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Results: 1-25 | 26-31
Results: 1-25/31
CLUSTER OF CREUTZFELDT-JAKOB-DISEASE IN FRANCE ASSOCIATED WITH THE CODON-200 MUTATION (E200K) IN THE PRION PROTEIN GENE
Authors: CHATELAIN J DELASNERIELAUPRETRE N LEMAIRE MH CATHALA F LAUNAY JM LAPLANCHE JL
Citation: J. Chatelain et al., CLUSTER OF CREUTZFELDT-JAKOB-DISEASE IN FRANCE ASSOCIATED WITH THE CODON-200 MUTATION (E200K) IN THE PRION PROTEIN GENE, European journal of neurology, 5(4), 1998, pp. 375-379
SEROTONIN TRANSPORTER GENE POLYMORPHISMS IN PATIENTS WITH UNIPOLAR ORBIPOLAR DEPRESSION
Authors: BELLIVIER F HENRY C SZOKE A SCHURHOFF F NOSTENBERTRAND M FEINGOLD J LAUNAY JM LEBOYER M LAPLANCHE JL
Citation: F. Bellivier et al., SEROTONIN TRANSPORTER GENE POLYMORPHISMS IN PATIENTS WITH UNIPOLAR ORBIPOLAR DEPRESSION, Neuroscience letters, 255(3), 1998, pp. 143-146
SEROTONIN TRANSPORTER GENE POLYMORPHISMS IN UNIPOLAR AND BIPOLAR DEPRESSION
Authors: BELLIVIER F SZOKE A HENRY C NOSTENBERTRAND M FEINGOLD J LAUNAY JM LAPLANCHE JL LEBOYER M
Citation: F. Bellivier et al., SEROTONIN TRANSPORTER GENE POLYMORPHISMS IN UNIPOLAR AND BIPOLAR DEPRESSION, American journal of medical genetics, 81(6), 1998, pp. 466-467
CREUTZFELDT-JAKOB-DISEASE - NEUROPHYSIOLOGIC VISUAL IMPAIRMENTS
Authors: DESEZE J HACHE JC VERMERSCH P ARNDT CF MAURAGE CA PASQUIER F LAPLANCHE JL RUCHOUX MM LEYS D DESTEE A PETIT H
Citation: J. Deseze et al., CREUTZFELDT-JAKOB-DISEASE - NEUROPHYSIOLOGIC VISUAL IMPAIRMENTS, Neurology, 51(4), 1998, pp. 962-967
CREUTZFELDT-JAKOB-DISEASE WITH LONG-DURATION AND PANENCEPHALOPATHIC LESIONS - MOLECULAR ANALYSIS OF ONE CASE
Authors: GHORAYEB I SERIES C PARCHI P SAWAN B GUEZ S LAPLANCHE JL CAPELLARI S GAMBETTI P VITAL C
Citation: I. Ghorayeb et al., CREUTZFELDT-JAKOB-DISEASE WITH LONG-DURATION AND PANENCEPHALOPATHIC LESIONS - MOLECULAR ANALYSIS OF ONE CASE, Neurology, 51(1), 1998, pp. 271-274
GENETIC-BASIS OF PHENOTYPIC VARIABILITY IN SPORADIC CREUTZFELDT-JAKOB-DISEASE
Authors: TRANCHANT C GERANTON L LAPLANCHE JL MOHR M WARTER JM
Citation: C. Tranchant et al., GENETIC-BASIS OF PHENOTYPIC VARIABILITY IN SPORADIC CREUTZFELDT-JAKOB-DISEASE, Neurology, 50(4), 1998, pp. 44002-44002
INCIDENCE OF CREUTZFELDT-JAKOB-DISEASE IN FRANCE, 1992-1995
Authors: RUFFIE A DELASNERIELAUPRETRE N BRANDEL JP JAUSSENT I DORMONT D LAPLANCHE JL HAUW JJ RICHARDSON S ALPEROVITCH A
Citation: A. Ruffie et al., INCIDENCE OF CREUTZFELDT-JAKOB-DISEASE IN FRANCE, 1992-1995, Revue d'epidemiologie et de sante publique, 45(6), 1997, pp. 448-453
APOLIPOPROTEIN-E GENE POLYMORPHISM IN EARLY AND LATE-ONSET BIPOLAR PATIENTS
Authors: BELLIVIER F LAPLANCHE JL SCHURHOFF F FEINGOLD J FELINE A JOUVENT R LAUNAY JM LEBOYER M
Citation: F. Bellivier et al., APOLIPOPROTEIN-E GENE POLYMORPHISM IN EARLY AND LATE-ONSET BIPOLAR PATIENTS, Neuroscience letters, 233(1), 1997, pp. 45-48
SEROTONIN TRANSPORTER GENE REGULATORY REGION AND MANIC-DEPRESSIVE ILLNESS - AN ASSOCIATION STUDY
Authors: LAPLANCHE JL NOSTENBERTRAND M BELLIVIER F LEBOYER M MALLET J LAUNAY JM
Citation: Jl. Laplanche et al., SEROTONIN TRANSPORTER GENE REGULATORY REGION AND MANIC-DEPRESSIVE ILLNESS - AN ASSOCIATION STUDY, American journal of medical genetics, 74(6), 1997, pp. 620-620
APOLIPOPROTEIN-E GENE POLYMORPHISM IN EARLY AND LATE-ONSET MANIC-DEPRESSIVE ILLNESS
Authors: BELLIVIER F LAPLANCHE JL SCHURHOFF F LEBOYER M FEINGOLD J FELINE A LAUNAY JM
Citation: F. Bellivier et al., APOLIPOPROTEIN-E GENE POLYMORPHISM IN EARLY AND LATE-ONSET MANIC-DEPRESSIVE ILLNESS, American journal of medical genetics, 74(6), 1997, pp. 632-632
FATAL FAMILIAL INSOMNIA - PHENOTYPIC DIFF ERENCE DETERMINED BY POLYMORPHISM AT CODON-129
Authors: COLOMBIER C GERAUD G DELISLE MB LAPLANCHE JL LETRAON AP ALIZE P DELPLA PA
Citation: C. Colombier et al., FATAL FAMILIAL INSOMNIA - PHENOTYPIC DIFF ERENCE DETERMINED BY POLYMORPHISM AT CODON-129, Revue neurologique, 153(4), 1997, pp. 239-243
CREUTZFELDT-JAKOB-DISEASE AFTER EXTRACRANIAL DURA-MATER EMBOLIZATION FOR A NASOPHARYNGEAL ANGIOFIBROMA
Authors: ANTOINE JC MICHEL D BERTHOLON P MOSNIER JF LAPLANCHE JL BEAUDRY P HAUW JJ VEYRET C
Citation: Jc. Antoine et al., CREUTZFELDT-JAKOB-DISEASE AFTER EXTRACRANIAL DURA-MATER EMBOLIZATION FOR A NASOPHARYNGEAL ANGIOFIBROMA, Neurology, 48(5), 1997, pp. 1451-1453
PROTEINS WHICH INTERACT WITH WILD-TYPE AND MUTANT N-TERMINAL DOMAINS OF HUMAN PRPC
Authors: SILVERMAN G YAO H STROME R LAPLANCHE JL FONCIN JF STGEORGEHYSLOP P FRASER PE WESTAWAY D
Citation: G. Silverman et al., PROTEINS WHICH INTERACT WITH WILD-TYPE AND MUTANT N-TERMINAL DOMAINS OF HUMAN PRPC, Journal of neuropathology and experimental neurology, 56(5), 1997, pp. 99-99
SEROTONIN TRANSPORTER GENE AND MANIC-DEPRESSIVE ILLNESS - AN ASSOCIATION STUDY
Authors: BELLIVIER F LAPLANCHE JL LEBOYER M FEINGOLD J BOTTOS C ALLILAIRE JF LAUNAY JM
Citation: F. Bellivier et al., SEROTONIN TRANSPORTER GENE AND MANIC-DEPRESSIVE ILLNESS - AN ASSOCIATION STUDY, Biological psychiatry, 41(6), 1997, pp. 750-752
MOLECULAR-GENETICS OF FAMILIAL AND SPORAD IC FORMS OF HUMAN PRION DISEASES
Authors: LAPLANCHE JL
Citation: Jl. Laplanche, MOLECULAR-GENETICS OF FAMILIAL AND SPORAD IC FORMS OF HUMAN PRION DISEASES, Medecine et maladies infectieuses, 26(BIS), 1996, pp. 264-270
CREUTZFELDT-JAKOB-DISEASE IN A 52-YEAR-OLD WOMAN WITH FLORID PLAQUES
Authors: KOPP N STREICHENBERGER N DESLYS JP LAPLANCHE JL CHAZOT G
Citation: N. Kopp et al., CREUTZFELDT-JAKOB-DISEASE IN A 52-YEAR-OLD WOMAN WITH FLORID PLAQUES, Lancet, 348(9036), 1996, pp. 1239-1240
DEMYELINATING PERIPHERAL NEUROPATHY WITH CREUTZFELDT-JAKOB-DISEASE AND MUTATION AT CODON-200 OF THE PRION PROTEIN GENE
Authors: ANTOINE JC LAPLANCHE JL MOSNIER JF BEAUDRY P CHATELAIN J MICHEL D
Citation: Jc. Antoine et al., DEMYELINATING PERIPHERAL NEUROPATHY WITH CREUTZFELDT-JAKOB-DISEASE AND MUTATION AT CODON-200 OF THE PRION PROTEIN GENE, Neurology, 46(4), 1996, pp. 1123-1127
2 NOVEL INSERTIONS IN THE PRION PROTEIN GENE IN PATIENTS WITH LATE-ONSET DEMENTIA
Authors: LAPLANCHE JL DELASNERIELAUPRETRE N BRANDEL JP DUSSAUCY M CHATELAIN J LAUNAY JM
Citation: Jl. Laplanche et al., 2 NOVEL INSERTIONS IN THE PRION PROTEIN GENE IN PATIENTS WITH LATE-ONSET DEMENTIA, Human molecular genetics, 4(6), 1995, pp. 1109-1111
PRION PROTEIN - STRUCTURE, FUNCTIONS AND HUMAN SPONGIFORM ENCEPHALOPATHIES-ASSOCIATED POLYMORPHISMS
Authors: LAPLANCHE JL BEAUDRY P RIPOLL L LAUNAY JM
Citation: Jl. Laplanche et al., PRION PROTEIN - STRUCTURE, FUNCTIONS AND HUMAN SPONGIFORM ENCEPHALOPATHIES-ASSOCIATED POLYMORPHISMS, Pathologie et biologie, 43(2), 1995, pp. 104-113
APOLIPOPROTEIN-E IN CREUTZFELDT-JAKOB-DISEASE
Authors: AMOUYEL P ALPEROVITCH A DELASNERIELAUPRETRE N LAPLANCHE JL
Citation: P. Amouyel et al., APOLIPOPROTEIN-E IN CREUTZFELDT-JAKOB-DISEASE, Lancet, 345(8949), 1995, pp. 595-596
DIFFERENT ALLELIC EFFECTS OF THE CODON-136 AND CODON-171 OF THE PRIONPROTEIN GENE IN SHEEP WITH NATURAL SCRAPIE
Authors: CLOUSCARD C BEAUDRY P ELSEN JM MILAN D DUSSAUCY M BOUNNEAU C SCHELCHER F CHATELAIN J LAUNAY JM LAPLANCHE JL
Citation: C. Clouscard et al., DIFFERENT ALLELIC EFFECTS OF THE CODON-136 AND CODON-171 OF THE PRIONPROTEIN GENE IN SHEEP WITH NATURAL SCRAPIE, Journal of General Virology, 76, 1995, pp. 2097-2101
MOLECULAR-BASIS OF FAMILIAL AND SPORADIC HUMAN PRION DISEASES
Authors: LAPLANCHE JL
Citation: Jl. Laplanche, MOLECULAR-BASIS OF FAMILIAL AND SPORADIC HUMAN PRION DISEASES, Transfusion clinique et biologique, 1(5), 1994, pp. 345-353
THE APOLIPOPROTEIN-E ALLELES AS MAJOR SUSCEPTIBILITY FACTORS FOR CREUTZFELDT-JAKOB-DISEASE
Authors: AMOUYEL P VIDAL O LAUNAY JM LAPLANCHE JL
Citation: P. Amouyel et al., THE APOLIPOPROTEIN-E ALLELES AS MAJOR SUSCEPTIBILITY FACTORS FOR CREUTZFELDT-JAKOB-DISEASE, Lancet, 344(8933), 1994, pp. 1315-1318
STUDY-GROUP ON HUMAN SPONGIFORM ENCEPHALO PATHIES - PRELIMINARY-RESULTS
Authors: BRANDEL JP DELASNERIELAUPRETRE N LAPLANCHE JL DORMONT D HAUW JJ ALPEROVITCH A
Citation: Jp. Brandel et al., STUDY-GROUP ON HUMAN SPONGIFORM ENCEPHALO PATHIES - PRELIMINARY-RESULTS, Revue neurologique, 150(10), 1994, pp. 684-688
MOLECULAR-GENETICS OF PRION DISEASES IN FRANCE
Authors: LAPLANCHE JL DELASNERIELAUPRETRE N BRANDEL JP CHATELAIN J BEAUDRY P ALPEROVITCH A LAUNAY JM
Citation: Jl. Laplanche et al., MOLECULAR-GENETICS OF PRION DISEASES IN FRANCE, Neurology, 44(12), 1994, pp. 2347-2351
Risultati: 1-25 | 26-31