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La ricerca find articoli where authors phrase all words ' WIJSMAN E' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 18 riferimenti
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    1. Poorkaj, P; Tsuang, D; Wijsman, E; Steinbart, E; Garruto, RM; Craig, UK; Chapman, NH; Anderson, L; Bird, TD; Plato, CC; Perl, DP; Weiderholt, W; Galasko, D; Schellenberg, GD
      TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonismdementia complex of Guam

      ARCHIVES OF NEUROLOGY
    2. Austin, MA; Stephens, K; Walden, CE; Wijsman, E
      Linkage analysis of candidate genes and the small, dense low-density lipoprotein phenotype

      ATHEROSCLEROSIS
    3. Kamino, K; Wijsman, E; Anderson, L; Nemens, E; Yamagata, H; Ohta, S; Bird, TD; Schellenberg, GD
      A family with late-onset Alzheimer's disease carrying a Val91Met mutation of the apolipoprotein A-II gene suggests altered plasma lipid metabolism inAlzheimer's disease

      ALZHEIMER'S DISEASE AND RELATED DISORDERS
    4. POORKAJ P; BIRD TD; WIJSMAN E; NEMENS E; GARRUTO RM; ANDERSON L; ANDREADIS A; WIEDERHOLT WC; RASKIND M; SCHELLENBERG GD
      TAU IS A CANDIDATE GENE FOR CHROMOSOME-17 FRONTOTEMPORAL DEMENTIA

      Annals of neurology
    5. BIRD TD; WIJSMAN E; NOCHLIN D; LEEHEY M; SUMI M; PAYAMI H; NEMENS E; SCHELLENBERG G
      GENETIC-STUDIES OF THE CHROMOSOME-17 FORM OF HEREDITARY DEMENTIA

      Neurology
    6. EDLAND SD; SILVERMAN JM; PESKIND ER; TSUANG D; WIJSMAN E; MORRIS JC
      INCREASED RISK OF DEMENTIA IN MOTHERS OF ALZHEIMERS-DISEASE CASES - EVIDENCE FOR MATERNAL INHERITANCE

      Neurology
    7. MARCOVINA SM; ALBERS JJ; WIJSMAN E; ZHANG ZH; CHAPMAN NH; KENNEDY H
      DIFFERENCES IN LP[A] CONCENTRATIONS AND APO[A] POLYMORPHS BETWEEN BLACK-AND-WHITE AMERICANS

      Journal of lipid research
    8. PAYAMI H; MONTEE K; ZAREPARSI S; KAVE J; BIRD T; YU C; WIJSMAN E; HESTON L; LITT M; SCHELLENBERG G
      FAMILIAL ALZHEIMER-DISEASE IN WOMEN

      American journal of human genetics
    9. STEPHENS K; ZLOTOGORSKI A; SMITH L; EHRLICH P; WIJSMAN E; LIVINGSTON RJ; SYBERT VP
      EPIDERMOLYSIS-BULLOSA SIMPLEX - A KERATIN-5 MUTATION IS A FULLY DOMINANT ALLELE IN EPIDERMAL CYTOSKELETON FUNCTION

      American journal of human genetics
    10. JARVIK GP; BRUNZELL JD; AUSTIN MA; KRAUSS RM; MOTULSKY AG; WIJSMAN E
      GENETIC PREDICTORS OF FCHL IN 4 LARGE PEDIGREES - INFLUENCE OF APO-B LEVEL MAJOR LOCUS PREDICTED GENOTYPE AND LDL SUBCLASS PHENOTYPE

      Arteriosclerosis and thrombosis
    11. COMMENGES D; OLSON J; WIJSMAN E
      THE WEIGHTED RANK PAIRWISE CORRELATION STATISTIC FOR LINKAGE ANALYSIS- SIMULATION STUDY AND APPLICATION TO ALZHEIMERS-DISEASE

      Genetic epidemiology
    12. STEPHENS K; ZLOTOGORSKI A; SMITH L; EHRLICH P; LE R; WIJSMAN E; SYBERT VP
      AN EPIDERMOLYSIS-BULLOSA-SIMPLEX PATIENT WITH A KERATIN-5 HOMOZYGOUS DEFECT

      Journal of investigative dermatology
    13. LIN S; THOMPSON E; WIJSMAN E
      AN ALGORITHM FOR MONTE-CARLO ESTIMATION OF GENOTYPE PROBABILITIES ON COMPLEX PEDIGREES

      Annals of Human Genetics
    14. LIN SL; THOMPSON E; WIJSMAN E
      FINDING NONCOMMUNICATING SETS FOR MARKOV-CHAIN MONTE-CARLO ESTIMATIONS ON PEDIGREES

      American journal of human genetics
    15. JARVIK GP; WIJSMAN E; LITTLE RE; ALBERS JJ; MOTULSKY AG; BRUNZELL JD
      HOST AND ENVIRONMENTAL-EFFECTS ON PLASMA APOLIPOPROTEIN-B

      International journal of clinical & laboratory research
    16. LIN SL; THOMPSON E; WIJSMAN E
      ACHIEVING IRREDUCIBILITY OF THE MARKOV-CHAIN MONTE-CARLO METHOD APPLIED TO PEDIGREE DATA

      IMA journal of mathematics applied in medicine and biology
    17. AUSTIN MA; STEPHENS K; WIJSMAN E; WALDEN C; LORETZ C
      EVIDENCE AGAINST LINKAGE OF SMALL, DENSE LOW-DENSITY LIPOPROTEINS (LDL) TO THE LDL RECEPTOR LOCUS ON CHROMOSOME-19

      Circulation
    18. COOK A; RASKIND W; BLANTON SH; PAULI RM; GREGG RG; FRANCOMANO CA; PUFFENBERGER E; CONRAD EU; SCHMALE G; SCHELLENBERG G; WIJSMAN E; HECHT JT; WELLS D; WAGNER MJ
      GENETIC-HETEROGENEITY IN FAMILIES WITH HEREDITARY MULTIPLE EXOSTOSES

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/01/21 alle ore 05:26:36