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    <link>http://hdl.handle.net/2328/1696</link>
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    <pubDate>Wed, 19 Jun 2013 09:06:34 GMT</pubDate>
    <dc:date>2013-06-19T09:06:34Z</dc:date>
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      <title>Are alcohol gels better than liquid hand rubs?</title>
      <link>http://hdl.handle.net/2328/2934</link>
      <description>Title: Are alcohol gels better than liquid hand rubs?
Authors: Maiwald, Matthias; Widmer, Andreas F.
Description: Letter</description>
      <pubDate>Fri, 06 Jul 2007 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2328/2934</guid>
      <dc:date>2007-07-06T00:00:00Z</dc:date>
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    <item>
      <title>Diversity of Helicobacter pylori vacA and cagA genes and relationship to VacA and CagA protein expression, cytotoxin production, and associated diseases</title>
      <link>http://hdl.handle.net/2328/1703</link>
      <description>Title: Diversity of Helicobacter pylori vacA and cagA genes and relationship to VacA and CagA protein expression, cytotoxin production, and associated diseases
Authors: Rudi, J; Kolb, C; Maiwald, Matthias; Kuck, D; Sieg, A; Galle, PR; Stremmel, W
Abstract: The vacuolating cytotoxin and the cytotoxin-associated protein, encoded by vacA and cagA, respectively, are important virulence determinants of Helicobacter pylori. Sixty-five H. pylori strains were isolated from dyspeptic patients (19 with peptic ulcer disease, 43 with chronic gastritis, and 3 with gastric cancer) and studied for differences in the vacA and cagA genes and their relationship to VacA and CagA expression, cytotoxin activity, and the clinical outcome of infection. By PCR, fifty-four (83.1%) of 65 strains had the vacA signal sequence genotype s1 and only 10 (15.4%) had the type s2. After primer modification, the vacA middle-region types m1 and m2 were detected in 24 (36.9%) and 41 (63.1%) strains, respectively. The combinations s1-m2 (31 [47.7%]) and s1-m1 (23 [35.4%]) occurred more frequently than s2-m2 (10 [15.4%]) (P = 0.01). No strain with the combination s2-m1 was found. All 19 patients with peptic ulcers harbored type s1 strains, in contrast to 32 (74.4%) of 43 patients with gastritis (P = 0.02). The vacA genotype s1 was associated with the presence of cagA (P &lt; 0.0001), VacA expression (P &lt; 0.0001), and cytotoxin activity (P = 0.003). The cagA gene was detectable in 48 (73.8%) of 65 isolates and present in 16 (84.2%) of 19 ulcer patients and 29 (67.4%) of 43 patients with gastritis (P = 0.17). The vacA genotypes of German H. pylori isolates are identical to those previously reported. H. pylori strains of vacA type s1 are associated with the occurrence of peptic ulceration and the presence of cagA, cytotoxin activity, and VacA expression.</description>
      <pubDate>Tue, 01 Jun 1999 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2328/1703</guid>
      <dc:date>1999-06-01T00:00:00Z</dc:date>
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    <item>
      <title>Comparison of urinary bladder and ear biopsy samples for determining prevalence of Borrelia burgdorferi in rodents in central Europe</title>
      <link>http://hdl.handle.net/2328/1702</link>
      <description>Title: Comparison of urinary bladder and ear biopsy samples for determining prevalence of Borrelia burgdorferi in rodents in central Europe
Authors: Petney, T N; Hassler, D; Bruckner, M; Maiwald, Matthias
Abstract: PCR was used to compare urinary bladder and ear biopsy samples from four European species of wild rodents for the presence of Borrelia burgdorferi sensu lato. From 60 paired comparisons of bladder and ear biopsy samples, the PCR results were concordantly positive or negative in 43 samples (71.7%). Of the 17 which differed, 14 bladder samples were positive and ear samples were negative while the converse occurred for three samples. Thus ear biopsy samples led to a significantly lower estimate of infection than bladder biopsy samples. This suggests that the use of ear biopsy samples in epidemiological studies of B. burgdorferi in Central European rodents is likely to lead to underestimates of the prevalence.</description>
      <pubDate>Wed, 01 May 1996 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2328/1702</guid>
      <dc:date>1996-05-01T00:00:00Z</dc:date>
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    <item>
      <title>Cultivation of Tropheryma whipplei from cerebrospinal fluid</title>
      <link>http://hdl.handle.net/2328/1701</link>
      <description>Title: Cultivation of Tropheryma whipplei from cerebrospinal fluid
Authors: Maiwald, Matthias; von Herbay, Axel; Fredricks, David N; Ouverney, Cleber C; Kosek, Jon C; Relman, David A
Abstract: Whipple disease (WD) is a systemic disorder caused by the bacterium Tropheryma whipplei. Since the recognition of a bacterial etiology in 1961, many attempts have been made to cultivate this bacterium in vitro. It was eventually isolated, in 2000, from an infected heart valve, in coculture with human fibroblasts. Here we report the isolation of 2 new strains of T. whipplei from cerebrospinal fluid (CSF) of 2 patients with intestinal WD but no neurological signs or symptoms. One culture-positive specimen was obtained before treatment; the other was obtained 12 months after discontinuation of therapy, at a time of intestinal remission. In both cases, 15 passages of the cultures were completed over 17 months. Bacterial growth was measured by quantitative polymerase chain reaction, which suggested a generation time of 4 days. Staining with YO-PRO nucleic-acid dye showed characteristic rod-shaped bacteria arranged in chains. Fluorescent in situ hybridization with a T. whipplei-specific oligonucleotide probe, a broad-range bacterial probe, and a nonspecific nucleic-acid stain indicated that all visible bacteria were T. whipplei. Scanning electron microscopy and transmission electron microscopy showed both intracellular and extracellular bacteria. This first isolation of T. whipplei from CSF provides clear evidence of viable bacteria in the central nervous system in individuals with WD, even after prolonged antibiotic therapy.</description>
      <pubDate>Mon, 01 Sep 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2328/1701</guid>
      <dc:date>2003-09-01T00:00:00Z</dc:date>
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