Search Results - "Gruenhage, F"

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    Gallstone disease in Swedish twins: risk is associated with ABCG8 D19H genotype by Katsika, D., Magnusson, P., Krawczyk, M., Grünhage, F., Lichtenstein, P., Einarsson, C., Lammert, F., Marschall, H.‐U.

    Published in Journal of internal medicine (01-09-2010)
    “…  Katsika D, Magnusson P, Krawczyk M, Grünhage F, Lichtenstein P, Einarsson C, Lammert F, Marschall H‐U (Karolinska University Hospital Huddinge, Karolinska…”
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    Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these loci by HAWI, Z, LOWER, N, KIRLEY, A, GRUENHAGE, F, NÖTHEN, M, GREENWOOD, T, KELSOE, J, FITZGERALD, M, GILL, M

    Published in Molecular psychiatry (01-03-2003)
    “…Abnormalities in dopaminergic neurotransmission are now accepted as factors in predisposing to ADHD. Evidence of associations between dopamine transporter gene…”
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    Graft‐versus‐host disease or toxic epidermal necrolysis: diagnostic dilemma after liver transplantation by Jeanmonod, P., Hubbuch, M., Grünhage, F., Meiser, A., Rass, K., Schilling, M.K., Kollmar, O.

    Published in Transplant infectious disease (01-08-2012)
    “…Graft‐versus‐host disease (GvHD) and toxic epidermal necrolysis (TEN) are rare and severe complications after liver transplantation. While mild acute GvHD is…”
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    The common adiponutrin variant p.I148M does not confer gallstone risk but affects fasting glucose and triglyceride levels by Krawczyk, M, Gruenhage, F, Mahler, M, Tirziu, S, Acalovschi, M, Lammert, F

    “…Recently the common adiponutrin (PNPLA3) polymorphism p.I148M has been identified as a genetic determinant of severe forms of non-alcoholic fatty liver disease…”
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    Heterozygosity for the alpha1‐antitrypsin Z allele may confer genetic risk of cholangiocarcinoma by Mihalache, F., Höblinger, A., Grünhage, F., Krawczyk, M., Gärtner, B. C., Acalovschi, M., Sauerbruch, T., Lammert, F., Zimmer, V.

    Published in Alimentary pharmacology & therapeutics (01-02-2011)
    “…Aliment Pharmacol Ther 2011; 33: 389–394 Summary Background  Alpha1‐antitrypsin (α1AT) deficiency caused by Z allele homozygosity represents a well‐established…”
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    Lymphoid pneumonitis as an immune reconstitution inflammatory syndrome in a patient with CD4 cell recovery after HAART initiation by Ingiliz, P, Appenrodt, B, Gruenhage, F, Vogel, M, Tschampa, H, Tasci, S, Rockstroh, JK

    Published in HIV medicine (01-09-2006)
    “…In the era of highly active antiretroviral therapy (HAART), immune reconstitution inflammatory syndrome (IRIS) has come to present a significant clinical…”
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    Toll-like receptor (TLR) 2 promoter and intron 2 polymorphisms are associated with increased risk for spontaneous bacterial peritonitis in liver cirrhosis by Nischalke, H.D, Berger, C, Aldenhoff, K, Thyssen, L, Gentemann, M, Grünhage, F, Lammert, F, Nattermann, J, Sauerbruch, T, Spengler, U, Appenrodt, B

    Published in Journal of hepatology (01-11-2011)
    “…Background & Aims Toll-like receptor (TLR) 2 and nucleotide-binding oligomerisation domain (NOD) 2 recognize distinct pathogen-associated molecular patterns…”
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    A genetic variant in the promoter of phosphate‐activated glutaminase is associated with hepatic encephalopathy by Mayer, L. B., Krawczyk, M., Grünhage, F., Lammert, F., Stokes, C. S.

    Published in Journal of internal medicine (01-09-2015)
    “…Background Hepatic encephalopathy (HE) is a serious complication of liver cirrhosis. Recently, a microsatellite in the promoter region of the…”
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    Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers by JÖNSSON, E. G, NÖTHEN, M. M, GRÜNHAGE, F, FARDE, L, NAKASHIMA, Y, PROPPING, P, SEDVALL, G. C

    Published in Molecular psychiatry (01-05-1999)
    “…The density of striatal dopamine D2 receptors has been shown to vary considerably among healthy subjects. This variability might be due to genetic or…”
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    Genome-wide association studies in hepatology by Weber, S, Grünhage, F, Hall, R, Lammert, F

    Published in Zeitschrift fur Gastroenterologie (01-01-2010)
    “…Genomewide association studies (GWAS) are being reported for an increasing number of common diseases, including first reports on GWAS for hepatobiliary…”
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    Progression of liver fibrosis in HIV/HCV genotype 1 co-infected patients is related to the T allele of the rs12979860 polymorphism of the IL28B gene by Lutz, P, Wasmuth, J-C, Nischalke, H-D, Vidovic, N, Grünhage, F, Lammert, F, Oldenburg, J, Rockstroh, J K, Sauerbruch, T, Spengler, Ulrich

    Published in European journal of medical research (08-08-2011)
    “…HIV/HCV co-infection is characterised by accelerated progression of liver disease. Recently, the rs12979860 C/T polymorphism in the IL28B gene has been linked…”
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    Transient elastography discloses identical distribution of liver fibrosis in chronic hepatitis C between HIV-negative and HIV-positive patients on HAART by Grünhage, F, Wasmuth, J-C, Herkenrath, S, Vidovic, N, Goldmann, G, Rockstroh, J, Lammert, F, Oldenburg, J, Sauerbruch, T, Spengler, Ulrich

    Published in European journal of medical research (08-04-2010)
    “…Progressive immunodeficiency associated with HIV-infection leads to a progressive course of liver disease in HIV/HCV-co-infected patients. Highly active…”
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