanche, JL Launay, JM
Citation: P. Manivet et al., Biochemical mechanisms in the physiopathology of migraines., PATH BIOL, 48(7), 2000, pp. 630-641
Functional expression of P-glycoprotein and multidrug resistance-associated protein (Mrp1) in primary cultures of rat astrocytes
Authors: Decleves, X Regina, A Laplanche, JL Roux, F Boval, B Launay, JM Scherrmann, JM
Citation: X. Decleves et al., Functional expression of P-glycoprotein and multidrug resistance-associated protein (Mrp1) in primary cultures of rat astrocytes, J NEUROSC R, 60(5), 2000, pp. 594-601
First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases
Authors: Peoc'h, K Guerin, C Brandel, JP Launay, JM Laplanche, JL
Citation: K. Peoc'H et al., First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases, NEUROSCI L, 286(2), 2000, pp. 144-148
A novel binding assay for detection of 14-3-3 protein in cerebrospinal fluid from Creutzfeldt-Jakob patients
Authors: Leuck, J Peoc'h, K Laplanche, JL Grabar, E Muller, WEG Schroder, HC
Citation: J. Leuck et al., A novel binding assay for detection of 14-3-3 protein in cerebrospinal fluid from Creutzfeldt-Jakob patients, CELL MOL B, 46(7), 2000, pp. 1291-1296
Novel approaches in diagnosis and therapy of Creutzfeldt-Jakob disease
Authors: Muller, WEG Laplanche, JL Ushijima, H Schroder, HC
Citation: Weg. Muller et al., Novel approaches in diagnosis and therapy of Creutzfeldt-Jakob disease, MECH AGE D, 116(2-3), 2000, pp. 193-218
Signal transduction through prion protein
Authors: Mouillet-Richard, S Ermonval, M Chebassier, C Laplanche, JL Lehmann, S Launay, JM Kellermann, O
Citation: S. Mouillet-richard et al., Signal transduction through prion protein, SCIENCE, 289(5486), 2000, pp. 1925-1928
Non familial Creutzfeldt-Jakob disease: a study of 53 cases.
Authors: Giraud, P Perret-Liaudet, A Biacabe, AG Deslys, JP Laplanche, JL Chazot, G Kopp, N
Citation: P. Giraud et al., Non familial Creutzfeldt-Jakob disease: a study of 53 cases., REV NEUROL, 156(6-7), 2000, pp. 616-621
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
Possible association between serotonin transporter gene polymorphism and violent suicidal behavior in mood disorders
Authors: Bellivier, F Szoke, A Henry, C Lacoste, J Bottos, C Nosten-Bertrand, M Hardy, P Rouillon, F Launay, JM Laplanche, JL Leboyer, M
Citation: F. Bellivier et al., Possible association between serotonin transporter gene polymorphism and violent suicidal behavior in mood disorders, BIOL PSYCHI, 48(4), 2000, pp. 319-322
The first case of new variant Creutzfeldt-Jakob disease in France: clinical data and neuropathological findings
Authors: Streichenberger, N Jordan, D Verejan, I Souchier, C Philippeau, F Gros, E Mottolese, C Ostrowsky, K Perret-Liaudet, A Laplanche, JL Hermier, M Deslys, JP Chazot, G Kopp, N
Citation: N. Streichenberger et al., The first case of new variant Creutzfeldt-Jakob disease in France: clinical data and neuropathological findings, ACT NEUROP, 99(6), 2000, pp. 704-708
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
Prion protein and neuronal differentiation: quantitative analysis of prnp gene expression in a murine inducible neuroectodermal progenitor
Authors: Mouillet-Richard, S Laurendeau, I Vidaud, M Kellermann, O Laplanche, JL
Citation: S. Mouillet-richard et al., Prion protein and neuronal differentiation: quantitative analysis of prnp gene expression in a murine inducible neuroectodermal progenitor, MICROBES IN, 1(12), 1999, pp. 969-976
Search for asymptomatic coeliac disease in patients with spongiform encephalopathy
Authors: Beaugerie, L Andre, C Laplanche, JL
Citation: L. Beaugerie et al., Search for asymptomatic coeliac disease in patients with spongiform encephalopathy, GASTRO CL B, 23(3), 1999, pp. 411-412
Genetic susceptibility and transmission factors in scrapie: detailed analysis of an epidemic in a closed flock of Romanov
Authors: Elsen, JM Amigues, Y Schelcher, F Ducrocq, V Andreoletti, O Eychenne, F Khang, JVT Poivey, JP Lantier, F Laplanche, JL
Citation: Jm. Elsen et al., Genetic susceptibility and transmission factors in scrapie: detailed analysis of an epidemic in a closed flock of Romanov, ARCH VIROL, 144(3), 1999, pp. 431-445
Scrapie, chronic wasting disease, and transmissible mink encephalopathy
Authors: Laplanche, JL Hunter, N Shinagawa, M Williams, E
Citation: Jl. Laplanche et al., Scrapie, chronic wasting disease, and transmissible mink encephalopathy, COLD S H MG, 38, 1999, pp. 393-429
Risultati: 1-25 | 26-30