385 research outputs found

    Sarcoma de la lengua

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    La vacunaterapia en la blenorragia

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    Kaposi's sarcoma in a patient with erythroblastopenia and thymoma: Reactivation after topical corticosteroids

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    We report a 69-year-old female with erythroblastopenia and thymoma who developed lesions of Kaposi's sarcoma (KS) after thymectomy, 2 months after the initiation of therapy with methylprednisolone. Control of mucocutaneous KS lesions was obtained with radiotherapy, interferon alfa-2b and withdrawal of systemic immunosuppressive therapy. Erosive oral lichen planus appeared later, and after therapy with topical corticosteroids a new lesion of KS developed that regressed after withdrawal of topical corticosteroids. The detection of HHV-8 only in lesional skin supports the hypothesis that this virus can trigger the development of KS lesions

    Probing IMF using nanodust measurements from inside Saturn's magnetosphere

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    We present a new concept of monitoring the interplanetary magnetic field (IMF) by using in situ measurements of nanodust stream particles in Saturn's magnetosphere. We show that the nanodust detection pattern obtained inside the magnetosphere resembles those observed in interplanetary space and is associated with the solar wind compression regions. Our dust dynamics model reproduces the observed nanodust dynamical properties as well as the detection pattern, suggesting that the ejected stream particles can reenter Saturn's magnetosphere at certain occasions due to the dynamical influence from the time‐varying IMF. This method provides information on the IMF direction and a rough estimation on the solar wind compression arrival time at Saturn. Such information can be useful for studies related to the solar wind‐magnetosphere interactions, especially when the solar wind parameters are not directly available. Key Points A new method to probe IMF with nanodust measurements inside the magnetosphere Under changing IMF, ejected nanoparticles can re‐enter Saturn‐s magnetosphere IMF direction and solar wind compression arrival time can be derivedPeer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/99078/1/grl50604.pd

    Infants’ behavioral and physiological profile and mother–infant interaction

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    This study aims to (a) identify and profile groups of infants according to their behavioral and physiological characteristics, considering their neurobehavioral organization, social withdrawal behavior, and endocrine reactivity to stress, and to (b) analyze group differences in the quality of mother–infant interaction. Ninety seven 8-week-old infants were examined using the Neonatal Behavioral Assessment Scale and the Alarm Distress Baby Scale. Cortisol levels were measured both before and after routine inoculation between 8 and 12 weeks. At 12 to 16 weeks mother–infant interaction was assessed using the Global Rating Scales of Mother–Infant Interaction. Three groups of infants were identified: (a) ‘‘withdrawn’’; (b) ‘‘extroverted’’; (c) ‘‘underaroused.’’ Differences between them were found regarding both infant and mother behaviors in the interaction and the overall quality of mother–infant interaction. The identification of behavioral and physiological profiles in infants is an important step in the study of developmental pathways

    (2S)-2-[(2S*,5R*,6R*)-5,6-Dimeth­oxy-5,6-dimethyl-1,4-dioxan-2-yl]-1-[(S)-1,1-dimethyl­ethylsulfon­yl]aziridine

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    The reaction of a sulfur ylide with a chiral non-racemic sulfinyl imine afforded the desired aziridine in excellent yield and subsequent oxidation of the sulfinyl moiety dissolved in anhydrous dichloro­methane using a 75% aqueous solution of 3-chloro­per­oxy­benzoic acid afforded the title compound, C14H27NO6S. The configuration of the newly formed stereogenic center at the point of attachment of the 1,4-dioxane ring to the aziridine ring is S. The configurations of the pre-existing sites 2-, 5-, and 6-positions of the 1,4-dioxane ring prior to reaction of sulfinyl imine with the sulfur ylide are S, R, and R, respectively. The C—N bond lengths of the aziridine are 1.478 (2) and 1.486 (2) Å
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