Search Results - "Horder, M M"

Current perspectives in the interpretation of gunshot residues in forensic science: A review by Maitre, M, Kirkbride, K.P, Horder, M, Roux, C, Beavis, A

“…Highlights • The challenges associated with GSR are moving from analysis to interpretation • Bayesian reasoning could allow for evaluation of evidence in…”
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Randomised controlled trial of structured personal care of type 2 diabetes mellitus by Olivarius, Niels de Fine, Beck-Nielsen, Henning, Andreasen, Anne Helms, Hørder, Mogens, Pedersen, Poul A

“…Abstract Objective: To assess the effect of a multifaceted intervention directed at general practitioners on six year mortality, morbidity, and risk factors of…”
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Thinking beyond the lab: organic gunshot residues in an investigative perspective by Maitre, M., Kirkbride, K. P., Horder, M., Roux, C., Beavis, A.

“…Gunshot residues (GSR) are a common form of evidence in cases involving questions related to the association of a person of interest (POI) to a firearm-related…”
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Independent prognostic value of serum creatine kinase isoenzyme MB mass, cardiac troponin T and myosin light chain levels in suspected acute myocardial infarction : analysis of 28 months of follow-up in 196 patients by RAVKILDE, J, NISSEN, H, HØRDER, M, THYGESEN, K

“…We sought to determine the incidence and independent prognostic value of increased serum levels of sensitive serologic markers in patients in whom a…”
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Mutations in endoglin and in activin receptor-like kinase 1 among Danish patients with hereditary haemorrhagic telangiectasia by Brusgaard, K, Kjeldsen, AD, Poulsen, L, Moss, H, Vase, P, Rasmussen, K, Kruse, TA, Hørder, M

“…Hereditary haemorrhagic telangiectasia (HHT) is a rare disorder with one per 6000–10,000 affected individuals in the general Caucasian population. HHT is…”
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Molecular genetic analysis of 1053 Danish individuals with clinical signs of familial hypercholesterolemia by Brusgaard, K, Jordan, P, Hansen, H, Hansen, AB, Hørder, M

“…The lipid disorder familial hypercholesterolemia (FH) predisposes to cardiovascular disease. With a prevalence of approximately one in 500 in the general…”
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Association between CYP1A2 polymorphism and susceptibility to porphyria cutanea tarda by CHRISTIANSEN, L, BYGUM, A, JENSEN, A, THOMSEN, K, BRANDRUP, F, HØRDER, M, PETERSEN, N. E

“…Individuals with the most common form of the porphyrias, porphyria cutanea tarda (PCT), are believed to be genetically predisposed to development of clinically…”
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Ultrasound-induced temperature increase in guinea-pig fetal brain in utero: third-trimester gestation by Horder, M M, Barnett, S B, Vella, G J, Edwards, M J, Wood, A K

“…Temperature increase was measured at various depths in the brain of living fetal guinea pigs during in utero exposure to unscanned pulsed ultrasound at ISPTA…”
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In vivo heating of the guinea-pig fetal brain by pulsed ultrasound and estimates of thermal index by Horder, M M, Barnett, S B, Vella, G J, Edwards, M J, Wood, A K

“…Temperature was measured in the brain in live near-term fetal guinea pigs (62-66 d gestational age), during in utero exposure to a fixed beam of pulsed…”
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An improved PCR-based method for site directed mutagenesis using megaprimers by Brøns-Poulsen, J, Petersen, N.E, Hørder, M, Kristiansen, K

“…An improved protocol for site-directed mutagenesis based on the two-step polymerase chain reaction (PCR) megaprimer method is described. Compared to previously…”
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Vitamin D Receptor Alleles Do Not Predict Bone Mineral Density or Bone Loss in Danish Perimenopausal Women by Hansen, T.S, Abrahamsen, B, Henriksen, F.L, Hermann, A.P, Jensen, L.B, Hørder, M, Gram, J

“…A BsmI restriction enzyme polymorphism in the vitamin D receptor (VDR) gene has been reported to be associated with bone mineral density (BMD) and bone…”
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Characterization of two isoalleles and three mutations in both isoforms of purified recombinant human porphobilinogen deaminase by Brøns-Poulsen, J., Christiansen, L., Petersen, N. E., Hørder, M., Kristiansen, K.

“…Defects in the enzyme porphobilinogen deaminase (PBG-D) are associated with acute intermittent porphyria (AIP). Human PBG-D is transcribed into a housekeeping…”
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Expression and characterization of six clinically relevant uroporphyrinogen decarboxylase gene mutations by Christiansen, L., Brøns-Poulsen, J., Hørder, M., Brock, A., Petersen, N. E.

“…The functional consequence of six uroporphyrinogen decarboxylase (UROD) gene mutations found in Danish patients with familial porphyria cutanea tarda was…”
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Phenotypes and genotypes for CYP2D6 and CYP2C19 in a black Tanzanian population by Bathum, Lise, Skjelbo, Erik, Mutabingwa, Theonest K., Madsen, Hanne, Hørder, Mogens, Brøsen, Kim

“…Aims CYP2D6 and CYP2C19 are polymorphically expressed enzymes that show marked interindividual and interethnic variation. The aim of this study was to…”
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Reference intervals for trace elements in blood: significance of risk factors by Grandjean, P, Nielsen, G D, Jørgensen, P J, Hørder, M

“…A random sample of 100 men and 100 women was examined for whole-blood concentrations of mercury, lead, cadmium and selenium, and the serum concentrations of…”
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Effect of Long-Term Monitoring of Glycosylated Hemoglobin Levels in Insulin-Dependent Diabetes Mellitus by Larsen, Mogens Lytken, Hørder, Mogens, Mogensen, Erik F

“…THE relation between glycosylated hemoglobin (hemoglobin A 1c ) and blood glucose concentrations in diabetes mellitus became clear over a decade ago, 1 , 2 but…”
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Diagnostic performance and prognostic value of serum troponin T in suspected acute myocardial infarction by Ravkilde, J, Hørder, M, Gerhardt, W, Ljungdahl, L, Pettersson, T, Tryding, N, Møller, B H, Hamfelt, A, Graven, T, Asberg, A

“…Cardiac troponin T (TnT) is a new serological marker for use as a diagnostic tool for myocardial damage. A blinded prospective multicentre study representing…”
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Self-respect through ability to keep fear of frailty at a distance: Successful ageing from the perspective of community-dwelling older people by Hörder, HelenaM, Frändin, Kerstin, Larsson, MariaE. H.

“…With population ageing, there is an increased interest in how to promote a good old age. A predominant concept in these discussions is successful ageing, which…”
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Screening for mutations in the uroporphyrinogen decarboxylase gene using denaturing gradient gel electrophoresis. Identification and characterization of six novel mutations associated with familial PCT by Christiansen, L., Ged, C., Hombrados, I., Brøns-Poulsen, J., Fontanellas, A., de Verneuil, H., Hørder, M., Petersen, N.E.

“…The two porphyrias, familial porphyria cutanea tarda (fPCT) and hepatoerythropoietic porphyria (HEP), are associated with mutations in the gene encoding the…”
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Mutation screening of the entire coding region of the protoporphyrinogen oxidase gene using denaturing gradient gel electrophoresis and denaturing HPLC by CHRISTIANSEN, Lene, BYGUM, Anette, KÄEHNE, Marianne, JENSEN, Alice, HORDER, Mogens, ERICK PETERSEN, Niels

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