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Results of search for 'au:"LAPLANCHE, J"', page 4 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
Genotype
Humans
Male
Middle Aged
Mutation
Polymorphism, Genetic
Prion Diseases
Prions
diagnosis
genetics
metabolism
pathology
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German
Your search returned 107 results.
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61.
The normal distribution of PRNP codon 129 polymorphism in the Moroccan population (Arabs and Casablanca residents).
[electronic resource]
by
Nadifi, S
Slassi, I
Hachimi, K M El
Gazzaz, B
Bellayou, H
Raddaoui, K
Laplanche, J L
Producer:
20080909
In:
Pathologie-biologie
vol. 56
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62.
[Non-familial Creutzfeldt-Jakob disease: a study of 53 cases].
[electronic resource]
by
Giraud, P
Perret-Liaudet, A
Biacabe, A G
Deslys, J P
Laplanche, J L
Chazot, G
Kop, N
Producer:
20001019
In:
Revue neurologique
vol. 156
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63.
14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.
[electronic resource]
by
Beaudry, P
Cohen, P
Brandel, J P
Delasnerie-Lauprêtre, N
Richard, S
Launay, J M
Laplanche, J L
Producer:
19990303
In:
Dementia and geriatric cognitive disorders
vol. 10
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64.
OPRM1 polymorphism and lifetime suicide attempts among stabilized, methadone-maintained outpatients.
[electronic resource]
by
Icick, R
Peoc'h, K
Ksouda, K
Bloch, V
Laplanche, J L
Lépine, J P
Bellivier, F
Vorspan, F
Producer:
20141205
In:
Psychiatry research
vol. 218
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65.
Inherited prion disease.
[electronic resource]
by
Laplanche, J L
Chatelain, J
Dussaucy, M
Bounneau, C
Launay, J M
Brandel, J P
Delasnerie-Laupretre, N
Producer:
19930615
In:
BMJ (Clinical research ed.)
vol. 306
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66.
Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies.
[electronic resource]
by
Laplanche, J L
Delasnerie-Lauprêtre, N
Brandel, J P
Chatelain, J
Beaudry, P
Alpérovitch, A
Launay, J M
Producer:
19950111
In:
Neurology
vol. 44
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67.
Fatal familial insomnia presenting as psychosis in an 18-year-old man.
[electronic resource]
by
Dimitri, D
Jehel, L
Dürr, A
Lévy-Soussan, M
Andreux, V
Laplanche, J-L
Fossati, P
Cohen, D
Producer:
20060814
In:
Neurology
vol. 67
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68.
Serotonin and human immunodeficiency viruses.
[electronic resource]
by
Launay, J M
Copel, L
Callebert, J
Corvaïa, N
Bricaire, F
Laplanche, J L
Saal, F
Peries, J
Producer:
19890927
In:
Nouvelle revue francaise d'hematologie
vol. 31
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69.
Apolipoprotein E gene polymorphism in early and late onset bipolar patients.
[electronic resource]
by
Bellivier, F
Laplanche, J L
Schürhoff, F
Feingold, J
Féline, A
Jouvent, R
Launay, J M
Leboyer, M
Producer:
19971113
In:
Neuroscience letters
vol. 233
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70.
This is really a case of new variant Creutzfeldt-Jakob. Response to C.J.G. Lang et al. concerning our article Acta Neuropathol (2000) 99:704-708.
[electronic resource]
by
Streichenberger, N
Biacabe, A G
Perret-Liaudet, A
Deslys, J P
Laplanche, J L
Chazot, G
Kopp, N
Producer:
20020523
In:
Acta neuropathologica
vol. 102
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71.
Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype.
[electronic resource]
by
Peoc'h, K
Manivet, P
Beaudry, P
Attane, F
Besson, G
Hannequin, D
Delasnerie-Lauprêtre, N
Laplanche, J L
Producer:
20000921
In:
Human mutation
vol. 15
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72.
Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one case.
[electronic resource]
by
Ghorayeb, I
Series, C
Parchi, P
Sawan, B
Guez, S
Laplanche, J L
Capellari, S
Gambetti, P
Vital, C
Producer:
19980730
In:
Neurology
vol. 51
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73.
Creutzfeldt-Jakob disease in French West Indies.
[electronic resource]
by
Caparros-Lefebvre, D
Sazdovitch, V
Roudier, M
Brandel, J P
Laplanche, J L
Deslys, J P
Hauw, J J
Producer:
19990525
In:
Lancet (London, England)
vol. 353
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74.
[Fatal familial insomnia: phenotypic changes determined by polymorphism of the codon 129].
[electronic resource]
by
Colombier, C
Géraud, G
Delisle, M B
Laplanche, J L
Pavy le Traon, A
Alizé, P
Delpla, P A
Producer:
19971001
In:
Revue neurologique
vol. 153
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75.
Dissociation in circadian rhythms in a pseudohypersomnia form of fatal familial insomnia.
[electronic resource]
by
Dauvilliers, Y
Cervena, K
Carlander, B
Espa, F
Bassetti, C
Claustrat, B
Laplanche, J L
Billiard, M
Touchon, J
Producer:
20050815
In:
Neurology
vol. 63
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76.
A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease.
[electronic resource]
by
Ripoll, L
Laplanche, J L
Salzmann, M
Jouvet, A
Planques, B
Dussaucy, M
Chatelain, J
Beaudry, P
Launay, J M
Producer:
19931112
In:
Neurology
vol. 43
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77.
Deletions in the prion protein gene are not associated with CJD.
[electronic resource]
by
Palmer, M S
Mahal, S P
Campbell, T A
Hill, A F
Sidle, K C
Laplanche, J L
Collinge, J
Producer:
19930727
In:
Human molecular genetics
vol. 2
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78.
Creutzfeldt-Jakob disease after extracranial dura mater embolization for a nasopharyngeal angiofibroma.
[electronic resource]
by
Antoine, J C
Michel, D
Bertholon, P
Mosnier, J F
Laplanche, J L
Beaudry, P
Hauw, J J
Veyret, C
Producer:
19970611
In:
Neurology
vol. 48
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79.
Serotonin transporter gene polymorphisms in patients with unipolar or bipolar depression.
[electronic resource]
by
Bellivier, F
Henry, C
Szöke, A
Schürhoff, F
Nosten-Bertrand, M
Feingold, J
Launay, J M
Leboyer, M
Laplanche, J L
Producer:
19990210
In:
Neuroscience letters
vol. 255
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80.
Prion-like protein Doppel expression is not modified in scrapie-infected cells and in the brains of patients with Creutzfeldt-Jakob disease.
[electronic resource]
by
Peoc'h, K
Volland, H
De Gassart, A
Beaudry, P
Sazdovitch, V
Sorgato, M C
Creminon, C
Laplanche, J-L
Lehmann, S
Producer:
20030310
In:
FEBS letters
vol. 536
Online resources:
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