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La ricerca find articoli where authors phrase all words ' Jensen, HK' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 48 riferimenti
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    1. Kim, WY; Sogaard, P; Mortensen, PT; Jensen, HK; Pedersen, AK; Kristensen, BO; Egeblad, H
      Three dimensional echocardiography documents haemodynamic improvement by biventricular pacing in patients with severe heart failure

      HEART
    2. Aune, AK; Holm, I; Risberg, MA; Jensen, HK; Steen, H
      Four-strand hamstring tendon autograft compared with patellar tendon-bone autograft for anterior cruciate ligament reconstruction - A randomized study with two-year follow-up

      AMERICAN JOURNAL OF SPORTS MEDICINE
    3. Ziegler, BK; Kristensen, SD; Vissinger, H; Jensen, HK; Nielsen, HK; Husted, SE
      Incomplete thromboxane inhibition with 100 mg of intravenous acetylsalicylic acid in patients with acute ST elevation myocardial infarction - A placebo-controlled pilot trial

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

      CLINICAL GENETICS
    5. Sogaard, P; Kim, WY; Jensen, HK; Mortensen, P; Pedersen, AK; Kristensen, BO; Egeblad, H
      Impact of acute biventricular pacing on left ventricular performance and volumes in patients with severe heart failure - A tissue Doppler and three-dimensional echocardiographic study

      CARDIOLOGY
    6. Jensen, JM; Gerdes, LU; Jensen, HK; Christiansen, TM; Brorholt-Petersen, JU; Faergeman, O
      Association of coronary heart disease with age-adjusted aortocoronary calcification in patients with familial hypercholesterolaemia

      JOURNAL OF INTERNAL MEDICINE
    7. Raungaard, B; Brorholt-Petersen, JU; Jensen, HK; Faergeman, O
      Flow cytometric assessment of effects of fluvastatin on low-density lipoprotein receptor activity in stimulated T-lymphocytes from patients with heterozygous familial hypercholesterolemia

      JOURNAL OF CLINICAL PHARMACOLOGY
    8. Raungaard, B; Jensen, HK; Brorholt-Petersen, JU; Heath, F; Faergeman, O
      Functional characterization of two low density lipoprotein receptor gene mutations by fluorescence flow cytometric assessment of receptor activity instimulated human T-lymphocytes

      CLINICAL GENETICS
    9. Raungaard, B; Heath, F; Hansen, PS; Brorholt-Petersen, JU; Jensen, HK; Faergeman, O
      Flow cytometric assessment of LDL ligand function for detection of heterozygous familial defective apolipoprotein B-100

      CLINICAL CHEMISTRY
    10. Frikke-Schmidt, R; Arlien-Soborg, P; Thorsen, S; Jensen, HK; Vorstrup, S
      LDL receptor mutations and ApoB mutations are not risk factors for ischemic cerebrovascular disease of the young, but lipids and lipoproteins are

      EUROPEAN JOURNAL OF NEUROLOGY
    11. Peeters, AV; Thiart, R; de Villiers, JNP; Jensen, HK; Van Gaal, LF; Kotze, MJ
      Intronic mutations at splice junctions in the low-density lipoprotein receptor gene

      MOLECULAR AND CELLULAR PROBES
    12. Raungaard, B; Heath, F; Brorholt-Petersen, JU; Jensen, HK; Faergeman, O
      Flow cytometric assessment of LDL receptor activity peripheral blood mononuclear cells compared to gene mutation detection in diagnosis of heterozygous familial hypercholesterolemia

      CYTOMETRY
    13. Jensen, HK; Jensen, LG; Meinertz, H; Hansen, PS; Gregersen, N; Faergeman, O
      Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemia

      ATHEROSCLEROSIS
    14. Cenarro, A; Casao, E; Civeira, F; Jensen, HK; Faergeman, O; Pocovi, M
      Pl(A1/A2) polymorphism of platelet glycoprotein IIIa and risk of acute coronary syndromes in heterozygous familial hypercholesterolemia

      ATHEROSCLEROSIS
    15. Jensen, HK; Jensen, LG; Holst, HU; Andreasen, PH; Hansen, PS; Larsen, ML; Kolvraa, S; Bolund, L; Gregersen, N; Faergeman, O
      Normolipidemia and hypercholesterolemia in persons heterozygous for the same 1592+5G -> A splice site mutation in the low-density lipoprotein receptor gene

      CLINICAL GENETICS
    16. Jensen, JM; Kruse, TA; Brorholt-Petersen, JU; Christiansen, TM; Jensen, HK; Kolvraa, S; Faergeman, O
      Linking genotype to aorto-coronary atherosclerosis: a model using familialhypercholesterolemia and aorto-coronary calcification

      ANNALS OF HUMAN GENETICS
    17. RAUNGAARD B; HEATH F; BRORHOLTPETERSEN JU; JENSEN HK; FAERGEMAN O
      FLOW-CYTOMETRY WITH A MONOCLONAL-ANTIBODY TO THE LOW-DENSITY-LIPOPROTEIN RECEPTOR COMPARED WITH GENE MUTATION DETECTION IN DIAGNOSIS OF HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

      Clinical chemistry
    18. LANGDAHL BL; KNUDSEN JY; JENSEN HK; GREGERSEN N; ERIKSEN EF
      A SEQUENCE VARIATION - 713-8DELC IN THE TRANSFORMING GROWTH-FACTOR-BETA-1 GENE HAS HIGHER PREVALENCE IN OSTEOPOROTIC WOMEN THAN IN NORMAL WOMEN AND IS ASSOCIATED WITH VERY-LOW BONE MASS IN OSTEOPOROTIC WOMEN AND INCREASED BONE TURNOVER IN BOTH OSTEOPOROTIC AND NORMAL WOMEN

      Bone
    19. HANSEN PS; DEFESCHE JC; KASTELEIN JJP; GERDES LU; FRAZA L; GERDES C; TATO F; JENSEN HK; JENSEN LG; KLAUSEN IC; FAERGEMAN O; SCHUSTER H
      PHENOTYPIC VARIATION IN PATIENTS HETEROZYGOUS FOR FAMILIAL DEFECTIVE APOLIPOPROTEIN-B (FDB) IN 3 EUROPEAN COUNTRIES

      Arteriosclerosis, thrombosis, and vascular biology
    20. JENSEN HK; JENSEN TG; FAERGEMAN O; JENSEN LG; ANDRESEN BS; CORYDON MJ; ANDREASEN PH; HANSEN PS; HEATH F; BOLUND L; GREGERSEN N
      2 MUTATIONS IN THE SAME LOW-DENSITY-LIPOPROTEIN RECEPTOR ALLELE ACT IN SYNERGY TO REDUCE RECEPTOR FUNCTION IN HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

      Human mutation
    21. JENSEN HK; MIKKELSEN N; NEUHARD J
      RECOMBINANT URACIL PHOSPHORIBOSYLTRANSFERASE FROM THE THERMOPHILE BACILLUS-CALDOLYTICUS - EXPRESSION, PURIFICATION, AND PARTIAL CHARACTERIZATION

      Protein expression and purification
    22. RAUNGAARD B; HEATH F; BRORHOLTPETERSEN JU; JENSEN HK; FAERGEMAN O
      FUNCTIONAL-CHARACTERIZATION OF LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE-MUTATIONS IN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA

      Atherosclerosis
    23. JENSEN HK; HOLST H; JENSEN LG; JORGENSEN MM; ANDREASEN PH; JENSEN TG; ANDRESEN BS; HEATH F; HANSEN PS; NEVE S; KRISTIANSEN K; FAERGEMAN O; KOLVRAA S; BOLUND L; GREGERSEN N
      A COMMON W556S MUTATION IN THE LDL RECEPTOR GENE OF DANISH PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA ENCODES A TRANSPORT-DEFECTIVE PROTEIN

      Atherosclerosis
    24. ANDERSEN LK; JENSEN HK; FAERGEMAN O
      CHANGES IN ATTITUDE TO DETECTION AND TREATMENT OF FAMILIAL HYPERCHOLESTEROLEMIA AFTER DNA-DIAGNOSIS

      Atherosclerosis
    25. ANDERSEN LK; JENSEN HK; JUUL S; FAERGEMAN O
      PATIENTS ATTITUDES TOWARD DETECTION OF HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

      Archives of internal medicine
    26. JENSEN LG; JENSEN HK; HEATH F; EIBERG H; KJELDSEN M; FAERGEMAN O; KOLVRAA S; BOLUND L; GREGERSEN N
      ALLELE-SPECIFIC MEASUREMENT OF LOW-DENSITY-LIPOPROTEIN RECEPTOR TRANSCRIPT LEVELS

      Human mutation
    27. JENSEN HK; JENSEN LG; HANSEN PS; FAERGEMAN O; GREGERSEN N
      2 POINT MUTATIONS (313-]A AND 313+1G-]T) IN THE SPLICE DONOR SITE OF INTRON-3 OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE ARE ASSOCIATED WITH FAMILIAL HYPERCHOLESTEROLEMIA(1G)

      Human mutation
    28. JENSEN LG; JENSEN HK; NISSEN H; KRISTIANSEN K; FAERGEMAN O; BOLUND L; GREGERSEN N
      AN LDL RECEPTOR PROMOTER MUTATION IN A HETEROZYGOUS FH PATIENT WITH DRAMATICALLY SKEWED RATIO BETWEEN THE 2 ALLELIC MESSENGER-RNA VARIANTS

      Human mutation
    29. CENARRO A; JENSEN HK; CASAO E; CIVEIRA F; GONZALEZBONILLO J; POCOVI M; GREGERSEN N
      IDENTIFICATION OF A NOVEL MUTATION IN EXON-13 OF THE LDL RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA IN 2 SPANISH FAMILIES

      Biochimica et biophysica acta. Molecular basis of disease
    30. JENSEN HK; JENSEN LG; HANSEN PS; FAERGEMAN O; GREGERSEN N
      THE TRP(23)-STOP AND TRP(66)-GLY MUTATIONS IN THE LDL RECEPTOR GENE -COMMON CAUSES OF FAMILIAL HYPERCHOLESTEROLEMIA IN DENMARK

      Atherosclerosis
    31. JENSEN HK; JENSEN LG; HEATH F; MELSEN F; HANSEN PS; MEINERTZ H; BOLUND L; GREGERSEN N; FAERGEMAN O
      PHENOTYPIC CHARACTERIZATION OF A PATIENT HOMOZYGOUS FOR THE D558N LDLRECEPTOR GENE MUTATION

      Clinical genetics
    32. JENSEN HK; JENSEN LG; HANSEN PS; BOLUND L; FAERGEMAN O; GREGERSEN N
      A G(-1)-TO-A ACCEPTOR SPLICE-SITE LDLR MUTANT ALLELE LEADS TO REDUCEDRELATIVE TRANSCRIPT LEVELS IN PATIENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

      Clinical genetics
    33. CENARRO A; JENSEN HK; CIVEIRA F; CASAO E; FERRANDO J; GONZALEZBONILLO J; POCOVI M; GREGERSEN N
      2 NOVEL MUTATIONS IN THE LDL RECEPTOR GENE - COMMON CAUSES OF FAMILIAL HYPERCHOLESTEROLEMIA IN A SPANISH POPULATION

      Clinical genetics
    34. JENSEN HK; JENSEN LG; HANSEN PS; FAERGEMAN O; GREGERSEN N
      AN IRANIAN ARMENIAN LDLR FRAMESHIFT MUTATION CAUSING FAMILIAL HYPERCHOLESTEROLEMIA

      Clinical genetics
    35. JENSEN HK; JENSEN LG; HANSEN PS; FAERGEMAN O; GREGERSEN N
      HIGH-SENSITIVITY OF THE SINGLE-STRAND CONFORMATION POLYMORPHISM METHOD FOR DETECTING SEQUENCE VARIATIONS IN THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE VALIDATED BY DNA-SEQUENCING

      Clinical chemistry
    36. LANGDAHL BL; BRIXEN K; JENSEN HK; GREGERSEN N; ERIKSEN EF
      MUTATIONS IN THE TGF-BETA-1 GENE ARE CORRELATED TO LOW BONE MASS AND INCREASED BONE TURNOVER

      Journal of bone and mineral research
    37. NISSEN H; HANSEN ABB; JENSEN HK
      A FREQUENT HHAL POLYMORPHISM IN INTRON-9 OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE DETECTED BY THE DENATURING GRADIENT GEL-ELECTROPHORESIS TECHNIQUE

      Clinical genetics
    38. JENSEN HK; HANSEN PS; JENSEN LG; KRISTENSEN MJ; KLAUSEN IC; KJELDSEN M; LEMMING L; BOLUND L; GREGERSEN N; FAERGEMAN O
      COMPLEXITY OF MOLECULAR-GENETICS OF DYSLIPIDEMIA IN A FAMILY HIGHLY SUSCEPTIBLE TO ISCHEMIC-HEART-DISEASE

      Clinical genetics
    39. JENSEN HK; JENSEN TG; JENSEN LG; HANSEN PS; KJELDSEN M; ANDRESEN BS; NIELSEN V; MEINERTZ H; HANSEN AB; BOLUND L; FAERGEMAN O; GREGERSEN N
      CHARACTERIZATION OF A DISEASE-CAUSING GLU119-LYS MUTATION IN THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE IN 2 DANISH FAMILIES WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

      Human mutation
    40. HANSEN PS; MEINERTZ H; JENSEN HK; FRUERGAARD P; LAUNBJERG J; KLAUSEN IC; LEMMING L; GERDES U; GREGERSEN N; FAERGEMAN O
      CHARACTERISTICS OF 46 HETEROZYGOUS CARRIERS AND 57 UNAFFECTED RELATIVES IN 5 DANISH FAMILIES WITH FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100

      Arteriosclerosis and thrombosis
    41. HANSEN PS; JENSEN HK; MEINERTZ H; HANSEN ABB; KLAUSEN IC; GERDES LU; HORDER M; GREGERSEN N; FAERGEMAN O
      APOLIPOPROTEIN-B AND APOLIPOPROTEIN-E GENE POLYMORPHISMS AND ASSOCIATION WITH PLASMA-LIPIDS AND ATHEROSCLEROTIC-DISEASE IN FAMILIAL HYPERCHOLESTEROLEMIA

      NMCD. Nutrition Metabolism and Cardiovascular Diseases
    42. KRISTENSEN T; JENSEN HK; MUNCHPETERSEN B
      OVEREXPRESSION OF HUMAN THYMIDINE KINASE MESSENGER-RNA WITHOUT CORRESPONDING ENZYMATIC-ACTIVITY IN PATIENTS WITH CHRONIC LYMPHATIC-LEUKEMIA

      Leukemia research
    43. JENSEN HK; JENSEN LG; HANSEN PS; PETERSEN LS; GERDES LU; BOLUND L; FAERGEMAN O; GREGERSEN N
      AN ALANINE(29)-SERINE VARIANT IN EXON-2 OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE - NO ASSOCIATION WITH HYPERCHOLESTEROLEMIA

      Clinical genetics
    44. JENSEN LG; JENSEN HK; KJELDSEN M; GERDES LU; HANSEN PS; FAERGEMAN O; KOLVRAA S; BOLUND L; GREGERSEN N
      A NEW, HIGHLY INFORMATIVE SMAI POLYMORPHISM IN INTRON-7 OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR (LDLR) GENE

      Clinical genetics
    45. JENSEN HK; JENSEN LG; HANSEN PS; KJELDSEN M; GERDES LU; BOLUND L; FAERGEMAN O; GREGERSEN N
      A RARE SILENT C-MUTATION TO T-MUTATION IN EXON-7 OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR (LDLR) GENE

      Clinical genetics
    46. HANSEN PS; NORGAARDPETERSEN B; MEINERTZ H; JENSEN HK; HANSEN ABB; KLAUSEN IC; GERDES LU; FAERGEMAN O
      INCIDENCE OF THE APOLIPOPROTEIN B-3500 MUTATION IN DENMARK

      Clinica chimica acta
    47. HANSEN PS; NORGAARDPETERSEN B; MEINERTZ H; JENSEN HK; HANSEN ABB; KLAUSEN IC; GERDES LU; FAERGEMAN O
      INCIDENCE OF THE APOLIPOPROTEIN B-3500 MUTATION IN DENMARK

      Clinica chimica acta
    48. BOTKER HE; JENSEN HK; KRUSELL LR; SORENSEN EV
      RENAL EFFECTS OF XAMOTEROL IN PATIENTS WITH MODERATE HEART-FAILURE

      Cardiovascular drugs and therapy


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/02/20 alle ore 00:05:51