Peoc'h K - Search Results

1

Diagnosis associated with Tau higher than 1200 pg/mL: Insights from the clinical and laboratory practice.

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 JL, Bouaziz-Amar E, Peoc'h K; ePLM Group. Lehmann S, et al. Clin Chim Acta. 2019 Aug;495:451-456. doi: 10.1016/j.cca.2019.04.081. Epub 2019 Apr 30. Clin Chim Acta. 2019. PMID: 31051163

2

[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].

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 JL, Hugon J, Paquet C; pour le groupe ePLM (étude des biomarqueurs de la Ponction Lombaire Multicentrique). Magnin E, et al. Rev Med Interne. 2017 Apr;38(4):250-255. doi: 10.1016/j.revmed.2016.10.383. Epub 2016 Nov 24. Rev Med Interne. 2017. PMID: 27890382 Review. French.

3

[Genetics of human subacute spongiform encephalopathies].

Peoc'h K, Laplanche JL. Peoc'h K, et al. Rev Prat. 1999 May 1;49(9):954-8. Rev Prat. 1999. PMID: 11865460 Review. French.

4

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

5

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. 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

6

First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases.

Peoc'h K, Guérin C, Brandel JP, Launay JM, Laplanche JL. Peoc'h K, et al. Neurosci Lett. 2000 Jun 2;286(2):144-8. doi: 10.1016/s0304-3940(00)01100-9. Neurosci Lett. 2000. PMID: 10825657

7

OPRM1 polymorphism and lifetime suicide attempts among stabilized, methadone-maintained outpatients.

Icick R, Peoc'h K, Ksouda K, Bloch V, Laplanche JL, Lépine JP, Bellivier F, Vorspan F. Icick R, et al. Psychiatry Res. 2014 Aug 15;218(1-2):259-60. doi: 10.1016/j.psychres.2014.04.035. Epub 2014 Apr 24. Psychiatry Res. 2014. PMID: 24813900 No abstract available.

8

Prion-like protein Doppel expression is not modified in scrapie-infected cells and in the brains of patients with Creutzfeldt-Jakob disease.

Peoc'h K, Volland H, De Gassart A, Beaudry P, Sazdovitch V, Sorgato MC, Creminon C, Laplanche JL, Lehmann S. Peoc'h K, et al. FEBS Lett. 2003 Feb 11;536(1-3):61-5. doi: 10.1016/s0014-5793(03)00012-7. FEBS Lett. 2003. PMID: 12586339 Free article.

9

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. Cell Mol Biol (Noisy-le-grand). 2000 Nov;46(7):1291-6. Cell Mol Biol (Noisy-le-grand). 2000. PMID: 11075958

10

Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype.

Peoc'h K, Manivet P, Beaudry P, Attane F, Besson G, Hannequin D, Delasnerie-Lauprêtre N, Laplanche JL. Peoc'h K, et al. Hum Mutat. 2000 May;15(5):482. doi: 10.1002/(SICI)1098-1004(200005)15:5<482::AID-HUMU16>3.0.CO;2-1. Hum Mutat. 2000. PMID: 10790216

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