Telomere length and mitochondrial DNA copy number in bipolar disorder: identification of a subgroup of young individuals with accelerated cellular aging von Spano, L., Etain, B., Meyrel, M., Hennion, V., Gross, G., Laplanche, J-L., Bellivier, F., Marie-Claire, C.

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Signal Transduction through Prion Protein von Mouillet-Richard, S., Ermonval, M., Chebassier, C., Laplanche, J. L., Lehmann, S., Launay, J. M., Kellermann, O.

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Acute pain Factors predictive of post-operative pain and opioid requirement in multimodal analgesia following knee replacement von Thomazeau, J., Rouquette, A., Martinez, V., Rabuel, C., Prince, N., Laplanche, J.L., Nizard, R., Bergmann, J.F., Perrot, S., Lloret-Linares, C.

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Genetic susceptibility and transmission factors in scrapie: detailed analysis of an epidemic in a closed flock of Romanov von Elsen, J.M, Amigues, Y, Schelcher, F, Ducrocq, V, Andreoletti, O, Eychenne, F, Tien Khang, J.V, Poivey, J.P, Lantier, F, Laplanche, J.L

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Amplification techniques and diagnosis of prion diseases von Brandel, J.-P., Culeux, A., Grznarova, K., Levavasseur, E., Lamy, P., Privat, N., Welaratne, A., Denouel, A., Laplanche, J.-L., Haik, S.

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Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease von ZERR, I, POCCHIARI, M, LADOGANA, A, BODEMER, M, FLETCHER, A, AWAN, T, RUIZ BREMON, A, BUDKA, H, LAPLANCHE, J. L, WILL, R. G, POSER, S, COLLINS, S, BRANDEL, J. P, DE PEDRO CUESTA, J, KNIGHT, R. S. G, BERNHEIMER, H, CARDONE, F, DELASNERIE-LAUPRETRE, N, CUADRADO CORRALES, N

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Sporadic Creutzfeldt-Jakob disease mimicking nonconvulsive status epilepticus von LAPERGUE, B, DEMERET, S, BOLGERT, F, BRANDEL, J. P, NAVARRO, V, DENYS, V, LAPLANCHE, J. L, GALANAUD, D, VERNY, M, SAZDOVITCH, V, BAULAC, M, HAÏK, S, HAUW, J. J

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A case of Gerstmann-Sträussler-Scheinker disease with a novel six octapeptide repeat insertion von Vital, A., Laplanche, J.-L., Bastard, J.-R., Xiao, X., Zou, W-Q., Vital, C.

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Long-standing Prion Dementia Manifesting as Posterior Cortical Atrophy von DEPAZ, Raphaë, HAIK, Stéphane, LAPLANCHE, J. L, FONTAINE, Bertrand, BRANDEL, Jean Philippe, PEOC'H, Katell, SEILHEAN, Danielle, GRABLI, David, VICART, Savine, SARAZIN, Marie, DETOFFOL, Bertrand, REMY, Catherine, FALLET-BIANCO, Catherine

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Functional expression of p-glycoprotein and multidrug resistance-associated protein (mrp1) in primary cultures of rat astrocytes von Declèves, X., Regina, A., Laplanche, J.-L., Roux, F., Boval, B., Launay, J.-M., Scherrmann, J.-M.

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Compassionate use of quinacrine in Creutzfeldt-Jakob disease fails to show significant effects von HAÏK, S, BRANDEL, J. P, HAUW, J. J, ALPEROVITCH, A, SALOMON, D, SAZDOVITCH, V, DELASNERIE-LAUPRETRE, N, LAPLANCHE, J. L, FAUCHEUX, B. A, SOUBRIE, C, BOHER, E, BELORGEY, C

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A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease von RODRIGUEZ, M.-M, PEOC'H, K, LAUNAY, J.-M, LAPLANCHE, J.-L, HAÏK, S, BOUCHET, C, VERNENGO, L, MANANA, G, SALAMANO, R, CARRASCO, L, LENNE, M, BEAUDRY, P

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Variant or sporadic Creutzfeldt-Jakob disease? von Brandel, J-P, Galanaud, D, Freeman, L, Laplanche, JL, Haik, S

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Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrP... von Faucheux, B. A., Morain, E., Diouron, V., Brandel, J.-P., Salomon, D., Sazdovitch, V., Privat, N., Laplanche, J.-L., Hauw, J.-J., Haïk, S.

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Diagnosis of Creutzfeldt-Jakob disease : Effect of clinical criteria on incidence estimates von BRANDEL, J.-P, DELASNERIE-LAUPRETRE, N, LAPLANCHE, J.-L, HAUW, J.-J, ALPEROVITCH, A

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Alzheimer's disease cerebro-spinal fluid biomarkers: A clinical research tool sometimes useful in daily clinical practice of memory clinics for the diagnosis of complex cases von Magnin, E, Dumurgier, J, Bouaziz-Amar, E, Bombois, S, Wallon, D, Gabelle, A, Lehmann, S, Blanc, F, Bousiges, O, Hannequin, D, Jung, B, Miguet-Alfonsi, C, Quillard, M, Pasquier, F, Peoc'h, K, Laplanche, J-L, Hugon, J, Paquet, C

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Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder von BETANCUR, C, CORBEX, M, NOSTEN-BERTRAND, M, LEBOYER, M, SPIELEWOY, C, PHILIPPE, A, LAPLANCHE, J-L, LAUNAY, J-M, GILLBERG, C, MOUREN-SIMEONI, M-C, HAMON, M, GIROS, B

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Antidepressant-induced mania, rapid cycling and the serotonin transporter gene polymorphism von Rousseva, A, Henry, C, van den Bulke, D, Fournier, G, Laplanche, J-L, Leboyer, M, Bellivier, F, Aubry, J-M, Baud, P, Boucherie, M, Buresi, C, Ferrero, F, Malafosse, A

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Possible association between serotonin transporter gene polymorphism and violent suicidal behavior in mood disorders von Bellivier, Frank, Szöke, Andreı̈, Henry, Chantal, Lacoste, Jérome, Bottos, Corinne, Nosten-Bertrand, Marika, Hardy, Patrick, Rouillon, Frederic, Launay, Jean-Marie, Laplanche, Jean-Louis, Leboyer, Marion

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Diagnosis associated with Tau higher than 1200 pg/mL: Insights from the clinical and laboratory practice von Lehmann, S., Paquet, C., Malaplate-Armand, C., Magnin, E., Schraen, S., Quillard-Muraine, M., Bousiges, O., Delaby, C., Dumurgier, J., Hugon, J., Sablonnière, B., Blanc, F., Wallon, D., Gabelle, A., Laplanche, J.L., Bouaziz-Amar, E., Peoc'h, K.

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