A simple method for variance shift detection at unknown time points

Financial literature considers volatility as a good proxy for the risk level and thus the crucial parameter in many financial techniques and strategies. As such, the aim of this paper is to analyse the evolution of time series volatility and detect significant long-term variance changes. Building up on the variance ratio detection technique introduced by Tsay (1988), our paper extends it in two ways: first, we propose the computation of a moving variance ratio implemented on a selected part of the series, thus reducing the amount of calculus and increasing the reliability and second, as in reality permanent variance changes are almost inexistent, we proceed to an adjustment on a specified part of the series only after the detected variance change. Our moving variance ratio technique proves its efficiency in detecting variance changes and removing them from the series, both on simulated and real financial data. More specifically, two significant variance changes are detected within the series of the Hang Seng daily log-returns between 1994 and 2007: the first one on August 15, 1997 and can be linked to the Asian financial crisis, and the second one on July 27, 2001 corresponding to the beginning of a high volatility regime in emerging markets following the Internet bubble crash along with the first signs of the financial crisis in Argentina.Moving Variance Ratio, Variance Changes, Series Adjustment

Two Cases of Orbital Myositis as a Rare Feature of Lyme Borreliosis

Myositis has been reported as a rare manifestation of Lyme disease, and the Lyme disease spirochetes can be an important consideration in the differential diagnosis of unusual cases of myositis, especially in patients who live in or travel to endemic areas. We report the case of two patients who presented with focal orbital myositis which are rare localization for Lyme disease. Myositis were confirmed by magnetic resonance imaging. Diagnosis criteria for Borrelia burgdorferi (B. burgdorferi) infection was supported by (i) medical history (tick bite in an endemic area), (ii) systemic clinical findings (Erythema migrans, neurological manifestation or arthritis), (iii) positive Lyme serology and/or the detection of B. burgdorferi DNA by polymerase chain reaction, as well as (iv) exclusion of other infectious and inflammatory causes. The current cases are reviewed in the context of findings from previous myositis descriptions

Atrophie cérébrale diffuse au cours d’un syndrome de Goldenhar : à propos d’un cas

Les auteurs rapportent un cas d'un syndrome de Goldenhar non décris dans la littérature chez un nourrisson de 3 mois, de sexe féminin présentant une atrophie cérébrale diffuse. Cette observation permet de décrire cette malformation rare et d'attirer l'attention de l'opinion scientifique à mettre en marche des études poussées afin de comprendre la survenue de cette pathologie.Key words: Syndrome de Goldenhar, atrophie cérébrale diffuse, nourrisso

Etude du strabisme chez des enfants de 0 à 15 ans suivis a Lubumbashi, République Démocratique du Congo: analyse des aspects épidémiologiques et cliniques

Introduction: Le strabisme est défini comme un syndrome à double composante : motrice et  sensorielle. Le but de ce travail est de décrire les aspects épidémiologiques et cliniques du strabisme chez l'enfant congolais de 0 à 15 ans dans la ville de Lubumbashi.Méthodes: Il s'agit d'une étude descriptive longitudinale sur les aspects épidémiologiques et cliniques du strabisme chez l'enfant congolais de 0 à 15 ans dans la ville de Lubumbashi entre Décembre 2012 à  Décembre 2013. Nous avons recueilli l'âge des patients, leur sexe, leur provenance, le type de strabisme, la réfraction, le fond d'oeil, les antécédents (hérédité) ainsi que le type de la déviation strabique observé sur 70 patients.Résultats: Nous avons observé 70 cas de strabisme manifeste dont 31 cas (44,28%) étaient dans la  tranche d'âge comprise entre 0 et 5 ans. L'âge moyen de nos patients était de 6,7 ans avec une  prédominance du sexe féminin, soit 51,42%. Le strabisme était convergent dans 65,71%, divergent dans 30%, et vertical dans 4,28%. Les ésotropies représentaient 65 cas (92,85%), quatre cas (5,71%)  avaient un antécédent familial de strabisme au premier degré de parenté, 21 cas (30%) au second degré de parenté, 45 cas (64,28%) n'avaient pas cet antécédent. L'oeil gauche était le plus dominé dans 30% des cas. Les facteurs favorisant le strabisme étaient inconnus dans 54 cas (77,14%). Le strabisme était secondaire à l'hypermétropie chez 32 patients (42,71%).Conclusion: La fréquence du strabisme dans la ville de Lubumbashi chez les enfants âgés de 0 à 15 ans  est de 0,50%. Comme dans la plupart des études sur le strabisme de l'enfant, c'est l'ésotropie qui est la  déviation la plus commune.Key words: Enfant congolais, strabisme, hypermétropie, ésotropi

Cytokine Profiles in Toxoplasmic and Viral Uveitis

BackgroundUveitis is a major cause of visual impairment throughout the world. Analysis of cytokine profiles in aqueous humor specimens may provide insight into the physiopathological processes that underly retinal damage in this context MethodsUsing a multiplex assay, we determined the concentrations of 17 cytokines and chemokines in aqueous humor specimens obtained from patients with ocular toxoplasmosis or viral uveitis and compared these concentrations with those in specimens obtained from patients with noninfectious intermediate uveitis or cataract ResultsFive mediators (interleukin [IL]-8, monocyte chemoattractant protein-1, tumor necrosis factor-α, IL-4, and IL-10) were detected in >50% of patients in all groups. In contrast, IL-5 and IL-12 were specific for ocular toxoplasmosis, and granulocyte monocyte colony-stimulating factor and IL-1 were specific for viral uveitis; these mediators could present specific markers for diagnostic purposes. Interferon-γ, IL-6, and macrophage inflammatory protein-1β were common markers of ocular toxoplasmosis and viral uveitis. IL-17 was a common marker of ocular toxoplasmosis and intermediate uveitis ConclusionsWe found specific cytokine profiles for each type of uveitis, with large interindividual variations and no etiological or clinical correlations. Ocular cytokine mapping contributes to a better understanding of the physiopathology of specific forms of uveitis and provides guidance for new targeted treatmen

Effect of ranitidine on acetaminophen-induced hepatotoxicity in dogs

The effect of ranitidine administration upon the hepatotoxic effect produced by a multidose acetaminophen administration regimen was examined. Seventy-two dogs received three subcutaneous injections of acetaminophen (750, 200, 200 mg/kg body wt) in DMSO (600 mg/ml) at time zero, 9 hr later, and 24 hr after the first dose. Ten control animals (group I) were not given ranitidine, the remaining 62 dogs received an intramus-cular injection of ranitidine 30 min before each acetaminophen dose. Three different doses of ranitidine were used (mg/kg body wt): 50 mg, group II (33 dogs); 75 mg, group III (14 dogs); 120 mg, group IV (15 dogs). Ranitidine reduced the expected acetaminophen-induced hepatoxicity in a dose-response manner. Moreover, a significant correlation was found between the ranitidine dose and the survival rate, as evidenced by transaminase levels in the serum and histology of the liver. This model of fulminant hepatic failure induced by acetaminophen and its modulation with ranitidine provides clinical investigators with a research tool that will be useful in the future investigation of putative medical and surgical therapies being investigated for use in the clinical management of fulminant hepatic failure. Because of the size of the animal used in this model, frequent and serial analyses of blood and liver were available for study to determine the effect of therapy within a given animal as opposed to within groups of animals. © 1990 Plenum Publishing Corporation

Proteasome subunit variants cause neurosensory syndrome combining deafness and cataract due to proteotoxic stress

The ubiquitin–proteasome system degrades ubiquitin‐modified proteins to maintain protein homeostasis and to control signalling. Whole‐genome sequencing of patients with severe deafness and early‐onset cataracts as part of a neurological, sensorial and cutaneous novel syndrome identified a unique deep intronic homozygous variant in the PSMC3 gene, encoding the proteasome ATPase subunit Rpt5, which lead to the transcription of a cryptic exon. The proteasome content and activity in patient\u27s fibroblasts was however unaffected. Nevertheless, patient\u27s cells exhibited impaired protein homeostasis characterized by accumulation of ubiquitinated proteins suggesting severe proteotoxic stress. Indeed, the TCF11/Nrf1 transcriptional pathway allowing proteasome recovery after proteasome inhibition is permanently activated in the patient\u27s fibroblasts. Upon chemical proteasome inhibition, this pathway was however impaired in patient\u27s cells, which were unable to compensate for proteotoxic stress although a higher proteasome content and activity. Zebrafish modelling for knockout in PSMC3 remarkably reproduced the human phenotype with inner ear development anomalies as well as cataracts, suggesting that Rpt5 plays a major role in inner ear, lens and central nervous system development

Dynamic competition between contour integration and contour segmentation probed with moving stimuli

AbstractLine-ends, corners and junctions are important singularities for form analysis, object recognition, depth ordering or motion processing. In this study, we investigate the extent to which processing the motion of line ends depends on the spatial configuration of their immediate surround. To that aim, we used two vertical collinear line segments, translating clockwise or anti-clockwise along a circular path, together with a direction discrimination task. Direction discrimination was measured independently for outer line-ends––at both segments extremities––and inner line-ends––in between collinear segments––using line segments partially occluded by invisible masks such that the direction of either inner or outer line-ends’ motion was restricted to a sinusoidal translation along a horizontal axis, and thus irrelevant for the motion task. Under these conditions, access to the direction of inner line-ends is longer and more difficult than it is for outer line-ends. Subsequent experiments show that these effects depend on the degree of collinearity between line segments. Similar experiments were performed after volunteers took a dose of Lorazepam, a benzodiazepine that facilitates the fixation of GABA on GABAa receptors. The results show that the differences between the processing of inner and outer line-ends is reduced, suggesting that the effect of the surround is modulated by inhibitory mechanisms. Using a simple model, we propose that this effect can be explained by a competition between a segmentation process based on surround suppression and contour integration through long-range horizontal connections, at or prior to motion processing stages