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    1. Derlon, JM; Chapon, F; Noel, MH; Khouri, S; Benali, K; Petit-Taboue, MC; Houtteville, JP; Chajari, MH; Bouvard, G
      Non-invasive grading of oligodendrogliomas: correlations between in vivo metabolic pattern and histopathology

      EUROPEAN JOURNAL OF NUCLEAR MEDICINE
    2. Fardeau, M; Vicart, P; Caron, A; Chateau, D; Chevallay, M; Collin, H; Chapon, F; Duboc, D; Eymard, B; Tome, FMS; Dupret, JM; Paulin, D; Guicheney, P
      Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alpha beta-cristallin gene

      REVUE NEUROLOGIQUE
    3. Adams, D; Schaeffer, S; Chapon, F
      Sensorial and motor peripheral neuropathy, high CSF protein and monoclonalIgG in a 38-year-old man

      REVUE NEUROLOGIQUE
    4. Iglesias, S; Chapon, F; Baron, JC
      Familial occipital calcifications, hemorrhagic strokes, leukoencephalopathy, dementia, and external carotid dysplasia

      NEUROLOGY
    5. Joutel, A; Andreux, F; Gaulis, S; Domenga, V; Cecillon, M; Battail, N; Piga, N; Chapon, F; Godfrain, C; Tournier-Lasserve, E
      The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients

      JOURNAL OF CLINICAL INVESTIGATION
    6. Macro, M; Andre, I; Comby, E; Cheze, S; Chapon, F; Ballet, JJ; Reman, O; Leporrier, M; Troussard, X
      IgE multiple myeloma

      LEUKEMIA & LYMPHOMA
    7. Xiang, FQ; Nicolao, P; Chapon, F; Edstrom, L; Anvret, M; Zhang, ZP
      A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21

      NEUROMUSCULAR DISORDERS
    8. Caron, A; Chapon, F
      Desmin phosphorylation abnormalities in cytoplasmic body and desmin-related myopathies

      MUSCLE & NERVE
    9. Sindou, P; Vallat, JM; Chapon, F; Archelos, JJ; Tabaraud, F; Anani, T; Braund, KG; Maisonobe, T; Hauw, JJ; Vandenberghe, A
      Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B disease

      MUSCLE & NERVE
    10. Guesmi, H; Houtteville, JP; Courtheoux, P; Derlon, JM; Chapon, F
      Dysembryoplastic neuroepithelial tumors. Features in eight cases, including two with unusual locations.

      NEUROCHIRURGIE
    11. Chapon, F; Latour, P; Diraison, P; Schaeffer, S; Vandenberghe, A
      Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutationin the myelin protein zero gene

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    12. Caron, A; Gohel, C; Mollaret, K; Morello, R; Chapon, F
      Study of some components of the cytoskeleton in muscular disorders with nonspecific cytoplasmic bodies

      ACTA NEUROPATHOLOGICA
    13. VICART P; CARON A; GUICHENEY P; LI ZL; PREVOST MC; FAURE A; CHATEAU D; CHAPON F; TOME F; DUPRET JM; PAULIN D; FARDEAU M
      A MISSENSE MUTATION IN THE ALPHA-B-CRYSTALLIN CHAPERONE GENE CAUSES ADESMIN-RELATED MYOPATHY

      Nature genetics
    14. BESANCON R; CHAPON F; LATOUR P; DIRAISON P; SCHAEFFER S; BOUCHERAT M; CHAMBA G; VANDENBERGHE A
      A MUTATION IN MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH-DISEASE TYPE-II

      European journal of human genetics
    15. BESANCON R; CHAPON F; LATOUR P; DIRAISON P; SCHAEFFER S; BOUCHERAT M; CHAMBA G; VANDENBERGHE A
      A MUTATION IN MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH DISEASE TYPE-II

      European journal of neuroscience
    16. LEMESTRIC C; CHAVOIX C; CHAPON F; MEZENGE F; EPELBAUM J; BARON JC
      EFFECTS OF DAMAGE TO THE BASAL FOREBRAIN ON BRAIN GLUCOSE-UTILIZATION- A REEVALUATION USING POSITRON-EMISSION-TOMOGRAPHY IN BABOONS WITH EXTENSIVE UNILATERAL EXCITOTOXIC LESION

      Journal of cerebral blood flow and metabolism
    17. DUBUC L; LEPORRIER N; QUESNEY A; MALLET JF; BERTHELIN C; VIDAUD M; LECHEVALIER B; CHAPON F
      AN UNUSUAL TYPE OF A FAMILIAL SENSORY NEUROPATHY WITH DYSAUTONOMIA

      Brain pathology
    18. REZNIK Y; CHAPON F; LAHLOU N; DEBOUCHER N; MAHOUDEAU J
      PITUITARY APOPLEXY OF A GONADOTROPH ADENOMA FOLLOWING GONADOTROPIN-RELEASING-HORMONE AGONIST THERAPY FOR PROSTATIC-CANCER

      Journal of endocrinological investigation
    19. DERLON JM; PETITTABOUE MC; CHAPON F; BEAUDOUIN V; NOEL MH; CREVEUIL C; COURTHEOUX P; HOUTTEVILLE JP
      THE IN-VIVO METABOLIC PATTERN OF LOW-GRADE BRAIN GLIOMAS - A POSITRONEMISSION TOMOGRAPHIC STUDY USING F-18 FLUORODEOXYGLUCOSE AND C-11 L-METHYLMETHIONINE

      Neurosurgery
    20. NOTELET L; HOUTTEVILLE JP; KHOURY S; LECHEVALIER B; CHAPON F
      PROLIFERATING CELL NUCLEAR ANTIGEN (PCNA) IN CEREBRAL CAVERNOMAS - ANIMMUNOCYTOCHEMICAL STUDY OF 42 CASES

      Surgical neurology
    21. GHERARDI R; BERTRAN F; CHAPON F
      DISTAL MUSCULAR WEAKNESS INVOLVING THE FO RELIMBS AND RUNNING FROM 3 YEARS IN A 61-YEAR-OLD MAN

      Revue neurologique
    22. CHAPON F
      THE LIFE AND WORK OF TERIADE, ART PUBLISH ER OF ILLUSTRATED BOOKS BY MATISSE, PICASSO, MIRO, AND CHAGALL

      L'Oeil
    23. NOTELET L; CHAPON F; KHOURY S; VAHEDI K; CHODKIEWICZ JP; COURTHEOUX P; IBAZIZEN M; CABANIS EA; LECHEVALIER B; TOURNIERLASSERVE E; HOUTTEVILLE JP
      FAMILIAL CAVERNOUS MALFORMATIONS IN A LARGE FRENCH KINDRED - MAPPING OF THE GENE TO THE CCM1 LOCUS ON CHROMOSOME 7Q

      Journal of Neurology, Neurosurgery and Psychiatry
    24. LATOUR P; FABREGUETTE A; RESSOT C; BLANQUETGROSSARD F; ANTOINE JC; CALVAS P; CHAPON F; CORBILLON E; OLLAGNON E; STURTZ F; BOUCHERAT M; CHAZOT G; DAUTIGNY A; PHAMDINH D; VANDENBERGHE A
      NEW MUTATIONS IN THE X-LINKED FORM OF CHARCOT-MARIE-TOOTH DISEASE

      European neurology
    25. BLANQUETGROSSARD E; PHAMDINH D; DAUTIGNY A; LATOUR P; BONNEBOUCHE C; DIRAISON P; CHAPON F; CHAZOT G; VANDENBERGHE A
      CHARCOT-MARIE-TOOTH TYPE-1B NEUROPATHY - A MUTATION AT THE SINGLE GLYCOSYLATION SITE IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN-P0

      Human mutation
    26. LECHEVALIER B; BERTRAN F; BUSSON P; CHAPON F; RAOUL G; DELASAYETTE V
      AKINETIC MUTISM WITH RIGHT HEMIPLEGIA DUE TO AN INFARCT IN THE TERRITORY OF THE LEFT ANTERIOR CEREBRAL-ARTERY

      Revue neurologique
    27. CHAPON F; DIRAISON P; LECHEVALIER B; CHAZOT G; VIADER F; BONNEBOUCHE C; VANDENBERGHE A; TIMMERMAN V; VANBROECKHOVEN C; VANDENBERGHE A
      HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES WITH A PARTIAL DELETION OF THE REGION OFTEN DUPLICATED IN CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A

      Journal of Neurology, Neurosurgery and Psychiatry
    28. STURTZ FG; CHAUVIN F; OLLAGNONROMAN E; BOST M; LATOUR P; BONNEBOUCHE C; GONNAUD PM; BADY B; CHAZOT G; VANDENBERGHE A; BEAUVAIS P; CHAPON F; CLAVELOU P; FLOCARD F; MATHIEU M; POUGET J; RENDU M
      MODELIZATION OF MOTOR-NERVE CONDUCTION VELOCITIES FOR CHARCOT-MARIE-TOOTH (TYPE-1) PATIENTS

      European neurology
    29. VANDENBERGHE A; LATOUR P; CHAUPLANNAZ G; CHAPON F; POUGET J; DUMAS R; LAGUENAY A; OLLAGNON E; BOST M; DUTHEL S; CHAZOT G; BOUCHERAT M
      MOLECULAR DIAGNOSIS OF CHARCOT-MARIE-TOOTH IA DISEASE AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES BY QUANTIFYING CMTIA-REPSEQUENCES - CONSEQUENCES OF RECOMBINATIONS AT VARIANT SITES ON CHROMOSOME 17P11.2-12

      Clinical chemistry
    30. LOPES J; LEGUERN E; GOUIDER R; TARDIEU S; ABBAS N; BIROUK N; GUGENHEIM M; BOUCHE P; AGID Y; BRICE A; ARNEBES MC; BRICHET B; CHAPON F; CHAZOT G; CLAVELOU P; DESNUELLE C; DIRAISON P; DUBAS F; GONNAUD PM; HURTEVENT JF; KUNTZER T; LAGUENY A; MABIN D; MAYER M; OCHSNER F; OLLAGNONROMAN E; POUGET J; TABARAUD F; VALLAT JM; VANDENBERGHE A
      RECOMBINATION HOT-SPOT IN A 3.2-KB REGION OF THE CHARCOT-MARIE-TOOTH TYPE 1A REPEAT SEQUENCES - NEW TOOLS FOR MOLECULAR DIAGNOSIS OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES AND OF CHARCOT-MARIE-TOOTH TYPE 1A

      American journal of human genetics
    31. DUCROS A; NAGY T; ALAMOWITCH S; NIBBIO A; JOUTEL A; VAHEDI K; CHABRIAT H; IBAZIZEN MT; JULIEN J; DAVOUS P; GOAS JY; LYONCAEN O; DUBOIS B; DUCROCQ X; SALSA F; RAGNO M; BURKHARD P; BASSETTI C; HUTCHINSON M; VERIN M; VIADER F; CHAPON F; LEVASSEUR M; MAS JL; DELRIEU O; MACIAZEK J; PRIEUR M; MOHRENWEISER H; BACH JF; BOUSSER MG; TOURNIERLASSERVE E
      CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, GENETIC HOMOGENEITY, AND MAPPING OF THE LOCUS WITHIN A 2-CM INTERVAL

      American journal of human genetics
    32. LATOUR P; BLANQUET F; NELIS E; BONNEBOUCHE C; CHAPON F; DIRAISON P; OLLAGNON E; DAUTIGNY A; PHAMDINH D; CHAZOT G; BOUCHERAT M; VANBROECKHOVEN C; VANDENBERGHE A
      MUTATIONS IN THE MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH DISEASE TYPE 1B

      Human mutation
    33. LEGUERN E; GOUIDER R; LOPES J; ABBAS N; GUGENHEIM M; TARDIEU S; RAVISE N; LEGER JM; VALLAT JM; BOUCHE P; AGID Y; BRICE A; ARNEBES MC; BRICHET B; BIROUK N; CHAPON F; CHAZOT G; CLAVELOU P; DESNUELLE C; DIRAISON P; DUBAS F; GONNAUD PM; HURTEVENT JF; KUNTZER T; LAGUENY A; MABIN D; OSHSNER F; OLLAGNONROMAN E; POUGET J; TABERAUD F; VANDENBERGHE A
      CONSTANT REARRANGEMENT OF THE CMT1A-REP SEQUENCES IN HNPP PATIENTS WITH A DELETION IN CHROMOSOME 17P11.2 - A STUDY OF 30 UNRELATED CASES

      Human molecular genetics
    34. PENNIELLO MJ; CHAPON F; OLIVIER D; LEROY F; GUILLOIS B; LECHEVALIER B
      MYOSITIS-OSSIFICANS PROGRESSIVA

      Archives de pediatrie
    35. VERMERSCH P; BORDET R; LEDOZE F; RUCHOUX MM; CHAPON F; THOMAS P; DESTEE A; LECHEVALLIER B; DELACOURTE A
      DEMONSTRATION OF A SPECIFIC PROFILE OF PA THOLOGICAL TAU-PROTEINS IN FRONTOTEMPORAL DEMENTIA CASES

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    36. VIADER F; CHAPON F; DAO T; RIVRAIN Y; LECHEVALIER B
      ADULT CELIAC-DISEASE REVEALED BY A SENSOR Y-MOTOR NEUROPATHY

      La Presse medicale
    37. DELASAYETTE V; MACRO M; DIRAISON P; BERTRAN F; LECHEVALIER B; CHAPON F
      ACUTE NECROTIZING VASCULITIS (POLYARTERITIS-NODOSA) CONFINED TO THE NERVE WITH SPONTANEOUS-RECOVERY

      British journal of rheumatology
    38. CARON A; VIADER F; LECHEVALIER B; CHAPON F
      CYTOPLASMIC BODY MYOPATHY - FAMILIAL CASES WITH ACCUMULATION OF DESMIN AND DYSTROPHIN - AN IMMUNOHISTOCHEMICAL, IMMUNOELECTRON MICROSCOPIC AND BIOCHEMICAL-STUDY

      Acta Neuropathologica
    39. LATOUR P; BONNEBOUCHE C; BOST M; DIRAISON P; CHAPON F; BOUCHERAT M; VANDENBERGHE A
      A RSAL RFLP AT THE HUMAN MYELIN PROTEIN ZERO (MPZ) FOCUS

      Clinical genetics
    40. ERMINE A; KHOURI S; CHAPON F; DERLON JM; LECHEVALIER B
      METABOLIC-FATE OF CH3-LABELED METHIONINE IN THE CNS TUMOR STUDIES WITH PET

      Journal of neurochemistry


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Documento generato il 29/10/20 alle ore 16:01:53