111 research outputs found
Utviklingen i energiforbruket i Norge i 2002-2003
Ă
rene 2002 og 2003 vil forelÞpig gÄ inn i historien som historiske Är i norsk kraftforsyning. Dette skyldes ekstremt lite nedbÞr og tilsig til kraftmagasinene gjennom hÞsten 2002. I motsetning til hva mange synes Ä tro var ikke hele Äret 2002 et nedbÞrmessig svakt Är. Det spesielle med dette Äret var at det var svÊrt lave tilsig til de norske kraftmagasinene gjennom noen fÄ hÞstuker. Resten av Äret var det normalt eller vÄtere enn normalt. PÄ grunn av at ekstremperioden var sÄ kort, og at forventningene om framtidige priser dermed endret seg raskt, var det heller ikke enkelt for produsentene Ä tilpasse produksjonen sin slik at verdien av vannet kunne optimaliseres. PÄ sommeren og tidlig hÞsten var magasinfyllingen langt over det normale for deretter Ä falle til langt under det normale i lÞpet av fÄ uker. Dette bidro til at prisen i markedet steg kraftig. Produsentene fikk dermed signaler fra markedet om at det var svÊrt lÞnnsomt Ä produsere. NedbÞrsvikten vedvarte, produksjonen var hÞy og forventinger om framtidig mangel pÄ vann medfÞrte etter hvert en enda kraftigere stigning i elektrisitetsprisene. Dette skapte problemer for mange forbrukere. Prisen pÄ ulike kontraktstyper steg i ulik grad, det ble vanskeligere for forbrukerne Ä danne seg forventninger om hvilke kontrakter som var de beste pÄ lenger sikt. I ettertid synes markedet Ä ha hÄndtert utfordringen det ble satt gjennom hÞsten og vinteren 2002-2003 pÄ tilfredsstillende mÄte. NÄr tilsigssvikten kom rasjonerte markedet forbruket gjennom prisene, handelen mellom Norge og Sverige skiftet fra eksport pÄ hÞsten 2002 til import vÄren 2003, og det var en relativt god magasinbeholdningen ved utgangen av fyringssesongen vÄren 2003.
I denne rapporten gĂ„r vi gjennom utviklingen i kraftmarkedet i perioden 2002 â 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
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
Đ Đ°ŃŃĐŒĐŸŃŃĐ”Đœ ĐœĐŸĐČŃĐč ŃĐżĐŸŃĐŸĐ± ĐŸĐ±ŃĐ°Đ±ĐŸŃĐșĐž ŃĐžĐłĐœĐ°Đ»Đ° ĐŒĐ”ŃĐ°Đ»Đ»ĐŸĐžŃĐșĐ°ŃДлŃ, ĐŸŃĐœĐŸĐČĐ°ĐœĐœŃĐč ĐœĐ° ĐžĐ·ĐŒĐ”ŃĐ”ĐœĐžŃŃ
ŃĐ°Đ·Ń ŃĐ°Đ·ĐœĐŸŃŃĐœĐŸĐłĐŸ ŃĐžĐłĐœĐ°Đ»Đ°. ĐĐżŃĐ”ĐŽĐ”Đ»Đ”ĐœŃ ĐżŃĐ”ĐžĐŒŃŃĐ”ŃŃĐČĐ° ĐœĐ°ĐŽ ŃĐ°Đ·ŃĐ°Đ±ĐŸŃĐ°ĐœĐœŃĐŒĐž ĐŒĐ”ŃĐ°Đ»Đ»ĐŸĐžŃĐșĐ°ŃДлŃĐŒĐž ĐžĐŒĐ”ŃŃĐžŃ
ŃĐ°Đ·ĐŸĐŒĐ”ŃŃĐžŃĐ”ŃĐșŃŃ ŃŃ
Đ”ĐŒŃ. ĐĐ·ŃŃĐ”ĐœĐ° Đ·Đ°ĐČĐžŃĐžĐŒĐŸŃŃŃ ŃĐ°Đ·Ń ŃĐ°Đ·ĐœĐŸŃŃĐœĐŸĐłĐŸ ŃĐžĐłĐœĐ°Đ»Đ° ĐŸŃ Đ°ĐŒĐżĐ»ĐžŃŃĐŽŃ ĐČŃ
ĐŸĐŽĐœŃŃ
ŃĐžĐłĐœĐ°Đ»ĐŸĐČ Đž ŃĐ°Đ·ĐœĐŸŃŃĐž ĐžŃ
ŃĐ°Đ·. ĐŃĐŸĐČĐ”ĐŽĐ”Đœ Đ°ĐœĐ°Đ»ĐžĐ· ŃŃĐČŃŃĐČĐžŃДлŃĐœĐŸŃŃĐ”Đč Đș ŃĐ°Đ·ĐœĐŸŃŃĐž Đ°ĐŒĐżĐ»ĐžŃŃĐŽ ĐČŃ
ĐŸĐŽĐœŃŃ
ŃĐžĐłĐœĐ°Đ»ĐŸĐČ Đž ŃĐ°Đ·ĐœĐŸŃŃĐž ŃĐ°Đ·. ĐŁŃŃĐ°ĐœĐŸĐČĐ»Đ”ĐœĐŸ, ŃŃĐŸ ĐŽĐ°ĐœĐœŃĐč ĐŒĐ”ŃĐ°Đ»Đ»ĐŸĐžŃĐșĐ°ŃĐ”Đ»Ń ĐŸĐ±Đ»Đ°ĐŽĐ°Đ”Ń Đ±ĐŸĐ»ŃŃĐ”Đč ŃŃĐČŃŃĐČĐžŃДлŃĐœĐŸŃŃĐž ĐżĐŸ ŃŃĐ°ĐČĐœĐ”ĐœĐžŃ Ń ĐžĐ·ĐČĐ”ŃŃĐœŃĐŒĐž ŃĐ°Đ·ŃĐ°Đ±ĐŸŃĐșĐ°ĐŒĐž Đž ŃĐżĐŸŃĐŸĐ±Đ”Đœ ĐŽĐ”ŃĐ”ĐșŃĐžŃĐŸĐČĐ°ŃŃ ĐŒĐ”Ńалл ĐżŃĐž ĐŒĐ°Đ»Đ”ĐčŃĐ”ĐŒ ĐžĐ·ĐŒĐ”ĐœĐ”ĐœĐžĐž ĐČŃŃ
ĐŸĐŽĐœĐŸĐłĐŸ ŃĐžĐłĐœĐ°Đ»Đ° пДŃĐČĐžŃĐœĐŸĐłĐŸ ĐżŃĐ”ĐŸĐ±ŃĐ°Đ·ĐŸĐČĐ°ŃДлŃ. Đ Đ°Đ·ŃĐ°Đ±ĐŸŃĐ°ĐœĐ° ŃŃŃŃĐșŃŃŃĐœĐ°Ń ŃŃ
Đ”ĐŒĐ° ĐŽĐ»Ń ĐżŃĐ”ĐŽĐ»Đ°ĐłĐ°Đ”ĐŒĐŸĐłĐŸ ĐŒĐ”ŃĐ°Đ»Đ»ĐŸĐžŃĐșĐ°ŃĐ”Đ»Ń Đž ĐżŃĐžĐČĐ”ĐŽĐ”ĐœĐŸ ĐŸĐżĐžŃĐ°ĐœĐžĐ” ĐżŃĐžĐœŃОпа ŃĐ°Đ±ĐŸŃŃ
The regularity of the Stokes operator and the FujitaâKato approach to the NavierâStokes initial value problem in Lipschitz domains
AbstractWe study the regularity of the NavierâStokes equations in arbitrary Lipschitz domains
Apheresis therapies for NMOSD attacks A retrospective study of 207 therapeutic interventions
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
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
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
- âŠ