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La ricerca find articoli where authors phrase all words ' MALAFOSSE A' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 67 riferimenti
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    1. Abbar, M; Courtet, P; Bellivier, F; Leboyer, H; Boulenger, JP; Castelhau, D; Ferreira, M; Lambercy, C; Mouthon, D; Paoloni-Giacobino, A; Vessaz, M; Malafosse, A; Buresi, C
      Suicide attempts and the tryptophan hydroxylase gene

      MOLECULAR PSYCHIATRY
    2. Courtet, P; Baud, P; Abbar, M; Boulenger, JP; Castelnau, D; Mouthon, D; Malafosse, A; Buresi, C
      Association between violent suicidal behavior and the low activity allele of the serotonin transporter gene

      MOLECULAR PSYCHIATRY
    3. Moulard, B; Picard, F; le Hellard, S; Agulhon, C; Weiland, S; Favre, I; Bertrand, S; Malafosse, A; Bertrand, D
      Ion channel variation causes epilepsies

      BRAIN RESEARCH REVIEWS
    4. Karege, F; Schwald, M; Lambercy, C; Murama, JJ; Cisse, M; Malafosse, A
      A non-radioactive assay for the cAMP-dependent protein kinase activity in rat brain homogenates and age-related changes in hippocampus and cortex

      BRAIN RESEARCH
    5. Paoloni-Giacobino, A; Mouthon, D; Lambercy, C; Vessaz, M; Coutant-Zimmerli, S; Rudolph, W; Malafosse, A; Buresi, C
      Identification and analysis of new sequence variants in the human tryptophan hydroxylase (TpH) gene

      MOLECULAR PSYCHIATRY
    6. Khoris, J; Moulard, B; Briolotti, V; Hayer, M; Durieux, A; Clavelou, P; Malafosse, A; Rouleau, GA; Camu, W
      Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country

      EUROPEAN JOURNAL OF NEUROLOGY
    7. Escayg, A; MacDonald, BT; Meisler, MH; Baulac, S; Huberfeld, G; An-Gourfinkel, I; Brice, A; LeGuern, E; Moulard, B; Chaigne, D; Buresi, C; Malafosse, A
      Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

      NATURE GENETICS
    8. Moulard, B; Buresi, C; Malafosse, A
      Study of the voltage-gated sodium channel beta 1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)

      HUMAN MUTATION
    9. Karege, F; Buresi, C; Golaz, J; Schwald, M; Malafosse, A
      Decreased expression of G alpha s mRNA and protein levels in lithium-treated bipolar affective disorder

      HUMAN PSYCHOPHARMACOLOGY-CLINICAL AND EXPERIMENTAL
    10. Moulard, B; Chaigne, D; Malafosse, A
      Clinical heterogeneity in pedigrees with 2q-linked febrile seizures

      ANNALS OF NEUROLOGY
    11. Chollet, D; Franken, P; Raffin, Y; Malafosse, A; Widmer, J; Tafti, M
      Blood and brain magnesium in inbred mice and their correlation with sleep quality

      AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
    12. Moulard, B; Crespel, A; Malafosse, A; Baldy-Moulinier, M
      Recent insights about genetics of human idiopathic epilepsies and febrilesseizures

      REVUE NEUROLOGIQUE
    13. Preisig, M; Bellivier, F; Fenton, BT; Baud, P; Berney, A; Courtet, P; Hardy, P; Golaz, J; Leboyer, M; Mallet, J; Matthey, ML; Mouthon, D; Neidhart, E; Nosten-Bertrand, M; Stadelmann-Dubuis, E; Guimon, J; Ferrero, F; Buresi, C; Malafosse, A
      Association between bipolar disorder and monoamine oxidase A gene polymorphisms: Results of a multicenter study

      AMERICAN JOURNAL OF PSYCHIATRY
    14. Serratosa, JM; Gomez-Garre, P; Gallardo, ME; Anta, B; de Bernabe, DBV; Lindhout, D; Augustijn, PB; Tassinari, CA; Michelucci, R; Malafosse, A; Topcu, M; Grid, D; Dravet, C; Berkovic, SF; de Cordoba, SR
      A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)

      HUMAN MOLECULAR GENETICS
    15. Agulhon, C; Abitbol, M; Bertrand, D; Malafosse, A
      Localization of mRNA for CHRNA7 in human fetal brain

      NEUROREPORT
    16. Echenne, B; Rivier, F; Humbertclaude, V; Roubertie, A; Cheminal, R; Malafosse, A
      Benign familial infantile convulsions.

      ARCHIVES DE PEDIATRIE
    17. Karege, F; Golaz, J; Schwald, M; Malafosse, A
      Lithium and haloperidol treatments differently affect the mononuclear leukocyte G alpha s protein levels in bipolar affective disorder

      NEUROPSYCHOBIOLOGY
    18. Agulhon, C; Charnay, Y; Vallet, P; Abitbol, M; Kobetz, A; Bertrand, D; Malafosse, A
      Distribution of mRNA for the alpha-subunit of the nicotinic acetylcholine receptor in the human fetal brain (vol 58, pg 123, 1998)

      MOLECULAR BRAIN RESEARCH
    19. Franken, P; Malafosse, A; Tafti, N
      Genetic determinants of sleep regulation in inbred mice

      SLEEP
    20. Agulhon, C; Blanchet, P; Kobetz, A; Marchant, D; Faucon, N; Sarda, P; Moraine, C; Sittler, A; Biancalana, V; Malafosse, A; Abitbol, M
      Expression of FMR1, FXR1, and FXR2 genes in human prenatal tissues

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    21. Picot, MC; Crespel, A; Tricot, M; Daures, JP; Valton, L; Malafosse, A; Baldy-Moulinier, M
      Validity of diagnosis using the French translation of the semi-structured interview for seizure classification

      EPILEPSIA
    22. Le Hellard, S; Neidhart, E; Thomas, P; Feingold, J; Malafosse, A; Tafti, M
      Lack of association between juvenile myoclonic epilepsy and HLA-DR13

      EPILEPSIA
    23. Bellivier, F; Leboyer, M; Courtet, P; Feingold, J; Buresi, C; Malafosse, A
      No allelic association between bipolar affective disorder and the tryptophan hydroxylase gene - In reply

      ARCHIVES OF GENERAL PSYCHIATRY
    24. Moulard, B; Guipponi, M; Chaigne, D; Mouthon, D; Buresi, C; Malafosse, A
      Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33

      AMERICAN JOURNAL OF HUMAN GENETICS
    25. LALIOTI MD; SCOTT HS; GENTON P; GRID D; OUAZZANI R; MRABET A; IBRAHIM S; GOUIDER R; DRAVET C; CHKILI T; BOTTANI A; BURESI C; MALAFOSSE A; ANTONARAKIS SE
      THE EXPANDED DODECAMER REPEAT IN PROGRESSIVE MYOCLONUS EPILEPSY (EPM1) IS UNSTABLE, SHOWS NO CORRELATION WITH AGE-OF-ONSET, AND RESULTS IN REDUCED EXPRESSION OF REPORTER GENES IN-VITRO

      European journal of human genetics
    26. PAOLONIGIACOBINO A; BURESI C; FENTON B; PREISIG M; GOLAZ J; GUIMON J; FERRERO F; MALAFOSSE A
      PRELIMINARY-RESULTS OF AN ASSOCIATION STUDY BETWEEN THE TRYPTOPHAN-HYDROXYLASE GENE AND MANIAC DEPRESSIVE-ILLNESS IN A SWISS SAMPLE

      European journal of human genetics
    27. GOMEZGARRE P; ANTA B; CASTROGAGO M; LINDHOUT D; TASSINARI CA; MICHELUCCI R; MALAFOSSE A; TOPCU M; GRID D; DRAVET C; SERRATOSA J
      REDUCTION OF THE LAFORA-DISEASE CANDIDATE GENE REGION TO A 2 CM INTERVAL IN CHROMOSOME 6Q24 AND EVIDENCE FOR GENETIC-HETEROGENEITY

      European journal of human genetics
    28. AGULHON C; KOBETZ A; BLANCHET P; SARDA P; BIANCALANA V; SITTLER A; MALAFOSSE A; ABITHOL M
      EXPRESSION OF FMR1, FXR1, AND FXR2 GENES IN HUMAN PRENATAL TISSUES

      European journal of neuroscience
    29. KAREGE F; BOVIER P; STEPANIAN R; MALAFOSSE A
      THE EFFECT OF CLINICAL OUTCOME ON PLATELET G-PROTEINS OF MAJOR DEPRESSED-PATIENTS

      European neuropsychopharmacology
    30. MOULARD B; SALACHAS F; CHASSANDE B; BRIOLOTTI V; MEININGER V; MALAFOSSE A; CAMU W
      ASSOCIATION BETWEEN CENTROMERIC DELETIONS OF THE SMN GENE AND SPORADIC ADULT-ONSET LOWER MOTOR-NEURON DISEASE

      Annals of neurology
    31. FRANKEN P; MALAFOSSE A; TAFTI M
      GENETIC-VARIATION IN EEG ACTIVITY DURING SLEEP IN INBRED MICE

      American journal of physiology. Regulatory, integrative and comparative physiology
    32. BOUKAFTANE Y; KHORIS J; MOULARD B; SALACHAS F; MEININGER V; MALAFOSSE A; CAMU W; ROULEAU GA
      IDENTIFICATION OF 6 NOVEL SOD1 GENE-MUTATIONS IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS

      Canadian journal of neurological sciences
    33. AGULHON C; CHARNAY Y; VALLET P; BERTRAND D; MALAFOSSE A
      DISTRIBUTION OF MESSENGER-RNA FOR THE ALPHA-4 SUBUNIT OF THE NICOTINIC ACETYLCHOLINE-RECEPTOR IN THE HUMAN FETAL BRAIN

      Molecular brain research
    34. KAREGE F; LAMBERCY C; RUDOLPH W; SCHWALD M; MALAFOSSE A
      IN-VITRO STUDY OF G-PROTEIN ACTIVATION BY S-35 GTP-GAMMA-S BINDING TOPLATELET MEMBRANE - EFFECTS OF DIFFERENT MODULATORS

      Biogenic amines
    35. PAOLONIGIACOBINO A; COURTET P; BELLIVIER F; ABBAR M; LAMBERCY C; MOUTHON D; VESSAZ M; MALLET J; BOULANGER JP; LEBOYER M; MALAFOSSE A; BURESI C
      STUDY OF TRYPTOPHANE HYDROXYLASE GENE (TPH) POLYMORPHISMS IN BIPOLAR PATIENTS (BP) AND SUICIDE ATTEMPTERS (SA)

      American journal of medical genetics
    36. BELLIVIER F; LEBOYER M; COURTET P; BURESI C; SAMOLYK D; MALLET J; ALLILAIRE JF; FEINGOLD J; MALAFOSSE A
      ASSOCIATION BETWEEN THE TRYPTOPHAN-HYDROXYLASE GENE AND SUICIDAL-BEHAVIOR IN BIPOLAR PATIENTS

      American journal of medical genetics
    37. GOUIDER R; IBRAHIM S; FREDJ M; GARGOURI A; SAIDI H; OUEZZANI R; MALAFOSSE A; YAHIAOUI M; GRID D; MRABET A
      UNVERRICHT-LUNDBORG-DISEASE - CLINICAL AND ELECTROPHYSIOLOGICAL ASPECTS IN 19 NORTH-AFRICAN FAMILIES

      Revue neurologique
    38. BELLIVIER F; LEBOYER M; COURTET P; BURESI C; BEAUFILS B; SAMOLYK D; ALLILAIRE JF; FEINGOLD J; MALLET J; MALAFOSSE A
      ASSOCIATION BETWEEN THE TRYPTOPHAN-HYDROXYLASE GENE AND MANIC-DEPRESSIVE ILLNESS

      Archives of general psychiatry
    39. LALIOTI MD; SCOTT HS; GENTON P; GRID D; OUAZZANI R; MRABET A; IBRAHIM S; GOUIDER R; DRAVET C; CHKILI T; BOTTANI A; BURESI C; MALAFOSSE A; ANTONARAKIS SE
      A PCR AMPLIFICATION METHOD REVEALS INSTABILITY OF THE DODECAMER REPEAT IN PROGRESSIVE MYOCLONUS EPILEPSY (EPM1) AND NO CORRELATION BETWEEN THE SIZE OF THE REPEAT AND AGE AT ONSET

      American journal of human genetics
    40. MALAFOSSE A; LEBOYER M; DAMATO T; AMADEO S; ABBAR M; CAMPION D; CANSEIL O; CASTELNAU D; GHEYSEN F; GRANGER B; HENRIKSON B; POIRIER MF; SABATE O; SAMOLYK D; FEINGOLD J; MALLET J
      MANIC-DEPRESSIVE ILLNESS AND TYROSINE-HYDROXYLASE GENE - LINKAGE HETEROGENEITY AND ASSOCIATION

      Neurobiology of disease
    41. GUIPPONI M; RIVIER F; VIGEVANO F; BECK C; CRESPEL A; ECHENNE B; LUCCHINI P; SEBASTIANELLI R; BALDYMOULINIER M; MALAFOSSE A
      LINKAGE MAPPING OF BENIGN FAMILIAL INFANTILE CONVULSIONS (BFIC) TO CHROMOSOME 19Q

      Human molecular genetics
    42. TAFTI M; FRANKEN P; KITAHAMA K; MALAFOSSE A; JOUVET M; VALATX JL
      LOCALIZATION OF CANDIDATE GENOMIC REGIONS INFLUENCING PARADOXICAL SLEEP IN MICE

      NeuroReport
    43. LABAUGE P; OUAZZANI R; MRABET A; GRID D; GENTON P; DRAVET C; CHKILI T; BECK C; BURESI C; BALDYMOULINIER M; MALAFOSSE A
      ALLELIC HETEROGENEITY OF MEDITERRANEAN MYOCLONUS AND THE CYSTATIN-B GENE

      Annals of neurology
    44. WIDMER J; MOUTHON D; RAFFIN Y; CHOLLET D; HILLERET H; MALAFOSSE A; BOVIER P
      WEAK ASSOCIATION BETWEEN BLOOD SODIUM, POTASSIUM, AND CALCIUM AND INTENSITY OF SYMPTOMS IN MAJOR DEPRESSED-PATIENTS

      Neuropsychobiology
    45. BELLIVIER F; LEBOYER M; COURTET P; BURESI C; BEAUFILS B; SAMOLYK D; FEINGOLD J; ALLILAIRE JF; MALLET J; MALAFOSSE A
      ASSOCIATION BETWEEN THE TRYPTOPHAN-HYDROXYLASE GENE AND MANIC-DEPRESSIVE ILLNESS

      American journal of medical genetics
    46. GUIPPONI M; THOMAS P; GIRARDREYDET C; FEINGOLD J; BALDYMOULINIER M; MALAFOSSE A
      LACK OF ASSOCIATION BETWEEN JUVENILE MYOCLONIC EPILEPSY AND GABRA5 AND GABRB3 GENES

      American journal of medical genetics
    47. MOULARD B; CAMU W; MALAFOSSE A; BILLIARD M; BALDYMOULINIER M
      CLINICAL ANALYSIS OF FAMILIAL AMYOTROPHIC -LATERAL-SCLEROSIS - REVIEWOF LITERATURE

      Revue neurologique
    48. LALIOTI MD; SCOTT HS; BURESI C; ROSSIER C; BOTTANI A; MORRIS MA; MALAFOSSE A; ANTONARAKIS SE
      DODECAMER REPEAT EXPANSION IN CYSTATIN-B GENE IN PROGRESSIVE MYOCLONUS EPILEPSY

      Nature
    49. GUIPPONI M; BALDYMOULINIER M; MALAFOSSE A
      A FOK1 POLYMORPHISM IN THE HUMAN NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTOR ALPHA-4 SUBUNIT GENE

      Clinical genetics
    50. LALIOTI MD; SCOTT HS; BURESI C; ROSSIER C; BOTTANI A; MORRIS MA; MALAFOSSE A; ANTONARAKIS SE
      DODECAMER REPEAT EXPANSION IN THE CYSTATIN-B GENE IN PROGRESSIVE MYOCLONUS EPILEPSY (EPM1)

      American journal of human genetics
    51. BURESI C; COURTET P; LEBOYER M; FEINGOLD J; MALAFOSSE A
      ASSOCIATION BETWEEN SUICIDE ATTEMPT AND THE TRYPTOPHANE HYDROXYLASE (TPH) GENE

      American journal of human genetics
    52. LALIOTI MD; MIROTSOU M; BURESI C; PEITSCH MC; ROSSIER C; OUAZZANI R; BALDYMOULINIER M; BOTTANI A; MALAFOSSE A; ANTONARAKIS SE
      IDENTIFICATION OF MUTATIONS IN CYSTATIN B, THE GENE RESPONSIBLE FOR THE UNVERRICHT-LUNDBORG TYPE OF PROGRESSIVE MYOCLONUS EPILEPSY (EPM1)

      American journal of human genetics
    53. MOULARD B; SEFIANI A; LAAMRI A; MALAFOSSE A; CAMU W
      APOLIPOPROTEIN-E GENOTYPING IN SPORADIC AMYOTROPHIC-LATERAL-SCLEROSIS- EVIDENCE FOR A MAJOR INFLUENCE ON THE CLINICAL PRESENTATION AND PROGNOSIS

      Journal of the neurological sciences
    54. DULAC O; BULTEAU C; MALAFOSSE A; AUBOURG P; FEINGOLD J
      GENETICS OF EPILEPSY IN CHILDHOOD

      Archives de pediatrie
    55. LABAUGE P; BECK C; BELLET H; COQUILLAT G; VESPIGNANI H; DULAC O; GILGENKRANTZ S; DRAVET C; GENTON P; PELLISSIER JF; CHERY M; BALDYMOULINIER M; MALAFOSSE A
      LAFORA DISEASE IS NOT LINKED TO THE UNVERRICHT-LUNDBORG LOCUS

      American journal of medical genetics
    56. BILLIARD M; PASQUIEMAGNETTO V; TARODO F; HECKMANN M; CARLANDER B; MALAFOSSE A
      FAMILY STUDIES IN NARCOLEPSY

      Neurology
    57. MALAFOSSE A; BECK C; BELLET H; OUAZZANI R; GRID D; MRABET A; GENTON P; DRAVET C; BALDYMOULINIER M
      MOLECULAR-GENETIC STUDY OF UNVERRICHT-LUNDBORG-DISEASE IN MAGHREBI (NORTH-AFRICAN) PEDIGREES

      Epilepsia
    58. GUIPPONI M; MONTPIED P; MARESCAUX C; MALAFOSSE A
      GENOME SCREENING BY SEARCHING FOR SHARED SEGMENTS IN GENETICALLY ABSENCE EPILEPSY RATS - TOWARD THE MAPPING OF EPILEPSY ABSENCE GENE

      Epilepsia
    59. LOPESCENDES I; ANDERMANN E; ROUSSEAU M; BECK C; SORENSEN T; YACUBIAN EMT; SANTOS MCD; ASHWAL S; TORO C; BERG MJ; LINDHOUT D; RESOR SR; ANDERMANN F; GENTON P; PANDOLFO M; MALAFOSSE A; ROULEAU GA
      SEARCHING FOR THE GENE CAUSING LAFORA BODY DISEASE

      Epilepsia
    60. BECK C; MONTPIED P; MALAFOSSE A
      A NONSENSE MUTATION IN THE ALPHA-4-SUBUNIT OF THE NICOTINIC ACETYLCHOLINE-RECEPTOR (CHRNA(4)) COSEGREGATES WITH 20Q-LINKED BENIGN NEONATAL FAMILIAL CONVULSION (EBN1)

      Epilepsia
    61. ABBAR M; COURTET P; AMADEO S; CAER Y; MALLET J; BALDYMOULINIER M; CASTELNAU D; MALAFOSSE A
      SUICIDAL BEHAVIORS AND THE TRYPTOPHAN-HYDROXYLASE GENE

      Archives of general psychiatry
    62. ECHENNE B; HUMBERTCLAUDE V; RIVIER F; MALAFOSSE A; CHEMINAL R
      BENIGN INFANTILE EPILEPSY WITH AUTOSOMAL-DOMINANT INHERITANCE

      Brain & development
    63. MALAFOSSE A; BECK C; BELLET H; DICAPUA M; DULAC O; ECHENNE B; FUSCO L; LUCCHINI P; RICCI S; SEBASTIANELLI R; FEINGOLD J; BALDYMOULINIER M; VIGEVANO F
      BENIGN INFANTILE FAMILIAL CONVULSIONS ARE NOT AN ALLELIC FORM OF THE BENIGN FAMILIAL NEONATAL CONVULSIONS GENE

      Annals of neurology
    64. SMITH CL; KEITH T; HANSMANN I; WEISSENBACH J; ASIMAKOPOULOS FA; BOWDEN DW; DELEUZE JF; DUTTON ER; FASMAN KH; GREEN T; HADCHOUEL M; HAZAN J; HILGARTNER S; KINGSBURY DK; LODER B; MALAFOSSE A; MEUNIERROTIVAL M; PEARSON PL; SIRACUSA LD; STEINLEIN O; WHITE N; WILLIAMSON CM
      REPORT OF THE FIRST ERNATIONAL-WORKSHOP-ON-HUMAN-CHROMOSOME-20-MAPPING 1993 HELD ON SEPTEMBER 6-8, 1993 AT GIF-SUR-YVETTE, FRANCE

      Cytogenetics and cell genetics
    65. BILLIARD M; PASQUIEMAGNETTO V; HECKMAN M; CARLANDER B; BESSET A; ZACHARIEV Z; ELIAOU JF; MALAFOSSE A
      FAMILY STUDIES IN NARCOLEPSY

      Sleep
    66. MEININGER V; MOULARD B; CAMU W; MALAFOSSE A; DIB M; NDIAYE B; BILLIARD M; BALDYMOULINIER M
      GENETIC-ANALYSIS OF 19 FRENCH FAMILIAL FORMS OF AMYOTROPHIC-LATERAL-SCLEROSIS - LACK OF SOD1 MUTATION

      Neurology
    67. HIRSCH E; VELEZ A; SELLAL F; MATON B; GRINSPAN A; MALAFOSSE A; MARESCAUX C
      ELECTROCLINICAL SIGNS OF BENIGN NEONATAL FAMILIAL CONVULSIONS

      Annals of neurology


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Documento generato il 26/02/20 alle ore 04:53:20