98 research outputs found

    Actuariële bedenkingen bij een eenvormig opgelegd bonus-malus stelsel.

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    Verscheidene actoren van het verzekeringswezen dringen sterk aan om het verplicht eenvormig bonus-malus stelsel in de verzekering B.A.-auto te behouden. In deze nota wordt aan de hand van een theoretisch voorbeeld aangetoond dat dit standpunt vanuit actuariëel oogpunt onhoudbaar is.

    Effect of Impurities on Pentacene Thin Film Growth for Field-Effect Transistors

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    Pentacenequinone (PnQ) impurities have been introduced into a pentacene source material at number densities from 0.001 to 0.474 to quantify the relative effects of impurity content and grain boundary structure on transport in pentacene thin-film transistors. Atomic force microscopy (AFM) and electrical measurements of top-contact pentacene thin-film transistors have been employed to directly correlate initial structure and final film structures, with the device mobility as a function of added impurity content. The results reveal a factor four decrease in mobility without significant changes in film morphology for source PnQ number fractions below ~0.008. For these low concentrations, the impurity thus directly influences transport, either as homogeneously distributed defects or by concentration at the otherwise-unchanged grain boundaries. For larger impurity concentrations, the continuing strong decrease in mobility is correlated with decreasing grain size, indicating an impurity-induced increase in the nucleation of grains during early stages of film growth.Comment: 18 pages, 4 Figures, 1 Tabl

    Myocardial infarction in a neonate with left-sided congenital diaphragmatic hernia.

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    Contains fulltext : 79830.pdf (publisher's version ) (Closed access)We present a case study of a newborn girl with a left-sided congenital diaphragmatic hernia and a myocardial infarction (MI). The occurrence of MI in newborns has been associated with cardiac malformations and abnormalities of the coronary arteries or thromboembolization. In our patient, echocardiography revealed left ventricular dysfunction, persistent pulmonary hypertension and an inferolateral MI. Within 24 hours cardiac function and oxygenation did not improve and the baby died. Autopsy showed massive MI, a small aortic valve and ascending aorta, and hypoplasia of the distal aortic arch and isthmus. An accessory spleen was also present. The present report underlines the importance of cardiac evaluation in patients with congenital diaphragmatic hernia

    Actuariële bedenkingen bij een eenvormig opgelegd bonus-malus stelsel

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    Verscheidene actoren van het verzekeringswezen dringen sterk aan om het verplicht eenvormig bonus-malus stelsel in de verzekering B.A.-auto te behouden. In deze nota wordt aan de hand van een theoretisch voorbeeld aangetoond dat dit standpunt vanuit actuariëel oogpunt onhoudbaar is.status: publishe

    Management of haemophilia in three premature infants.

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    Contains fulltext : 69134.pdf (publisher's version ) (Closed access

    Inherited multicentric osteolysis with carpal-tarsal localisation mimicking juvenile idiopathic arthritis.

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    Contains fulltext : 58064.pdf (publisher's version ) (Closed access)Five patients with multicentric carpal-tarsal osteolysis are presented: a mother and her three children with an autosomal dominant mode of inheritance and one of the children with nephropathy, the fifth a sporadic case also with renal involvement. The main findings common to these five patients are symptoms and signs simulating arthritis of the wrists and/or ankles starting at a young age and mimicking juvenile idiopathic arthritis. Early signs of osteolysis and shortening of the carpus or tarsus are radiological characteristic. The disease may be associated with a peculiar face, but most importantly with nephropathy. The pathogenesis is still unknown. Conclusion: Recognition of this disease and differentiation from juvenile idiopathic arthritis is important to avoid unnecessary investigations and treatment. Follow-up of renal function is indicated

    Posttransplantation cytomegalovirus-induced recurrence of atypical hemolytic uremic syndrome associated with a factor H mutation: successful treatment with intensive plasma exchanges and ganciclovir.

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    Item does not contain fulltextAtypical hemolytic uremic syndrome (HUS) can recur after renal transplantation and often leads to graft loss. In some series of familial HUS, the risk of early graft loss due to recurrence of HUS approaches 100% despite any therapy. This led some authors to claim that kidney transplantation is contraindicated in those patients. The authors describe an 8-year-old girl with end-stage renal failure owing to familial atypical HUS with a factor H mutation who underwent successful transplantation using continuous prophylactic plasma exchange (PE). Twenty-four months after transplantation, plasma creatinine level is 1.2 mg/dL (106 micromol/L) despite 2 recurrences of HUS contemporaneous to 2 cytomegalovirus infections, which resolved with PE intensification and ganciclovir. This strongly suggests that cytomegalovirus infection may trigger posttransplant recurrent HUS. The feasibility of kidney transplantation in case of atypical HUS related to factor H mutation using continuous prophylactic PE intensified during relapses should be confirmed in prospective studies
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