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    1. de Cid, R; Chomel, JC; Lazaro, C; Sunyer, J; Baudis, M; Casals, T; Le Moual, N; Kitzis, A; Feingold, J; Anto, J; Estivill, X; Kauffmann, F
      CFTR and asthma in the French EGEA study

      EUROPEAN JOURNAL OF HUMAN GENETICS
    2. Levy, M; Gubler, MC; Feingold, J
      Contribution of genetics to knowledge and management of hereditary renal diseases progressing to renal failure

      ARCHIVES DE PEDIATRIE
    3. Kauffmann, F; Dizier, MH; Annesi-Maesano, I; Bousquet, J; Charpin, D; Demenais, F; Ecochard, D; Feingold, J; Gormand, F; Grimfeld, A; Lathrop, M; Matran, R; Neukirch, F; Paty, E; Pison, C; Scheinmann, P; Vervloet, D; Lockhart, A
      Epidemiological study of the Genetics and Environment of Asthma, bronchialhyperresponsiveness and atopy (EGEA). Protocol and potential selection factors

      REVUE D EPIDEMIOLOGIE ET DE SANTE PUBLIQUE
    4. Baulac, S; Picard, F; Herman, A; Feingold, J; Genin, E; Hirsch, E; Prud'homme, JF; Baulac, M; Brice, A; LeGuern, E
      Evidence for digenic inheritance in a family with both febrile convulsionsand temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31

      ANNALS OF NEUROLOGY
    5. Fang, LJ; Chalhoub, N; Li, WT; Feingold, J; Ortenberg, J; Lemieux, B; Thirion, JP
      Genotype analysis of the NF1 gene in the French Canadians from the Quebec population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    6. Gabolde, M; Hubert, D; Guilloud-Bataille, M; Lenaerts, C; Feingold, J; Besmond, C
      The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis

      JOURNAL OF MEDICAL GENETICS
    7. Benlounis, A; Nabbout, R; Feingold, J; Parmeggiani, A; Guerrini, R; Kaminska, A; Dulac, O
      Genetic predisposition to severe myoclonic epilepsy in infancy

      EPILEPSIA
    8. Frebourg, T; Ebel, A; Bonaiti-Pellie, C; Brugieres, L; Berthet, P; Bressac-De Paillerets, B; Chevrier, A; Chompret, A; Cohen-Haguenauer, O; Delattre, O; Feingold, J; Feunteun, J; Frappaz, D; Fricker, JP; Gesta, P; Jonveaux, P; Kalifa, C; Lasset, C; Leheup, B; Limacher, JM; Longy, M; Nogues, C; Oppenheim, D; Sommelet, D; Soubrier, F; Stoll, C; Stoppa-Lyonnet, D; Tristant, H
      Li-Fraumeni syndrome: update, new data and guidelines for clinical management

      BULLETIN DU CANCER
    9. Sylvius, N; Tesson, F; Gayet, C; Charron, P; Benaiche, A; Mangin, L; Peuchmaurd, M; Duboscq-Bidot, L; Feingold, J; Beckmann, JS; Bouchier, C; Komajda, M
      A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q14

      AMERICAN JOURNAL OF HUMAN GENETICS
    10. Dizier, MH; Besse-Schmittler, C; Guilloud-Bataille, M; Annesi-Maesano, I; Boussaha, M; Bousquet, J; Charpin, D; Degioanni, A; Gormand, F; Grimfeld, A; Hochez, J; Hyne, G; Lockhart, A; Luillier-Lacombe, M; Matran, R; Meunier, F; Neukirch, F; Pacheco, Y; Parent, V; Paty, E; Pin, I; Pison, C; Scheinmann, P; Thobie, N; Vervloet, D; Kauffmann, F; Feingold, J; Lathrop, M; Demenais, F
      Genome screen for asthma and related phenotypes in the French EGEA study

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    11. Gorwood, P; Batel, P; Gouya, L; Courtois, F; Feingold, J; Ades, J
      Reappraisal of the association between the DRD2 gene, alcoholism and addiction

      EUROPEAN PSYCHIATRY
    12. Neonato, MG; Guilloud-Bataille, M; Beauvais, P; Begue, P; Belloy, M; Benkerrou, M; Ducrocq, R; Maier-Redelsperger, M; de Montalembert, M; Quinet, B; Elion, J; Feingold, J; Girot, R
      Acute clinical events in 299 homozygous sickle cell patients living in France

      EUROPEAN JOURNAL OF HAEMATOLOGY
    13. Feingold, J
      Modifiying genes in hereditary diseases

      M S-MEDECINE SCIENCES
    14. Sampogna, F; Demenais, F; Hochez, J; Oryszczyn, MP; Maccario, J; Kauffmann, F; Feingold, J; Dizier, MH
      Segregation analysis of IgE levels in 335 French families (EGEA) using different strategies to correct for the ascertainment through a correlated trait (asthma)

      GENETIC EPIDEMIOLOGY
    15. Levy, M; Feingold, J
      Estimating prevalence in single-gene kidney diseases progressing to renal failure

      KIDNEY INTERNATIONAL
    16. Mouele, R; Bodo, JM; Mpele, DMB; Feingold, J; Galacteros, F
      beta-globin gene haplotypes and alpha-thalassemia analysis in Babinga pygmies from Congo-Brazzaville

      HUMAN BIOLOGY
    17. Mouele, R; Pambou, O; Feingold, J; Galacteros, F
      alpha-thalassemia in Bantu population from Congo-Brazzaville: Its interaction with sickle cell anemia

      HUMAN HEREDITY
    18. Guilloud-Bataille, M; De Crozes, D; Rault, G; Degioanni, A; Feingold, J
      Cystic fibrosis mutations: Report from the French registry

      HUMAN HEREDITY
    19. Garcia, A; Abel, L; Cot, M; Richard, P; Ranque, S; Feingold, J; Demenais, F; Boussinesq, M; Chippaux, JP
      Genetic epidemiology of host predisposition microfilaraemia in human loiasis

      TROPICAL MEDICINE & INTERNATIONAL HEALTH
    20. Neonato, MG; Lu, CY; Guilloud-Bataille, M; Lapoumeroulie, C; Nabeel-Jassim, H; Dabit, D; Girot, R; Krishnamoorthy, R; Feingold, J; Besmond, C; Elion, J
      Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections

      EUROPEAN JOURNAL OF HUMAN GENETICS
    21. Philippe, A; Martinez, M; Guilloud-Bataille, M; Gillberg, C; Rastam, M; Sponheim, E; Coleman, M; Zappella, M; Aschauer, H; Van Maldergem, L; Penet, C; Feingold, J; Brice, A; Leboyer, M
      Genome-wide scan for autism susceptibility genes (vol 8, pg 805, 1999)

      HUMAN MOLECULAR GENETICS
    22. Philippe, A; Martinez, M; Guilloud-Bataille, M; Gillberg, C; Rastam, M; Sponheim, E; Coleman, M; Zappella, M; Aschauer, H; van Malldergerme, L; Penet, C; Feingold, J; Brice, A; Leboyer, M
      Genome-wide scan for autism susceptibility genes

      HUMAN MOLECULAR GENETICS
    23. Gabolde, M; Guilloud-Bataille, M; Feingold, J; Besmond, C
      Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study

      BRITISH MEDICAL JOURNAL
    24. Favier, R; Neonato, MG; Maillet, F; Feingold, J; Cayre, Y; Girot, R
      Incidence of G20210A mutation in severe vaso-occlusive events complicatingsickle cell anemia

      BLOOD COAGULATION & FIBRINOLYSIS
    25. Kauffmann, F; Dizier, MH; Annesi-Maesano, I; Bousquet, J; Charpin, D; Demenais, F; Ecochard, D; Feingold, J; Gormand, F; Grimfeld, A; Lathrop, M; Matran, R; Neukirch, F; Paty, E; Pin, I; Pison, C; Scheinmann, P; Vervloet, D; Lockhart, A
      EGEA (Epidemiological study on the Genetics and Environment of Asthma, bronchial hyperresponsiveness and atopy) - descriptive characteristics

      CLINICAL AND EXPERIMENTAL ALLERGY
    26. Mouele, R; Galacteros, F; Feingold, J
      Haemoglobin F (HbF) levels in sickle-cell anaemia patients homozygous for the Bantu haplotype

      EUROPEAN JOURNAL OF HAEMATOLOGY
    27. Feingold, J
      Misuse of genetic testing by insurance

      REVUE D EPIDEMIOLOGIE ET DE SANTE PUBLIQUE
    28. Durr, A; Hahn-Barma, V; Brice, A; Pecheux, C; Dode, C; Feingold, J
      Homozygosity in Huntington's disease

      JOURNAL OF MEDICAL GENETICS
    29. Le Hellard, S; Neidhart, E; Thomas, P; Feingold, J; Malafosse, A; Tafti, M
      Lack of association between juvenile myoclonic epilepsy and HLA-DR13

      EPILEPSIA
    30. Eisinger, F; Alby, N; Bremond, A; Dauplat, J; Espie, M; Janiaud, P; Kuttenn, F; Lebrun, JP; Lefranc, JP; Pierret, J; Sobol, H; Stoppa-Lyonnet, D; Thouvenin, D; Tristant, H; Feingold, J
      Recommendations for medical management of hereditary breast and ovarian cancer: the Inserm-FNCLCC ad hoc committee

      BULLETIN DU CANCER
    31. Leboyer, M; Philippe, A; Bouvard, M; Guilloud-Bataille, M; Bondoux, D; Tabuteau, F; Feingold, J; Mouren-Simeoni, MC; Launay, JM
      Whole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives

      BIOLOGICAL PSYCHIATRY
    32. 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
    33. Fang, LJ; Feingold, J; Lemieux, B; Thirion, JP
      A novel and very peculiar HincII polymorphism in the 5 ' region of the human neurofibromatosis type 1 (NF1) gene

      ANNALES DE GENETIQUE
    34. Yaouanq, J; Feingold, J; Lacombe, D
      French Society for Human Genetics. "Genetics in practice" commission. Corescientific data of use in genetic counseling. Hemochromatosis.

      ANNALES DE GENETIQUE
    35. Feingold, J; Guilloud-Bataille, M
      Genetic comparisons of patients with cystic fibrosis with or without meconium ileus

      ANNALES DE GENETIQUE
    36. Houdayer, C; Soupre, V; Rosenberg-Bourgin, M; Martinez, H; Tredano, M; Feldmann, D; Feingold, J; Aymard, P; Munnich, A; Le Bouc, Y; Vazquez, MP; Bahuau, M
      Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait

      ANNALES DE GENETIQUE
    37. Eisinger, F; Alby, N; Bremond, A; Dauplat, J; Espie, M; Janiaud, P; Kuttenn, F; Lebrun, JP; Lefranc, JP; Pierret, J; Sobol, H; Stoppa-Lyonnet, D; Thouvenin, D; Tristant, H; Feingold, J
      Recommendations for medical management of hereditary breast and ovarian cancer: the INSERM-FNCLCC ad hoc committee

      ANNALES DE GENETIQUE
    38. Mouele, R; Boukila, V; Fourcade, V; Feingold, J; Galacteros, F
      Sickle-cell disease in Brazzaville, Congo: Genetical, hematological, biochemical and clinical aspects

      ACTA HAEMATOLOGICA
    39. Gargiulo, M; Prouvost, B; Hahn-Barma, V; Lagroua, I; Brice, A; Feingold, J; Durr, A
      Scope and temporality in predictive test. Predictive test for the diagnosis of potential Huntington's disease: the experience of a French hospital (La Pitie-Salpetriere, Paris).

      PUBLIC HEALTH AND UNIVERSAL ETHICS
    40. VONKLEISTRETZOW JC; CORMIERDAIRE V; DELONLAY P; PARFAIT B; CHRETIEN D; RUSTIN P; FEINGOLD J; ROTIG A; MUNNICH A
      A HIGH-RATE OF PARENTAL CONSANGUINITY (20-30-PERCENT) IN CYTOCHROME-OXIDASE DEFICIENCY

      European journal of human genetics
    41. EISINGER F; ALBY N; BREMOND A; DAUPLAT J; ESPIE M; JANIAUD P; KUTTENN F; LEBRUN JP; LEFRANC JP; PIERRET J; SOBOL H; STOPPALYONNET D; THOUVENIN D; TRISTANT H; FEINGOLD J
      RECOMMENDATIONS FOR MEDICAL-MANAGEMENT OF HEREDITARY BREAST AND OVARIAN-CANCER - THE FRENCH NATIONAL AD HOC COMMITTEE

      Annals of oncology
    42. Feingold, J
      Prevalence and incidence of hereditary diseases

      M S-MEDECINE SCIENCES
    43. FEINGOLD J
      MULTIPLE MUTATIONS IN A SPECIFIC GENE IN A SMALL POPULATION

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    44. Feingold, J
      Identification of a genetic component in common diseases.

      PATHOLOGIE BIOLOGIE
    45. SEGBENA AY; PREHU C; WAJCMAN H; BARDAKDJIANMICHAU J; MESSIE K; FETEKE L; VOVOR A; DAVID M; FEINGOLD J; GALACTEROS F
      HEMOGLOBINS IN TOGOLESE NEWBORNS - HB-S, HB-C, HB-BARTS, AND ALPHA-GLOBIN GENE STATUS

      American journal of hematology
    46. 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
    47. FEINGOLD J
      THE DILEMMA OF GENETIC TESTING

      Biofutur (Puteaux)
    48. CHARRON P; DUBOURG O; DESNOS M; ISNARD R; HAGEGE A; BONNE G; CARRIER L; TESSON F; BOUHOUR JB; BUZZI JC; FEINGOLD J; SCHWARTZ K; KOMAJDA M
      GENOTYPE-PHENOTYPE CORRELATIONS IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - A COMPARISON BETWEEN MUTATIONS IN THE CARDIAC PROTEIN-C AND THE BETA-MYOSIN HEAVY-CHAIN GENES

      European heart journal
    49. Leboyer, M; Bellivier, F; McKeon, P; Albus, M; Borrman, M; Perez-Diaz, F; Mynett-Johnson, L; Feingold, J; Maier, W
      Age at onset and gender resemblance in bipolar siblings

      PSYCHIATRY RESEARCH
    50. 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
    51. PHILIPPE A; GUILLOUDBATAILLE M; MARTINEZ M; BRICE A; FEINGOLD J; GILLBERG C; LEBOYER M
      A GENOME-WIDE SEARCH FOR AUTISM SUSCEPTIBILITY GENES

      American journal of medical genetics
    52. CORBEX M; NOSTENBERTRAND M; BELLIVIER F; FEINGOLD J; LEBAYER M; MALLET J
      GENETIC-ANALYSIS OF BIPOLAR DISORDERS - EPISTATIC EFFECTS BETWEEN CANDIDATE GENES

      American journal of medical genetics
    53. 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
    54. DUBERTRET C; GORWOOD P; ADES J; FEINGOLD J; SCHWARTZ JC; SOKOLOFF P
      METAANALYSIS OF DRD3 GENE AND SCHIZOPHRENIA - ETHNIC HETEROGENEITY AND SIGNIFICANT ASSOCIATION IN CAUCASIANS

      American journal of medical genetics
    55. BELLIVIER F; SCHURHOFF F; NOSTENBERTRAND M; MALLET J; FEINGOLD J; LEBOYER M
      METHODOLOGICAL PROBLEMS IN METAANALYSIS OF ASSOCIATION STUDIES BETWEEN BIPOLAR AFFECTIVE-DISORDER AND THE TYROSINE-HYDROXYLASE GENE

      American journal of medical genetics
    56. KAUFFMANN F; CHOMEL JC; KITZIS A; FEINGOLD J
      DELTA-F508 HETEROZYGOSITY AND ASTHMA

      Lancet
    57. HAHNBARMA V; DEWEER B; DURR A; DODE C; FEINGOLD J; PILLON B; AGID Y; BRICE A; DUBOIS B
      ARE COGNITIVE CHANGES THE FIRST SYMPTOMS OF HUNTINGTONS-DISEASE - A STUDY OF GENE CARRIERS

      Journal of Neurology, Neurosurgery and Psychiatry
    58. CARTAULT F; STEFFANN J; VIDAUD D; BOUSQUET S; LESURE F; RENOUIL M; MCDONNELL N; FEINGOLD J; BELDJORD C; BIENVENU T
      DETECTION OF MORE THAN 91-PERCENT CYSTIC-FIBROSIS MUTATIONS IN A SAMPLE OF THE POPULATION FROM REUNION-ISLAND AND IDENTIFICATION OF 2 NOVELMUTATIONS (A309G, S1255L) AND ONE NOVEL POLYMORPHISM (L49L)

      Clinical genetics
    59. BRUINSSLOT L; GORWOOD P; BOUVARD M; BLOT P; ADES J; FEINGOLD J; SCHWARTZ JC; MOURENSIMEONI MC
      LACK OF ASSOCIATION BETWEEN ANOREXIA-NERVOSA AND D3 DOPAMINE-RECEPTORGENE

      Biological psychiatry
    60. 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
    61. Eisinger, F; Alby, N; Bremond, A; Dauplat, J; Espie, M; Janiaud, P; Kuttenn, F; Lebrun, JP; Lefranc, JP; Pierret, J; Sobol, H; Stoppa-Lyonnet, D; Thouvenin, D; Tristant, H; Feingold, J
      Recommendations for medical management of hereditary breast and ovarian cancer: The INSERM-FNCLCC ad hoc committee

      ANNALES D ENDOCRINOLOGIE
    62. FEINGOLD J; GUILLOUDBATAILLE M; DECROZES D
      AN ABNORMAL DISTRIBUTION OF DELTA-F508 GENOTYPES IN CYSTIC-FIBROSIS PATIENT REGISTRIES

      Annales de genetique
    63. Jouanolle, AM; Fergelot, P; Raoul, ML; Gandon, G; Roussey, M; Deugnier, Y; Feingold, J; Le Gall, JY; David, V
      Prevalence of the C282Y mutation in Brittany: Penetrance of genetic hemochromatosis?

      ANNALES DE GENETIQUE
    64. GARCIA A; COT M; CHIPPAUX JP; RANQUE S; FEINGOLD J; DEMENAIS F; ABEL L
      GENETIC-CONTROL OF BLOOD INFECTION LEVELS IN HUMAN MALARIA - EVIDENCEFOR A COMPLEX GENETIC MODEL

      The American journal of tropical medicine and hygiene
    65. SOUIED EH; BENLIAN P; AMOUYEL P; FEINGOLD J; LAGARDE JP; MUNNICH A; KAPLAN J; COSCAS G; SOUBRANE G
      THE EPSILON-4 ALLELE OF THE APOLIPOPROTEIN-E GENE AS A POTENTIAL PROTECTIVE FACTOR FOR EXUDATIVE AGE-RELATED MACULAR DEGENERATION

      American journal of ophthalmology
    66. VONKLEISTRETZOW JC; CORMIERDAIRE V; DELONLAY P; PARFAIT B; CHRETIEN D; RUSTIN P; FEINGOLD J; ROTIG A; MUNNICH A
      A HIGH-RATE (20-PERCENT-30-PERCENT) OF PARENTAL CONSANGUINITY IN CYTOCHROME-OXIDASE DEFICIENCY

      American journal of human genetics
    67. BOUANGA JC; MOUELE R; PREHU C; WAJCMAN H; FEINGOLD J; GALACTEROS F
      GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY AND HOMOZYGOUS SICKLE-CELL DISEASE IN CONGO

      Human heredity
    68. Eisinger, F; Feingold, J
      Summary of the INSERM-FNCLCC recommendations on the management of women genetically predisposed to breast or ovarian cancer

      EUROCANCER 98
    69. KAUFFMANN F; DIZIER MH; PIN I; PATY E; GORMAND F; VERVLOET D; BOUSQUET J; NEUKIRCH F; ANNESI I; ORYSZCZYN MP; LATHROP M; DEMENAIS F; LOCKHART A; FEINGOLD J
      EPIDEMIOLOGIC-STUDY OF THE GENETICS AND ENVIRONMENT OF ASTHMA, BRONCHIAL HYPERRESPONSIVENESS, AND ATOPY - PHENOTYPE ISSUES

      American journal of respiratory and critical care medicine
    70. 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
    71. JAY M; GORWOOD P; FEINGOLD J; LEBOYER M
      A ONE-YEAR PREVALENCE STUDY OF SCHIZOPHRENIA ON REUNION ISLAND

      European psychiatry
    72. GORWOOD P; LEBOYER M; FALISSARD B; ROUILLON F; JAY M; FEINGOLD J
      FURTHER EPIDEMIOLOGIC EVIDENCE FOR ANTICIPATION IN SCHIZOPHRENIA

      Biomedicine & pharmacotherapy
    73. FEINGOLD J; DURR A
      GENETIC PRESYMPTOMATIC TESTING - THE HUNT INGTONS-DISEASE TYPICAL DISORDER

      Pathologie et biologie
    74. 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
    75. TELVI L; DUPUY O; ION R; FEINGOLD J; PONSOT G
      THE POSSIBLE IMPLICATION OF RARE AUTOSOMAL FRAGILE SITES IN MENTAL-RETARDATION - STUDY OF 9 FAMILIES

      Cytogenetics and cell genetics
    76. ABRAHAM J; BILGRAMI S; DORSKY D; EDWARDS RL; FEINGOLD J; HILL DR; TUTSCHKA PJ
      STOMATOCOCCUS-MUCILAGINOSUS MENINGITIS IN A PATIENT WITH MULTIPLE-MYELOMA FOLLOWING AUTOLOGOUS STEM-CELL TRANSPLANTATION

      Bone marrow transplantation
    77. BELLIVIER F; NOSTENBERTRAND M; LEBOYER M; SCHURHOFF F; FEINGOLD J; MELONI R; ALLILAIRE JF; MALLET J
      ASSOCIATION BETWEEN LATE-ONSET BIPOLAR AFFECTIVE-DISORDER AND TYROSINE-HYDROXYLASE GENE POLYMORPHISM

      American journal of medical genetics
    78. GORWOOD P; ADES J; BATEL P; GOUYA L; NORDMAN Y; FEINGOLD J
      THE DRD2 TAQ1 POLYMORPHISM IS INDIRECTLY INVOLVED IN SEVERE ADDICTION, NOT IN ALCOHOL-DEPENDENCE

      American journal of medical genetics
    79. 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
    80. 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
    81. 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
    82. NEUKIRCH F; LYONCAEN O; CLANET M; BOUSQUET J; FEINGOLD J; DRUET P
      ASTHMA, NASAL ALLERGIES, AND MULTIPLE-SCLEROSIS

      Journal of allergy and clinical immunology
    83. HAHNBARMA V; DEWEER B; DURR A; DODE C; FEINGOLD J; PILLON B; AGID Y; BRICE A; DUBOIS B
      ARE COGNITIVE CHANGES THE FIRST SYMPTOM OF HUNTINGTONS-DISEASE - A STUDY OF GENE CARRIERS

      Neurology
    84. EMERIT I; OGANESIAN N; ARUTYUNIAN R; POGOSSIAN A; SARKISIAN T; CERNJAVSKI L; LEVY A; FEINGOLD J
      OXIDATIVE STRESS-RELATED CLASTOGENIC FACTORS IN PLASMA FROM CHERNOBYLLIQUIDATORS - PROTECTIVE EFFECTS OF ANTIOXIDANT PLANT PHENOLS, VITAMINS AND OLIGOELEMENTS

      Mutation research
    85. DURR A; MEDJBEUR S; DIDIERJEAN O; VIDAILHET M; BONNET AM; GRID D; PENET C; BRICE A; AGID Y; MARTINEZ M; FEINGOLD J; AMOUYEL P; BORG M; BROUSSOLLE E; DESTEE A; DURIF F; FENELON G; FEVE JR; POLLAK P; RASCOL O; TISON F; TRANCHANT C; WARTER JM; VERIN M; VIALLET F
      APOLIPOPROTEIN-E GENOTYPE IN FAMILIAL PARKINSONS-DISEASE

      Journal of Neurology, Neurosurgery and Psychiatry
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/06/20 alle ore 06:21:10