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La ricerca find articoli where soggetti phrase all words 'FRENCH-CANADIANS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 70 riferimenti
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    1. Miller, WL; Portale, AA
      Genetics of vitamin D biosynthesis and its disorders

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    2. Demetriou, K; H'Maltezou, E; Pierides, AM
      Familial homozygous hypercholesterolemia: Effective long-term treatment with cascade double filtration plasmapheresis

      BLOOD PURIFICATION
    3. Pausova, Z; Gossard, F; Gaudet, D; Tremblay, J; Kotchen, TA; Cowley, AW; Hamet, P
      Heritability estimates of obesity measures in siblings with and without hypertension

      HYPERTENSION
    4. 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
    5. Myerowitz, R
      The search for the genetic lesion in Ashkenazi Jews with classic Tay-Sachsdisease

      TAY-SACHS DISEASE
    6. Dardenne, O; Prud'homme, J; Arabian, A; Glorieux, FH; St-Arnaud, R
      Targeted inactivation of the 25-hydroxyvitamin D-3-1 alpha-hydroxylase gene (CYP27B1) creates an animal model of pseudovitamin D-deficiency rickets

      ENDOCRINOLOGY
    7. Brorholt-Petersen, JU; Jensen, HK; Raungaard, B; Gregersen, N; Faergeman, O
      LDL-receptor gene mutations and the hypocholesterolemic response to statintherapy

      CLINICAL GENETICS
    8. Chappuis, PO; Hamel, N; Paradis, AJ; Deschenes, J; Robidoux, A; Potvin, C; Cantin, J; Tonin, P; Ghadirian, P; Foulkes, WD
      Prevalence of founder BRCA1 and BRCA2 mutations in unselected French Canadian women with breast cancer

      CLINICAL GENETICS
    9. Gagnon, A; Heyer, E
      Fragmentation of the Quebec population genetic pool (Canada): Evidence from the genetic contribution of founders per region in the 17th and 18th centuries

      AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY
    10. Durst, R; Colombo, R; Shpitzen, S; Ben Avi, L; Friedlander, Y; Wexler, R; Raal, FJ; Marais, DA; Defesche, JC; Mandelshtam, MY; Kotze, MJ; Leitersdorf, E; Meiner, V
      Recent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: Positive selection is not always necessary to account for disease incidence among Ashkenazi Jews

      AMERICAN JOURNAL OF HUMAN GENETICS
    11. Lee, N; Daly, MJ; Delmonte, T; Lander, ES; Xu, FH; Hudson, TJ; Mitchell, GA; Morin, CC; Robinson, BH; Rioux, JD
      A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16

      AMERICAN JOURNAL OF HUMAN GENETICS
    12. Cordeiro, P; Hechtman, P; Kaplan, F
      The G(M2) gangliosidoses databases: Allelic variation at the HEXA, HEKB, and GM2A gene loci

      GENETICS IN MEDICINE
    13. Miller, WL; Portale, AA
      Vitamin D 1 alpha-hydroxylase

      TRENDS IN ENDOCRINOLOGY AND METABOLISM
    14. Austerlitz, F; Heyer, E
      Allelic association is increased by correlation of effective family size

      EUROPEAN JOURNAL OF HUMAN GENETICS
    15. Portale, AA; Miller, WL
      Human 25-hydroxyvitamin D-1 alpha-hydroxylase: cloning, mutations, and gene expression

      PEDIATRIC NEPHROLOGY
    16. Ghadirian, P; Maisonneuve, P; Perret, C; Kennedy, G; Boyle, P; Krewski, D; Lacroix, A
      A case-control study of toenail selenium and cancer of the breast, colon, and prostate

      CANCER DETECTION AND PREVENTION
    17. Colombo, R; Bignamini, AA; Carobene, A; Sasaki, J; Tachikawa, M; Kobayashi, K; Toda, T
      Age and origin of the FCMD 3 '-untranslated-region retrotransposal insertion mutation causing Fukuyama-type congenital muscular dystrophy in the Japanese population

      HUMAN GENETICS
    18. Laprise, C; Boulet, LP; Morissette, J; Winstall, E; Raymond, V
      Evidence for association and linkage between atopy, airway hyper-responsiveness, and the beta subunit Glu237Gly variant of the high-affinity receptorfor immunoglobulin E in the French-Canadian population

      IMMUNOGENETICS
    19. Blumen, SC; Korczyn, AD; Lavoie, H; Medynski, S; Chapman, J; Asherov, A; Nisipeanu, P; Inzelberg, R; Carasso, RL; Bouchard, JP; Tome, FMS; Rouleau, GA; Brais, B
      Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene

      NEUROLOGY
    20. Labuda, M; Labuda, D; Miranda, C; Poirier, J; Soong, BW; Barucha, NE; Pandolfo, M
      Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion

      NEUROLOGY
    21. Malyshev, PP
      Heterozygous familial hypercholesterolemia: Diagnosis and drug therapy

      KARDIOLOGIYA
    22. Vohl, MC; Lepage, P; Gaudet, D; Brewer, CG; Betard, C; Perron, P; Houde, G; Cellier, C; Faith, JM; Despres, JP; Morgan, K; Hudson, TJ
      Molecular scanning of the human PPAR alpha gene: association of the L162V mutation with hyperapobetalipoproteinemia

      JOURNAL OF LIPID RESEARCH
    23. Carmena, R; Roy, M; Roederer, G; Minnich, A; Davignon, J
      Coexisting dysbetalipoproteinemia and familial hypercholesterolemia - Clinical and laboratory observations

      ATHEROSCLEROSIS
    24. Colombo, R
      Age estimate of the N370S mutation causing Gaucher disease in Ashkenazi Jews and European populations: A reappraisal of haplotype data

      AMERICAN JOURNAL OF HUMAN GENETICS
    25. Rinat, C; Wanders, RJA; Drukker, A; Halle, D; Frishberg, Y
      Primary hyperoxaluria type I: A model for multiple mutations in a monogenic disease within a distinct ethnic group

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    26. Walker, ARP; Halse, J
      Pattern of cancer in Indian patients hospitalized in Durban, South Africa

      EUROPEAN JOURNAL OF CANCER PREVENTION
    27. Couture, P; Morissette, J; Gaudet, D; Vohl, MC; Gagne, C; Bergeron, J; Despres, JP; Simard, J
      Fine mapping of low-density lipoprotein receptor gene by genetic linkage on chromosome 19p13.1-p13.3 and study of the founder effect of four French Canadian low-density lipoprotein receptor gene mutations

      ATHEROSCLEROSIS
    28. Gaudet, D; Vohl, MC; Couture, P; Moorjani, S; Tremblay, G; Perron, P; Gagne, C; Despres, JP
      Contribution of receptor negative versus receptor defective mutations in the LDL-receptor gene to angiographically assessed coronary artery disease among young (25-49 years) versus middle-aged (50-64 years) men

      ATHEROSCLEROSIS
    29. BERGMAN AJIW; VANDENBERG IET; BRINK W; POLLTHE BT; PLOOSVANAMSTEL JK; BERGER R
      SPECTRUM OF MUTATIONS IN THE FUMARYLACETOACETATE HYDROLASE GENE OF TYROSINEMIA TYPE-1 PATIENTS IN NORTHWESTERN EUROPE AND MEDITERRANEAN COUNTRIES

      Human mutation
    30. MINNICH A; BALOUKAS J; ROEDERER G; LUSSIERCACAN S; DAVIGNON J; GENEST J
      LIPOPROTEIN-LIPASE GENE-MUTATIONS IN CORONARY-ARTERY DISEASE

      Canadian journal of cardiology
    31. STARKEY LJ; KUHNLEIN HV; GRAYDONALD K
      FOOD BANK USERS - SOCIODEMOGRAPHIC AND NUTRITIONAL CHARACTERISTICS

      CMAJ. Canadian Medical Association journal
    32. GHADIRIAN P; LACROIX A; PERRET C; MAISONNEUVE P; BOYLE P
      SOCIODEMOGRAPHIC CHARACTERISTICS, SMOKING, MEDICAL AND FAMILY HISTORY, AND BREAST-CANCER

      Cancer detection and prevention
    33. GHADIRIAN P; MAISONNEUVE P; PERRET C; LACROIX A; BOYLE P
      EPIDEMIOLOGY OF SOCIODEMOGRAPHIC CHARACTERISTICS, LIFE-STYLE, MEDICALHISTORY, AND COLON-CANCER - A CASE-CONTROL STUDY AMONG FRENCH-CANADIANS IN MONTREAL

      Cancer detection and prevention
    34. MORASH BA; TAN MH; NASSAR BA; TOO CKL; GUERNSEY DL
      A NOVEL MUTATION IN EXON-4 OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE RESULTING IN HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA ASSOCIATED WITH DECREASED LIGAND-BINDING

      Atherosclerosis
    35. STLOUIS M; TANGUAY RM
      MUTATIONS IN THE FUMARYLACETOACETATE HYDROLASE GENE CAUSING HEREDITARY TYROSINEMIA TYPE-I - OVERVIEW

      Human mutation
    36. MYEROWITZ R
      TAY-SACHS DISEASE-CAUSING MUTATIONS AND NEUTRAL POLYMORPHISMS IN THE HEX-A GENE

      Human mutation
    37. MAILLY F; PALMEN J; MULLER DPR; GIBBS T; LLOYD J; BRUNZELL J; DURRINGTON P; MITROPOULOS K; BETTERIDGE J; WATTS G; LITHELL H; ANGELICO F; HUMPHRIES SE; TALMUD PJ
      FAMILIAL LIPOPROTEIN-LIPASE (LPL) DEFICIENCY - A CATALOG OF LPL GENE-MUTATIONS IDENTIFIED IN 20 PATIENTS FROM THE UK, SWEDEN, AND ITALY

      Human mutation
    38. GUDNASON V; SIGURDSSON G; NISSEN H; HUMPHRIES SE
      COMMON FOUNDER MUTATION IN THE LDL RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA IN THE ICELANDIC POPULATION

      Human mutation
    39. STEWART GJ; TEUTSCH SM; CASTLE M; HEARD RNS; BENNETTS BH
      HLA-DR, HLA-DQA1 AND HLA-DQB1 ASSOCIATIONS IN AUSTRALIAN MULTIPLE-SCLEROSIS PATIENTS

      European journal of immunogenetics
    40. WEBER M; MCNICOLL S; MARCIL M; CONNELLY P; LUSSIERCACAN S; DAVIGNON J; LATOUR Y; GENEST J
      METABOLIC FACTORS CLUSTERING, LIPOPROTEIN CHOLESTEROL, APOLIPOPROTEIN-B, LIPOPROTEIN (A) AND APOLIPOPROTEIN-E PHENOTYPES IN PREMATURE CORONARY-ARTERY DISEASE IN FRENCH-CANADIANS

      Canadian journal of cardiology
    41. FOUBERT L; DEGENNES JL; LAGARDE JP; EHRENBORG E; RAISONNIER A; GIRARDET JP; HAYDEN MR; BENLIAN P
      ASSESSMENT OF FRENCH PATIENTS WITH LPL DEFICIENCY FOR FRENCH-CANADIANMUTATIONS

      Journal of Medical Genetics
    42. HEYER E; TREMBLAY M; DESJARDINS B
      17TH-CENTURY EUROPEAN ORIGINS OF HEREDITARY-DISEASES IN THE SAGUENAY POPULATION (QUEBEC, CANADA)

      Human biology
    43. VOHL MC; MOORJANI S; ROY M; GAUDET D; TORRES AL; MINNICH A; GAGNE C; TREMBLAY G; LAMBERT M; BERGERON J; COUTURE P; PERRON P; BLAICHMAN S; BRUN LD; DAVIGNON J; LUPIEN PJ; DESPRES JP
      GEOGRAPHIC-DISTRIBUTION OF FRENCH-CANADIAN LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE-MUTATIONS IN THE PROVINCE OF QUEBEC

      Clinical genetics
    44. GHADIRIAN P; LACROIX A; MAISONNEUVE P; PERRET C; POTVIN C; GRAVEL D; BERNARD D; BOYLE P
      NUTRITIONAL FACTORS AND COLON-CARCINOMA - A CASE-CONTROL STUDY INVOLVING FRENCH-CANADIANS IN MONTREAL, QUEBEC, CANADA

      Cancer
    45. AKERMAN BR; NATOWICZ MR; KABACK MM; LOYER M; CAMPEAU E; GRAVEL RA
      NOVEL MUTATIONS AND DNA-BASED SCREENING IN NON-JEWISH CARRIERS OF TAY-SACHS-DISEASE

      American journal of human genetics
    46. GHADIRIAN P; LACROIX A; MAISONNEUVE P; PERRET C; DROUIN G; PERRAULT JP; BELAND G; ROHAN TE; HOWE GR
      NUTRITIONAL FACTORS AND PROSTATE-CANCER - A CASE-CONTROL STUDY OF FRENCH-CANADIANS IN MONTREAL, CANADA

      CCC. Cancer causes & control
    47. VANBAEL M; NATOWICZ MR; TOMCZAK J; GREBNER EE; PRENCE EM
      HETEROZYGOSITY FOR TAY-SACHS-DISEASE IN NON-JEWISH AMERICANS WITH ANCESTRY FROM IRELAND OR GREAT-BRITAIN

      Journal of Medical Genetics
    48. TORRES AL; MOORJANI S; VOHL MC; GAGNE C; LAMARCHE B; BRUN LD; LUPIEN PJ; DESPRES JP
      HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA IN CHILDREN - LOW-DENSITY-LIPOPROTEIN RECEPTOR MUTATIONAL ANALYSIS AND VARIATION IN THE EXPRESSION OF PLASMA LIPOPROTEIN-LIPID CONCENTRATIONS

      Atherosclerosis
    49. HSIA SH; CONNELLY PW; HEGELE RA
      GENETIC DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA IN AFFECTED RELATIVES USING PEDIGREE TRACING

      Clinical biochemistry
    50. MINNICH A; DELANGAVANT G; LAVIGNE J; ROEDERER G; LUSSIERCACAN S; DAVIGNON J
      G-]A SUBSTITUTION AT POSITION-75 OF THE APOLIPOPROTEIN-A-I GENE PROMOTER - EVIDENCE AGAINST A DIRECT EFFECT ON HDL CHOLESTEROL LEVELS

      Arteriosclerosis, thrombosis, and vascular biology
    51. MCNICOLL S; LATOUR Y; RONDEAU C; BOUTHILLIER D; DAVIGNON J; GENEST J
      CARDIOVASCULAR RISK-FACTORS AND LIPOPROTEIN PROFILE IN FRENCH-CANADIANS WITH PREMATURE CAD - IMPACT OF THE NATIONAL-CHOLESTEROL-EDUCATION-PROGRAM-II

      Canadian journal of cardiology
    52. GHADIRIAN P; SHATENSTEIN B; LAMBERT J; THOUEZ JP; PETITCLERC C; PARENT ME; MAILHOT M; GOULET MC
      FOOD-HABITS OF FRENCH-CANADIANS IN MONTREAL, QUEBEC

      Journal of the American College of Nutrition
    53. LANGLOIS A; RAZIN E
      SELF-EMPLOYMENT AMONG FRENCH-CANADIANS - THE ROLE OF THE REGIONAL MILIEU

      Ethnic and racial studies
    54. MINNICH A; ROY M; CHAMBERLAND A; LAVIGNE J; DAVIGNON J
      NEW METHODS FOR RAPID DETECTION OF LOW-DENSITY-LIPOPROTEIN RECEPTOR AND APOLIPOPROTEIN-B GENE-MUTATIONS CAUSING FAMILIAL HYPERCHOLESTEROLEMIA

      Clinical biochemistry
    55. FERRIERES J; LAMBERT J; LUSSIERCACAN S; DAVIGNON J
      CORONARY-ARTERY DISEASE IN HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIAPATIENTS WITH THE SAME LDL RECEPTOR GENE MUTATION

      Circulation
    56. EISENSMITH RC; GOLTSOV AA; ONEILL C; TYFIELD LA; SCHWARTZ EI; KUZMIN AI; BARANOVSKAYA SS; TSUKERMAN GL; TREACY E; SCRIVER CR; GUTTLER F; GULDBERG P; EIKEN HG; APOLD J; SVENSSON E; NAUGHTEN E; CAHALANE SF; CROKE DT; COCKBURN F; WOO SLC
      RECURRENCE OF THE R408W MUTATION IN THE PHENYLALANINE-HYDROXYLASE LOCUS IN EUROPEANS

      American journal of human genetics
    57. FERRIERES J; SING CF; ROY M; DAVIGNON J; LUSSIERCACAN S
      APOLIPOPROTEIN-E POLYMORPHISM AND HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA - SEX-SPECIFIC EFFECTS

      Arteriosclerosis and thrombosis
    58. PERUSSE D
      MATE CHOICE IN MODERN SOCIETIES - TESTING EVOLUTIONARY HYPOTHESES WITH BEHAVIORAL-DATA

      Human nature
    59. EISENSMITH RC; WOO SLC
      POPULATION-GENETICS OF PHENYLKETONURIA

      Acta paediatrica
    60. HAEGERT DG; MARROSU MG
      GENETIC SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS

      Annals of neurology
    61. TANAKA A; SAKAZAKI H; MURAKAMI H; ISSHIKI G; SUZUKI K
      MOLECULAR-GENETICS OF TAY-SACHS-DISEASE IN JAPAN

      Journal of inherited metabolic disease
    62. DEBRAEKELEER M; DAO TN
      HEREDITARY DISORDERS IN THE FRENCH-CANADIAN POPULATION OF QUEBEC .1. IN SEARCH OF FOUNDERS

      Human biology
    63. HUMPHRIES SE
      THE APPLICATION OF MOLECULAR-BIOLOGY TECHNIQUES TO THE DIAGNOSIS OF HYPERLIPEMIA AND OTHER RISK-FACTORS FOR CARDIOVASCULAR-DISEASE

      Annales de biologie clinique
    64. ROZEN R; MASCISCH A; LAMBERT M; LAFRAMBOISE R; SCRIVER CR
      MUTATION PROFILES OF PHENYLKETONURIA IN QUEBEC POPULATIONS - EVIDENCEOF STRATIFICATION AND NOVEL MUTATIONS

      American journal of human genetics
    65. HECHTMAN P; KAPLAN F
      TAY-SACHS-DISEASE SCREENING AND DIAGNOSIS - EVOLVING TECHNOLOGIES

      DNA and cell biology
    66. SCRIVER CR
      1992 GENETICS-SOCIETY-OF-CANADA AWARD OF EXCELLENCE LECTURE - GENES, SCIENCE, AND SOCIETY

      Genome
    67. MEIJER H; JONGBLOED RJE; HEKKING M; SPAAPEN LJM; GERAEDTS JPM
      RFLP HAPLOTYPING AND MUTATION ANALYSIS OF THE PHENYLALANINE-HYDROXYLASE GENE IN DUTCH PHENYLKETONURIA FAMILIES

      Human genetics
    68. PERUSSE D
      CULTURAL AND REPRODUCTIVE SUCCESS IN INDUSTRIAL-SOCIETIES - TESTING THE RELATIONSHIP AT THE PROXIMATE AND ULTIMATE LEVELS

      Behavioral and brain sciences
    69. DEBRAEKELEER M; DAO TN
      FOUNDER EFFECT IN BETA-THALASSEMIA IN PORTNEUF, QUEBEC

      Nouvelle revue francaise d'hematologie
    70. HAEGERT DG; FRANCIS GS
      HLA-DQ POLYMORPHISMS DO NOT EXPLAIN HLA CLASS-II ASSOCIATIONS WITH MULTIPLE-SCLEROSIS IN 2 CANADIAN PATIENT GROUPS

      Neurology


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Documento generato il 05/08/20 alle ore 10:41:44