Rune Hjelen ENGLISH
S states of health. The composition of the associated microbiome will be assessed based on ribosomal dna and rna sequences, and attention will be given to richness (diversity), evenness (relative abundance), and variation with respect to time, person, and anatomic niche. Host response at the adjacent mucosal surface will be assessed based on genome-wide gene expression patterns. Condition intervention phase primary sclerosing cholangitis biliary atresia drug: vancomycin phase 1 study type: interventional study design: allocation: non-randomizedendpoint classification: efficacy studyintervention model: single group assignmentmasking: open labelprimary purpose: treatment official title: the human gastrointestinal tract microbiota in the setting of treating primary sclerosing cholangitis and biliary atresia with vancomycin. Resource links provided by nlm: genetics home reference related topics: primary sclerosing cholangitis drug information available for: vancomycin vancomycin hydrochloride u. S. can you buy viagra without prescriptions viagra for sale cheap viagra buy cheap viagra generic viagra online generic viagra online buy cheap viagra buy cheap viagra viagra online cheap generic viagra Fda resources further study details as provided by stanford university: primary outcome measures: determine the benefit of oral vancomycin therapy for primary sclerosing cholangitis and biliary atresia [ time frame: within 3 months of therapy ] [ designated as safety issue: no ]blood tests(liver enzymes - alt and ggt), imaging studies (mri, ercp) and/or liver biopsy changes before and while on oral vancomycin will assess the benefit of the therapy. Enrollment: 21 study start date: may 2007 estimated study completion date: october 2011 estimated primary completion date: october 2011 (final data collection date for primary outcome measure) arms assigned interventions experimental: oral vancomycin drug: vancomycin oral 50mg/kg per day up to maximum of 1500 mg a day for three months. Other name: vancocin   eligibility ages eligible for study:   1 month to 20 years genders eligible for study:   both accepts healthy volunteers:   no criteria inclusion criteria: clinical diagnosis of biliary atresia or primary sclerosing cholangitis. Clinical controls who are undergoing upper endoscopy or colonoscopy and do not have biliary atresia or primary sclerosing cholangitis. Subjects who have been on oral vancomycin for 1 year for biliary atresia or - exclusion criteria: patients that have taken antibiotics within the last 3 month will be excluded as this will alter the original bacterial flora.   contacts and locations please refer to.
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