111 research outputs found

    Utviklingen i energiforbruket i Norge i 2002-2003

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    Årene 2002 og 2003 vil forelĂžpig gĂ„ inn i historien som historiske Ă„r i norsk kraftforsyning. Dette skyldes ekstremt lite nedbĂžr og tilsig til kraftmagasinene gjennom hĂžsten 2002. I motsetning til hva mange synes Ă„ tro var ikke hele Ă„ret 2002 et nedbĂžrmessig svakt Ă„r. Det spesielle med dette Ă„ret var at det var svĂŠrt lave tilsig til de norske kraftmagasinene gjennom noen fĂ„ hĂžstuker. Resten av Ă„ret var det normalt eller vĂ„tere enn normalt. PĂ„ grunn av at ekstremperioden var sĂ„ kort, og at forventningene om framtidige priser dermed endret seg raskt, var det heller ikke enkelt for produsentene Ă„ tilpasse produksjonen sin slik at verdien av vannet kunne optimaliseres. PĂ„ sommeren og tidlig hĂžsten var magasinfyllingen langt over det normale for deretter Ă„ falle til langt under det normale i lĂžpet av fĂ„ uker. Dette bidro til at prisen i markedet steg kraftig. Produsentene fikk dermed signaler fra markedet om at det var svĂŠrt lĂžnnsomt Ă„ produsere. NedbĂžrsvikten vedvarte, produksjonen var hĂžy og forventinger om framtidig mangel pĂ„ vann medfĂžrte etter hvert en enda kraftigere stigning i elektrisitetsprisene. Dette skapte problemer for mange forbrukere. Prisen pĂ„ ulike kontraktstyper steg i ulik grad, det ble vanskeligere for forbrukerne Ă„ danne seg forventninger om hvilke kontrakter som var de beste pĂ„ lenger sikt. I ettertid synes markedet Ă„ ha hĂ„ndtert utfordringen det ble satt gjennom hĂžsten og vinteren 2002-2003 pĂ„ tilfredsstillende mĂ„te. NĂ„r tilsigssvikten kom rasjonerte markedet forbruket gjennom prisene, handelen mellom Norge og Sverige skiftet fra eksport pĂ„ hĂžsten 2002 til import vĂ„ren 2003, og det var en relativt god magasinbeholdningen ved utgangen av fyringssesongen vĂ„ren 2003. I denne rapporten gĂ„r vi gjennom utviklingen i kraftmarkedet i perioden 2002 – 2003. Vi beskriver hvorfor situasjonen ble som den ble, og hvordan markedet responderte sammenlignet med hva en kunne forvente Ă„ fĂ„ i et slikt marked

    Kidney failure in mice lacking the tetraspanin CD151

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    The tetraspanin CD151 is a cell-surface molecule known for its strong lateral interaction with the laminin-binding integrin α3ÎČ1. Patients with a nonsense mutation in CD151 display end-stage kidney failure associated with regional skin blistering and sensorineural deafness, and mice lacking the integrin α3 subunit die neonatally because of severe abnormalities in the lung and kidney epithelia. We report the generation of Cd151-null mice that recapitulate the renal pathology of human patients, i.e., with age they develop massive proteinuria caused by focal glomerulosclerosis, disorganization of the glomerular basement membrane, and tubular cystic dilation. However, neither skin integrity nor hearing ability are impaired in the Cd151-null mice. Furthermore, we generated podocyte-specific conditional knockout mice for the integrin α3 subunit that show renal defects similar to those in the Cd151 knockout mice. Our results support the hypothesis that CD151 plays a key role in strengthening α3ÎČ1-mediated adhesion in podocytes

    Metal detector by the principle phasemeter

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    Đ Đ°ŃŃĐŒĐŸŃ‚Ń€Đ”Đœ ĐœĐŸĐČыĐč ŃĐżĐŸŃĐŸĐ± ĐŸĐ±Ń€Đ°Đ±ĐŸŃ‚ĐșĐž ŃĐžĐłĐœĐ°Đ»Đ° ĐŒĐ”Ń‚Đ°Đ»Đ»ĐŸĐžŃĐșĐ°Ń‚Đ”Đ»Ń, ĐŸŃĐœĐŸĐČĐ°ĐœĐœŃ‹Đč ĐœĐ° ĐžĐ·ĐŒĐ”Ń€Đ”ĐœĐžŃŃ… Ń„Đ°Đ·Ń‹ Ń€Đ°Đ·ĐœĐŸŃŃ‚ĐœĐŸĐłĐŸ ŃĐžĐłĐœĐ°Đ»Đ°. ĐžĐżŃ€Đ”ĐŽĐ”Đ»Đ”ĐœŃ‹ ĐżŃ€Đ”ĐžĐŒŃƒŃ‰Đ”ŃŃ‚ĐČĐ° ĐœĐ°ĐŽ Ń€Đ°Đ·Ń€Đ°Đ±ĐŸŃ‚Đ°ĐœĐœŃ‹ĐŒĐž ĐŒĐ”Ń‚Đ°Đ»Đ»ĐŸĐžŃĐșĐ°Ń‚Đ”Đ»ŃĐŒĐž ĐžĐŒĐ”ŃŽŃ‰ĐžŃ… Ń„Đ°Đ·ĐŸĐŒĐ”Ń‚Ń€ĐžŃ‡Đ”ŃĐșую ŃŃ…Đ”ĐŒŃƒ. Đ˜Đ·ŃƒŃ‡Đ”ĐœĐ° Đ·Đ°ĐČĐžŃĐžĐŒĐŸŃŃ‚ŃŒ Ń„Đ°Đ·Ń‹ Ń€Đ°Đ·ĐœĐŸŃŃ‚ĐœĐŸĐłĐŸ ŃĐžĐłĐœĐ°Đ»Đ° ĐŸŃ‚ Đ°ĐŒĐżĐ»ĐžŃ‚ŃƒĐŽŃ‹ ĐČŃ…ĐŸĐŽĐœŃ‹Ń… ŃĐžĐłĐœĐ°Đ»ĐŸĐČ Đž Ń€Đ°Đ·ĐœĐŸŃŃ‚Đž ох Ń„Đ°Đ·. ĐŸŃ€ĐŸĐČĐ”ĐŽĐ”Đœ Đ°ĐœĐ°Đ»ĐžĐ· чуĐČстĐČĐžŃ‚Đ”Đ»ŃŒĐœĐŸŃŃ‚Đ”Đč Đș Ń€Đ°Đ·ĐœĐŸŃŃ‚Đž Đ°ĐŒĐżĐ»ĐžŃ‚ŃƒĐŽ ĐČŃ…ĐŸĐŽĐœŃ‹Ń… ŃĐžĐłĐœĐ°Đ»ĐŸĐČ Đž Ń€Đ°Đ·ĐœĐŸŃŃ‚Đž Ń„Đ°Đ·. ĐŁŃŃ‚Đ°ĐœĐŸĐČĐ»Đ”ĐœĐŸ, Ń‡Ń‚ĐŸ ĐŽĐ°ĐœĐœŃ‹Đč ĐŒĐ”Ń‚Đ°Đ»Đ»ĐŸĐžŃĐșĐ°Ń‚Đ”Đ»ŃŒ ĐŸĐ±Đ»Đ°ĐŽĐ°Đ”Ń‚ Đ±ĐŸĐ»ŃŒŃˆĐ”Đč чуĐČстĐČĐžŃ‚Đ”Đ»ŃŒĐœĐŸŃŃ‚Đž ĐżĐŸ сраĐČĐœĐ”ĐœĐžŃŽ с ОзĐČĐ”ŃŃ‚ĐœŃ‹ĐŒĐž Ń€Đ°Đ·Ń€Đ°Đ±ĐŸŃ‚ĐșĐ°ĐŒĐž Đž ŃĐżĐŸŃĐŸĐ±Đ”Đœ ЎДтДĐșŃ‚ĐžŃ€ĐŸĐČать ĐŒĐ”Ń‚Đ°Đ»Đ» про ĐŒĐ°Đ»Đ”ĐčŃˆĐ”ĐŒ ĐžĐ·ĐŒĐ”ĐœĐ”ĐœĐžĐž ĐČŃ‹Ń…ĐŸĐŽĐœĐŸĐłĐŸ ŃĐžĐłĐœĐ°Đ»Đ° пДрĐČĐžŃ‡ĐœĐŸĐłĐŸ ĐżŃ€Đ”ĐŸĐ±Ń€Đ°Đ·ĐŸĐČĐ°Ń‚Đ”Đ»Ń. Đ Đ°Đ·Ń€Đ°Đ±ĐŸŃ‚Đ°ĐœĐ° струĐșŃ‚ŃƒŃ€ĐœĐ°Ń ŃŃ…Đ”ĐŒĐ° ĐŽĐ»Ń ĐżŃ€Đ”ĐŽĐ»Đ°ĐłĐ°Đ”ĐŒĐŸĐłĐŸ ĐŒĐ”Ń‚Đ°Đ»Đ»ĐŸĐžŃĐșĐ°Ń‚Đ”Đ»Ń Đž проĐČĐ”ĐŽĐ”ĐœĐŸ ĐŸĐżĐžŃĐ°ĐœĐžĐ” ĐżŃ€ĐžĐœŃ†ĐžĐżĐ° Ń€Đ°Đ±ĐŸŃ‚Ń‹

    Apheresis therapies for NMOSD attacks A retrospective study of 207 therapeutic interventions

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    Objective To analyze whether 1 of the 2 apheresis techniques, therapeutic plasma exchange (PE) or immunoadsorption (IA), is superior in treating neuromyelitis optica spectrum disorder (NMOSD) attacks and to identify predictive factors for complete remission (CR). Methods This retrospective cohort study was based on the registry of the German Neuromyelitis Optica Study Group, a nationwide network established in 2008. It recruited patients with neuromyelitis optica diagnosed according to the 2006 Wingerchuk criteria or with aquaporin-4 (AQP4-ab)-antibody-seropositive NMOSD treated at 6 regional hospitals and 16 tertiary referral centers until March 2013. Besides descriptive data analysis of patient and attack characteristics, generalized estimation equation (GEE) analyses were applied to compare the effectiveness of the 2 apheresis techniques. A GEE model was generated to assess predictors of outcome. Results Two hundred and seven attacks in 105 patients (87% AQP4-ab-antibody seropositive) were treated with at least 1 apheresis therapy. Neither PE nor IA was proven superior in the therapy of NMOSD attacks. CR was only achieved with early apheresis therapy. Strong predictors for CR were the use of apheresis therapy as first-line therapy (OR 12.27, 95% CI: 1.04-144.91, p = 0.047), time from onset of attack to start of therapy in days (OR 0.94, 95% CI: 0.89-0.99, p = 0.014), the presence of AQP4-abantibodies (OR 33.34, 95% CI: 1.76-631.17, p = 0.019), and monofocal attack manifestation (OR 4.71, 95% CI: 1.03-21.62, p = 0.046). Conclusion: s Our findings suggest early use of an apheresis therapy in NMOSD attacks, particularly in AQP4-ab-seropositive patients. No superiority was shown for one of the 2 apheresis techniques

    Influence of female sex and fertile age on neuromyelitis optica spectrum disorders

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    Background: Gender and age at onset are important epidemiological factors influencing prevalence, clinical presentation, and treatment response in autoimmune diseases. Objective: To evaluate the impact of female sex and fertile age on aquaporin-4-antibody (AQP4-ab) status, attack localization, and response to attack treatment in patients with neuromyelitis optica (NMO) and its spectrum disorders (neuromyelitis optica spectrum disorder (NMOSD)). Methods: Female-to-male ratios, diagnosis at last visit (NMO vs NMOSD), attack localization, attack treatment, and outcome were compared according to sex and age at disease or attack onset. Results: A total of 186 NMO/SD patients (82% female) were included. In AQP4-ab-positive patients, female predominance was most pronounced during fertile age (female-to-male ratio 23:1). Female patients were more likely to be positive for AQP4-abs (92% vs 55%;p40years. Conclusion: Our data suggest an influence of sex and age on susceptibility to AQP4-ab-positive NMO/SD. Genetic and hormonal factors might contribute to pathophysiology of NMO/SD

    Contrasting disease patterns in seropositive and seronegative neuromyelitis optica: A multicentre study of 175 patients

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    BACKGROUND: The diagnostic and pathophysiological relevance of antibodies to aquaporin-4 (AQP4-Ab) in patients with neuromyelitis optica spectrum disorders (NMOSD) has been intensively studied. However, little is known so far about the clinical impact of AQP4-Ab seropositivity. OBJECTIVE: To analyse systematically the clinical and paraclinical features associated with NMO spectrum disorders in Caucasians in a stratified fashion according to the patients' AQP4-Ab serostatus. METHODS: Retrospective study of 175 Caucasian patients (AQP4-Ab positive in 78.3%). RESULTS: Seropositive patients were found to be predominantly female (p 1 myelitis attacks in the first year were identified as possible predictors of a worse outcome. CONCLUSION: This study provides an overview of the clinical and paraclinical features of NMOSD in Caucasians and demonstrates a number of distinct disease characteristics in seropositive and seronegative patients
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