Laplanche JL - Search Results

1

14-3-3 Protein in the cerebrospinal fluid of patients with acute transverse myelitis and multiple sclerosis.

de Seze J, Peoc'h K, Ferriby D, Stojkovic T, Laplanche JL, Vermersch P. de Seze J, et al. Among authors: laplanche jl. J Neurol. 2002 May;249(5):626-7. doi: 10.1007/s004150200074. J Neurol. 2002. PMID: 12021955 No abstract available.

2

14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients.

Brandel JP, Peoc'h K, Beaudry P, Welaratne A, Bottos C, Agid Y, Laplanche JL. Brandel JP, et al. Among authors: laplanche jl. Ann Neurol. 2001 Feb;49(2):257-60. doi: 10.1002/1531-8249(20010201)49:2<257::aid-ana48>3.0.co;2-x. Ann Neurol. 2001. PMID: 11220747

3

Creutzfeldt-Jakob disease: neurophysiologic visual impairments.

de Seze J, Hache JC, Vermersch P, Arndt CF, Maurage CA, Pasquier F, Laplanche JL, Ruchoux MM, Leys D, Destée A, Petit H. de Seze J, et al. Among authors: laplanche jl. Neurology. 1998 Oct;51(4):962-7. doi: 10.1212/wnl.51.4.962. Neurology. 1998. PMID: 9781513

4

Diagnostic value of CSF 14-3-3 detection in sporadic CJD diagnosis according to the age of the patient.

Peoc'h K, Delasnerie-Lauprêtre N, Beaudry P, Laplanche JL. Peoc'h K, et al. Among authors: laplanche jl. Eur J Neurol. 2006 Apr;13(4):427-8. doi: 10.1111/j.1468-1331.2006.01180.x. Eur J Neurol. 2006. PMID: 16643327 No abstract available.

5

Determination of 14-3-3 protein levels in cerebrospinal fluid from Creutzfeldt-Jakob patients by a highly sensitive capture assay.

Peoc'h K, Schröder HC, Laplanche J, Ramljak S, Müller WE. Peoc'h K, et al. Neurosci Lett. 2001 Apr 6;301(3):167-70. doi: 10.1016/s0304-3940(01)01619-6. Neurosci Lett. 2001. PMID: 11257424

6

A novel binding assay for detection of 14-3-3 protein in cerebrospinal fluid from Creutzfeldt-Jakob patients.

Leuck J, Peoch K, Laplanche JL, Grabar E, Müller WE, Schröder HC. Leuck J, et al. Among authors: laplanche jl. Cell Mol Biol (Noisy-le-grand). 2000 Nov;46(7):1291-6. Cell Mol Biol (Noisy-le-grand). 2000. PMID: 11075958

7

Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease.

Haïk S, Brandel JP, Sazdovitch V, Delasnerie-Lauprêtre N, Peoc'h K, Laplanche JL, Privat N, Duyckaerts C, Kemeny JL, Kopp N, Laquerrière A, Mohr M, Deslys JP, Dormont D, Hauw JJ. Haïk S, et al. Among authors: laplanche jl. Neurology. 2000 Nov 14;55(9):1401-4. doi: 10.1212/wnl.55.9.1401. Neurology. 2000. PMID: 11087793

8

A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease.

Rodriguez MM, Peoc'h K, Haïk S, Bouchet C, Vernengo L, Mañana G, Salamano R, Carrasco L, Lenne M, Beaudry P, Launay JM, Laplanche JL. Rodriguez MM, et al. Among authors: laplanche jl. Neurology. 2005 Apr 26;64(8):1455-7. doi: 10.1212/01.WNL.0000158618.39527.93. Neurology. 2005. PMID: 15851745

9

Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene.

Hauw JJ, Sazdovitch V, Laplanche JL, Peoc'h K, Kopp N, Kemeny J, Privat N, Delasnerie-Lauprêtre N, Brandel JP, Deslys JP, Dormont D, Alpérovitch A. Hauw JJ, et al. Among authors: laplanche jl. Neurology. 2000 Apr 25;54(8):1641-6. doi: 10.1212/wnl.54.8.1641. Neurology. 2000. PMID: 10762506

10

A French cluster of Creutzfeldt-Jakob disease: a molecular analysis.

Beaudry P, Parchi P, Peoc'h K, Desbordes P, Dartigues JF, Vital A, Vital C, Capellari S, Gambetti P, Delasnerie-Lauprêtre N, Mary JY, Laplanche JL. Beaudry P, et al. Among authors: laplanche jl. Eur J Neurol. 2002 Sep;9(5):457-62. doi: 10.1046/j.1468-1331.2002.00456.x. Eur J Neurol. 2002. PMID: 12220376

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