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    1. LABERGE S; LABAUGE P; MARECHAL E; AUVERGNON M; TOURNIERLASSERVE E
      FAMILIAL CAVERNOUS ANGIOMAS CCM1 GENE IDENTIFICATION

      European journal of human genetics
    2. TAILLIA H; CHABRIAT H; KURTZ A; VERIN M; LEVY C; VAHEDI K; TOURNIERLASSERVE E; BOUSSER MG
      COGNITIVE ALTERATIONS IN NONDEMENTED CADASIL PATIENTS

      Cerebrovascular diseases
    3. FURBY A; VAHEDI K; FORCE M; LARROUY S; RUCHOUX MM; JOUTEL A; TOURNIERLASSERVE E
      DIFFERENTIAL-DIAGNOSIS OF A VASCULAR LEUKOENCEPHALOPATHY WITHIN A CADASIL FAMILY - USE OF SKIN BIOPSY ELECTRON-MICROSCOPY STUDY AND DIRECT GENOTYPIC SCREENING

      Journal of neurology
    4. MICHEL M; MEYER O; FRANCES C; TOURNIERLASSERVE E; PIETTE JC
      IMMUNOGENETICS BASIS OF HUMAN SYSTEMIC LUPUS-ERYTHEMATOSUS

      La Revue de medecine interne (Paris)
    5. CHABRIAT H; LEVY C; TAILLIA H; IBAZIZEN MT; VAHEDI K; JOUTEL A; TOURNIERLASSERVE E; BOUSSER MG
      PATTERNS OF MRI LESIONS IN CADASIL

      Neurology
    6. MELLIES JK; BAUMER T; MULLER JA; TOURNIERLASSERVE E; CHABRIAT H; KNOBLOCH O; HACKELOER HJ; GOEBEL HH; WETZIG L; HALLER P
      SPECT STUDY OF A GERMAN CADASIL FAMILY - A PHENOTYPE WITH MIGRAINE AND PROGRESSIVE DEMENTIA ONLY

      Neurology
    7. HEINZLEF O; JOHANNET C; SAZDOVITCH V; VERDIERTAILLEFER MH; TOURNIERLASSERVE E; ROULLET E
      ANTICARDIOLIPIN ANTIBODIES (ACL ABS) IN MULTIPLE-SCLEROSIS (MS) - A PROSPECTIVE-STUDY OF 285 PATIENTS

      Neurology
    8. LABAUGE P; LABERGE S; BRUNEREAU L; LEVY C; MARECHAL E; TOURNIERLASSERVE E
      CLINICAL AND GENETIC-STUDY OF 57 FRENCH FAMILIAL CAVERNOMAS PEDIGREES

      Neurology
    9. JOUTEL A; CHABRIAT H; VAHEDI K; DOMENGA V; VAYSSIERE C; MACIAZEK J; CRUAUD C; BOUSSER MG; TOURNIERLASSERVE E
      NOTCH3 SPLICE-SITE MUTATION CAUSING AUTOSOMAL-DOMINANT MIGRAINE WITH MRI WHITE-MATTER ABNORMALITIES

      Neurology
    10. DUCROS A; JOUTEL A; VAHEDI K; BOUSSER MG; TOURNIERLASSERVE E
      GENOTYPE-PHENOTYPE CORRELATIONS IN FAMILIAL HEMIPLEGIC MIGRAINE (FHM)

      Neurology
    11. PIETTE JC; MICHEL M; TINCANI A; CERVERA R; SHOENFELD Y; CRASSARD I; BIOUSSE V; MEYER O; TOURNIERLASSERVE E; BOFFA MC
      CHARACTERIZATION OF FAMILIAL, ANTIPHOSPHOLIPID SYNDROME - A EUROPEAN ANTIPHOSPHOLIPID FORUM PROJECT

      Arthritis and rheumatism
    12. MICHEL M; WITTKE F; MEYER O; FRANCES C; PIETTE JC; TOURNIERLASSERVE E
      SCREENING FOR CHROMOSOME-1 SUSCEPTIBILITY LOCI AND GENES IN 125 LUPUSMULTIPLEX FAMILIES

      Arthritis and rheumatism
    13. MICHEL M; MEYER O; FRANCES C; MICHEL C; JOHANNET C; ARFI S; TOURNIERLASSERVE E; PIETTE JC
      CLINICAL CHARACTERIZATION OF 125 FRENCH LUPUS MULTIPLEX FAMILIES

      Arthritis and rheumatism
    14. GILGENKRANTZ S; TOURNIERLASSERVE E
      CADASIL AND ALAGILLE-SYNDROME, 2 DEFECTS IN NOTCH SIGNALING

      MS. Medecine sciences
    15. DUCROS A; JOUTEL A; VAHEDI K; CECILLON M; FERREIRA A; BERNARD E; VERIER A; ECHENNE B; DEMUNAIN AL; BOUSSER MG; TOURNIERLASSERVE E
      MAPPING OF A 2ND LOCUS FOR FAMILIAL HEMIPLEGIC MIGRAINE TO 1Q21-Q23 AND EVIDENCE OF FURTHER HETEROGENEITY

      Annals of neurology
    16. BENTOLILA S; RIPOLL L; DROUET L; CRASSARD I; TOURNIERLASSERVE E; PIETTE JC
      LACK OF ASSOCIATION BETWEEN THROMBOSIS IN PRIMACY ANTIPHOSPHOLIPID SYNDROME AND THE RECENTLY DESCRIBED THROMBOPHILIC 3'-UNTRANSLATED PROTHOMBIN GENE POLYMORPHISM

      Thrombosis and haemostasis
    17. JOUTEL A; VAHEDI K; CORPECHOT C; TROESCH A; CHABRIAT H; VAYSSIERE C; CRUAUD C; MACIAZEK J; WEISSENBACH J; BOUSSER MG; BACH JF; TOURNIERLASSERVE E
      STRONG CLUSTERING AND STEREOTYPED NATURE OF NOTCH3 MUTATIONS IN CADASIL PATIENTS

      Lancet
    18. JOUTEL A; CORPECHOT C; DUCROS A; VAHEDI K; CHABRIAT H; MOUTON P; ALAMOWITCH S; DOMENGA V; CECILLION M; MARECHAL E; MACIAZEK J; VAYSSIERE C; CRUAUD C; CABANIS EA; RUCHOUX MM; WEISSENBACH J; BACH JF; BOUSSER MG; TOURNIERLASSERVE E
      IDENTIFICATION OF THE CADASIL GENE

      Stroke
    19. CHABRIAT H; JOUTEL A; VAHEDI K; IBAZIZEN MT; TOURNIERLASSERVE E; BOUSSER MG
      CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY

      Revue neurologique
    20. JOUTEL A; CORPECHOT C; VAYSSIERE C; VAHEDI K; CHABRIAT H; MARECHAL E; MACIAZEK J; CRUAUD C; RUCHOUX MM; WEISSENBACH J; BOUSSER MG; TOURNIERLASSERVE E
      CHARACTERIZATION OF NOTCH3 MUTATIONS IN CADASIL PATIENTS

      Neurology
    21. MELLIES JK; TOURNIERLASSERVE E; BAUMER T; MULLER JA; KNOBLOCH O; GOEBEL HH; HACKELOER HJ; WETZIG L; HALLER P
      A CLINICAL, MRI, SPECT AND PATHOLOGICAL-STUDY OF A LARGE GERMAN CADASIL FAMILY

      Neurology
    22. 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
    23. BENTOLILA S; RIPOLL L; DROUET L; CRASSARD I; TOURNIERLASSERVE E; PIETTE JC
      COMMON PROTHROMBOTIC GENETIC-FACTORS ARE ADDITIONAL RISKS FOR THROMBOSIS IN MEN WITH PRIMARY ANTIPHOSPHOLIPID SYNDROME (PAPS)

      Arthritis and rheumatism
    24. JOUTEL A; DUCROS A; ALAMOWITCH S; CRUAUD C; DOMENGA V; MARECHAL E; VAHEDI K; CHABRIAT H; BOUSSER MG; TOURNIERLASSERVE E
      A HUMAN HOMOLOG OF BACTERIAL ACETOLACTATE SYNTHASE GENES MAPS WITHIN THE CADASIL CRITICAL REGION

      Genomics
    25. CHABRIAT H; JOUTEL A; VAHEDI K; IBAZIZEN MT; TOURNIERLASSERVE E; BOUSSER MG
      CADASIL (CEREBRAL AUTOSOMAL-DOMINANT ARTE RIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY)

      Journal des maladies vasculaires
    26. VAHEDI K; TOURNIERLASSERVE E; CHABRIAT H; BOUSSER MG
      AN ADDITIONAL MONOGENIC DISORDER THAT MASQUERADES AS MULTIPLE-SCLEROSIS

      American journal of medical genetics
    27. DUCROS A; PICO F; VAHEDI K; JOUTEL A; MICHEL A; DARCEL F; JULIEN J; MOULIN T; BISGAARD C; ECHENNE B; LABAUQE P; BOUSSER MG; TOURNIERLASSERVE E
      FAMILIAL HEMIPLEGIC MIGRAINE - GENETIC-ANALYSIS OF 21 FAMILIES WITH CHROMOSOME 19P MARKERS

      Neurology
    28. ALAMOWITCH S; DUCROS A; NAGY T; NIBBIO A; JOUTEL A; VAHEDI K; CHABRIAT H; MACIAZEK J; BOUSSER MG; TOURNIERLASSERVE E
      CADASIL - GENETIC HOMOGENEITY AND MAPPING OF THE LOCUS WITHIN A 2-CM INTERVAL

      Neurology
    29. VAHEDI K; CHABRIAT H; DUCROS A; ALAMOWITCH S; JOUTEL A; IBAZIZEN MT; CABANIS EA; TOURNIERLASSERVE E; BOUSSER MG
      ANALYSIS OF CADASIL CLINICAL NATURAL-HISTORY IN A SERIES OF 136 PATIENTS BELONGING TO 17 FAMILIES LINKED TO CHROMOSOME-19

      Neurology
    30. CHABRIAT H; TAILLA H; IBAZIZEN MT; LEVY C; VAHEDI K; ABANOU A; JOUTEL A; TOURNIERLASSERVE E; CABANIS EA; BOUSSER MG
      MRI FEATURES OF CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY

      Neurology
    31. BIOUSSE V; FRANCES C; PIETTE JC; TOURNIERLASSERVE E; AIACH M
      ACTIVATED PROTEIN-C RESISTANCE CAUSED BY FACTOR-V ARG-506-]GLN MUTATION IN 14 PATIENTS WITH SNEDDONS-SYNDROME

      Neurology
    32. JOUTEL A; CORPECHOT C; DUCROS A; VAHEDI K; CHABRIAT H; MOUTON P; ALAMOWITCH S; DOMENGA V; CECILLION M; MARECHAL E; MACIAZEK J; VAYSSIERE C; CRUAUD C; CABANIS EA; RUCHOUX MM; WEISSENBACH J; BACH JF; BOUSSER MG; TOURNIERLASSERVE E
      NOTCH3 MUTATIONS IN CADASIL, A HEREDITARY ADULT-ONSET CONDITION CAUSING STROKE AND DEMENTIA

      Nature
    33. HEINZLEF O; ROULLET E; JOHANET C; TOURNIERLASSERVE E; CHAZOUILLERES O
      PREVALENCE OF SERUM ANTIBODIES TO HEPATITIS-C VIRUS IS NOT INCREASED PATIENTS WITH MULTIPLE-SCLEROSIS

      Journal of Neurology, Neurosurgery and Psychiatry
    34. SHANMUGAM A; COPIEBERGMAN C; FALISSARD B; DELRIEU O; JAIS JP; REBIBO D; BACH JB; TOURNIERLASSERVE E
      TCR ALPHA-BETA GENE USAGE FOR MYELIN BASIC-PROTEIN RECOGNITION IN HEALTHY MONOZYGOTIC TWINS

      The Journal of immunology
    35. CRASSARD I; BIOUSSE V; MICHEL C; BLETRY O; PIETTE AM; LABAUGE P; TOURNIERLASSERVE E; PIETTE JC
      FAMILIAL PRIMARY ANTIPHOSPHOLIPID SYNDROME (PAPS)

      Arthritis and rheumatism
    36. 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
    37. JOUTEL A; TOURNIERLASSERVE E; BOUSSER MG
      HEMIPLEGIC MIGRAINE

      La Presse medicale
    38. HUTCHINSON M; ORIORDAN J; JAVED M; QUIN E; MACERLAINE D; WILLCOX T; PARFREY N; NAGY TG; TOURNIERLASSERVE E
      FAMILIAL HEMIPLEGIC MIGRAINE AND AUTOSOMAL-DOMINANT ARTERIOPATHY WITHLEUKOENCEPHALOPATHY (CADASIL)

      Annals of neurology
    39. RAGNO M; TOURNIERLASSERVE E; FIORI MG; MANCA A; PATROSSO MC; FERLINI A; SIROCCHI G; TROJANO L; CHABRIAT H; SALVI F
      AN ITALIAN KINDRED WITH CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITHSUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY (CADASIL)

      Annals of neurology
    40. VAHEDI K; JOUTEL A; VANBOGAERT P; DUCROS A; MACIAZECK J; BACH JF; BOUSSER MG; TOURNIERLASSERVE E
      A GENE FOR HEREDITARY PAROXYSMAL CEREBELLAR-ATAXIA MAPS TO CHROMOSOME19P

      Annals of neurology
    41. BIOUSSE V; PIETTE JC; FRANCES C; BLETRY O; PAPO T; TOURNIERLASSERVE E; DUCHEMIN J; AIACH M
      PRIMARY ANTIPHOSPHOLIPID SYNDROME IS NOT ASSOCIATED WITH ACTIVATED PROTEIN-C RESISTANCE CAUSED BY FACTOR-V ARG 506-]GLN MUTATION

      Journal of rheumatology
    42. SHANMUGAM A; COPIEBERGMAN C; CAILLAT S; BACH JF; TOURNIERLASSERVE E
      IN-VIVO CLONAL EXPANSION OF T-LYMPHOCYTES SPECIFIC FOR AN IMMUNODOMINANT N-TERMINAL MYELIN BASIC-PROTEIN EPITOPE IN HEALTHY-INDIVIDUALS

      Journal of neuroimmunology
    43. CHABRIAT H; TOURNIERLASSERVE E; VAHEDI K; LEYS D; JOUTEL A; NIBBIO A; ESCAILLAS JP; BRACARD S; IBAZIZEN MT; TEHINDRAZANARIVELO A; GASTAUT JL; BOUSSER MG
      AUTOSOMAL-DOMINANT MIGRAINE WITH MRI WHITE-MATTER ABNORMALITIES MAPPING AT THE CADASIL (CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY) LOCUS

      Stroke
    44. CHABRIAT H; TOURNIERLASSERVE E; VAHEDI K; LEYS D; JOUTEL A; NIBBIO A; ESCAILLAS JP; IBAZIZEN MT; BRACARD S; TEHINDRAZANARIVELO A; GASTAUT JL; BOUSSER MG
      AUTOSOMAL-DOMINANT MIGRAINE WITH MRI WHITE-MATTER ABNORMALITIES MAPPING TO THE CADASIL LOCUS

      Neurology
    45. DUCROS A; JOUTEL A; LABAUGE P; PAGES M; BOUSSER MG; TOURNIERLASSERVE E
      MONOZYGOTIC TWINS DISCORDANT FOR FAMILIAL HEMIPLEGIC MIGRAINE

      Neurology
    46. BIOUSSE V; FRANCES C; BLETRY O; PAPOP T; GODEAU P; TOURNIERLASSERVE E; PIETTE JC
      FAMILIAL INCIDENCE OF PRIMARY ANTIPHOSPHOLIPID SYNDROME (PAPS) - AN ANALYSIS OF 17 UNRELATED FAMILIES

      Neurology
    47. DUCROS A; JOUTEL A; VAHEDI K; FERREIRA A; BERNARD E; VERIER A; TOURNIERLASSERVE E
      LOCALIZATION OF A 2ND GENE FOR FAMILIAL HEMIPLEGIC MIGRAINE

      Neurology
    48. TOURNIERLASSERVE E; JOUTEL A; CHABRIAT H; VAHEDI K; NAGY T; DUCROS A; NIBBIO A; VERIN M; MAS JL; DAVOUS P; DUCROCQ X; LEVASSEUR M; DUBOIS B; LYONCAEN O; RAGNO M; HUTCHINSON M; BURKHARD P; JULIEN J; VIADER F; BURGUNDER JM; IBAZIZEN MT; BOUSSER MG
      CADASIL - CLINICAL PHENOTYPES AND GENETIC DATA IN 15 UNRELATED FAMILIES

      Neurology
    49. FRANCES C; BIOUSSE V; SAADA V; LAGRANGE S; GODEAU P; TOURNIERLASSERVE E; PIETTE JC
      FAMILIAL INCIDENCE OF SNEDDONS-SYNDROME - AN ANALYSIS OF 17 UNRELATEDFAMILIES

      Neurology
    50. HEINZLEF O; JOHANNET C; TOURNIERLASSERVE E; ROULLET E
      ANTINUCLEAR ANTIBODIES IN MULTIPLE-SCLEROSIS

      Neurology
    51. VERIN M; ROLLAND Y; LANDGRAF F; CHABRIAT H; BOMPAIS B; MICHEL A; VAHEDI K; MARTINET JP; TOURNIERLASSERVE E; LEMAITRE MH; EDAN G
      NEW PHENOTYPE OF THE CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY MAPPED TO CHROMOSOME-19 - MIGRAINE AS THE PROMINENT CLINICAL-FEATURE

      Journal of Neurology, Neurosurgery and Psychiatry
    52. JUNG HH; BASSETTI C; TOURNIERLASSERVE E; VAHEDI K; ARNABOLDI M; ARIFI VB; BURGUNDER JM
      CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY - A CLINICOPATHOLOGICAL AND GENETIC-STUDY OF A SWISS FAMILY

      Journal of Neurology, Neurosurgery and Psychiatry
    53. BIOUSSE V; FRANCES C; BLETRY O; PAPO T; WECHSLER B; GODEAU P; TOURNIERLASSERVE E; PIETTE JC
      FAMILIAL STUDY OF PRIMARY ANTIPHOSPHOLIPID SYNDROME (PAPS) - ANALYSISOF 29 UNRELATED FAMILIES

      Arthritis and rheumatism
    54. DUCROS A; JOUTEL A; VAHEDI K; FERRERIA A; BERNARD E; CECILLON M; VERRIER A; BOUSSER MG; TOURNIERLASSERVE E
      FAMILIAL HEMIPLEGIC MIGRAINE - IDENTIFICATION OF A 2ND LOCUS

      American journal of human genetics
    55. JOUTEL A; DUCROS A; ALAMOWITCH S; VAHEDI K; CHABRIAT H; DOMENGA V; RONI V; MACIAZEK J; PRIEUR M; MOHRENWEISER H; BOUSSER MG; TOURNIERLASSERVE E
      IDENTIFICATION OF EXPRESSED SEQUENCES FROM THE CADASIL REGION ON 19P

      American journal of human genetics
    56. HUTCHINSON M; ORIORDAN J; JAVED M; MACERLAINE D; WILLCOX T; PARPHREY N; TOURNIERLASSERVE E
      CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY AND LEUKOENCEPHALOPATHY ASSOCIATED WITH FAMILIAL HEMIPLEGIC MIGRAINE

      Annals of neurology
    57. VAHEDI K; TOURNIERLASSERVE E; LUTZ G; JOUTEL A; DUCROS A; TEHINDRAZANARIVELO A; CHABRIAT H; MASSIOU H; BOUSSER MG
      FAMILIAL MIGRAINE WITH CEREBRAL MAGNETIC-RESONANCE-IMAGING T2W1 HYPERSIGNALS

      Annals of neurology
    58. BOUSSER MG; TOURNIERLASSERVE E
      SUMMARY OF THE PROCEEDINGS OF THE FIRST INTERNATIONAL WORKSHOP ON CADASIL - PARIS, MAY 19-21, 1993

      Stroke
    59. RUCHOUX MM; CHABRIAT H; BOUSSER MG; TOURNIERLASSERVE E; BAUDRIMONT M
      PRESENCE OF ULTRASTRUCTURAL ARTERIAL LESIONS IN MUSCLE AND SKIN VESSELS OF PATIENTS WITH CADASIL

      Stroke
    60. RUCHOUX MM; CHABRIAT H; BOUSSER MG; TOURNIERLASSERVE E; BAUDRIMONT M
      PRESENCE OF ULTRASTRUCTURAL ARTERIAL LESIONS IN MUSCLE AND SKIN VESSELS OF PATIENTS WITH CADASIL

      Stroke
    61. JOUTEL A; BOUSSER MG; BIOUSSE V; LABAUGE P; CHABRIAT H; NIBBIO A; MACIAZEK J; MEYER B; BACH MA; WEISSENBACH J; LATHROP GM; TOURNIERLASSERVE E
      FAMILIAL HEMIPLEGIC MIGRAINE - LOCALIZATI ON OF A RESPONSIBLE GENE ONCHROMOSOME-19

      Revue neurologique
    62. VERIN M; ROLLAND Y; LANDGRAF F; BOMPAIS B; CHABRIAT H; TOURNIERLASSERVE E; LEMAITRE MH; EDAN G
      NEW PHENOTYPE OF CADASIL IN BRITTANY WITH MIGRAINE AND BIPOLAR PSYCHOTIC DISORDERS AS PROMINENT CLINICAL-FEATURES

      Neurology
    63. JOUTEL A; BOUSSER MG; BIOUSSE V; LABAUGE P; CHABRIAT H; JULIEN J; GOUTTIERE F; PONSOT G; PINSARD N; NIBBIO A; MACIAZEK J; WEISSENBACH J; LATHROP GM; TOURNIERLASSERVE E
      LINKAGE ANALYSIS IN FAMILIAL HEMIPLEGIC MIGRAINE FAMILIES, WITH CHROMOSOME-19 MARKERS

      Neurology
    64. SHANMUGAM A; COPIEBERGMAN C; HASHIM G; REBIBO D; JAIS JP; BACH JF; BACH MA; TOURNIERLASSERVE E
      HEALTHY MONOZYGOTIC TWINS DO NOT RECOGNIZE IDENTICAL T-CELL EPITOPES ON THE MYELIN BASIC-PROTEIN AUTOANTIGEN

      European Journal of Immunology
    65. JOUTEL A; DUCROS A; VAHEDI K; LABAUGE P; DELRIEU O; PINSARD N; MANCINI J; PONSOT G; GOUTTIERE F; GASTAUT JL; MAZIACECK J; WEISSENBACH J; BOUSSER MG; TOURNIERLASSERVE E
      GENETIC-HETEROGENEITY OF FAMILIAL HEMIPLEGIC MIGRAINE

      American journal of human genetics
    66. JOUTEL A; BOUSSER MG; BIOUSSE V; LABAUGE P; CHABRIAT H; NIBBIO A; MACIAZEK J; MEYER B; BACH MA; WEISSENBACH J; LATHROP GM; TOURNIERLASSERVE E
      A GENE FOR FAMILIAL HEMIPLEGIC MIGRAINE MAPS TO CHROMOSOME-19

      Nature genetics
    67. TOURNIERLASSERVE E; BACH JF
      THE IMMUNOGENETICS OF MYASTHENIA-GRAVIS, MULTIPLE-SCLEROSIS AND THEIRANIMAL-MODELS

      Journal of neuroimmunology
    68. TOURNIERLASSERVE E; JOUTEL A; MELKI J; WEISSENBACH J; LATHROP GM; CHABRIAT H; MAS JL; NIBBIO A; CABANIS EA; BAUDRIMONT M; MACIAZEK J; BACH MA; BOUSSER MG
      CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS MAPS TO CHROMOSOME-19Q12

      American journal of human genetics


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Documento generato il 31/10/20 alle ore 15:27:36