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Results of search for 'au:"LAPLANCHE, J"', page 2 of 6
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Authors
Alpérovitch, A
Beaudry, P
Bellivier, F
Bottos, C
Brandel, J P
Chatelain, J
Chazot, G
Delasnerie-Lauprêtre, N
Deslys, J P
Dreux, C
Dussaucy, M
Hauw, J J
Laplanche, J
Laplanche, J L
Laplanche, J-L
Launay, J M
Leboyer, M
Lehmann, S
Peoc'h, K
Sazdovitch, V
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Adult
Aged
Animals
Brain
Codon
Creutzfeldt-Jakob Syndrome
Female
France
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Middle Aged
Mutation
Polymorphism, Genetic
Prion Diseases
Prions
diagnosis
genetics
metabolism
pathology
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Your search returned 107 results.
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21.
Apolipoprotein E in Creutzfeldt-Jakob disease. French Research Group on Epidemiology of Human Spongiform Encephalopathies.
[electronic resource]
by
Amouyel, P
Alpérovitch, A
Delasnerie-Lauprêtre, N
Laplanche, J L
Producer:
19950707
In:
Lancet (London, England)
vol. 345
Online resources:
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22.
Diagnostic value of CSF 14-3-3 detection in sporadic CJD diagnosis according to the age of the patient.
[electronic resource]
by
Peoc'h, K
Delasnerie-Lauprêtre, N
Beaudry, P
Laplanche, J-L
Producer:
20060616
In:
European journal of neurology
vol. 13
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23.
[Proteins, genes and early diagnosis of Alzheimer's disease].
[electronic resource]
by
Laplanche, J L
Chatelain, J
Launay, J M
Dreux, C
Producer:
19900813
In:
Annales de biologie clinique
vol. 48
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24.
The apolipoprotein E alleles as major susceptibility factors for Creutzfeldt-Jakob disease. The French Research Group on Epidemiology of Human Spongiform Encephalopathies.
[electronic resource]
by
Amouyel, P
Vidal, O
Launay, J M
Laplanche, J L
Producer:
19941213
In:
Lancet (London, England)
vol. 344
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25.
[Prion protein: structure, functions and polymorphisms associated with human spongiform encephalopathies].
[electronic resource]
by
Laplanche, J L
Beaudry, P
Ripoll, L
Launay, J M
Producer:
19950712
In:
Pathologie-biologie
vol. 43
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26.
[Transmissible animal spongiform encephalopathies].
[electronic resource]
by
Brugère-Picoux, J
Chatelain, J
Laplanche, J L
Brugère, H
Producer:
19941215
In:
Bulletin de l'Academie nationale de medecine
vol. 178
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27.
[Bovine spongiform encephalopathy: a new entity caused by a non-conventional transmissible agent].
[electronic resource]
by
Parodi, A L
Brugère-Picoux, J
Chatelain, J
Laplanche, J L
Producer:
19910222
In:
Bulletin de l'Academie nationale de medecine
vol. 174
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28.
[Creutzfeldt-Jakob disease: diagnostic value of protein 14-3-3 and neuronal specific enolase assay in cerebrospinal fluid].
[electronic resource]
by
Brandel, J P
Beaudry, P
Delasnerie-Lauprêtre, N
Laplanche, J L
Producer:
19990618
In:
Revue neurologique
vol. 155
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29.
[Analysis of the PrP gene in a Tunisian family with Creutzfeldt-Jakob disease].
[electronic resource]
by
Laplanche, J L
Chatelain, J
Thomas, S
Brown, P
Cathala, F
Producer:
19920310
In:
Revue neurologique
vol. 147
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30.
A new polymorphism (N21D) in the exon 2 of the human MDR1 gene encoding the P-glycoprotein.
[electronic resource]
by
Declèves, X
Chevillard, S
Charpentier, C
Vielh, P
Laplanche, J L
Producer:
20000921
In:
Human mutation
vol. 15
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31.
Novel approaches in diagnosis and therapy of Creutzfeldt-Jakob disease.
[electronic resource]
by
Müller, W E
Laplanche, J L
Ushijima, H
Schröder, H C
Producer:
20001121
In:
Mechanisms of ageing and development
vol. 116
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32.
PrP immunohistochemistry: different protocols, including a procedure for long formalin fixation, and a proposed schematic classification for deposits in sporadic Creutzfeldt-Jakob disease.
[electronic resource]
by
Privat, N
Sazdovitch, V
Seilhean, D
LaPlanche, J L
Hauw, J J
Producer:
20000822
In:
Microscopy research and technique
vol. 50
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33.
Creutzfeldt-Jakob disease in a 52-year-old woman with florid plaques.
[electronic resource]
by
Kopp, N
Streichenberger, N
Deslys, J P
Laplanche, J L
Chazot, G
Producer:
19961204
In:
Lancet (London, England)
vol. 348
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34.
Valine homozygous 129 PrP genotype in a French growth-hormone-related Creutzfeldt-Jakob disease patient.
[electronic resource]
by
Labauge, P
Pagès, M
Blard, J M
Chatelain, J
Laplanche, J L
Producer:
19930323
In:
Neurology
vol. 43
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35.
Prion protein and neuronal differentiation: quantitative analysis of prnp gene expression in a murine inducible neuroectodermal progenitor.
[electronic resource]
by
Mouillet-Richard, S
Laurendeau, I
Vidaud, M
Kellermann, O
Laplanche, J L
Producer:
20000621
In:
Microbes and infection
vol. 1
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36.
Variant or sporadic Creutzfeldt-Jakob disease?
[electronic resource]
by
Brandel, J-P
Galanaud, D
Freeman, L
Laplanche, J L
Haik, S
Producer:
20100330
In:
Lancet (London, England)
vol. 375
Online resources:
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37.
Deletion in prion protein gene in a Moroccan family.
[electronic resource]
by
Laplanche, J L
Chatelain, J
Launay, J M
Gazengel, C
Vidaud, M
Producer:
19910115
In:
Nucleic acids research
vol. 18
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38.
HLA in French patients with variant Creutzfeldt-Jakob disease.
[electronic resource]
by
Laplanche, J L
Lepage, V
Peoc'h, K
Delasnerie-Lauprêtre, N
Charron, D
Producer:
20030321
In:
Lancet (London, England)
vol. 361
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39.
Determination of 14-3-3 protein levels in cerebrospinal fluid from Creutzfeldt-Jakob patients by a highly sensitive capture assay.
[electronic resource]
by
Peoc'h, K
Schröder, H C
Laplanche, J
Ramljak, S
Müller, W E
Producer:
20010524
In:
Neuroscience letters
vol. 301
Online resources:
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40.
[A signaling function for the prion protein].
[electronic resource]
by
Chebassier, C
Mouillet-Richard, S
Laplanche, J L
Kellermann, O
Launay, J M
Producer:
20010628
In:
Pathologie-biologie
vol. 49
Online resources:
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