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    1. Chebassier, C; Mouillet-Richard, S; Laplanche, JL; Kellermann, O; Launay, JM
      A signalling fuction for the prion protein

      PATHOLOGIE BIOLOGIE
    2. Brandel, JP; Peoc'h, K; Beaudry, P; Welaratne, A; Bottos, C; Agid, Y; Laplanche, JL
      14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients

      ANNALS OF NEUROLOGY
    3. Peoc'h, K; Schroder, HC; Laplanche, JL; Ramljak, S; Muller, WEG
      Determination of 14-3-3 protein levels in cerebrospinal fluid from Creutzfeldt-Jakob patients by a highly sensitive capture assay

      NEUROSCIENCE LETTERS
    4. Bellivier, F; Laplanche, JL; Fournier, G; Wolkenstein, P
      Serotonin transporter gene polymorphism and psychiatric disorders in NF1 patients

      AMERICAN JOURNAL OF MEDICAL GENETICS
    5. Streichenberger, N; Biacabe, AG; Perret-Liaudet, A; Deslys, JP; Laplanche, JL; Chazot, G; Kopp, N
      This is really a case of new variant Creutzfeldt-Jakob - Response

      ACTA NEUROPATHOLOGICA
    6. Privat, N; Sazdovitch, V; Seilhean, D; Laplanche, JL; Hauw, JJ
      PrP immunohistochemistry: Different protocols, including a procedure for long formalin fixation, and a proposed schematic classification for depositsin sporadic Creutzfeldt-Jakob disease

      MICROSCOPY RESEARCH AND TECHNIQUE
    7. Manivet, P; Soliman, HR; Callebert, J; Laplanche, JL; Launay, JM
      Biochemical mechanisms in the physiopathology of migraines.

      PATHOLOGIE BIOLOGIE
    8. Decleves, X; Regina, A; Laplanche, JL; Roux, F; Boval, B; Launay, JM; Scherrmann, JM
      Functional expression of P-glycoprotein and multidrug resistance-associated protein (Mrp1) in primary cultures of rat astrocytes

      JOURNAL OF NEUROSCIENCE RESEARCH
    9. Peoc'h, K; Guerin, C; Brandel, JP; Launay, JM; Laplanche, JL
      First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases

      NEUROSCIENCE LETTERS
    10. Leuck, J; Peoc'h, K; Laplanche, JL; Grabar, E; Muller, WEG; Schroder, HC
      A novel binding assay for detection of 14-3-3 protein in cerebrospinal fluid from Creutzfeldt-Jakob patients

      CELLULAR AND MOLECULAR BIOLOGY
    11. Muller, WEG; Laplanche, JL; Ushijima, H; Schroder, HC
      Novel approaches in diagnosis and therapy of Creutzfeldt-Jakob disease

      MECHANISMS OF AGEING AND DEVELOPMENT
    12. Mouillet-Richard, S; Ermonval, M; Chebassier, C; Laplanche, JL; Lehmann, S; Launay, JM; Kellermann, O
      Signal transduction through prion protein

      SCIENCE
    13. Giraud, P; Perret-Liaudet, A; Biacabe, AG; Deslys, JP; Laplanche, JL; Chazot, G; Kopp, N
      Non familial Creutzfeldt-Jakob disease: a study of 53 cases.

      REVUE NEUROLOGIQUE
    14. Haik, S; Brandel, JP; Sazdovitch, V; Delasnerie-Laupretre, N; Peoc'h, K; Laplanche, JL; Privat, N; Duyckaerts, C; Kemeny, JL; Kopp, N; Laquerriere, A; Mohr, M; Deslys, JP; Dormont, D; Hauw, JJ
      Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease

      NEUROLOGY
    15. Zerr, I; Pocchiari, M; Collins, S; Brandel, JP; Cuesta, JD; Knight, RSG; Bernheimer, H; Cardone, F; Delasnerie-Laupretre, N; Corrales, NC; Ladogana, A; Bodemer, M; Fletcher, A; Awan, T; Bremon, AR; Budka, H; Laplanche, JL; Will, RG; Poser, S
      Analysis of EEG and CSF 14-3-3 protein as aids to the diagnosis of Creutzfeldt-Jakob disease

      NEUROLOGY
    16. Hauw, JJ; Sazdovitch, V; Laplanche, JL; Peoc'h, K; Kopp, N; Kemeny, J; Privat, N; Delasnerie-Laupretre, N; Brandel, JP; Deslys, JP; Dormont, D; Alperovitch, A
      Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene

      NEUROLOGY
    17. Brandel, JP; Delasnerie-Laupretre, N; Laplanche, JL; Hauw, JJ; Alperovitch, A
      Diagnosis of Creutzfeldt-Jakob disease - Effect of clinical criteria on incidence estimates

      NEUROLOGY
    18. d'Aignaux, JH; Laplanche, JL; Delasnerie-Laupretre, N; Brandel, JP; Peoc'h, K; Salomon, D; Hauw, JJ; Alperovitch, A
      Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    19. Bellivier, F; Szoke, A; Henry, C; Lacoste, J; Bottos, C; Nosten-Bertrand, M; Hardy, P; Rouillon, F; Launay, JM; Laplanche, JL; Leboyer, M
      Possible association between serotonin transporter gene polymorphism and violent suicidal behavior in mood disorders

      BIOLOGICAL PSYCHIATRY
    20. Streichenberger, N; Jordan, D; Verejan, I; Souchier, C; Philippeau, F; Gros, E; Mottolese, C; Ostrowsky, K; Perret-Liaudet, A; Laplanche, JL; Hermier, M; Deslys, JP; Chazot, G; Kopp, N
      The first case of new variant Creutzfeldt-Jakob disease in France: clinical data and neuropathological findings

      ACTA NEUROPATHOLOGICA
    21. Beaudry, P; Cohen, P; Brandel, JP; Delasnerie-Laupretre, N; Richard, S; Launay, JM; Laplanche, JL
      14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    22. Mouillet-Richard, S; Laurendeau, I; Vidaud, M; Kellermann, O; Laplanche, JL
      Prion protein and neuronal differentiation: quantitative analysis of prnp gene expression in a murine inducible neuroectodermal progenitor

      MICROBES AND INFECTION
    23. Beaugerie, L; Andre, C; Laplanche, JL
      Search for asymptomatic coeliac disease in patients with spongiform encephalopathy

      GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE
    24. Elsen, JM; Amigues, Y; Schelcher, F; Ducrocq, V; Andreoletti, O; Eychenne, F; Khang, JVT; Poivey, JP; Lantier, F; Laplanche, JL
      Genetic susceptibility and transmission factors in scrapie: detailed analysis of an epidemic in a closed flock of Romanov

      ARCHIVES OF VIROLOGY
    25. Laplanche, JL; Hunter, N; Shinagawa, M; Williams, E
      Scrapie, chronic wasting disease, and transmissible mink encephalopathy

      PRION BIOLOGY AND DISEASES
    26. Caparros-Lefebvre, D; Sazdovitch, V; Roudier, M; Brandel, JP; Laplanche, JL; Deslys, JP; Hauw, JJ
      Creutzfeldt-Jakob disease in French West Indies

      LANCET
    27. Brandel, JP; Beaudry, P; Delasnerie-Laupretre, N; Laplanche, JL
      Creutzfeldt Jakob disease: diagnostic value of protein 14-3-3 and neuronalspecific enolase assay in cerebrospinal fluid.

      REVUE NEUROLOGIQUE
    28. Mouillet-Richard, S; Teil, C; Lenne, M; Hugon, S; Taleb, O; Laplanche, JL
      Mutation at codon 210 (V210I) of the prion protein gene in a North Africanpatient with Creutzfeldt-Jakob disease

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    29. Gidon-Jeangirard, C; Hugel, B; Holl, V; Toti, F; Laplanche, JL; Meyer, D; Freyssinet, JM
      Annexin V delays apoptosis while exerting an external constraint preventing the release of CD4(+) and PrPc+ membrane particles in a human T lymphocyte model

      JOURNAL OF IMMUNOLOGY
    30. Laplanche, JL; El Hachimi, KH; Durieux, I; Thuillet, P; Defebvre, L; Delasnerie-Laupretre, N; Peoc'h, K; Foncin, JF; Destee, A
      Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene

      BRAIN
    31. CHATELAIN J; DELASNERIELAUPRETRE N; LEMAIRE MH; CATHALA F; LAUNAY JM; LAPLANCHE JL
      CLUSTER OF CREUTZFELDT-JAKOB-DISEASE IN FRANCE ASSOCIATED WITH THE CODON-200 MUTATION (E200K) IN THE PRION PROTEIN GENE

      European journal of neurology
    32. BELLIVIER F; HENRY C; SZOKE A; SCHURHOFF F; NOSTENBERTRAND M; FEINGOLD J; LAUNAY JM; LEBOYER M; LAPLANCHE JL
      SEROTONIN TRANSPORTER GENE POLYMORPHISMS IN PATIENTS WITH UNIPOLAR ORBIPOLAR DEPRESSION

      Neuroscience letters
    33. BELLIVIER F; SZOKE A; HENRY C; NOSTENBERTRAND M; FEINGOLD J; LAUNAY JM; LAPLANCHE JL; LEBOYER M
      SEROTONIN TRANSPORTER GENE POLYMORPHISMS IN UNIPOLAR AND BIPOLAR DEPRESSION

      American journal of medical genetics
    34. DESEZE J; HACHE JC; VERMERSCH P; ARNDT CF; MAURAGE CA; PASQUIER F; LAPLANCHE JL; RUCHOUX MM; LEYS D; DESTEE A; PETIT H
      CREUTZFELDT-JAKOB-DISEASE - NEUROPHYSIOLOGIC VISUAL IMPAIRMENTS

      Neurology
    35. GHORAYEB I; SERIES C; PARCHI P; SAWAN B; GUEZ S; LAPLANCHE JL; CAPELLARI S; GAMBETTI P; VITAL C
      CREUTZFELDT-JAKOB-DISEASE WITH LONG-DURATION AND PANENCEPHALOPATHIC LESIONS - MOLECULAR ANALYSIS OF ONE CASE

      Neurology
    36. TRANCHANT C; GERANTON L; LAPLANCHE JL; MOHR M; WARTER JM
      GENETIC-BASIS OF PHENOTYPIC VARIABILITY IN SPORADIC CREUTZFELDT-JAKOB-DISEASE

      Neurology
    37. RUFFIE A; DELASNERIELAUPRETRE N; BRANDEL JP; JAUSSENT I; DORMONT D; LAPLANCHE JL; HAUW JJ; RICHARDSON S; ALPEROVITCH A
      INCIDENCE OF CREUTZFELDT-JAKOB-DISEASE IN FRANCE, 1992-1995

      Revue d'epidemiologie et de sante publique
    38. BELLIVIER F; LAPLANCHE JL; SCHURHOFF F; FEINGOLD J; FELINE A; JOUVENT R; LAUNAY JM; LEBOYER M
      APOLIPOPROTEIN-E GENE POLYMORPHISM IN EARLY AND LATE-ONSET BIPOLAR PATIENTS

      Neuroscience letters
    39. LAPLANCHE JL; NOSTENBERTRAND M; BELLIVIER F; LEBOYER M; MALLET J; LAUNAY JM
      SEROTONIN TRANSPORTER GENE REGULATORY REGION AND MANIC-DEPRESSIVE ILLNESS - AN ASSOCIATION STUDY

      American journal of medical genetics
    40. BELLIVIER F; LAPLANCHE JL; SCHURHOFF F; LEBOYER M; FEINGOLD J; FELINE A; LAUNAY JM
      APOLIPOPROTEIN-E GENE POLYMORPHISM IN EARLY AND LATE-ONSET MANIC-DEPRESSIVE ILLNESS

      American journal of medical genetics
    41. COLOMBIER C; GERAUD G; DELISLE MB; LAPLANCHE JL; LETRAON AP; ALIZE P; DELPLA PA
      FATAL FAMILIAL INSOMNIA - PHENOTYPIC DIFF ERENCE DETERMINED BY POLYMORPHISM AT CODON-129

      Revue neurologique
    42. ANTOINE JC; MICHEL D; BERTHOLON P; MOSNIER JF; LAPLANCHE JL; BEAUDRY P; HAUW JJ; VEYRET C
      CREUTZFELDT-JAKOB-DISEASE AFTER EXTRACRANIAL DURA-MATER EMBOLIZATION FOR A NASOPHARYNGEAL ANGIOFIBROMA

      Neurology
    43. SILVERMAN G; YAO H; STROME R; LAPLANCHE JL; FONCIN JF; STGEORGEHYSLOP P; FRASER PE; WESTAWAY D
      PROTEINS WHICH INTERACT WITH WILD-TYPE AND MUTANT N-TERMINAL DOMAINS OF HUMAN PRPC

      Journal of neuropathology and experimental neurology
    44. BELLIVIER F; LAPLANCHE JL; LEBOYER M; FEINGOLD J; BOTTOS C; ALLILAIRE JF; LAUNAY JM
      SEROTONIN TRANSPORTER GENE AND MANIC-DEPRESSIVE ILLNESS - AN ASSOCIATION STUDY

      Biological psychiatry
    45. LAPLANCHE JL
      MOLECULAR-GENETICS OF FAMILIAL AND SPORAD IC FORMS OF HUMAN PRION DISEASES

      Medecine et maladies infectieuses
    46. KOPP N; STREICHENBERGER N; DESLYS JP; LAPLANCHE JL; CHAZOT G
      CREUTZFELDT-JAKOB-DISEASE IN A 52-YEAR-OLD WOMAN WITH FLORID PLAQUES

      Lancet
    47. ANTOINE JC; LAPLANCHE JL; MOSNIER JF; BEAUDRY P; CHATELAIN J; MICHEL D
      DEMYELINATING PERIPHERAL NEUROPATHY WITH CREUTZFELDT-JAKOB-DISEASE AND MUTATION AT CODON-200 OF THE PRION PROTEIN GENE

      Neurology
    48. LAPLANCHE JL; DELASNERIELAUPRETRE N; BRANDEL JP; DUSSAUCY M; CHATELAIN J; LAUNAY JM
      2 NOVEL INSERTIONS IN THE PRION PROTEIN GENE IN PATIENTS WITH LATE-ONSET DEMENTIA

      Human molecular genetics
    49. LAPLANCHE JL; BEAUDRY P; RIPOLL L; LAUNAY JM
      PRION PROTEIN - STRUCTURE, FUNCTIONS AND HUMAN SPONGIFORM ENCEPHALOPATHIES-ASSOCIATED POLYMORPHISMS

      Pathologie et biologie
    50. AMOUYEL P; ALPEROVITCH A; DELASNERIELAUPRETRE N; LAPLANCHE JL
      APOLIPOPROTEIN-E IN CREUTZFELDT-JAKOB-DISEASE

      Lancet
    51. CLOUSCARD C; BEAUDRY P; ELSEN JM; MILAN D; DUSSAUCY M; BOUNNEAU C; SCHELCHER F; CHATELAIN J; LAUNAY JM; LAPLANCHE JL
      DIFFERENT ALLELIC EFFECTS OF THE CODON-136 AND CODON-171 OF THE PRIONPROTEIN GENE IN SHEEP WITH NATURAL SCRAPIE

      Journal of General Virology
    52. LAPLANCHE JL
      MOLECULAR-BASIS OF FAMILIAL AND SPORADIC HUMAN PRION DISEASES

      Transfusion clinique et biologique
    53. AMOUYEL P; VIDAL O; LAUNAY JM; LAPLANCHE JL
      THE APOLIPOPROTEIN-E ALLELES AS MAJOR SUSCEPTIBILITY FACTORS FOR CREUTZFELDT-JAKOB-DISEASE

      Lancet
    54. BRANDEL JP; DELASNERIELAUPRETRE N; LAPLANCHE JL; DORMONT D; HAUW JJ; ALPEROVITCH A
      STUDY-GROUP ON HUMAN SPONGIFORM ENCEPHALO PATHIES - PRELIMINARY-RESULTS

      Revue neurologique
    55. LAPLANCHE JL; DELASNERIELAUPRETRE N; BRANDEL JP; CHATELAIN J; BEAUDRY P; ALPEROVITCH A; LAUNAY JM
      MOLECULAR-GENETICS OF PRION DISEASES IN FRANCE

      Neurology
    56. GRAY F; CHRETIEN E; CESARO P; CHATELAIN J; BEAUDRY P; LAPLANCHE JL; MIKOL J; BELL J; GAMBETTI P; DEGOS JD
      CREUTZFELDT-JAKOB-DISEASE AND CEREBRAL AMYLOID ANGIOPATHY

      Acta Neuropathologica
    57. BRUGEREPICOUX J; CHATELAIN J; LAPLANCHE JL; BRUGERE H
      TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES OF ANIMALS

      Bulletin de l'Academie nationale de medecine
    58. PALMER MS; MAHAL SP; CAMPBELL TA; HILL AF; SIDLE KC; LAPLANCHE JL; COLLINGE J
      DELETIONS IN THE PRION PROTEIN GENE ARE NOT ASSOCIATED WITH CJD

      Human molecular genetics
    59. LAPLANCHE JL; CHATELAIN J; BEAUDRY P; DUSSAUCY M; BOUNNEAU C; LAUNAY JM
      FRENCH AUTOCHTHONOUS SCRAPIED SHEEP WITHOUT THE 136VAL PRP POLYMORPHISM

      Mammalian genome
    60. RIPOLL L; LAPLANCHE JL; SALZMANN M; JOUVET A; PLANQUES B; DUSSAUCY M; CHATELAIN J; BEAUDRY P; LAUNAY JM
      A NEW POINT MUTATION IN THE PRION PROTEIN GENE AT CODON 210 IN CREUTZFELDT-JAKOB-DISEASE

      Neurology
    61. DREUX C; LAPLANCHE JL; CHATELAIN J
      THE HUMAN TRANSMISSIBLE DEMENTIA - PRION DISEASES

      Bulletin de l'Academie nationale de medecine


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Documento generato il 25/05/20 alle ore 04:25:27